PCGF1 - polycomb group ring finger 1 Gene

Also Known as NSPC1; RNF68; RNF3A-2; 2010002K04Rik

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 84759

About PCGF1

Cytogenetic location: 2p13.1 Genomic coordinates (GRCh38): 2:74,505,043-74,507,695 (from NCBI)

This gene has 7 transcripts (splice variants), 203 orthologues and 7 paralogues. Ubiquitous expression in thyroid (RPKM 3.8), testis (RPKM 3.8) and 25 other tissues.

Summary

PCGF1 is a mammalian homolog of the Drosophila polycomb group genes, which act as transcriptional repressors to regulate anterior-posterior patterning in early embryonic development (Nunes et al., 2001 [PubMed 11287196]). See also PCGF2 (MIM 600346).[supplied by OMIM, Aug 2008]

PCGF1 Products (1)

mRNA Protein Name
NM_032673.3 NP_116062.2 polycomb group RING finger protein 1
Molecular Function GO Annotation Evidence Verweise Source
enables protein binding IPI
IPI: Inferred from physical interaction
16943429 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in chromatin remodeling IDA
IDA: Inferred from direct assay
16943429 GOA
involved in chromatin remodeling IMP
IMP: Inferred from mutant phenotype
26151332 GOA
Cellular Component GO Annotation Evidence Verweise Source
part of PcG protein complex IDA
IDA: Inferred from direct assay
16943429 GOA
located in nucleus IDA
IDA: Inferred from direct assay
21282530 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

PCGF1 Protein Structure

zf-C3HC4

zf-C3HC4: Zinc finger, C3HC4 type (RING finger) (47 - 85)

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

polycomb group RING finger protein 1

  • RING finger protein 68

PCGF1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
PCGF1 Q9BSM1 FCHO1 Homo sapiens A0A0C3SFZ9 32296183
Intra
PCGF1 Q9BSM1 FCHO1 Homo sapiens A0A0C3SFZ9 32296183
Intra
PCGF1 Q9BSM1 CBX7 Homo sapiens O95931 21282530
Intra
PCGF1 Q9BSM1 CBX6 Homo sapiens O95503 21282530
Intra
PCGF1 Q9BSM1 CBX8 Homo sapiens Q9HC52
TAP
27705803
Intra
PCGF1 Q9BSM1 CBX8 Homo sapiens Q9HC52 27505670
Intra
PCGF1 Q9BSM1 CBX8 Homo sapiens Q9HC52
TAP
27505670
Intra
PCGF1 Q9BSM1 CBX8 Homo sapiens Q9HC52 33961781
Intra
PCGF1 Q9BSM1 RNF2 Homo sapiens Q99496 32296183
Intra
PCGF1 Q9BSM1 RNF2 Homo sapiens Q99496
TAP
27705803
Intra
PCGF1 Q9BSM1 RNF2 Homo sapiens Q99496 16943429
Intra
PCGF1 Q9BSM1 RNF2 Homo sapiens Q99496 33961781
Intra
PCGF1 Q9BSM1 RNF2 Homo sapiens Q99496
TAP
27505670
Intra
PCGF1 Q9BSM1 RNF2 Homo sapiens Q99496 27505670
Intra
PCGF1 Q9BSM1 RNF2 Homo sapiens Q99496 32296183
Intra
PCGF1 Q9BSM1 RING1 Homo sapiens Q06587
TAP
27505670
Intra
PCGF1 Q9BSM1 RING1 Homo sapiens Q06587 33961781
Intra
PCGF1 Q9BSM1 RING1 Homo sapiens Q06587 22493164
Intra
PCGF1 Q9BSM1 RING1 Homo sapiens Q06587
TAP
27705803
Intra
PCGF1 Q9BSM1 RING1 Homo sapiens Q06587 22493164
Intra
PCGF1 Q9BSM1 RING1 Homo sapiens Q06587 16943429
Intra
PCGF1 Q9BSM1 BCOR Homo sapiens Q6W2J9 16943429
Intra
PCGF1 Q9BSM1 BCOR Homo sapiens Q6W2J9 16943429
Intra
PCGF1 Q9BSM1 BCOR Homo sapiens Q6W2J9
TAP
27505670
Intra
PCGF1 Q9BSM1 BCOR Homo sapiens Q6W2J9 16943429
Intra
PCGF1 Q9BSM1 BCOR Homo sapiens Q6W2J9 33961781
Intra
PCGF1 Q9BSM1 BCOR Homo sapiens Q6W2J9 27505670
Intra
PCGF1 Q9BSM1 BCOR Homo sapiens Q6W2J9
TAP
27705803
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Pontocerebellar Hypoplasia, Type 13
  • PCH13

  • Pontocerebellar Hypoplasia Type 13

  • Pontocerebellar Hypoplasia 13

  • Doid:0112332

  • Hypoplasia, Pontocerebellar, Type 13

Microphthalmia, Syndromic 2
  • Oculofaciocardiodental Syndrome

  • Ofcd Syndrome

  • MCOPS2

  • Microphthalmia, Cataracts, Radiculomegaly, And Septal Heart Defects

  • Syndromic Microphthalmia 2

  • Anop2

  • Cataract-Microphthalmia-Radiculomegaly-Cardiac Septal Defect Syndrome

  • Maa2

  • Microphthalmia Cataracts Radiculomegaly And Septal Heart Defects

  • Syndromic Microphthalmia Type 2

  • Oculo-Facio-Cardio-Dental Syndrome

  • Anop2, Formerly

  • Maa2, Formerly

  • Microphthalmia Syndromic 2

  • Oculo Facio Cardio Dental Syndrome

  • Microphthalmia, Syndromic, 2

  • Marashi-Gorlin Syndrome

  • Microphthalmia, Cataracts, Radiculomegaly And Septal Heart Defects

  • Microphthalmia, Syndromic, Type 2

Syndromic Microphthalmia
  • Microphthalmia, Syndromic

Diffuse Large B-Cell Lymphoma
  • Dlbcl

  • Diffuse Large B-Cell Lymphoma, Not Otherwise Specified

  • Large B-Cell Diffuse Lymphoma

  • Lymphoma, Large B-Cell, Diffuse

  • Dlbcl - [Diffuse Large B-Cell Lymphoma]

  • Diffuse Large Beta Cell Lymphoma

Microphthalmia, Syndromic 1
  • MCOPS1

  • Lenz Microphthalmia Syndrome

  • Lenz Dysplasia

  • Mcops4

  • Syndromic Microphthalmia 1

  • Lenz Microphthalmia

  • Maa

  • Microphthalmia Or Anophthalmos With Associated Anomalies

  • Syndromic Microphthalmia Type 4

  • Microphthalmia, Syndromic 4

  • Microphthalmia, Syndromic 4, Formerly

  • Mcops4, Formerly

  • Anop1, Formerly

  • Maa, Formerly

  • Lenz Type Microphthalmia

  • Syndromic Microphthalmia 4

  • Microphthalmia Lenz Type

  • Microphthalmia Syndromic 1

  • Syndromic Microphthalmia Type 1

  • Microphthalmia Syndromic 4

  • Microphthalmia With Ankyloblepharon And Intellectual Disability

  • Microphthalmia, Lenz Type

  • Microphthalmia-Ankyloblepharon-Intellectual Disability Syndrome

  • Microphthalmia, Syndromic, 1

  • Anop1

  • Microphthalmia, Syndromic, Type 1

Kidney Clear Cell Sarcoma
  • Clear Cell Sarcoma Of Kidney

  • Childhood Kidney Clear Cell Sarcoma

  • Renal Clear Cell Sarcoma

  • Ccsk

  • Clear Cell Sarcoma Of The Kidney

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

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 PCGF1 MGD MGI:1917087
Felis catus PCGF1 VGNC VGNC:81141
Canis familiaris PCGF1 VGNC VGNC:44300
Bos taurus PCGF1 VGNC VGNC:32626
Macaca mulatta PCGF1 VGNC VGNC:75640
Rattus norvegicus PCGF1 RGD RGD:1549782
Others PCGF1 NCBI