TARDBP - TAR DNA binding protein Gene

Also Known as ALS10; TDP-43

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 23435

About TARDBP

Cytogenetic location: 1p36.22 Genomic coordinates (GRCh38): 1:11,012,654-11,030,528 (from NCBI)

This gene has 38 transcripts (splice variants), 291 orthologues, 24 paralogues and is associated with 3 phenotypes. Ubiquitous expression in lymph node (RPKM 32.8), appendix (RPKM 30.2) and 25 other tissues.

Summary

HIV-1, the causative agent of acquired immunodeficiency syndrome (AIDS), contains an RNA genome that produces a chromosomally integrated DNA during the replicative cycle. Activation of HIV-1 gene expression by the transactivator Tat is dependent on an RNA regulatory element (TAR) located downstream of the transcription initiation site. The protein encoded by this gene is a transcriptional repressor that binds to chromosomally integrated TAR DNA and represses HIV-1 transcription. In addition, this protein regulates alternate splicing of the CFTR gene. A similar pseudogene is present on chromosome 20. [provided by RefSeq, Jul 2008]

TARDBP Products (1)

mRNA Protein Name
NM_007375.4 NP_031401.1 TAR DNA-binding protein 43
Molecular Function GO Annotation Evidence Referencias Source
enables DNA binding EXP
EXP: Inferred from Experiment
26735904 GOA
enables RNA binding IDA
IDA: Inferred from direct assay
11285240 GOA
enables RNA binding IMP
IMP: Inferred from mutant phenotype
25678563 GOA
enables double-stranded DNA binding IDA
IDA: Inferred from direct assay
7745706 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
19383787 GOA
enables lipid binding EXP
EXP: Inferred from Experiment
26735904 GOA
enables mRNA 3'-UTR binding IDA
IDA: Inferred from direct assay
17481916 GOA
enables molecular condensate scaffold activity IDA
IDA: Inferred from direct assay
27545621 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
15231747 GOA
Biological Process GO Annotation Evidence Referencias Source
involved in 3'-UTR-mediated mRNA destabilization IDA
IDA: Inferred from direct assay
28335005 GOA
involved in 3'-UTR-mediated mRNA stabilization IDA
IDA: Inferred from direct assay
17481916 GOA
involved in RNA splicing IDA
IDA: Inferred from direct assay
11285240 GOA
involved in amyloid fibril formation IDA
IDA: Inferred from direct assay
26735904 GOA
involved in negative regulation by host of viral transcription IDA
IDA: Inferred from direct assay
7745706 GOA
involved in negative regulation of gene expression IMP
IMP: Inferred from mutant phenotype
18305152 GOA
involved in negative regulation of protein phosphorylation IMP
IMP: Inferred from mutant phenotype
18305152 GOA
involved in nuclear inner membrane organization IMP
IMP: Inferred from mutant phenotype
18305152 GOA
involved in regulation of apoptotic process IMP
IMP: Inferred from mutant phenotype
18305152 GOA
involved in regulation of cell cycle IMP
IMP: Inferred from mutant phenotype
18305152 GOA
involved in regulation of protein stability IMP
IMP: Inferred from mutant phenotype
27123980 GOA
Cellular Component GO Annotation Evidence Referencias Source
is active in intracellular non-membrane-bounded organelle EXP
EXP: Inferred from Experiment
26735904 GOA
is active in intracellular non-membrane-bounded organelle IDA
IDA: Inferred from direct assay
26735904 GOA
located in nucleus IDA
IDA: Inferred from direct assay
11285240 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TARDBP Protein Structure

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (106 - 171)

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (193 - 241)

  • 0
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  • 200
  • 300
  • 414 a.a.
Protein Preferred Names Protein Names

TAR DNA-binding protein 43

  • TAR DNA-binding protein-43

TARDBP Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Referencias
Intra
TARDBP Q13148 HNRNPUL1 Homo sapiens Q9BUJ2 32814053
Intra
TARDBP Q13148 HNRNPUL1 Homo sapiens Q9BUJ2 32814053
Intra
TARDBP Q13148 HNRNPUL1 Homo sapiens Q9BUJ2 32814053
Intra
TARDBP Q13148 ESRP1 Homo sapiens Q6NXG1 32814053
Intra
TARDBP Q13148 ESRP1 Homo sapiens Q6NXG1 32814053
Intra
TARDBP Q13148 ESRP1 Homo sapiens Q6NXG1 32814053
Intra
TARDBP Q13148 BEX5 Homo sapiens Q5H9J7 32814053
Intra
TARDBP Q13148 BEX5 Homo sapiens Q5H9J7 32814053
Intra
TARDBP Q13148 BEX5 Homo sapiens Q5H9J7 32814053
Intra
TARDBP Q13148 IGF2BP2 Homo sapiens Q9Y6M1 32814053
Intra
TARDBP Q13148 IGF2BP2 Homo sapiens Q9Y6M1 32814053
Intra
TARDBP Q13148 IGF2BP2 Homo sapiens Q9Y6M1 32814053
Intra
TARDBP Q13148 TRIM74 Homo sapiens Q86UV6-2 32814053
Intra
TARDBP Q13148 TRIM74 Homo sapiens Q86UV6-2 32814053
Intra
TARDBP Q13148 TRIM74 Homo sapiens Q86UV6-2 32814053
Intra
TARDBP Q13148 VPS37A Homo sapiens Q8NEZ2-2 32814053
Intra
TARDBP Q13148 VPS37A Homo sapiens Q8NEZ2-2 32814053
Intra
TARDBP Q13148 VPS37A Homo sapiens Q8NEZ2-2 32814053
Intra
TARDBP Q13148 JADE3 Homo sapiens Q92613 32814053
Intra
TARDBP Q13148 JADE3 Homo sapiens Q92613 32814053
Intra
TARDBP Q13148 JADE3 Homo sapiens Q92613 32814053
Intra
TARDBP Q13148 HNRPUL1 Homo sapiens Q9BTB7 32814053
Intra
TARDBP Q13148 HNRPUL1 Homo sapiens Q9BTB7 32814053
Intra
TARDBP Q13148 HNRPUL1 Homo sapiens Q9BTB7 32814053
Intra
TARDBP Q13148 PBX4 Homo sapiens Q9BYU1 32814053
Intra
TARDBP Q13148 PBX4 Homo sapiens Q9BYU1 32814053
Intra
TARDBP Q13148 PBX4 Homo sapiens Q9BYU1 32814053
Intra
TARDBP Q13148 q9h669_human Homo sapiens Q9H669 32814053
Intra
TARDBP Q13148 q9h669_human Homo sapiens Q9H669 32814053
Intra
TARDBP Q13148 q9h669_human Homo sapiens Q9H669 32814053
Intra
TARDBP Q13148 KRTAP9-2 Homo sapiens Q9BYQ4 32814053
Intra
TARDBP Q13148 KRTAP9-2 Homo sapiens Q9BYQ4 32814053
Intra
TARDBP Q13148 KRTAP9-2 Homo sapiens Q9BYQ4 32814053
Intra
TARDBP Q13148 UBE2V1 Homo sapiens Q13404 32814053
Intra
TARDBP Q13148 UBE2V1 Homo sapiens Q13404 32814053
Intra
TARDBP Q13148 UBE2V1 Homo sapiens Q13404 32814053
Intra
TARDBP Q13148 CLPP Homo sapiens Q16740 32814053
Intra
TARDBP Q13148 CLPP Homo sapiens Q16740 32814053
Intra
TARDBP Q13148 CLPP Homo sapiens Q16740 32814053
Intra
TARDBP Q13148 OTUB1 Homo sapiens Q96FW1 32814053
Intra
TARDBP Q13148 OTUB1 Homo sapiens Q96FW1 32814053
Intra
TARDBP Q13148 OTUB1 Homo sapiens Q96FW1 32814053
Intra
TARDBP Q13148 NUP43 Homo sapiens Q8NFH3 32814053
Intra
TARDBP Q13148 NUP43 Homo sapiens Q8NFH3 32814053
Intra
TARDBP Q13148 NUP43 Homo sapiens Q8NFH3 32814053
Intra
TARDBP Q13148 MAGEC3 Homo sapiens Q8TD91-2 32814053
Intra
TARDBP Q13148 MAGEC3 Homo sapiens Q8TD91-2 32814053
Intra
TARDBP Q13148 MAGEC3 Homo sapiens Q8TD91-2 32814053
Intra
TARDBP Q13148 C6orf141 Homo sapiens Q5SZD1 32814053
Intra
TARDBP Q13148 C6orf141 Homo sapiens Q5SZD1 32814053
Intra
TARDBP Q13148 C6orf141 Homo sapiens Q5SZD1 32814053
Intra
TARDBP Q13148 MTF2 Homo sapiens Q9Y483-4 32814053
Intra
TARDBP Q13148 MTF2 Homo sapiens Q9Y483-4 32814053
Intra
TARDBP Q13148 MTF2 Homo sapiens Q9Y483-4 32814053
Intra
TARDBP Q13148 KLHL36 Homo sapiens Q8N4N3-2 32814053
Intra
TARDBP Q13148 KLHL36 Homo sapiens Q8N4N3-2 32814053
Intra
TARDBP Q13148 KLHL36 Homo sapiens Q8N4N3-2 32814053
Intra
TARDBP Q13148 HNRNPUL1 Homo sapiens Q9BUJ2-2 32814053
Intra
TARDBP Q13148 HNRNPUL1 Homo sapiens Q9BUJ2-2 32814053
Intra
TARDBP Q13148 HNRNPUL1 Homo sapiens Q9BUJ2-2 32814053
Intra
TARDBP Q13148 PATZ1 Homo sapiens Q9HBE1-4 32814053
Intra
TARDBP Q13148 PATZ1 Homo sapiens Q9HBE1-4 32814053
Intra
TARDBP Q13148 PATZ1 Homo sapiens Q9HBE1-4 32814053
Intra
TARDBP Q13148 LDHAL6B Homo sapiens Q9BYZ2 32814053
Intra
TARDBP Q13148 LDHAL6B Homo sapiens Q9BYZ2 32814053
Intra
TARDBP Q13148 LDHAL6B Homo sapiens Q9BYZ2 32814053
Intra
TARDBP Q13148 SIAH1 Homo sapiens Q8IUQ4-2 32814053
Intra
TARDBP Q13148 SIAH1 Homo sapiens Q8IUQ4-2 32814053
Intra
TARDBP Q13148 SIAH1 Homo sapiens Q8IUQ4-2 32814053
Intra
TARDBP Q13148 TRIM69 Homo sapiens Q86WT6-2 32814053
Intra
TARDBP Q13148 TRIM69 Homo sapiens Q86WT6-2 32814053
Intra
TARDBP Q13148 TRIM69 Homo sapiens Q86WT6-2 32814053
Intra
TARDBP Q13148 CEP70 Homo sapiens Q8NHQ1-3 32814053
Intra
TARDBP Q13148 CEP70 Homo sapiens Q8NHQ1-3 32814053
Intra
TARDBP Q13148 CEP70 Homo sapiens Q8NHQ1-3 32814053
Intra
TARDBP Q13148 DNAJA3 Homo sapiens Q96EY1-3 32814053
Intra
TARDBP Q13148 DNAJA3 Homo sapiens Q96EY1-3 32814053
Intra
TARDBP Q13148 DNAJA3 Homo sapiens Q96EY1-3 32814053
Intra
TARDBP Q13148 CFAP100 Homo sapiens Q494V2-2 32814053
Intra
TARDBP Q13148 CFAP100 Homo sapiens Q494V2-2 32814053
Intra
TARDBP Q13148 CFAP100 Homo sapiens Q494V2-2 32814053
Intra
TARDBP Q13148 SPAG8 Homo sapiens Q99932-2 32814053
Intra
TARDBP Q13148 SPAG8 Homo sapiens Q99932-2 32814053
Intra
TARDBP Q13148 SPAG8 Homo sapiens Q99932-2 32814053
Intra
TARDBP Q13148 CBX2 Homo sapiens Q14781-2 32814053
Intra
TARDBP Q13148 CBX2 Homo sapiens Q14781-2 32814053
Intra
TARDBP Q13148 CBX2 Homo sapiens Q14781-2 32814053
Intra
TARDBP Q13148 L3MBTL3 Homo sapiens Q96JM7-2 32814053
Intra
TARDBP Q13148 L3MBTL3 Homo sapiens Q96JM7-2 32814053
Intra
TARDBP Q13148 L3MBTL3 Homo sapiens Q96JM7-2 32814053
Intra
TARDBP Q13148 TRIM45 Homo sapiens Q9H8W5-2 32814053
Intra
TARDBP Q13148 TRIM45 Homo sapiens Q9H8W5-2 32814053
Intra
TARDBP Q13148 TRIM45 Homo sapiens Q9H8W5-2 32814053
Intra
TARDBP Q13148 ZSCAN1 Homo sapiens Q8NBB4-2 32814053
Intra
TARDBP Q13148 ZSCAN1 Homo sapiens Q8NBB4-2 32814053
Intra
TARDBP Q13148 ZSCAN1 Homo sapiens Q8NBB4-2 32814053
Intra
TARDBP Q13148 RBM46 Homo sapiens Q8TBY0 32814053
Intra
TARDBP Q13148 RBM46 Homo sapiens Q8TBY0 32814053
Intra
TARDBP Q13148 RBM46 Homo sapiens Q8TBY0 32814053
Intra
TARDBP Q13148 CHD2 Homo sapiens O14647 29153328
Intra
TARDBP Q13148 UBQLNL Homo sapiens Q8IYU4 32814053
Intra
TARDBP Q13148 UBQLNL Homo sapiens Q8IYU4 32814053
Intra
TARDBP Q13148 UBQLNL Homo sapiens Q8IYU4 32814053
Intra
TARDBP Q13148 KCTD15 Homo sapiens Q96SI1-2 32814053
Intra
TARDBP Q13148 KCTD15 Homo sapiens Q96SI1-2 32814053
Intra
TARDBP Q13148 KCTD15 Homo sapiens Q96SI1-2 32814053
Intra
TARDBP Q13148 ASB3 Homo sapiens Q9Y575-3 32814053
Intra
TARDBP Q13148 ASB3 Homo sapiens Q9Y575-3 32814053
Intra
TARDBP Q13148 ASB3 Homo sapiens Q9Y575-3 32814053
Intra
TARDBP Q13148 PARP11 Homo sapiens Q9NR21-5 32814053
Intra
TARDBP Q13148 PARP11 Homo sapiens Q9NR21-5 32814053
Intra
TARDBP Q13148 PARP11 Homo sapiens Q9NR21-5 32814053
Intra
TARDBP Q13148 THAP3 Homo sapiens Q8WTV1 32814053
Intra
TARDBP Q13148 THAP3 Homo sapiens Q8WTV1 32814053
Intra
TARDBP Q13148 THAP3 Homo sapiens Q8WTV1 32814053
Intra
TARDBP Q13148 KLHL22 Homo sapiens Q53GT1 32814053
Intra
TARDBP Q13148 KLHL22 Homo sapiens Q53GT1 32814053
Intra
TARDBP Q13148 KLHL22 Homo sapiens Q53GT1 32814053
Intra
TARDBP Q13148 RNF14 Homo sapiens Q9UBS8 32814053
Intra
TARDBP Q13148 RNF14 Homo sapiens Q9UBS8 32814053
Intra
TARDBP Q13148 RNF14 Homo sapiens Q9UBS8 32814053
Intra
TARDBP Q13148 RNF166 Homo sapiens Q96A37 32814053
Intra
TARDBP Q13148 RNF166 Homo sapiens Q96A37 32814053
Intra
TARDBP Q13148 RNF166 Homo sapiens Q96A37 32814053
Intra
TARDBP Q13148 KLHL17 Homo sapiens Q6TDP4 32814053
Intra
TARDBP Q13148 KLHL17 Homo sapiens Q6TDP4 32814053
Intra
TARDBP Q13148 KLHL17 Homo sapiens Q6TDP4 32814053
Intra
TARDBP Q13148 CELF1 Homo sapiens Q92879-3 32814053
Intra
TARDBP Q13148 CELF1 Homo sapiens Q92879-3 32814053
Intra
TARDBP Q13148 CELF1 Homo sapiens Q92879-3 32814053
Intra
TARDBP Q13148 SLC44A5 Homo sapiens Q8NCS7 32814053
Intra
TARDBP Q13148 SLC44A5 Homo sapiens Q8NCS7 32814053
Intra
TARDBP Q13148 SLC44A5 Homo sapiens Q8NCS7 32814053
Intra
TARDBP Q13148 DPP9 Homo sapiens Q86TI2-2 32814053
Intra
TARDBP Q13148 DPP9 Homo sapiens Q86TI2-2 32814053
Intra
TARDBP Q13148 DPP9 Homo sapiens Q86TI2-2 32814053
Intra
TARDBP Q13148 SYMPK Homo sapiens Q92797-2 32814053
Intra
TARDBP Q13148 SYMPK Homo sapiens Q92797-2 32814053
Intra
TARDBP Q13148 SYMPK Homo sapiens Q92797-2 32814053
Intra
TARDBP Q13148 IQSEC1 Homo sapiens Q6DN90-2 32814053
Intra
TARDBP Q13148 IQSEC1 Homo sapiens Q6DN90-2 32814053
Intra
TARDBP Q13148 IQSEC1 Homo sapiens Q6DN90-2 32814053
Intra
TARDBP Q13148 RAD18 Homo sapiens Q9NS91 32814053
Intra
TARDBP Q13148 RAD18 Homo sapiens Q9NS91 32814053
Intra
TARDBP Q13148 RAD18 Homo sapiens Q9NS91 32814053
Intra
TARDBP Q13148 TRIM8 Homo sapiens Q9BZR9 32814053
Intra
TARDBP Q13148 TRIM8 Homo sapiens Q9BZR9 32814053
Intra
TARDBP Q13148 TRIM8 Homo sapiens Q9BZR9 32814053
Intra
TARDBP Q13148 RBCK1 Homo sapiens Q9BYM8 32814053
Intra
TARDBP Q13148 RBCK1 Homo sapiens Q9BYM8 32814053
Intra
TARDBP Q13148 RBCK1 Homo sapiens Q9BYM8 32814053
Intra
TARDBP Q13148 LNX2 Homo sapiens Q8N448 32814053
Intra
TARDBP Q13148 LNX2 Homo sapiens Q8N448 32814053
Intra
TARDBP Q13148 LNX2 Homo sapiens Q8N448 32814053
Intra
TARDBP Q13148 MKRN2 Homo sapiens Q9H000 32814053
Intra
TARDBP Q13148 MKRN2 Homo sapiens Q9H000 32814053
Intra
TARDBP Q13148 MKRN2 Homo sapiens Q9H000 32814053
Intra
TARDBP Q13148 CBLC Homo sapiens Q9ULV8 32814053
Intra
TARDBP Q13148 CBLC Homo sapiens Q9ULV8 32814053
Intra
TARDBP Q13148 CBLC Homo sapiens Q9ULV8 32814053
Intra
TARDBP Q13148 DPF1 Homo sapiens Q92782-2 32814053
Intra
TARDBP Q13148 DPF1 Homo sapiens Q92782-2 32814053
Intra
TARDBP Q13148 DPF1 Homo sapiens Q92782-2 32814053
Intra
TARDBP Q13148 WDR12 Homo sapiens Q9GZL7 32814053
Intra
TARDBP Q13148 WDR12 Homo sapiens Q9GZL7 32814053
Intra
TARDBP Q13148 WDR12 Homo sapiens Q9GZL7 32814053
Intra
TARDBP Q13148 LONRF2 Homo sapiens Q1L5Z9 32814053
Intra
TARDBP Q13148 LONRF2 Homo sapiens Q1L5Z9 32814053
Intra
TARDBP Q13148 LONRF2 Homo sapiens Q1L5Z9 32814053
Intra
TARDBP Q13148 USP48 Homo sapiens Q86UV5 32814053
Intra
TARDBP Q13148 USP48 Homo sapiens Q86UV5 32814053
Intra
TARDBP Q13148 USP48 Homo sapiens Q86UV5 32814053
Intra
TARDBP Q13148 MPND Homo sapiens Q8N594 32814053
Intra
TARDBP Q13148 MPND Homo sapiens Q8N594 32814053
Intra
TARDBP Q13148 MPND Homo sapiens Q8N594 32814053
Intra
TARDBP Q13148 PACS1 Homo sapiens Q6VY07 32814053
Intra
TARDBP Q13148 PACS1 Homo sapiens Q6VY07 32814053
Intra
TARDBP Q13148 PACS1 Homo sapiens Q6VY07 32814053
Intra
TARDBP Q13148 RNF112 Homo sapiens Q9ULX5 32814053
Intra
TARDBP Q13148 RNF112 Homo sapiens Q9ULX5 32814053
Intra
TARDBP Q13148 RNF112 Homo sapiens Q9ULX5 32814053
Intra
TARDBP Q13148 OTUD7B Homo sapiens Q6GQQ9-2 32814053
Intra
TARDBP Q13148 OTUD7B Homo sapiens Q6GQQ9-2 32814053
Intra
TARDBP Q13148 OTUD7B Homo sapiens Q6GQQ9-2 32814053
Intra
TARDBP Q13148 MIER1 Homo sapiens Q8N108-16 32814053
Intra
TARDBP Q13148 MIER1 Homo sapiens Q8N108-16 32814053
Intra
TARDBP Q13148 MIER1 Homo sapiens Q8N108-16 32814053
Intra
TARDBP Q13148 PPP1R21 Homo sapiens Q6ZMI0-5 32814053
Intra
TARDBP Q13148 PPP1R21 Homo sapiens Q6ZMI0-5 32814053
Intra
TARDBP Q13148 PPP1R21 Homo sapiens Q6ZMI0-5 32814053
Intra
TARDBP Q13148 TERF2 Homo sapiens Q15554-4 32814053
Intra
TARDBP Q13148 TERF2 Homo sapiens Q15554-4 32814053
Intra
TARDBP Q13148 TERF2 Homo sapiens Q15554-4 32814053
Intra
TARDBP Q13148 ANKRD13D Homo sapiens Q6ZTN6-2 32814053
Intra
TARDBP Q13148 ANKRD13D Homo sapiens Q6ZTN6-2 32814053
Intra
TARDBP Q13148 ANKRD13D Homo sapiens Q6ZTN6-2 32814053
Intra
TARDBP Q13148 DCAF8 Homo sapiens Q5TAQ9-2 32814053
Intra
TARDBP Q13148 DCAF8 Homo sapiens Q5TAQ9-2 32814053
Intra
TARDBP Q13148 DCAF8 Homo sapiens Q5TAQ9-2 32814053
Intra
TARDBP Q13148 ASB9 Homo sapiens Q96DX5-3 32814053
Intra
TARDBP Q13148 ASB9 Homo sapiens Q96DX5-3 32814053
Intra
TARDBP Q13148 ASB9 Homo sapiens Q96DX5-3 32814053
Intra
TARDBP Q13148 DDI2 Homo sapiens Q5TDH0-2 32814053
Intra
TARDBP Q13148 DDI2 Homo sapiens Q5TDH0-2 32814053
Intra
TARDBP Q13148 DDI2 Homo sapiens Q5TDH0-2 32814053
Intra
TARDBP Q13148 KBTBD4 Homo sapiens Q9NVX7-2 32814053
Intra
TARDBP Q13148 KBTBD4 Homo sapiens Q9NVX7-2 32814053
Intra
TARDBP Q13148 KBTBD4 Homo sapiens Q9NVX7-2 32814053
Intra
TARDBP Q13148 CCIN Homo sapiens Q13939 32814053
Intra
TARDBP Q13148 CCIN Homo sapiens Q13939 32814053
Intra
TARDBP Q13148 CCIN Homo sapiens Q13939 32814053
Intra
TARDBP Q13148 PDZRN4 Homo sapiens Q6ZMN7-2 32814053
Intra
TARDBP Q13148 PDZRN4 Homo sapiens Q6ZMN7-2 32814053
Intra
TARDBP Q13148 PDZRN4 Homo sapiens Q6ZMN7-2 32814053
Intra
TARDBP Q13148 TNFRSF14 Homo sapiens Q92956-2 32814053
Intra
TARDBP Q13148 TNFRSF14 Homo sapiens Q92956-2 32814053
Intra
TARDBP Q13148 TNFRSF14 Homo sapiens Q92956-2 32814053
Intra
TARDBP Q13148 SPSB1 Homo sapiens Q96BD6 32814053
Intra
TARDBP Q13148 SPSB1 Homo sapiens Q96BD6 32814053
Intra
TARDBP Q13148 SPSB1 Homo sapiens Q96BD6 32814053
Intra
TARDBP Q13148 HES4 Homo sapiens Q9HCC6 32814053
Intra
TARDBP Q13148 HES4 Homo sapiens Q9HCC6 32814053
Intra
TARDBP Q13148 HES4 Homo sapiens Q9HCC6 32814053
Intra
TARDBP Q13148 FBXL5 Homo sapiens Q9UKA1 32814053
Intra
TARDBP Q13148 FBXL5 Homo sapiens Q9UKA1 32814053
Intra
TARDBP Q13148 FBXL5 Homo sapiens Q9UKA1 32814053
Intra
TARDBP Q13148 KLF15 Homo sapiens Q9UIH9 32814053
Intra
TARDBP Q13148 KLF15 Homo sapiens Q9UIH9 32814053
Intra
TARDBP Q13148 KLF15 Homo sapiens Q9UIH9 32814053
Intra
TARDBP Q13148 RMND5A Homo sapiens Q9H871 32814053
Intra
TARDBP Q13148 RMND5A Homo sapiens Q9H871 32814053
Intra
TARDBP Q13148 RMND5A Homo sapiens Q9H871 32814053
Intra
TARDBP Q13148 ZNF366 Homo sapiens Q8N895 32814053
Intra
TARDBP Q13148 ZNF366 Homo sapiens Q8N895 32814053
Intra
TARDBP Q13148 ZNF366 Homo sapiens Q8N895 32814053
Intra
TARDBP Q13148 ZNF366 Homo sapiens Q8N895 32814053
Intra
TARDBP Q13148 VPS37A Homo sapiens Q8NEZ2 32814053
Intra
TARDBP Q13148 VPS37A Homo sapiens Q8NEZ2 32814053
Intra
TARDBP Q13148 VPS37A Homo sapiens Q8NEZ2 32814053
Intra
TARDBP Q13148 CRLF3 Homo sapiens Q8IUI8 32814053
Intra
TARDBP Q13148 CRLF3 Homo sapiens Q8IUI8 32814053
Intra
TARDBP Q13148 CRLF3 Homo sapiens Q8IUI8 32814053
Intra
TARDBP Q13148 MAPK11 Homo sapiens Q15759 32814053
Intra
TARDBP Q13148 MAPK11 Homo sapiens Q15759 32814053
Intra
TARDBP Q13148 MAPK11 Homo sapiens Q15759 32814053
Intra
TARDBP Q13148 HDAC6 Homo sapiens Q9UBN7 32814053
Intra
TARDBP Q13148 HDAC6 Homo sapiens Q9UBN7 32814053
Intra
TARDBP Q13148 HDAC6 Homo sapiens Q9UBN7 32814053
Intra
TARDBP Q13148 SF3B3 Homo sapiens Q15393 32814053
Intra
TARDBP Q13148 SF3B3 Homo sapiens Q15393 32814053
Intra
TARDBP Q13148 SF3B3 Homo sapiens Q15393 32814053
Intra
TARDBP Q13148 GPSM3 Homo sapiens Q9Y4H4 32814053
Intra
TARDBP Q13148 GPSM3 Homo sapiens Q9Y4H4 32814053
Intra
TARDBP Q13148 GPSM3 Homo sapiens Q9Y4H4 32814053
Intra
TARDBP Q13148 PSMD2 Homo sapiens Q13200 32814053
Intra
TARDBP Q13148 PSMD2 Homo sapiens Q13200 32814053
Intra
TARDBP Q13148 PSMD2 Homo sapiens Q13200 32814053
Intra
TARDBP Q13148 SMARCD1 Homo sapiens Q96GM5 32814053
Intra
TARDBP Q13148 SMARCD1 Homo sapiens Q96GM5 32814053
Intra
TARDBP Q13148 SMARCD1 Homo sapiens Q96GM5 32814053
Intra
TARDBP Q13148 SKIC8 Homo sapiens Q9GZS3 32814053
Intra
TARDBP Q13148 SKIC8 Homo sapiens Q9GZS3 32814053
Intra
TARDBP Q13148 SKIC8 Homo sapiens Q9GZS3 32814053
Intra
TARDBP Q13148 XRN2 Homo sapiens Q9H0D6 32814053
Intra
TARDBP Q13148 XRN2 Homo sapiens Q9H0D6 32814053
Intra
TARDBP Q13148 XRN2 Homo sapiens Q9H0D6 32814053
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148
NMR
26735904
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148 26099433
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148 23384725
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148
GMS
23384725
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148 22193716
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148
AFM
21666678
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148 19383787
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148
GMS
21666678
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148 26735904
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148 21666678
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148 23384725
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148
TEM
26735904
Intra
TARDBP Q13148 TARDBP Homo sapiens Q13148
TEM
21666678
Intra
TARDBP Q13148 ELAVL1 Homo sapiens Q15717 32814053
Intra
TARDBP Q13148 ELAVL1 Homo sapiens Q15717 32814053
Intra
TARDBP Q13148 ELAVL1 Homo sapiens Q15717 32814053
Intra
TARDBP Q13148 ELAVL1 Homo sapiens Q15717 32814053
Intra
TARDBP Q13148 FAM117B Homo sapiens Q6P1L5 32814053
Intra
TARDBP Q13148 FAM117B Homo sapiens Q6P1L5 32814053
Intra
TARDBP Q13148 FAM117B Homo sapiens Q6P1L5 32814053
Intra
TARDBP Q13148 CDC23 Homo sapiens Q9UJX2 32814053
Intra
TARDBP Q13148 CDC23 Homo sapiens Q9UJX2 32814053
Intra
TARDBP Q13148 CDC23 Homo sapiens Q9UJX2 32814053
Intra
TARDBP Q13148 KPNA4 Homo sapiens O00629 26571498
Intra
TARDBP Q13148 MGARP Homo sapiens Q8TDB4 32814053
Intra
TARDBP Q13148 MGARP Homo sapiens Q8TDB4 32814053
Intra
TARDBP Q13148 MGARP Homo sapiens Q8TDB4 32814053
Intra
TARDBP Q13148 PRPF8 Homo sapiens Q6P2Q9 32814053
Intra
TARDBP Q13148 PRPF8 Homo sapiens Q6P2Q9 32814053
Intra
TARDBP Q13148 PRPF8 Homo sapiens Q6P2Q9 32814053
Intra
TARDBP Q13148 FAM98C Homo sapiens Q17RN3 32814053
Intra
TARDBP Q13148 FAM98C Homo sapiens Q17RN3 32814053
Intra
TARDBP Q13148 FAM98C Homo sapiens Q17RN3 32814053
Intra
TARDBP Q13148 PCMTD2 Homo sapiens Q9NV79 32814053
Intra
TARDBP Q13148 PCMTD2 Homo sapiens Q9NV79 32814053
Intra
TARDBP Q13148 PCMTD2 Homo sapiens Q9NV79 32814053
Intra
TARDBP Q13148 KLHL32 Homo sapiens Q96NJ5 32814053
Intra
TARDBP Q13148 KLHL32 Homo sapiens Q96NJ5 32814053
Intra
TARDBP Q13148 KLHL32 Homo sapiens Q96NJ5 32814053
Intra
TARDBP Q13148 TBX22 Homo sapiens Q9Y458 32814053
Intra
TARDBP Q13148 TBX22 Homo sapiens Q9Y458 32814053
Intra
TARDBP Q13148 TBX22 Homo sapiens Q9Y458 32814053
Intra
TARDBP Q13148 ATXN2 Homo sapiens Q99700 20740007
Intra
TARDBP Q13148 ATXN2 Homo sapiens Q99700 20740007
Intra
TARDBP Q13148 SPATA22 Homo sapiens Q8NHS9 32814053
Intra
TARDBP Q13148 SPATA22 Homo sapiens Q8NHS9 32814053
Intra
TARDBP Q13148 SPATA22 Homo sapiens Q8NHS9 32814053
Intra
TARDBP Q13148 ASB13 Homo sapiens Q8WXK3 32814053
Intra
TARDBP Q13148 ASB13 Homo sapiens Q8WXK3 32814053
Intra
TARDBP Q13148 ASB13 Homo sapiens Q8WXK3 32814053
Intra
TARDBP Q13148 RNF10 Homo sapiens Q8N5U6 32814053
Intra
TARDBP Q13148 RNF10 Homo sapiens Q8N5U6 32814053
Intra
TARDBP Q13148 RNF10 Homo sapiens Q8N5U6 32814053
Intra
TARDBP Q13148 USP13 Homo sapiens Q92995 32814053
Intra
TARDBP Q13148 USP13 Homo sapiens Q92995 32814053
Intra
TARDBP Q13148 USP13 Homo sapiens Q92995 32814053
Intra
TARDBP Q13148 KLHL20 Homo sapiens Q9Y2M5 32814053
Intra
TARDBP Q13148 KLHL20 Homo sapiens Q9Y2M5 32814053
Intra
TARDBP Q13148 KLHL20 Homo sapiens Q9Y2M5 32814053
Intra
TARDBP Q13148 PPP1R15A Homo sapiens O75807 29109149
Intra
TARDBP Q13148 PPP1R15A Homo sapiens O75807 29109149
Intra
TARDBP Q13148 TRIM9 Homo sapiens Q9C026 32814053
Intra
TARDBP Q13148 TRIM9 Homo sapiens Q9C026 32814053
Intra
TARDBP Q13148 TRIM9 Homo sapiens Q9C026 32814053
Intra
TARDBP Q13148 NSFL1C Homo sapiens Q9UNZ2 32814053
Intra
TARDBP Q13148 NSFL1C Homo sapiens Q9UNZ2 32814053
Intra
TARDBP Q13148 NSFL1C Homo sapiens Q9UNZ2 32814053
Intra
TARDBP Q13148 ABTB1 Homo sapiens Q969K4 32814053
Intra
TARDBP Q13148 ABTB1 Homo sapiens Q969K4 32814053
Intra
TARDBP Q13148 ABTB1 Homo sapiens Q969K4 32814053
Intra
TARDBP Q13148 TOB1 Homo sapiens P50616
TAP
18377426
Intra
TARDBP Q13148 KLHL26 Homo sapiens Q53HC5 32814053
Intra
TARDBP Q13148 KLHL26 Homo sapiens Q53HC5 32814053
Intra
TARDBP Q13148 KLHL26 Homo sapiens Q53HC5 32814053
Intra
TARDBP Q13148 LNX1 Homo sapiens Q8TBB1 32814053
Intra
TARDBP Q13148 LNX1 Homo sapiens Q8TBB1 32814053
Intra
TARDBP Q13148 LNX1 Homo sapiens Q8TBB1 32814053
Intra
TARDBP Q13148 GTPBP3 Homo sapiens Q969Y2 32814053
Intra
TARDBP Q13148 GTPBP3 Homo sapiens Q969Y2 32814053
Intra
TARDBP Q13148 GTPBP3 Homo sapiens Q969Y2 32814053
Intra
TARDBP Q13148 BAHD1 Homo sapiens Q8TBE0 32814053
Intra
TARDBP Q13148 BAHD1 Homo sapiens Q8TBE0 32814053
Intra
TARDBP Q13148 BAHD1 Homo sapiens Q8TBE0 32814053
Intra
TARDBP Q13148 RNF183 Homo sapiens Q96D59 32814053
Intra
TARDBP Q13148 RNF183 Homo sapiens Q96D59 32814053
Intra
TARDBP Q13148 RNF183 Homo sapiens Q96D59 32814053
Intra
TARDBP Q13148 KCTD17 Homo sapiens Q8N5Z5 32814053
Intra
TARDBP Q13148 KCTD17 Homo sapiens Q8N5Z5 32814053
Intra
TARDBP Q13148 KCTD17 Homo sapiens Q8N5Z5 32814053
Intra
TARDBP Q13148 ILF3 Homo sapiens Q9NXX0 32814053
Intra
TARDBP Q13148 ILF3 Homo sapiens Q9NXX0 32814053
Intra
TARDBP Q13148 ILF3 Homo sapiens Q9NXX0 32814053
Intra
TARDBP Q13148 CBLB Homo sapiens Q13191 32814053
Intra
TARDBP Q13148 CBLB Homo sapiens Q13191 32814053
Intra
TARDBP Q13148 CBLB Homo sapiens Q13191 32814053
Intra
TARDBP Q13148 RMND5B Homo sapiens Q96G75 32814053
Intra
TARDBP Q13148 RMND5B Homo sapiens Q96G75 32814053
Intra
TARDBP Q13148 RMND5B Homo sapiens Q96G75 32814053
Intra
TARDBP Q13148 ZNF581 Homo sapiens Q9P0T4 32814053
Intra
TARDBP Q13148 ZNF581 Homo sapiens Q9P0T4 32814053
Intra
TARDBP Q13148 ZNF581 Homo sapiens Q9P0T4 32814053
Intra
TARDBP Q13148 ASB9 Homo sapiens Q96DX5 32814053
Intra
TARDBP Q13148 ASB9 Homo sapiens Q96DX5 32814053
Intra
TARDBP Q13148 ASB9 Homo sapiens Q96DX5 32814053
Intra
TARDBP Q13148 TASOR2 Homo sapiens Q5VWN6 32814053
Intra
TARDBP Q13148 TASOR2 Homo sapiens Q5VWN6 32814053
Intra
TARDBP Q13148 TASOR2 Homo sapiens Q5VWN6 32814053
Intra
TARDBP Q13148 DDX17 Homo sapiens Q92841 32814053
Intra
TARDBP Q13148 DDX17 Homo sapiens Q92841 32814053
Intra
TARDBP Q13148 DDX17 Homo sapiens Q92841 32814053
Intra
TARDBP Q13148 RNF138 Homo sapiens Q8WVD3 32814053
Intra
TARDBP Q13148 RNF138 Homo sapiens Q8WVD3 32814053
Intra
TARDBP Q13148 RNF138 Homo sapiens Q8WVD3 32814053
Intra
TARDBP Q13148 GMPPA Homo sapiens Q96IJ6 32814053
Intra
TARDBP Q13148 GMPPA Homo sapiens Q96IJ6 32814053
Intra
TARDBP Q13148 GMPPA Homo sapiens Q96IJ6 32814053
Intra
TARDBP Q13148 C8orf48 Homo sapiens Q96LL4 32814053
Intra
TARDBP Q13148 C8orf48 Homo sapiens Q96LL4 32814053
Intra
TARDBP Q13148 C8orf48 Homo sapiens Q96LL4 32814053
Intra
TARDBP Q13148 RYBP Homo sapiens Q8N488 32814053
Intra
TARDBP Q13148 RYBP Homo sapiens Q8N488 32814053
Intra
TARDBP Q13148 RYBP Homo sapiens Q8N488 32814053
Intra
TARDBP Q13148 WDR83 Homo sapiens Q9BRX9 32814053
Intra
TARDBP Q13148 WDR83 Homo sapiens Q9BRX9 32814053
Intra
TARDBP Q13148 WDR83 Homo sapiens Q9BRX9 32814053
Intra
TARDBP Q13148 FAM9A Homo sapiens Q8IZU1 32814053
Intra
TARDBP Q13148 FAM9A Homo sapiens Q8IZU1 32814053
Intra
TARDBP Q13148 FAM9A Homo sapiens Q8IZU1 32814053
Intra
TARDBP Q13148 MLC1 Homo sapiens Q15049 32814053
Intra
TARDBP Q13148 MLC1 Homo sapiens Q15049 32814053
Intra
TARDBP Q13148 MLC1 Homo sapiens Q15049 32814053
Intra
TARDBP Q13148 METTL27 Homo sapiens Q8N6F8 32814053
Intra
TARDBP Q13148 METTL27 Homo sapiens Q8N6F8 32814053
Intra
TARDBP Q13148 METTL27 Homo sapiens Q8N6F8 32814053
Intra
TARDBP Q13148 LGALS9C Homo sapiens Q6DKI2 32814053
Intra
TARDBP Q13148 LGALS9C Homo sapiens Q6DKI2 32814053
Intra
TARDBP Q13148 LGALS9C Homo sapiens Q6DKI2 32814053
Intra
TARDBP Q13148 ASIC4 Homo sapiens Q96FT7-4 32814053
Intra
TARDBP Q13148 ASIC4 Homo sapiens Q96FT7-4 32814053
Intra
TARDBP Q13148 ASIC4 Homo sapiens Q96FT7-4 32814053
Intra
TARDBP Q13148 ENKUR Homo sapiens Q8TC29 32814053
Intra
TARDBP Q13148 ENKUR Homo sapiens Q8TC29 32814053
Intra
TARDBP Q13148 ENKUR Homo sapiens Q8TC29 32814053
Intra
TARDBP Q13148 BTBD1 Homo sapiens Q9H0C5 32814053
Intra
TARDBP Q13148 BTBD1 Homo sapiens Q9H0C5 32814053
Intra
TARDBP Q13148 BTBD1 Homo sapiens Q9H0C5 32814053
Intra
TARDBP Q13148 FBXO4 Homo sapiens Q9UKT5 32814053
Intra
TARDBP Q13148 FBXO4 Homo sapiens Q9UKT5 32814053
Intra
TARDBP Q13148 FBXO4 Homo sapiens Q9UKT5 32814053
Intra
TARDBP Q13148 SMURF1 Homo sapiens Q9HCE7-2 32814053
Intra
TARDBP Q13148 SMURF1 Homo sapiens Q9HCE7-2 32814053
Intra
TARDBP Q13148 SMURF1 Homo sapiens Q9HCE7-2 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant TARDBP Proteins

Referencia número Nombre del producto Accession Pureza
HY-P71788 TARDBP Protein, Human (His) Q13148-1 (M1-M414) ≥ 90%, as determined by reducing SDS-PAGE.

TARDBP Antibodies

Referencia número Nombre del producto Aplicación Reactivity
HY-P82427 TDP43 Antibody (YA2172) WB, IHC-F, IHC-P, ICC/IF, IP Human, Mouse, Rat
HY-P82427A TDP43 Antibody (YA2172)(PBS only) WB, IHC-F, IHC-P, ICC/IF, IP Human, Mouse, Rat
HY-P84529 TDP43 Antibody (YA4226) WB, IHC-P, ICC/IF, FC, ELISA Human
HY-P84529A TDP43 Antibody (YA4226)(PBS only) WB, IHC-P, ICC/IF, FC, ELISA Human
HY-P86503 TDP43 Antibody (YA6195) WB, IHC-P, ICC/IF, IP, ELISA Human, Mouse, Rat

Related Diseases

Diseases Alias
Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia
  • Amyotrophic Lateral Sclerosis Type 10

  • ALS10

  • Amyotrophic Lateral Sclerosis 10, With Or Without Ftd

  • Frontotemporal Lobar Degeneration, Tardbp-Related

  • Amyotrophic Lateral Sclerosis 10

  • Amyotrophic Lateral Sclerosis 10, With Or Without Frontotemporal Dementia

  • Tardbp-Related Frontotemporal Lobar Degeneration With Tdp43 Inclusions

  • Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia And With Tdp43 Inclusions

  • Sclerosis, Lateral, Amyotrophic, Type Type 10

Motor Neuron Disease
  • Anterior Horn Cell Disease

  • Motor Neuron Diseases

  • Mnd - [Motor Neurone Disease]

  • Lou Gehrig Disease

  • Creeping Palsy

  • Creeping Paralysis

  • Bulbar Motor Neuron Disease

  • Bulbar Syndrome

  • Anterior Horn Cell Disorder

  • Hereditary Motor Neuron Disease

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1
  • FTDALS1

  • Frontotemporal Dementia And/Or Motor Neuron Disease

  • Ftdmnd

  • Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia

  • Alsftd

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-1

  • Frontotemporal Dementia With Motor Neuron Disease

  • Ftdals

  • Ftd-Als

  • Ftd-Mnd

  • Frontotemporal Dementia With Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis With Frontotemporal Dementia 1

  • Amyotrophic Lateral Sclerosis/Frontotemporal Dementia

  • Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia 1

  • Frontotemporal Lobar Degeneration

  • Grn-Related Frontotemporal Dementia

Amyotrophic Lateral Sclerosis 1
  • Amyotrophic Lateral Sclerosis

  • ALS

  • Lou Gehrig Disease

  • Amyotrophic Lateral Sclerosis Type 1

  • Charcot Disease

  • ALS1

  • Amyotrophic Lateral Sclerosis, Susceptibility To

  • Fals

  • Lou Gehrig'S Disease

  • Mnd

  • Motor Neuron Disease

  • Familial Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis 1, Familial

  • Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

  • Motor Neuron Disease, Bulbar

  • Motor Neurone Disease

  • Amyotrophic Lateral Sclerosis With Dementia

  • Dementia With Amyotrophic Lateral Sclerosis

  • Motor Neuron Disease, Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic

  • Sclerosis, Lateral, Amyotrophic, Type 1

  • Amyotrophic Sclerosis

  • Als - [Amyotrophic Lateral Sclerosis]

  • Wasting Palsy

  • Amyotrophic Paralysis

  • Amyotrophy Lateral Sclerosis

  • Wasting Paralysis

  • Spinal Progressive Amyotrophy

  • Progressive Atrophic Paralysis

Frontotemporal Dementia
  • Pallidopontonigral Degeneration

  • Frontotemporal Lobar Degeneration

  • Semantic Dementia

  • FTD

  • Frontotemporal Lobe Dementia

  • Multiple System Tauopathy With Presenile Dementia

  • Dementia, Frontotemporal

  • Frontotemporal Dementia With Parkinsonism

  • Mstd

  • Frontotemporal Lobar Degeneration With Tau Inclusions

  • Ftld With Tau Inclusions

  • Dementia, Frontotemporal, With Parkinsonism

  • Fldem

  • Ftdp17

  • Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

  • Ddpac

  • Wilhelmsen-Lynch Disease

  • Wld

  • Ppnd

  • Dementia, Frontotemporal, With Or Without Parkinsonism

  • Semantic Primary Progressive Aphasia

  • Semantic Variant Ppa

  • Wilhemsen-Lynch Disease

  • Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

  • Ftd-Als

  • Ftld

  • Pick Complex

  • Pick Disease Of The Brain

  • Frontotemporal Dementia With Parkinsonism-17

  • Grn-Related Frontotemporal Dementia

  • Frontotemporal Dementia With Motor Neuron Disease

  • Dementia In Fronto-Temporal Lobar Degeneration

  • Ftd - [Frontotemporal Dementia]

  • Temple Dementia

  • Frontal Lobe Dementia

Aphasia
Lateral Sclerosis
  • Primary Lateral Sclerosis

  • Adult-Onset Primary Lateral Sclerosis

  • Adult-Onset Pls

  • Motor Neuron Disease

  • Pls

  • Pls - [Primary Lateral Sclerosis]

  • Lateral Spinal Sclerosis

  • Lateral Complete Paralysis

  • Lateral Incomplete Paralysis

  • Lateral Paralysis

Corticobasal Degeneration
Pick Disease Of Brain
  • Pick Disease

  • Pick'S Disease

  • Pick Disease Of The Brain

  • Lobar Atrophy Of Brain

  • Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions

  • Behavioral Variant Of Frontotemporal Dementia

  • Dementia In Pick'S Disease

  • Lobar Atrophy Of The Brain

  • Bvftd

  • Bv-Ftd

  • PIDB

  • Picks Disease

Dementia
  • Dementias

  • Presenile Dementia

  • Alzheimer Type Dementia

  • Alzheimer Sclerosis

  • Alzheimer Disease Dementia

  • Alzheimer Dementia

  • Primary Degenerative Alzheimer Type Dementia

  • End Stage Alzheimer'S Dementia

  • Alzheimer'S Type Atypical Dementia

  • Alzheimer Type Presenile Dementia

  • Early Onset Alzheimer Dementia

  • Dementia In Alzheimer Disease Type 2

  • Dementia In Alzheimer Disease With Early Onset

  • Early Onset Alzheimer Type Dementia, Uncomplicated

  • Primary Degenerative Alzheimer Type Dementia, Early Onset

  • Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated

  • Alzheimer Disease Dementia With Early Onset

  • Presenile Sclerosis

  • Presenile Brain Sclerosis

  • Presenile Alzheimer Brain Sclerosis

  • Late Onset Alzheimer Dementia

  • Dementia In Alzheimer Disease Type 1

  • Dementia In Alzheimer Disease With Late Onset

  • Primary Degenerative Alzheimer Type Dementia, Late Onset

  • Sdat - [Senile Dementia, Alzheimer Type]

  • Alzheimer Disease Dementia With Late Onset

  • Late Onset Alzheimer Brain Sclerosis

  • Senile Alzheimer Brain Disease

  • Senile Alzheimer Brain Sclerosis

  • Senile Primary Degenerative Alzheimer Type Dementia

  • Senile Dementia Of The Alzheimer Type

  • Arteriosclerotic Dementia

  • Strategic-Infarct Dementia

  • Post Stroke Dementia

  • Vascular Cognitive Impairment

  • Vascular Dementia

  • Dementia Of The Lewy Body Type

  • Dementia With Lewy Bodies

  • Sdlt - [Senile Dementia Of The Lewy Body Type]

  • Senile Dementia Of The Lewy Body Type

  • Alcohol-Related Dementia

  • Alcoholic Dementia Nos

  • Alcohol-Induced Dementia

  • Alcoholic Brain Syndrome

  • Chronic Alcoholic Brain Syndrome

  • Alcohol Dementia

  • Late Onset Alcoholic Psychosis

  • Residual And Late-Onset Alcohol-Induced Psychotic Disorder

  • Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder

  • Late-Onset Psychoactive Substance-Induced Psychotic Disorder

  • Inhalant Dementia

  • Volatile Solvents Dementia

  • Dementia In Paralysis Agitans

  • Pdd - [Parkinson Disease Dementia]

  • Dementia Syndrome Of Parkinson Disease

  • Dementia In Parkinson Disease

  • Parkinson Related Dementia

  • Dementia In Huntington Chorea

  • Hiv - [Human Immunodeficiency Virus] Dementia

  • Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex

  • Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex

  • Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex

  • Aids Related Dementia

  • Dementia Due To Niacin Deficiency

Perry Syndrome
  • Parkinsonism With Alveolar Hypoventilation And Mental Depression

  • PERRYS

Speech And Communication Disorders
  • Language Disorder

  • Communication Disorder

  • Language Disorders

  • Communication Disorders

  • Speech Language Disorder

  • Speech-Language Disorder

  • Communication Impairment

  • Speech And Language Disorder

Nominal Aphasia
  • Anomia

  • Anomic Aphasia

Spinocerebellar Ataxia 2
  • Spinocerebellar Ataxia Type 2

  • SCA2

  • Amyotrophic Lateral Sclerosis 13

  • Spinocerebellar Degeneration With Slow Eye Movements

  • SDSEM

  • Spinocerebellar Atrophy Ii

  • Olivopontocerebellar Atrophy Ii

  • Opca2

  • Cerebellar Degeneration With Slow Eye Movements

  • Wadia-Swami Syndrome

  • Amyotrophic Lateral Sclerosis Type 13

  • ALS13

  • Olivopontocerebellar Atrophy Holguin Type

  • Spinocerebellar Ataxia Cuban Type

  • Olivopontocerebellar Atrophy, Holguin Type

  • Spinocerebellar Ataxia, Cuban Type

  • Amyotrophic Lateral Sclerosis, Susceptibility To, 13

  • Olivopontocerebellar Atrophy 2

  • Sca 2

  • Spinocerebellar Ataxia With Slow Eye Movements

  • Spinocerebellar Atrophy 2

  • Wadia Swami Syndrome

  • Opca Ii

  • Spinocerebellar Ataxia-2

  • Ataxia, Spinocerebellar, Type 2

Associative Agnosia
Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia
  • Ibmpfd

  • Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia

  • Pagetoid Amyotrophic Lateral Sclerosis

  • Pagetoid Neuroskeletal Syndrome

  • Inclusion Body Myopathy With Paget Disease Of Bone And/Or Frontotemporal Dementia

  • Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone And/Or Frontotemporal Dementia

  • Multisystem Proteinopathy

  • Limb-Girdle Muscular Dystrophy With Paget Disease Of Bone

  • Inclusion Body Myopathy With Paget'S Disease Of Bone And Frontotemporal Dementia

  • Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dement

  • Lower Motor Neuron Degeneration With Paget-Like Bone Disease

  • Muscular Dystrophy, Limb-Girdle, With Paget Disease Of Bone

  • Myopathy, Inclusion Body, With Early-Onset Paget Disease And Frontotemporal Dementia

Alzheimer Disease 7
  • Ad7

  • Alzheimer'S Disease 7

  • Alzheimer Disease, Familial, 7

  • Alzheimer Disease-7

  • Alzheimer Disease, Familial 7

Prosopagnosia
Niemann-Pick Disease
  • Sphingomyelin/Cholesterol Lipidosis

  • Niemann-Pick Diseases

  • Lipoid Histiocytosis

  • Sphingomyelin Lipidosis

  • Sphingomyelinase Deficiency Disease

  • Lipid Histiocytosis

  • Neuronal Cholesterol Lipidosis

  • Neuronal Lipidosis

  • Npd

  • Sphingomyelinase Deficiency

  • Niemann-Pick Disease, Type A

Ideomotor Apraxia
  • Apraxia, Ideomotor

  • Classic Apraxia

  • Ideomotor Dyspraxia

  • Limb-Kinetic Apraxia

  • Transcortical Apraxia

Machado-Joseph Disease
  • SCA3

  • MJD

  • Spinocerebellar Ataxia 3

  • Azorean Disease

  • Spinocerebellar Ataxia Type 3

  • Spinocerebellar Atrophy

  • Azorean Neurologic Disease

  • Spinopontine Atrophy

  • Nigrospinodentatal Degeneration

  • Spinocerebellar Atrophy Iii

  • Spinocerebellar Atrophy Type 3

  • Azorean Ataxia

  • Azorean Disease Of The Nervous System

  • Machado Disease

  • Nigro-Spino-Dentatal Degeneration With Nuclear Ophthalmoplegia

  • Disease, Machado-Joseph

  • Ataxia, Spinocerebellar

Agraphia
Multisystem Proteinopathy
Arteriolosclerosis
Writing Disorder
Amyotrophic Lateral Sclerosis Type 6
  • Amyotrophic Lateral Sclerosis 6, Autosomal Recessive

  • Als6

  • Amyotrophic Lateral Sclerosis 6, With Or Without Frontotemporal Dementia

  • Autosomal Recessive Amyotrophic Lateral Sclerosis 6

  • Sclerosis, Lateral, Amyotrophic, Type Type 6

  • Amyotrophic Lateral Sclerosis 6

Amyotrophic Lateral Sclerosis Type 22
  • Als 22

  • Amyotrohpic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia

  • Amyotrophic Lateral Sclerosis 22

Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1
  • Guam Disease

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex Of Guam

  • Als-Pdc

  • Lytico-Bodig Disease

  • Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1, Susceptibility To

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex, Susceptibility To

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex

  • Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Of Guam Syndrome

  • Parkinsonism-Dementia-Als Complex

  • Pdals

  • Amyotrophic Lateral Sclerosis, Parkinsonism/Dementia Complex Of Guam

  • Parkinson-Dementia Complex Of Guam

  • G-Pdc

  • Guam Parkinsonism-Dementia Complex

  • ALS-PDC1

  • Als/Pdc Of Guam

  • Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic/Parkinsonism/Dementia Complex 1

  • Amyotrophic Lateral Sclerosis, Guam Form

  • Parkinsonian Disorders

Muscular Atrophy
  • Muscle Wasting

  • Amyotrophia

  • Wasting - Muscle

  • Skeletal Muscle Atrophy

Dysgraphia
  • Agraphia

Amyotrophic Lateral Sclerosis 8
  • Amyotrophic Lateral Sclerosis Type 8

  • ALS8

  • Sclerosis, Lateral, Amyotrophic, Type Type 8

Progressive Muscular Atrophy
  • Progressive Spinal Muscular Atrophy

  • Pure Progressive Muscular Atrophy

  • Pma

  • Hereditary Spinal Muscle Atrophy

  • Pma - [Progressive Muscular Atrophy]

  • Progressive Muscle Atrophy

  • Progressive Spinal Muscle Atrophy

  • Duchenne-Aran Atrophy

  • Duchenne-Aran Muscle Atrophy

  • Hereditary Sma - [Spinal Muscle Atrophy]

Amyotrophic Lateral Sclerosis 11
  • Amyotrophic Lateral Sclerosis Type 11

  • ALS11

  • Sclerosis, Lateral, Amyotrophic, Type Type 11

Parkinsonism
  • Parkinsonism-Plus

  • Idiopathic Parkinsonism

  • Primary Parkinsonism

  • Paralysis Agitans Syndrome

  • Parkinsonian Syndrome

  • Trembling Paralysis

  • Paralysis Agitans

  • Shaking Palsy

  • Shaking Paralysis

Liposarcoma
  • Lipomatous Cancer

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 2
  • FTDALS2

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-2

  • Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 2

Creutzfeldt-Jakob Disease
  • Variant Creutzfeldt-Jakob Disease

  • CJD

  • Bovine Spongiform Encephalopathy

  • Vcjd

  • Inherited Creutzfeldt-Jakob Disease

  • Creutzfeldt-Jakob Disease, Familial

  • Creutzfeldt Jakob Disease

  • Creutzfeldt-Jacob Disease

  • Creutzfeldt Jacob Disease

  • Sporadic Creutzfeldt-Jakob Disease

  • Encephalopathy, Bovine Spongiform

  • Creutzfeldt-Jakob Disease, Variant, Resistance To

  • Creutzfeldt-Jakob Disease, Variant

  • Creutzfeldt Jacob Syndrome

  • Jakob-Creutzfeldt Disease

  • Subacute Spongiform Encephalopathy

  • Transmissible Virus Dementia

  • New Variant Of Cjd

  • Nv-Cjd

  • Variant Cjd

  • Variant Creutzfeldt-Jacob Disease

  • Sporadic Cjd

  • Inherited Cjd

  • Acquired Creutzfeldt-Jakob Disease

  • Variant Mcj

  • Encephalopathy Bovine Spongiform

  • Familial Creutzfeldt-Jakob Disease

  • Creutzfeldt-Jakob Syndrome

  • New Variant Creutzfeldt-Jakob Disease

  • Creutzfeldt-Jakob Disease, Sporadic

  • Acquired Cjd

  • Scjd - [Sporadic Creutzfeldt-Jakob Disease]

  • Idiopathic Creutzfeldt-Jakob Disease

  • Creutzfeld-Jakob Disease Nos

  • Vcjd - [Variant Creutzfeldt-Jakob Disease]

Amyotrophic Lateral Sclerosis 4, Juvenile
  • Amyotrophic Lateral Sclerosis Type 4

  • ALS4

  • Amyotrophic Lateral Sclerosis 4

  • Dhmn With Upper Motor Neuron Signs

  • Distal Hereditary Motor Neuropathy With Upper Motor Neuron Signs

  • Neuronopathy, Distal Hereditary Motor, With Pyramidal Features

  • Als 4

  • Distal Hereditary Motor Neuropathy With Pyramidal Features

  • Amyotrophic Lateral Sclerosis Juvenile 4

  • Neuronopathy Distal Hereditary Motor With Pyramidal Features

  • Sclerosis, Lateral, Amyotrophic, Type Type 4

Postencephalitic Parkinson Disease
  • Postencephalitic Parkinsonism

  • Parkinson Disease, Postencephalitic

Cerebral Amyloid Angiopathy, Cst3-Related
  • Cerebral Amyloid Angiopathy

  • Hereditary Cerebral Hemorrhage With Amyloidosis

  • Hchwa

  • Hereditary Cystatin C Amyloid Angiopathy

  • Cerebral Amyloid Angiopathy, Familial

  • Amyloidosis, Cerebroarterial, Icelandic Type

  • Amyloidosis Vi

  • Cerebral Hemorrhage, Hereditary, With Amyloidosis

  • Cst3-Related Cerebral Amyloid Angiopathy

  • Cerebral Hemorrhage, Hereditary, With Amyloidosis, Icelandic Variant

  • Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Variant

  • Caa, Familial

  • Cerebral Amyloid Angiopathy, Genetic

  • Acys Amyloidosis

  • Cst3-Related Amyloidosis

  • Cystatin Amyloidosis

  • Hchwa, Icelandic Type

  • Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Type

  • Amyloidosis 6

  • AMYL6

  • Acys

  • Caa

  • Cerebral Amyloid Angiopathy Cst3-Related

  • Cerebroarterial Amyloidosis Icelandic Type

  • Cystatin C Amyloidosis

  • Hccaa

  • Hchwai

  • Hchwa-I

  • Hereditary Cerebral Hemorrhage With Amyloidosis Icelandic Type

  • Cerebral Amyloid Angiopathy Familial

  • Angiopathy, Amyloid, Cerebral, Cst3-Related

  • Hereditary Cerebral Amyloid Angiopathy, Icelandic Type

  • Familial Cerebral Amyloid Angiopathy

  • Cerebral Amyloid Angiopathy, Hereditary

Amyotrophic Lateral Sclerosis 19
  • Amyotrophic Lateral Sclerosis Type 19

  • ALS19

  • Sclerosis, Lateral, Amyotrophic, Type 19

Huntington Disease
  • Huntington'S Disease

  • Huntington Chorea

  • Huntington'S Chorea

  • HD

  • Huntington Chronic Progressive Hereditary Chorea

  • Juvenile Huntington Disease

  • Chronic Progressive Chorea

  • Chronic Progressive Hereditary Chorea

  • Hc - [Huntington Chorea]

  • Hereditary Chorea

  • Progressive Hereditary Chorea

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3
  • FTDALS3

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-3

  • Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 3

Amyotrophic Lateral Sclerosis, Juvenile, With Dementia
  • Juvenile Amyotrophic Lateral Sclerosis With Dementia

  • Als-Dementia Complex

Nonaka Myopathy
  • Gne Myopathy

  • Hibm

  • Distal Myopathy With Rimmed Vacuoles

  • Hereditary Inclusion Body Myopathy

  • Ibm2

  • Inclusion Body Myopathy, Quadriceps-Sparing

  • Qsm

  • Dmrv

  • Distal Myopathy, Nonaka Type

  • Inclusion Body Myopathy 2

  • Inclusion Body Myopathy, Autosomal Recessive

  • NM

  • Nonaka Distal Myopathy

  • Myopathy, Distal, With Or Without Rimmed Vacuoles

  • Inclusion Body Myopathy, Hereditary, Autosomal Recessive

  • Inclusion Body Myopathy Type 2

  • Quadriceps-Sparing Myopathy

  • Quadriceps Sparing Myopathy

  • Rimmed Vacuole Myopathy

  • Inclusion Body Myopathy 2, Autosomal Recessive, Formerly

  • Ibm2, Formerly

  • Hibm2

  • Hereditary Inclusion Body Myopathy Type 2

  • Inclusion Body Myopathy 2, Autosomal Recessive

  • Myopathy, Distal, With Rimmed Vacuoles

  • Inclusion Body Myopathy Autosomal Recessive

  • Myopathy, Inclusion Body, Type 2

  • Myopathy, Nonaka

Simultanagnosia
Pseudobulbar Palsy
  • Pseudobulbar Paralysis

Paget'S Disease Of Bone
  • Osteitis Deformans

  • Paget Disease Of Bone

  • Osseous Paget'S Disease

  • Paget Disease Of Bone, Familial

  • Bone Paget Disease

  • Familial Paget'S Disease Of Bone

  • Paget'S Bone Disease

  • Familial Paget Disease Of Bone

  • Paget Disease, Bone

  • Pdb

  • Pagets Bone Disease

Alzheimer Disease, Familial, 1
  • Alzheimer Disease

  • Alzheimer'S Disease

  • Presenile And Senile Dementia

  • AD1

  • Alzheimer Disease, Susceptibility To

  • Alzheimer Disease, Late-Onset, Susceptibility To

  • Alzheimer Disease 1, Familial

  • AD

  • Familial Alzheimer Disease

  • Alzheimer Disease, Late-Onset

  • Alzheimers Dementia

  • Alzheimer Dementia

  • Alzheimer Sclerosis

  • Alzheimer Syndrome

  • Alzheimer-Type Dementia

  • Dat

  • Primary Senile Degenerative Dementia

  • Sdat

  • Alzheimer Disease 1

  • Autosomal Dominant Alzheimer Disease

  • Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

  • Late Onset Alzheimer Disease

  • Alzheimers Disease

  • Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

  • Late-Onset Alzheimers Disease

  • Alzheimer'S Disease Pathway Kegg

  • Dementia Due To Alzheimer'S Disease

  • Alzheimer Disease Type 1

  • Alzheimers

Neuronopathy, Distal Hereditary Motor, Type Viib
  • HMN7B

  • Hmn Viib

  • Dhmn7b

  • Neuropathy, Distal Hereditary Motor, Type Viib

  • Distal Hereditary Motor Neuronopathy Type 7b

  • Distal Hereditary Motor Neuropathy Type Viib

  • Neuronopathy, Distal Hereditary Motor, Type 7b

  • Neuropathy, Distal Hereditary Motor, With Vocal Cord Paralysis, Type Viib

  • Lower Motor Neuron Disease, Dynactin Type

  • Distal Spinal Muscular Atrophy With Vocal Cord Paralysis Type 7b

  • Harper-Young Myopathy

  • Neuronopathy, Distal Hereditary Motor, 7b

  • Distal Hereditary Motor Neuropathy With Vocal Cord Paralysis Type Viib

  • Lower Motor Neuron Disease Dynactin Type

  • Plmnd

  • Progressive Lower Motor Neuron Disease

  • Neuropathy, Motor, Distal, Hereditary, Type Viib

Supranuclear Palsy, Progressive, 1
  • Progressive Supranuclear Palsy

  • Steele-Richardson-Olszewski Syndrome

  • Supranuclear Palsy, Progressive

  • Progressive Supranuclear Ophthalmoplegia

  • Psp

  • PSNP1

  • Familial Progressive Supranuclear Palsy

  • Richardson'S Syndrome

  • Psp Syndrome

  • Progressive Supranuclear Palsy 1

  • Supranuclear Palsy Progressive

  • Ophthalmoplegia, Supranuclear, Progressive

  • Steele-Richardson-Olszewksi Syndrome

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7
  • Ftd3

  • Frontotemporal Dementia, Chromosome 3-Linked

  • Amyotrophic Lateral Sclerosis, Chmp2b-Related

  • Chromosome 3-Linked Frontotemporal Dementia

  • FTDALS7

  • Chmp2b-Related Frontotemporal Dementia

  • Amyotrophic Lateral Sclerosis 17, Formerly

  • Als17, Formerly

  • Amyotrophic Lateral Sclerosis Type 17

  • Dtm1

  • Ftd-3

  • Ftd-Chmp2b

  • Als17

  • Amyotrophic Lateral Sclerosis 17

  • Sclerosis, Lateral, Amyotrophic, Type 17

  • Dementia, Frontotemporal, Chromosome 3-Linked

Dementia, Lewy Body
  • Lewy Body Dementia

  • Lewy Body Disease

  • Diffuse Lewy Body Disease

  • Dementia With Lewy Bodies

  • DLB

  • Autosomal Dominant Diffuse Lewy Body Disease

  • Cortical Lewy Body Disease

  • Dementia, Lewy Body, Susceptibility To

  • Lewy Body Dementia, Susceptibility To

  • Senile Dementia Of The Lewy Body Type

  • Dementia Of The Lewy Body Type

  • Lbd

  • Diffuse Lewy Body Disease With Gaze Palsy

  • Dysphasic Dementia Hereditary

  • Lewy Body Type Senile Dementia

  • Lewy Body Variant Of Alzheimer Disease

  • Lewy Bodies

  • Lewy Body

  • Dlbd - [Diffuse Lewy Body Disease]

  • Clbd - [Cortical Lewy Body Disease]

Locked-In Syndrome
  • Locked In Syndrome

  • Cerebromedullospinal Disconnection

  • Locked-In State

  • Quadriplegia

Fragile X Syndrome
  • FXS

  • Martin-Bell Syndrome

  • Fraxa Syndrome

  • Marker X Syndrome

  • X-Linked Mental Retardation And Macroorchidism

  • Fragile X Mental Retardation Syndrome

  • Fra Syndrome

  • Mental Retardation, X-Linked, Associated With Marxq28

  • X-Linked Intellectual Disability And Macroorchidism

  • Frax Syndrome

  • Symptomatic Form Of Fragile X Syndrome In Female Carriers

  • Fragile-X Syndrome

  • Fraxe Syndrome

Gerstmann Syndrome
  • Aphasia-Angular Gyrus Syndrome

  • Developmental Gerstmann Syndrome

  • Gs

  • Gerstmann Badal Syndrome

  • Gerstmann Tetrad

  • Gerstmann'S Syndrome

  • Developmental Gerstmann'S Syndrome

Alexia
  • Dyslexia

  • Dyslexia, Acquired

  • Acquired Dyslexia

  • Aphemesthaesia

Spinal And Bulbar Muscular Atrophy, X-Linked 1
  • Kennedy Disease

  • Sbma

  • Spinal And Bulbar Muscular Atrophy

  • Kennedy'S Disease

  • X-Linked Spinal And Bulbar Muscular Atrophy

  • SMAX1

  • Kd

  • Kennedy Spinal And Bulbar Muscular Atrophy

  • Spinobulbar Muscular Atrophy

  • Bulbospinal Muscular Atrophy, X-Linked

  • Bulbospinal Neuronopathy, X-Linked Recessive

  • Xbsn

  • Spinal And Bulbar Muscular Atrophy Of Kennedy

  • Bulbospinal Muscular Atrophy

  • X-Linked Bulbospinal Amyotrophy

  • Bulbo-Spinal Atrophy, X-Linked

  • Spinal Bulbar Muscular Atrophy

  • X-Linked Bulbo-Spinal Atrophy

  • X-Linked Spinal Bulbar Muscular Atrophy

  • X-Linked Bsma

  • X-Linked Bulbospinal Muscular Atrophy

  • Spinal And Bulbar Muscular Atrophy X-Linked 1

  • Bulbospinal Muscular Atrophy X-Linked

  • Bulbospinal Neuronopathy X-Linked Recessive

  • Kennedy Disease)

  • Kennedy Syndrome

  • Atrophy, Muscular, Spinal And Bulbar, Kennedy Type

  • Atrophy, Muscular, Spinobulbar

  • Bulbospinal Neuronopathy

Akinetic Mutism
  • Coma Vigilans

Gerstmann-Straussler Disease
  • Gerstmann-Straussler-Scheinker Disease

  • Gerstmann-Straussler-Scheinker Syndrome

  • Prion Dementia

  • Cerebral Amyloid Angiopathy, Prnp-Related

  • GSD

  • Gss

  • Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In Cns

  • Amyloidosis, Cerebral, With Spongiform Encephalopathy

  • Subacute Spongiform Encephalopathy, Gerstmann-Straussler Type

  • Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type

  • Amyloidosis Cerebral With Spongiform Encephalopathy

  • Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In The Central Nervous System

  • Encephalopathy Subacute Spongiform Gerstmann-Straussler Type

  • Gssd

  • Gerstmann Straussler Scheinker Syndrome

  • Cerebral Amyloidosis With Spongiform Encephalopathy

  • Subacute Spongiform Encephalopathy Gerstmann-Straussler Type

  • Gluthathione Synthetase Deficiency

  • Gerstmann Straussler Syndrome

Kuru
  • Kuru, Susceptibility To

  • Kuru Encephalopathy

  • Kuru Encephalitis

  • Kuru Disease

Distal Hereditary Motor Neuronopathy Type 7
  • Dhmn7

  • Dhmnvpy

  • Distal Spinal Muscular Atrophy With Vocal Cord Paralysis

Amyotrophic Lateral Sclerosis Type 12
  • Amyotrophic Lateral Sclerosis 12

  • Als12

  • Sclerosis, Lateral, Amyotrophic, Type Type 12

Fatal Familial Insomnia
  • Insomnia, Fatal Familial

  • FFI

  • Familial Fatal Insomnia

  • Insomnia Familial Fatal

  • Insomnia Fatal Familial

  • Insomnia, Fatal, Familial

  • Ffi - [Fatal Familial Insomnia]

Rett Syndrome
  • Atypical Rett Syndrome

  • RTT

  • Rett Disorder

  • Rts

  • Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use

  • Rett Syndrome, Preserved Speech Variant

  • Rett Syndrome, Atypical

  • Rett'S Disorder

  • Rett Syndrome Variant

  • Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome

  • Cerebroatrophic Hyperammonemia

  • Rett Like Syndrome

  • Rett'S Syndrome

  • Atypical Rtt

  • Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use

  • Rett Syndrome Preserved Speech Variant

  • Rett Syndrome Zappella Variant

  • Rett Syndrome, Zappella Variant

Movement Disease
  • Movement Disorders

  • Movement Disorder

Epilepsy, Idiopathic Generalized 2
  • EIG2

  • Epilepsy, Idiopathic Generalized, Susceptibility To, 2

  • Idiopathic Generalized Epilepsy 2

  • Epilepsy, Idiopathic Generalized Locus On Chromosome 14

  • Epilepsy, Idiopathic Generalized, Susceptibility To, Locus On Chromosome 14

Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 2
  • Ibmpfd2

  • Msp2

  • Multisystem Proteinopathy 2

Disease Of Mental Health
  • Mental Health

  • Mental Disorders

Giant Axonal Neuropathy 2
Neuronal Ceroid Lipofuscinosis
  • Hereditary Ceroid Lipofuscinosis

  • Batten Disease

  • Ncl

  • Neuronal Ceroid-Lipofuscinoses

  • Lipofuscinosis, Ceroid, Neuronal

  • Juvenile Neuronal Ceroid Lipofuscinosis

  • Cerebromacular Dystrophy

  • Cerebromacular Degeneration

  • Ceroid-Lipofuscinosis

  • Ncl - [Neuronal Ceroid Lipofuscinosis]

  • Amaurotic Familial Idiocy

  • Amaurotic Idiocy

  • Amaurotic Idiot

  • Neuronal Lipofuscinosis

  • Pigmentary Retinal Lipoid Neuronal Heredodegeneration

Autosomal Dominant Cerebellar Ataxia
  • Spinocerebellar Ataxia

  • Adca

  • Pierre Marie Cerebellar Ataxia

  • Ataxia, Spinocerebellar

  • Sca

  • Autosomal Dominant Spinocerebellar Ataxia

  • Spinocerebellar Ataxias

Speech Disorder
  • Speech Disorders

Cerebellar Disease
  • Cerebellar Diseases

  • Cerebellar Dysfunction

  • Cerebellar Abnormality

  • Cerebellar Disorders

Neuromuscular Disease
  • Neuromuscular Diseases

  • Neuromuscular Disorders

  • Neuromuscular Disorder

Hereditary Spastic Paraplegia
  • Familial Spastic Paraplegia

  • Hereditary Spastic Paraparesis

  • Strumpell-Lorrain Disease

  • Familial Spastic Paraparesis

  • Hsp

  • Spg

  • Strümpell-Lorrain Disease

  • Spastic Paraplegia, Hereditary

  • French Settlement Disease

  • Strumpell-Lorrain Syndrome

  • Fsp

  • Spastic Paraplegia, Familial

  • Spastic Paraplegia Hereditary

  • Spastic Paraplegia 3, Autosomal Dominant

  • Spastic Paraparesis

  • Hereditary Spastic Paralysis

  • Familial Spastic Paralysis

  • Hereditary Spastic Ataxia

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

Charcot-Marie-Tooth Disease
  • Cmt

  • Hmsn

  • Hereditary Motor And Sensory Neuropathy

  • Pma

  • Cmt - Charcot-Marie-Tooth Disease

  • Charcot Marie Tooth Disease

  • Charcot-Marie-Tooth Hereditary Neuropathy

  • Charcot-Marie-Tooth Syndrome

  • Peroneal Muscular Atrophy

  • Hereditary Motor And Sensory Neuropathies

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris TARDBP VGNC VGNC:47109
Macaca mulatta TARDBP VGNC VGNC:100153
Mus musculus TARDBP MGD MGI:2387629
Rattus norvegicus TARDBP RGD RGD:1310906
Bos taurus TARDBP VGNC VGNC:35603
Felis catus TARDBP VGNC VGNC:80374
Others TARDBP NCBI