1. Gene
  2. REV1 - REV1 DNA directed polymerase Gene

REV1 - REV1 DNA directed polymerase Gene

Homo sapiens

Also known as REV1L; AIBP80

Gene ID: 51455 | Gene type: protein coding

About REV1

Cytogenetic location: 2q11.2 Genomic coordinates (GRCh38): 2:99,400,477-99,490,202 (from NCBI)

This gene has 16 transcripts (splice variants), 208 orthologues and 5 paralogues. Ubiquitous expression in endometrium (RPKM 6.5), testis (RPKM 6.4) and 25 other tissues.

Summary

This gene encodes a protein with similarity to the S. cerevisiae mutagenesis protein Rev1. The Rev1 proteins contain a BRCT domain, which is important in protein-protein interactions. A suggested role for the human Rev1-like protein is as a scaffold that recruits DNA polymerases involved in translesion synthesis (TLS) of damaged DNA. [provided by RefSeq, Mar 2016]

REV1 Products(7)

mRNA Protein Name
NM_001037872.3 NP_001032961.1 DNA repair protein REV1 isoform 2
NM_001321454.2 NP_001308383.1 DNA repair protein REV1 isoform 3
NM_001321455.2 NP_001308384.1 DNA repair protein REV1 isoform 4
NM_001321458.2 NP_001308387.1 DNA repair protein REV1 isoform 5
NM_001321459.2 NP_001308388.1 DNA repair protein REV1 isoform 6
NM_001321460.2 NP_001308389.1 DNA repair protein REV1 isoform 6
NM_016316.4 NP_057400.1 DNA repair protein REV1 isoform 1

REV1 Protein Structure

BRCT

BRCT: BRCA1 C Terminus (BRCT) domain (46 - 118)

IMS

IMS: impB/mucB/samB family (422 - 621)

IMS_C

IMS_C: impB/mucB/samB family C-terminal domain (700 - 825)

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Protein Preferred Names Protein Names

DNA repair protein REV1

REV1 homolog

Related Diseases

Diseases Alias
Xeroderma Pigmentosum, Variant Type

Xeroderma Pigmentosum

XPV

Xeroderma Pigmentosum Variant Type

Xeroderma Pigmentosum With Normal Dna Repair Rates

Photosensitivity With Defective Dna Synthesis

Xp

De Sanctis-Cacchione Syndrome

Desanctis-Cacchione Syndrome

Xeroderma Pigmentosa

Xerodermic Idiocy

Xeroderma Pigmentosum Variant

Xp - [Xeroderma Pigmentosum]

Atrophoderma Pigmentosum

Fanconi Anemia, Complementation Group F

Fanconi Anemia Complementation Group F

FANCF

Interstitial Nephritis, Karyomegalic

Karyomegalic Interstitial Nephritis

KMIN

Kin

Systemic Karyomegaly

Karyomegalic Tubulointerstitial Nephritis

Ktn

Aplastic Anemia

Aplastic Anemia, Susceptibility To

Anemia Aplastic

Idiopathic Aplastic Anemia

Secondary Aplastic Anemia

Idiopathic Bone Marrow Failure

Aplastic Anemia Idiopathic

AA

Anemia, Aplastic

Aplastic Anemia, Idiopathic

Erythroid Aplasia

Aa - [Aplastic Anaemia]

Haematopoietic Aplasia

Aleukia Haemorrhagica

Anaemia Due To Decreased Red Cell Production

Aplasia Bone Marrow

Aplastic Bone Marrow

Hypoplastic Anaemia Nos

Myeloid Bone Marrow Aplasia

Pancytopenia

Panhaematopenia

Hypoproliferative Anaemia

Medullary Hypoplasia

Red Blood Cells Hypoplastic Anaemia

Panmyelophthisis

Panhemocytopenia

Refractive Hypoproliferative Anaemia

Toxic Anaemia

Toxic Aplastic Anaemia

Aplastic Anaemia Due To Toxic Cause

Idiopathic Aplastic Anaemia Nos

Fanconi Anemia, Complementation Group A

Fanconi Anemia

Fanconi Pancytopenia

Fanconi Anemia Complementation Group A

FANCA

Fa

Fanconi Panmyelopathy

Fanconi'S Anemia

Fanconi Anaemia

Fanconi'S Anaemia

Fanconi Hypoplastic Anemia

Estren-Dameshek Variant Of Fanconi Anemia

Estren-Dameshek Variant Of Fanconi Pancytopenia

Fanconi Anemia Estren-Dameshek Variant

Fanconis Anemia

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
Rattus norvegicus REV1 RGD RGD:1306715
Canis familiaris REV1 VGNC VGNC:45487
Felis catus REV1 VGNC VGNC:64579
Macaca mulatta REV1 VGNC VGNC:106209
Bos taurus REV1 VGNC VGNC:33882
Mus musculus REV1 MGD MGI:1929074
Others REV1 NCBI