STUB1 - STIP1 homology and U-box containing protein 1 Gene

Also Known as CHIP; SCA48; UBOX1; SCAR16; HSPABP2; NY-CO-7; SDCCAG7

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10273

About STUB1

Cytogenetic location: 16p13.3 Genomic coordinates (GRCh38): 16:680,410-682,801 (from NCBI)

This gene has 11 transcripts (splice variants), 236 orthologues, 18 paralogues and is associated with 3 phenotypes. Ubiquitous expression in fat (RPKM 42.9), kidney (RPKM 39.1) and 25 other tissues.

Summary

This gene encodes a protein containing tetratricopeptide repeat and a U-box that functions as a ubiquitin Ligase/cochaperone. The encoded protein binds to and ubiquitinates shock cognate 71 kDa protein (Hspa8) and DNA Polymerase beta (Polb), among Other targets. Mutations in this gene cause spinocerebellar ataxia, autosomal recessive 16. Alternative splicing results in multiple transcript variants. There is a pseudogene for this gene on chromosome 2. [provided by RefSeq, Jun 2014]

STUB1 Products (2)

mRNA Protein Name
NM_001293197.2 NP_001280126.1 E3 ubiquitin-protein ligase CHIP isoform b
NM_005861.4 NP_005852.2 E3 ubiquitin-protein ligase CHIP isoform a
Molecular Function GO Annotation Evidence References Source
enables G protein-coupled receptor binding IPI
IPI: Inferred from physical interaction
12150907 GOA
enables Hsp70 protein binding IDA
IDA: Inferred from direct assay
10330192 GOA
enables Hsp70 protein binding IPI
IPI: Inferred from physical interaction
24613385 GOA
enables Hsp90 protein binding IDA
IDA: Inferred from direct assay
11146632 GOA
enables R-SMAD binding IPI
IPI: Inferred from physical interaction
15781469 GOA
enables SMAD binding IPI
IPI: Inferred from physical interaction
24613385 GOA
enables TPR domain binding IDA
IDA: Inferred from direct assay
11146632 GOA
enables enzyme binding IPI
IPI: Inferred from physical interaction
16280320 GOA
enables heat shock protein binding IPI
IPI: Inferred from physical interaction
16207813 GOA
enables kinase binding IPI
IPI: Inferred from physical interaction
17512523 GOA
enables misfolded protein binding IDA
IDA: Inferred from direct assay
16831871 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11146632 GOA
enables protein homodimerization activity IPI
IPI: Inferred from physical interaction
23990462 GOA
enables protein-folding chaperone binding IPI
IPI: Inferred from physical interaction
16207813 GOA
enables ubiquitin protein ligase activity IDA
IDA: Inferred from direct assay
14610072 GOA
enables ubiquitin protein ligase activity IGI
IGI: Inferred from genetic interaction
16207813 GOA
enables ubiquitin protein ligase activity IMP
IMP: Inferred from mutant phenotype
15781469 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
12150907 GOA
enables ubiquitin-protein transferase activity IDA
IDA: Inferred from direct assay
15466472 GOA
enables ubiquitin-protein transferase activity IMP
IMP: Inferred from mutant phenotype
19713937 GOA
Biological Process GO Annotation Evidence References Source
involved in ERAD pathway IMP
IMP: Inferred from mutant phenotype
23990462 GOA
involved in cellular response to misfolded protein IDA
IDA: Inferred from direct assay
16831871 GOA
involved in negative regulation of smooth muscle cell apoptotic process IMP
IMP: Inferred from mutant phenotype
20724525 GOA
involved in negative regulation of transforming growth factor beta receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
15781469 GOA
involved in positive regulation of ERAD pathway IMP
IMP: Inferred from mutant phenotype
26265139 GOA
involved in positive regulation of chaperone-mediated protein complex assembly IDA
IDA: Inferred from direct assay
16831871 GOA
involved in positive regulation of proteasomal ubiquitin-dependent protein catabolic process IDA
IDA: Inferred from direct assay
11146632 GOA
involved in positive regulation of protein ubiquitination IDA
IDA: Inferred from direct assay
11146632 GOA
involved in positive regulation of proteolysis IMP
IMP: Inferred from mutant phenotype
26634371 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IDA
IDA: Inferred from direct assay
15781469 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
29883609 GOA
involved in protein K63-linked ubiquitination IDA
IDA: Inferred from direct assay
16307917 GOA
involved in protein autoubiquitination IDA
IDA: Inferred from direct assay
16307917 GOA
involved in protein monoubiquitination IDA
IDA: Inferred from direct assay
24043303 GOA
involved in protein polyubiquitination IDA
IDA: Inferred from direct assay
15781469 GOA
involved in protein polyubiquitination IMP
IMP: Inferred from mutant phenotype
19713937 GOA
involved in protein quality control for misfolded or incompletely synthesized proteins IDA
IDA: Inferred from direct assay
16831871 GOA
involved in protein stabilization IDA
IDA: Inferred from direct assay
24043303 GOA
involved in protein ubiquitination IDA
IDA: Inferred from direct assay
14610072 GOA
involved in protein ubiquitination IMP
IMP: Inferred from mutant phenotype
16809764 GOA
involved in regulation of glucocorticoid metabolic process IDA
IDA: Inferred from direct assay
11146632 GOA
involved in regulation of protein stability IDA
IDA: Inferred from direct assay
16809764 GOA
involved in ubiquitin-dependent protein catabolic process IGI
IGI: Inferred from genetic interaction
18292230 GOA
involved in ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
19713937 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
10330192 GOA
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
12150907 GOA
located in nuclear inclusion body IDA
IDA: Inferred from direct assay
16831871 GOA
is active in nucleus IDA
IDA: Inferred from direct assay
23973223 GOA
part of protein folding chaperone complex IPI
IPI: Inferred from physical interaction
16207813 GOA
part of ubiquitin ligase complex IDA
IDA: Inferred from direct assay
12150907 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

STUB1 Protein Structure

TPR_11

TPR_11: TPR repeat (26 - 90)

TPR_1

TPR_1: Tetratricopeptide repeat (94 - 123)

U-box

U-box: U-box domain (227 - 299)

  • 0
  • 100
  • 200
  • 303 a.a.
Protein Preferred Names Protein Names

E3 ubiquitin-protein ligase CHIP

  • CLL-associated antigen KW-8

STUB1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
STUB1 Q9UNE7 NF2 Homo sapiens P35240 32814053
Intra
STUB1 Q9UNE7 NF2 Homo sapiens P35240 32814053
Intra
STUB1 Q9UNE7 NF2 Homo sapiens P35240 32814053
Intra
STUB1 Q9UNE7 OLFM3 Homo sapiens Q96PB7 25416956
Intra
STUB1 Q9UNE7 BAG1 Homo sapiens Q99933 25036637
Intra
STUB1 Q9UNE7 CISD2 Homo sapiens Q8N5K1 32814053
Intra
STUB1 Q9UNE7 CISD2 Homo sapiens Q8N5K1 32814053
Intra
STUB1 Q9UNE7 CISD2 Homo sapiens Q8N5K1 32814053
Intra
STUB1 Q9UNE7 MLF2 Homo sapiens Q15773 25036637
Intra
STUB1 Q9UNE7 MLF2 Homo sapiens Q15773 33961781
Intra
STUB1 Q9UNE7 MLF2 Homo sapiens Q15773 25036637
Intra
STUB1 Q9UNE7 UBE2N Homo sapiens P61088 25036637
Intra
STUB1 Q9UNE7 RAB7A Homo sapiens P51149 32814053
Intra
STUB1 Q9UNE7 RAB7A Homo sapiens P51149 32814053
Intra
STUB1 Q9UNE7 RAB7A Homo sapiens P51149 32814053
Intra
STUB1 Q9UNE7 DMWD Homo sapiens G5E9A7 32814053
Intra
STUB1 Q9UNE7 DMWD Homo sapiens G5E9A7 32814053
Intra
STUB1 Q9UNE7 DMWD Homo sapiens G5E9A7 32814053
Intra
STUB1 Q9UNE7 SEPTIN2 Homo sapiens Q15019-2 32814053
Intra
STUB1 Q9UNE7 SEPTIN2 Homo sapiens Q15019-2 32814053
Intra
STUB1 Q9UNE7 SEPTIN2 Homo sapiens Q15019-2 32814053
Intra
STUB1 Q9UNE7 BSCL2 Homo sapiens J3KQ12 32814053
Intra
STUB1 Q9UNE7 BSCL2 Homo sapiens J3KQ12 32814053
Intra
STUB1 Q9UNE7 BSCL2 Homo sapiens J3KQ12 32814053
Intra
STUB1 Q9UNE7 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
STUB1 Q9UNE7 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
STUB1 Q9UNE7 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
STUB1 Q9UNE7 NGFR Homo sapiens P08138 32814053
Intra
STUB1 Q9UNE7 NGFR Homo sapiens P08138 32814053
Intra
STUB1 Q9UNE7 NGFR Homo sapiens P08138 32814053
Intra
STUB1 Q9UNE7 MOS Homo sapiens P00540 25036637
Intra
STUB1 Q9UNE7 UBE2Q1 Homo sapiens Q7Z7E8 16275660
Intra
STUB1 Q9UNE7 UBE2Q1 Homo sapiens Q7Z7E8 16275660
Intra
STUB1 Q9UNE7 ATCAY Homo sapiens Q86WG3 16275660
Intra
STUB1 Q9UNE7 ATCAY Homo sapiens Q86WG3 16275660
Intra
STUB1 Q9UNE7 GLE1 Homo sapiens Q53GS7 32814053
Intra
STUB1 Q9UNE7 GLE1 Homo sapiens Q53GS7 32814053
Intra
STUB1 Q9UNE7 GLE1 Homo sapiens Q53GS7 32814053
Intra
STUB1 Q9UNE7 MPO Homo sapiens P05164 32814053
Intra
STUB1 Q9UNE7 MPO Homo sapiens P05164 32814053
Intra
STUB1 Q9UNE7 MPO Homo sapiens P05164 32814053
Intra
STUB1 Q9UNE7 COL25A1 Homo sapiens Q8NE08 32814053
Intra
STUB1 Q9UNE7 COL25A1 Homo sapiens Q8NE08 32814053
Intra
STUB1 Q9UNE7 COL25A1 Homo sapiens Q8NE08 32814053
Intra
STUB1 Q9UNE7 PEX7 Homo sapiens O00628-2 32814053
Intra
STUB1 Q9UNE7 PEX7 Homo sapiens O00628-2 32814053
Intra
STUB1 Q9UNE7 PEX7 Homo sapiens O00628-2 32814053
Intra
STUB1 Q9UNE7 SPTLC1 Homo sapiens O15269-2 32814053
Intra
STUB1 Q9UNE7 SPTLC1 Homo sapiens O15269-2 32814053
Intra
STUB1 Q9UNE7 SPTLC1 Homo sapiens O15269-2 32814053
Intra
STUB1 Q9UNE7 ALS2 Homo sapiens A0A0S2Z5Q7 32814053
Intra
STUB1 Q9UNE7 ALS2 Homo sapiens A0A0S2Z5Q7 32814053
Intra
STUB1 Q9UNE7 ALS2 Homo sapiens A0A0S2Z5Q7 32814053
Intra
STUB1 Q9UNE7 PANK2 Homo sapiens Q9BZ23-2 32814053
Intra
STUB1 Q9UNE7 PANK2 Homo sapiens Q9BZ23-2 32814053
Intra
STUB1 Q9UNE7 PANK2 Homo sapiens Q9BZ23-2 32814053
Intra
STUB1 Q9UNE7 NCAM1 Homo sapiens P13591 32814053
Intra
STUB1 Q9UNE7 NCAM1 Homo sapiens P13591 32814053
Intra
STUB1 Q9UNE7 NCAM1 Homo sapiens P13591 32814053
Intra
STUB1 Q9UNE7 TXN2 Homo sapiens Q99757 25416956
Intra
STUB1 Q9UNE7 HSP90AA1 Homo sapiens P07900 16307917
Intra
STUB1 Q9UNE7 HSP90AA1 Homo sapiens P07900
Y2H
16275660
Intra
STUB1 Q9UNE7 EGFR Homo sapiens P00533 20029029
Intra
STUB1 Q9UNE7 EGFR Homo sapiens P00533 24658140
Intra
STUB1 Q9UNE7 SQSTM1 Homo sapiens Q13501 32814053
Intra
STUB1 Q9UNE7 SQSTM1 Homo sapiens Q13501 32814053
Intra
STUB1 Q9UNE7 SQSTM1 Homo sapiens Q13501 32814053
Intra
STUB1 Q9UNE7 HSPA8 Homo sapiens P11142
Y2H
16275660
Intra
STUB1 Q9UNE7 HSPA8 Homo sapiens P11142 16293251
Intra
STUB1 Q9UNE7 HSPA8 Homo sapiens P11142 33961781
Intra
STUB1 Q9UNE7 HSP90AB1 Homo sapiens P08238 16293251
Intra
STUB1 Q9UNE7 HSP90AB1 Homo sapiens P08238
ITC
20618441
Intra
STUB1 Q9UNE7 HSPB1 Homo sapiens P04792 32814053
Intra
STUB1 Q9UNE7 HSPB1 Homo sapiens P04792 32814053
Intra
STUB1 Q9UNE7 HSPB1 Homo sapiens P04792 25277244
Intra
STUB1 Q9UNE7 HSPB1 Homo sapiens P04792 32814053
Intra
STUB1 Q9UNE7 BAG2 Homo sapiens O95816 25036637
Intra
STUB1 Q9UNE7 MAP3K2 Homo sapiens Q9Y2U5 20588253
Intra
STUB1 Q9UNE7 MAP3K2 Homo sapiens Q9Y2U5 20588253
Intra
STUB1 Q9UNE7 DAPK1 Homo sapiens P53355 29513927
Intra
STUB1 Q9UNE7 RAF1 Homo sapiens P04049 25036637
Intra
STUB1 Q9UNE7 MAPT Homo sapiens P10636 16275660
Intra
STUB1 Q9UNE7 MAPT Homo sapiens P10636 16275660
Intra
STUB1 Q9UNE7 RGS17 Homo sapiens Q9UGC6 32296183
Intra
STUB1 Q9UNE7 RGS17 Homo sapiens Q9UGC6 32296183
Intra
STUB1 Q9UNE7 PRKACA Homo sapiens P17612 32814053
Intra
STUB1 Q9UNE7 PRKACA Homo sapiens P17612 32814053
Intra
STUB1 Q9UNE7 PRKACA Homo sapiens P17612 32814053
Intra
STUB1 Q9UNE7 FYN Homo sapiens P06241 32814053
Intra
STUB1 Q9UNE7 FYN Homo sapiens P06241 32814053
Intra
STUB1 Q9UNE7 FYN Homo sapiens P06241 32814053
Intra
STUB1 Q9UNE7 SPRED1 Homo sapiens Q7Z699 32814053
Intra
STUB1 Q9UNE7 SPRED1 Homo sapiens Q7Z699 32814053
Intra
STUB1 Q9UNE7 SPRED1 Homo sapiens Q7Z699 32814053
Intra
STUB1 Q9UNE7 LRRK2 Homo sapiens Q5S007 29513927
Intra
STUB1 Q9UNE7 RUSC1 Homo sapiens Q9BVN2 25416956
Intra
STUB1 Q9UNE7 RUSC1 Homo sapiens Q9BVN2 25416956
Intra
STUB1 Q9UNE7 HSPA1A Homo sapiens P08107 25036637
Intra
STUB1 Q9UNE7 HSPA1A Homo sapiens P08107
Y2H
16275660
Intra
STUB1 Q9UNE7 HSPA1A Homo sapiens P08107
GMS
20618441
Intra
STUB1 Q9UNE7 HSPA1A Homo sapiens P08107 16275660
Intra
STUB1 Q9UNE7 A2M Homo sapiens P01023 32814053
Intra
STUB1 Q9UNE7 A2M Homo sapiens P01023 32814053
Intra
STUB1 Q9UNE7 A2M Homo sapiens P01023 32814053
Intra
STUB1 Q9UNE7 GAL Homo sapiens P22466 32814053
Intra
STUB1 Q9UNE7 GAL Homo sapiens P22466 32814053
Intra
STUB1 Q9UNE7 GAL Homo sapiens P22466 32814053
Intra
STUB1 Q9UNE7 UBE2L3 Homo sapiens P68036 32814053
Intra
STUB1 Q9UNE7 UBE2L3 Homo sapiens P68036 32814053
Intra
STUB1 Q9UNE7 UBE2L3 Homo sapiens P68036 32814053
Intra
STUB1 Q9UNE7 ACD Homo sapiens Q96AP0 21044950
Intra
STUB1 Q9UNE7 ACD Homo sapiens Q96AP0 21044950
Intra
STUB1 Q9UNE7 WFS1 Homo sapiens O76024 32814053
Intra
STUB1 Q9UNE7 WFS1 Homo sapiens O76024 32814053
Intra
STUB1 Q9UNE7 WFS1 Homo sapiens O76024 32814053
Intra
STUB1 Q9UNE7 MLF1 Homo sapiens P58340 25036637
Intra
STUB1 Q9UNE7 MLF1 Homo sapiens P58340 33961781
Intra
STUB1 Q9UNE7 BAG3 Homo sapiens O95817 25036637
Intra
STUB1 Q9UNE7 CCL28 Homo sapiens Q9NRJ3 25416956
Intra
STUB1 Q9UNE7 CCL28 Homo sapiens Q9NRJ3 25416956
Intra
STUB1 Q9UNE7 CCL28 Homo sapiens Q9NRJ3 25416956
Intra
STUB1 Q9UNE7 REC8 Homo sapiens O95072 25036637
Intra
STUB1 Q9UNE7 FOXP3 Homo sapiens Q9BZS1 23973223
Intra
STUB1 Q9UNE7 CYTH1 Homo sapiens Q15438 32814053
Intra
STUB1 Q9UNE7 CYTH1 Homo sapiens Q15438 32814053
Intra
STUB1 Q9UNE7 CYTH1 Homo sapiens Q15438 32814053
Cross
STUB1 Q9UNE7 Bag5 Rattus norvegicus Q5QJC9 21358815
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant STUB1 Proteins

Cat. No. Product Name Accession Purity
HY-P71340 STUB1 Protein, Human Q9UNE7 (M1-Y303) ≥ 95%, as determined by reducing SDS-PAGE.

STUB1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82351 STUB1 Antibody (YA2096) WB, ICC/IF, IP Human, Mouse, Rat

Related Diseases

Diseases Alias
Spinocerebellar Ataxia, Autosomal Recessive 16
  • Autosomal Recessive Spinocerebellar Ataxia 16

  • SCAR16

  • Autosomal Recessive Cerebellar Ataxia Due To Stub1 Deficiency

  • Spinocerebellar Ataxia Autosomal Recessive Type 16

  • Spinocerebellar Ataxia, Autosomal Recessive, 16

  • Ataxia, Spinocerebellar, Autosomal Recessive, Type 16

Spinocerebellar Ataxia 48
  • SCA48

Cerebellar Ataxia Type 48
  • Sca48

Gordon Holmes Syndrome
  • Cerebellar Ataxia And Hypogonadotropic Hypogonadism

  • Lhrh Deficiency And Ataxia

  • Cerebellar Ataxia-Hypogonadism Syndrome

  • GDHS

  • Cahh

  • Luteinizing Hormone-Releasing Hormone Deficiency With Ataxia

  • Gordon-Holmes Syndrome

  • Deficiency Of Luteinizing Hormone-Releasing Hormone With Ataxia

  • Luteinizing Hormone-Releasing Hormone, Deficiency Of, With Ataxia

  • Cerebellar Ataxia - Hypogonadism

  • Luteinizing Hormone Releasing Hormone, Deficiency Of With Ataxia

  • Ataxia, Cerebellar, And Hypogonadotropic Hypogonadism

Spinocerebellar Ataxia 15
  • SCA15

  • Spinocerebellar Ataxia Type 15

  • Spinocerebellar Ataxia Type 16

  • Sca16

  • Spinocerebellar Ataxia Type 15/16

  • Spinocerebellar Ataxia 16, Formerly

  • Sca16, Formerly

  • Spinocerebellar Ataxia 16

  • Sca15/16

  • Ataxia, Spinocerebellar, Type 15

Siderosis
  • Pulmonary Siderosis

  • Deposition Of Iron

  • Arc-Welders' Disease

  • Arc-Welders' Lung

  • Arc-Welders' Nodulation

  • Arc-Welders' Pneumoconiosis

  • Iron Oxide Lung

  • Iron Pneumoconiosis

  • Pneumoconiosis Siderotico

  • Siderotic Lung Disease

  • Steel Grinders' Disease

  • Welders' Lung

  • Welders' Siderosis

  • Lung Fibrosis With Siderosis

Dyslexia
Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Parkinson Disease, Late-Onset
  • Parkinson Disease

  • Parkinson'S Disease

  • PD

  • PARK

  • Parkinson Disease, Susceptibility To

  • Late Onset Parkinson'S Disease

  • Late Onset Parkinson Disease

  • Paralysis Agitans

  • Primary Parkinsonism

  • Idiopathic Parkinson Disease

  • Parkinson'S

  • Parkinson Disease, Late-Onset, Susceptibility To

  • Parkinson Disease, Age Of Onset, Modifier

  • Lewy Body Parkinson Disease

  • Idiopathic Parkinson'S Disease

  • Pd - [Parkinson Disease]

  • Parkinson Disease Nos

  • Parkinson, Nos

  • Primary Parkinson Disease

Hematuria, Benign Familial
  • Benign Familial Hematuria

  • BFH

  • Thin Membrane Nephropathy

  • Tmn

  • Thin Basement Membrane Nephropathy

  • Thin-Basement-Membrane Nephropathy

  • Hematuria, Familial Benign

  • Hematuria Benign Familial

  • Hematuria, Benign, Familial

  • Thin Basement Membrane Disease

Acute Tympanitis
  • Acute Myringitis

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

Cystic Fibrosis
  • Mucoviscidosis

  • CF

  • Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

  • Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

  • Cystic Fibrosis Lung Disease, Modifier Of

  • Cystic Fibrosis Of Pancreas

  • Fibrocystic Disease Of Pancreas

  • Cf - [Cystic Fibrosis]

  • Cystic Fibrosis Nos

  • Fibrocystic Disease

  • Fibrocystic Disease Of The Pancreas

  • Mucoviscidosis Of Pancreas

  • Nonproliferative Fibrocystic Disease

  • Pancreatic Cystic Fibrosis

Spondylocostal Dysostosis 3, Autosomal Recessive
  • SCDO3

  • Spondylocostal Dysostosis, Autosomal Recessive 3

  • Spondylocostal Dysostosis 3

  • Autosomal Recessive Spondylocostal Dysostosis 3

  • Doid:0112361

  • Dysostosis, Spondylocostal, Autosomal Recessive, Type 3

  • Jarcho-Levin Syndrome

Dystonia
  • Dystonic Disease

  • Dystonic Disorder

  • Dystonia Disorders

  • Neuroleptic Dyskinesia

Autosomal Dominant Cerebellar Ataxia
  • Spinocerebellar Ataxia

  • Adca

  • Pierre Marie Cerebellar Ataxia

  • Ataxia, Spinocerebellar

  • Sca

  • Autosomal Dominant Spinocerebellar Ataxia

  • Spinocerebellar Ataxias

Myelodysplastic Syndrome
  • Myelodysplastic Syndromes

  • Myelodysplasia

  • MDS

  • Myelodysplastic Syndrome Included

  • Myelodysplastic Syndrome, Susceptibility To, Included

  • Myelodysplastic Syndrome, Somatic

  • Myelodysplastic Syndrome, Susceptibility To

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

Attention Deficit-Hyperactivity Disorder
  • Attention Deficit Hyperactivity Disorder

  • ADHD

  • Attention Deficit Disorder

  • Attention Deficit-Hyperactivity Disorder, Susceptibility To

  • Attention Deficit Disorder With Hyperactivity

  • Hyperkinetic Disorder

  • Hyperactivity Of Childhood

  • Attention-Deficit/Hyperactivity Disorder

  • Add

  • Addh

  • Attention Deficit

  • Attention Deficit Disorder Of Childhood With Hyperactivity

  • Attention Deficit Disorder With Hyperactivity Syndrome

  • Hyperkinetic Syndrome

  • Attention-Deficit Hyperactivity Disorder

  • Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type

  • Disturbance Of Activity And Attention

  • Disorder Of Activity And Attention

  • Adhd - [Attention Deficit Hyperactivity Disorder]

  • Hyperkinetic Disorders

  • Disorder Of Activity And Attention With Hyperkinesia

  • Attention Deficit Syndrome With Hyperactivity

Leukemia, Acute Myeloid
  • Acute Myeloid Leukemia

  • Leukemia, Acute Myelogenous

  • Acute Myelogenous Leukemia

  • AML

  • Leukemia, Acute Myeloid, Susceptibility To

  • Acute Myeloblastic Leukemia

  • Leukemia, Acute Myeloid, Reduced Survival In, Somatic

  • Acute Myeloid Leukaemia

  • Leukemia, Myelocytic, Acute

  • Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

  • Secondary Aml

  • Acute Myelocytic Leukemia

  • Acute Myeloid Leukemia, Somatic

  • Leukemia, Acute Myeloid, Somatic

  • Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

  • Acute Myeloblastic Leukaemia

  • Acute Myelogenous Leukaemia

  • Aml - Acute Myeloid Leukemia

  • Acute Myeloid Leukemia With Cebpa Somatic Mutations

  • Aml With Cebpa Somatic Mutations

  • Inherited Acute Myeloid Leukemia

  • Familial Aml

  • Inherited Aml

  • Pure Familial Aml

  • Pure Familial Acute Myeloid Leukemia

  • Secondary Acute Myeloid Leukemia

  • Therapy-Related Aml And Myelodysplastic Syndrome

  • Acute Myeloid Leukemia, Secondary

  • Acute Non-Lymphoblastic Leukemia

  • Acute Non-Lymphocytic Leukemia

  • Acute Biphenotypic Leukemia

  • Acute Undifferentiated Leukemia

  • Acute Myeloblastic Leukaemia With Multilineage Dysplasia

  • Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

  • Acute Myeloid Leukaemia With Myelodysplasia-Related Features

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
Bos taurus STUB1 VGNC VGNC:58615
Rattus norvegicus STUB1 RGD RGD:1306167
Canis familiaris STUB1 VGNC VGNC:54073
Macaca mulatta STUB1 VGNC VGNC:99598
Felis catus STUB1 VGNC VGNC:65805
Mus musculus STUB1 MGD MGI:1891731
Others STUB1 NCBI