PHF1 - PHD finger protein 1 Gene

Also Known as PCL1; PHF2; hPHF1; MTF2L2; TDRD19C

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5252

About PHF1

Cytogenetic location: 6p21.32 Genomic coordinates (GRCh38): 6:33,410,412-33,416,439 (from NCBI)

This gene has 11 transcripts (splice variants), 1 gene allele, 193 orthologues and 2 paralogues. Ubiquitous expression in ovary (RPKM 47.5), testis (RPKM 44.7) and 25 other tissues.

Summary

This gene encodes a Polycomb group protein. The protein is a component of a histone H3 lysine-27 (H3K27)-specific methyltransferase complex, and functions in transcriptional repression of homeotic genes. The protein is also recruited to double-strand breaks, and reduced protein levels results in X-ray sensitivity and increased homologous recombination. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]

PHF1 Products (2)

mRNA Protein Name
NM_002636.5 NP_002627.2 PHD finger protein 1 isoform a
NM_024165.3 NP_077084.2 PHD finger protein 1 isoform b
Molecular Function GO Annotation Evidence References Source
enables histone methyltransferase binding IPI
IPI: Inferred from physical interaction
29628311 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
29628311 GOA
enables methylated histone binding IDA
IDA: Inferred from direct assay
23142980 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11571280 GOA
enables transcription corepressor binding IPI
IPI: Inferred from physical interaction
29628311 GOA
Biological Process GO Annotation Evidence References Source
involved in DNA repair-dependent chromatin remodeling IDA
IDA: Inferred from direct assay
23142980 GOA
Cellular Component GO Annotation Evidence References Source
part of ESC/E(Z) complex IDA
IDA: Inferred from direct assay
23273982 GOA
colocalizes with centrosome IDA
IDA: Inferred from direct assay
20873783 GOA
located in nucleus IDA
IDA: Inferred from direct assay
23273982 GOA
located in site of double-strand break IDA
IDA: Inferred from direct assay
23142980 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

PHF1 Protein Structure

PHD

PHD: PHD-finger (90 - 140)

Mtf2_C

Mtf2_C: Polycomb-like MTF2 factor 2 (528 - 564)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 567 a.a.
Protein Preferred Names Protein Names

PHD finger protein 1

  • hPCl1

PHF1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
PHF1 O43189 KRT40 Homo sapiens Q6A162 32296183
Intra
PHF1 O43189 KRT40 Homo sapiens Q6A162 32296183
Intra
PHF1 O43189 KRT40 Homo sapiens Q6A162 32296183
Intra
PHF1 O43189 PATZ1 Homo sapiens Q9HBE1-4 32296183
Intra
PHF1 O43189 PATZ1 Homo sapiens Q9HBE1-4 32296183
Intra
PHF1 O43189 PATZ1 Homo sapiens Q9HBE1-4 32296183
Intra
PHF1 O43189 ZNF526 Homo sapiens Q8TF50 32296183
Intra
PHF1 O43189 ZNF526 Homo sapiens Q8TF50 32296183
Intra
PHF1 O43189 ZNF526 Homo sapiens Q8TF50 32296183
Intra
PHF1 O43189 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
PHF1 O43189 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
PHF1 O43189 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
PHF1 O43189 ABI2 Homo sapiens Q9NYB9-2 32296183
Intra
PHF1 O43189 ABI2 Homo sapiens Q9NYB9-2 32296183
Intra
PHF1 O43189 ABI2 Homo sapiens Q9NYB9-2 32296183
Intra
PHF1 O43189 RBBP8NL Homo sapiens Q8NC74 32296183
Intra
PHF1 O43189 RBBP8NL Homo sapiens Q8NC74 32296183
Intra
PHF1 O43189 RBBP8NL Homo sapiens Q8NC74 32296183
Intra
PHF1 O43189 GPRASP3 Homo sapiens Q6PI77 32296183
Intra
PHF1 O43189 GPRASP3 Homo sapiens Q6PI77 32296183
Intra
PHF1 O43189 GPRASP3 Homo sapiens Q6PI77 32296183
Intra
PHF1 O43189 TLE5 Homo sapiens Q08117-2 32296183
Intra
PHF1 O43189 TLE5 Homo sapiens Q08117-2 32296183
Intra
PHF1 O43189 TLE5 Homo sapiens Q08117-2 32296183
Intra
PHF1 O43189 TP53BP2 Homo sapiens Q05BL1 32296183
Intra
PHF1 O43189 TP53BP2 Homo sapiens Q05BL1 32296183
Intra
PHF1 O43189 TP53BP2 Homo sapiens Q05BL1 32296183
Intra
PHF1 O43189 SPAG8 Homo sapiens Q99932-2 32296183
Intra
PHF1 O43189 SPAG8 Homo sapiens Q99932-2 32296183
Intra
PHF1 O43189 SPAG8 Homo sapiens Q99932-2 32296183
Intra
PHF1 O43189 ZIM2 Homo sapiens Q9NZV7 32296183
Intra
PHF1 O43189 ZIM2 Homo sapiens Q9NZV7 32296183
Intra
PHF1 O43189 ZIM2 Homo sapiens Q9NZV7 32296183
Intra
PHF1 O43189 USP54 Homo sapiens Q70EL1-9 32296183
Intra
PHF1 O43189 USP54 Homo sapiens Q70EL1-9 32296183
Intra
PHF1 O43189 USP54 Homo sapiens Q70EL1-9 32296183
Intra
PHF1 O43189 BOLL Homo sapiens Q8N9W6-4 32296183
Intra
PHF1 O43189 BOLL Homo sapiens Q8N9W6-4 32296183
Intra
PHF1 O43189 BOLL Homo sapiens Q8N9W6-4 32296183
Intra
PHF1 O43189 DISC1 Homo sapiens Q9NRI5-2 32296183
Intra
PHF1 O43189 DISC1 Homo sapiens Q9NRI5-2 32296183
Intra
PHF1 O43189 DISC1 Homo sapiens Q9NRI5-2 32296183
Intra
PHF1 O43189 ZBTB10 Homo sapiens Q96DT7-3 32296183
Intra
PHF1 O43189 ZBTB10 Homo sapiens Q96DT7-3 32296183
Intra
PHF1 O43189 ZBTB10 Homo sapiens Q96DT7-3 32296183
Intra
PHF1 O43189 PRR20D Homo sapiens P86480 32296183
Intra
PHF1 O43189 PRR20D Homo sapiens P86480 32296183
Intra
PHF1 O43189 PRR20D Homo sapiens P86480 32296183
Intra
PHF1 O43189 PRR20D Homo sapiens P86480 32296183
Intra
PHF1 O43189 TOX2 Homo sapiens Q96NM4-3 32296183
Intra
PHF1 O43189 TOX2 Homo sapiens Q96NM4-3 32296183
Intra
PHF1 O43189 TOX2 Homo sapiens Q96NM4-3 32296183
Intra
PHF1 O43189 CSTPP1 Homo sapiens Q9H6J7-2 32296183
Intra
PHF1 O43189 CSTPP1 Homo sapiens Q9H6J7-2 32296183
Intra
PHF1 O43189 CSTPP1 Homo sapiens Q9H6J7-2 32296183
Intra
PHF1 O43189 PIBF1 Homo sapiens Q4G0R1 32296183
Intra
PHF1 O43189 PIBF1 Homo sapiens Q4G0R1 32296183
Intra
PHF1 O43189 PIBF1 Homo sapiens Q4G0R1 32296183
Intra
PHF1 O43189 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
PHF1 O43189 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
PHF1 O43189 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
PHF1 O43189 ZNF500 Homo sapiens O60304 32296183
Intra
PHF1 O43189 ZNF500 Homo sapiens O60304 32296183
Intra
PHF1 O43189 ZNF500 Homo sapiens O60304 32296183
Intra
PHF1 O43189 LBX1 Homo sapiens P52954 32296183
Intra
PHF1 O43189 LBX1 Homo sapiens P52954 32296183
Intra
PHF1 O43189 LBX1 Homo sapiens P52954 32296183
Intra
PHF1 O43189 VAC14 Homo sapiens Q08AM6 25416956
Intra
PHF1 O43189 VAC14 Homo sapiens Q08AM6 25416956
Intra
PHF1 O43189 EFHC2 Homo sapiens Q5JST6 32296183
Intra
PHF1 O43189 EFHC2 Homo sapiens Q5JST6 32296183
Intra
PHF1 O43189 EFHC2 Homo sapiens Q5JST6 32296183
Intra
PHF1 O43189 DPF1 Homo sapiens Q92782-2 32296183
Intra
PHF1 O43189 DPF1 Homo sapiens Q92782-2 32296183
Intra
PHF1 O43189 DPF1 Homo sapiens Q92782-2 32296183
Intra
PHF1 O43189 FOSB Homo sapiens P53539 32296183
Intra
PHF1 O43189 FOSB Homo sapiens P53539 32296183
Intra
PHF1 O43189 FOSB Homo sapiens P53539 32296183
Intra
PHF1 O43189 SMG9 Homo sapiens Q9H0W8 32296183
Intra
PHF1 O43189 ARRDC3 Homo sapiens Q96B67 32296183
Intra
PHF1 O43189 ARRDC3 Homo sapiens Q96B67 32296183
Intra
PHF1 O43189 ARRDC3 Homo sapiens Q96B67 32296183
Intra
PHF1 O43189 ATXN7L1 Homo sapiens Q9ULK2 25416956
Intra
PHF1 O43189 ATXN7L1 Homo sapiens Q9ULK2 25416956
Intra
PHF1 O43189 ATXN7L1 Homo sapiens Q9ULK2 25416956
Intra
PHF1 O43189 PDLIM7 Homo sapiens Q9NR12 25416956
Intra
PHF1 O43189 PDLIM7 Homo sapiens Q9NR12 25416956
Intra
PHF1 O43189 PDLIM7 Homo sapiens Q9NR12 25416956
Intra
PHF1 O43189 PFDN5 Homo sapiens Q99471 32296183
Intra
PHF1 O43189 PFDN5 Homo sapiens Q99471 32296183
Intra
PHF1 O43189 PFDN5 Homo sapiens Q99471 32296183
Intra
PHF1 O43189 ZNF688 Homo sapiens P0C7X2 32296183
Intra
PHF1 O43189 ZNF688 Homo sapiens P0C7X2 32296183
Intra
PHF1 O43189 ZNF688 Homo sapiens P0C7X2 32296183
Intra
PHF1 O43189 BIRC7 Homo sapiens Q96CA5 31515488
Intra
PHF1 O43189 BIRC7 Homo sapiens Q96CA5 25416956
Intra
PHF1 O43189 BIRC7 Homo sapiens Q96CA5 25416956
Intra
PHF1 O43189 BIRC7 Homo sapiens Q96CA5 25416956
Intra
PHF1 O43189 ZRANB1 Homo sapiens Q9UGI0 32296183
Intra
PHF1 O43189 ZRANB1 Homo sapiens Q9UGI0 32296183
Intra
PHF1 O43189 ZRANB1 Homo sapiens Q9UGI0 32296183
Intra
PHF1 O43189 EZH2 Homo sapiens Q15910 33961781
Intra
PHF1 O43189 EZH2 Homo sapiens Q15910 23142980
Intra
PHF1 O43189 EZH2 Homo sapiens Q15910
Y2H
11571280
Intra
PHF1 O43189 EZH2 Homo sapiens Q15910
TAP
24981860
Intra
PHF1 O43189 EZH2 Homo sapiens Q15910
TAP
27705803
Intra
PHF1 O43189 GOLGA6L9 Homo sapiens A6NEM1 32296183
Intra
PHF1 O43189 GOLGA6L9 Homo sapiens A6NEM1 32296183
Intra
PHF1 O43189 INCA1 Homo sapiens Q0VD86 32296183
Intra
PHF1 O43189 INCA1 Homo sapiens Q0VD86 32296183
Intra
PHF1 O43189 INCA1 Homo sapiens Q0VD86 32296183
Intra
PHF1 O43189 FHL2 Homo sapiens Q14192 32296183
Intra
PHF1 O43189 BHLHE40 Homo sapiens O14503 32296183
Intra
PHF1 O43189 BHLHE40 Homo sapiens O14503 32296183
Intra
PHF1 O43189 ZBTB16 Homo sapiens Q05516 32296183
Intra
PHF1 O43189 ZBTB16 Homo sapiens Q05516 32296183
Intra
PHF1 O43189 ZBTB16 Homo sapiens Q05516 32296183
Intra
PHF1 O43189 ZNF71 Homo sapiens Q9NQZ8 32296183
Intra
PHF1 O43189 ZNF71 Homo sapiens Q9NQZ8 32296183
Intra
PHF1 O43189 ZNF71 Homo sapiens Q9NQZ8 32296183
Intra
PHF1 O43189 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
PHF1 O43189 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
PHF1 O43189 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
PHF1 O43189 TFCP2 Homo sapiens Q12800 25416956
Intra
PHF1 O43189 TFCP2 Homo sapiens Q12800 25416956
Intra
PHF1 O43189 MDFI Homo sapiens Q99750 32296183
Intra
PHF1 O43189 MDFI Homo sapiens Q99750 32296183
Intra
PHF1 O43189 MDFI Homo sapiens Q99750 32296183
Intra
PHF1 O43189 KIAA0408 Homo sapiens Q6ZU52 32296183
Intra
PHF1 O43189 KIAA0408 Homo sapiens Q6ZU52 32296183
Intra
PHF1 O43189 KIAA0408 Homo sapiens Q6ZU52 32296183
Intra
PHF1 O43189 KIAA0408 Homo sapiens Q6ZU52 32296183
Intra
PHF1 O43189 CALCOCO2 Homo sapiens Q13137 25416956
Intra
PHF1 O43189 CALCOCO2 Homo sapiens Q13137 25416956
Intra
PHF1 O43189 CALCOCO2 Homo sapiens Q13137 25416956
Intra
PHF1 O43189 TRIM23 Homo sapiens P36406 25416956
Intra
PHF1 O43189 TRIM23 Homo sapiens P36406 25416956
Intra
PHF1 O43189 TRIM23 Homo sapiens P36406 25416956
Intra
PHF1 O43189 RBPMS Homo sapiens Q93062 25416956
Intra
PHF1 O43189 RBPMS Homo sapiens Q93062 25416956
Intra
PHF1 O43189 RBPMS Homo sapiens Q93062 16189514
Intra
PHF1 O43189 RBPMS Homo sapiens Q93062-3 32296183
Intra
PHF1 O43189 RBPMS Homo sapiens Q93062-3 32296183
Intra
PHF1 O43189 RBPMS Homo sapiens Q93062-3 32296183
Intra
PHF1 O43189 LZTS2 Homo sapiens Q9BRK4 32296183
Intra
PHF1 O43189 LZTS2 Homo sapiens Q9BRK4 32296183
Intra
PHF1 O43189 LZTS2 Homo sapiens Q9BRK4 32296183
Intra
PHF1 O43189 SORBS3 Homo sapiens O60504 32296183
Intra
PHF1 O43189 SORBS3 Homo sapiens O60504 32296183
Intra
PHF1 O43189 SORBS3 Homo sapiens O60504 32296183
Intra
PHF1 O43189 THAP1 Homo sapiens Q9NVV9 32296183
Intra
PHF1 O43189 THAP1 Homo sapiens Q9NVV9 32296183
Intra
PHF1 O43189 THAP1 Homo sapiens Q9NVV9 32296183
Intra
PHF1 O43189 THAP1 Homo sapiens Q9NVV9 16189514
Intra
PHF1 O43189 HSD17B14 Homo sapiens Q9BPX1 32296183
Intra
PHF1 O43189 HSD17B14 Homo sapiens Q9BPX1 31515488
Intra
PHF1 O43189 HSD17B14 Homo sapiens Q9BPX1 25416956
Intra
PHF1 O43189 HSD17B14 Homo sapiens Q9BPX1 32296183
Intra
PHF1 O43189 HSD17B14 Homo sapiens Q9BPX1 25416956
Intra
PHF1 O43189 HSD17B14 Homo sapiens Q9BPX1 32296183
Intra
PHF1 O43189 GPKOW Homo sapiens Q92917 32296183
Intra
PHF1 O43189 AVPI1 Homo sapiens Q5T686 32296183
Intra
PHF1 O43189 AVPI1 Homo sapiens Q5T686 32296183
Intra
PHF1 O43189 AVPI1 Homo sapiens Q5T686 32296183
Intra
PHF1 O43189 NAB2 Homo sapiens Q15742 32296183
Intra
PHF1 O43189 NAB2 Homo sapiens Q15742 32296183
Intra
PHF1 O43189 NAB2 Homo sapiens Q15742 32296183
Intra
PHF1 O43189 ARID5A Homo sapiens Q03989 32296183
Intra
PHF1 O43189 ARID5A Homo sapiens Q03989 32296183
Intra
PHF1 O43189 ARID5A Homo sapiens Q03989 32296183
Intra
PHF1 O43189 TNS2 Homo sapiens Q63HR2 32296183
Intra
PHF1 O43189 TNS2 Homo sapiens Q63HR2 32296183
Intra
PHF1 O43189 TNS2 Homo sapiens Q63HR2 32296183
Intra
PHF1 O43189 IRAK1BP1 Homo sapiens Q5VVH5 32296183
Intra
PHF1 O43189 IRAK1BP1 Homo sapiens Q5VVH5 32296183
Intra
PHF1 O43189 IRAK1BP1 Homo sapiens Q5VVH5 32296183
Intra
PHF1 O43189 MORN3 Homo sapiens Q6PF18 32296183
Intra
PHF1 O43189 MORN3 Homo sapiens Q6PF18 32296183
Intra
PHF1 O43189 MORN3 Homo sapiens Q6PF18 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

PHF1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P810243 PHF1 Antibody (YA9587) WB, IP, ELISA human
HY-P811113 PHF1 Antibody WB, IHC-P Human, Bovine

Related Diseases

Diseases Alias
Ossifying Fibromyxoid Tumor
  • Ossifying Fibromyxoid Tumour

  • Ossifying Fibromyxoma

Endometrial Stromal Nodule
Endometrial Stromal Tumor
  • Endometrial Stromal Neoplasm

  • Endometrial Stromal Tumors

Myxoid Leiomyosarcoma
  • Leiomyosarcoma, Myxoid

Endometrial Stromal Sarcoma
  • Ess

  • Endometrial Stromal Sarcoma, High Grade

  • Undifferentiated Endometrial Sarcoma

  • Stromal Sarcoma Of The Corpus Uteri

  • Sarcoma Endometrial Stromal

  • Sarcoma, Endometrial Stromal

  • Undifferentiated Stromal Sarcoma

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

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

Adenosarcoma
  • Mullerian Adenosarcoma

Cellular Leiomyoma
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

Vaginal Endometrial Stromal Sarcoma
Vagina Sarcoma
  • Sarcoma Of The Vagina

  • Vaginal Sarcoma

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

Ovarian Sex-Cord Stromal Tumor
  • Ovarian Sex Cord Tumor With Annular Tubules

  • Ovarian Sex Cord-Stromal Tumor

  • Stromal Tumor Of Ovary

Arteriolosclerosis
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

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]

Movement Disease
  • Movement Disorders

  • Movement Disorder

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

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

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
Mus musculus PHF1 MGD MGI:98647
Rattus norvegicus PHF1 RGD RGD:1303205
Macaca mulatta PHF1 VGNC VGNC:75973
Canis familiaris PHF1 VGNC VGNC:44479
Felis catus PHF1 VGNC VGNC:102482
Bos taurus PHF1 VGNC VGNC:32812
Others PHF1 NCBI