Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51455
Gene name Gene Name - the full gene name approved by the HGNC.
REV1 DNA directed polymerase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
REV1
Synonyms (NCBI Gene) Gene synonyms aliases
AIBP80, REV1L
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q11.2
Summary Summary of gene provided in NCBI Entrez Gene.
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
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT006779 hsa-miR-96-5p Immunofluorescence, Luciferase reporter assay, qRT-PCR, Western blot 22761336
MIRT030984 hsa-miR-21-5p Microarray 18591254
MIRT296871 hsa-miR-106b-5p HITS-CLIP 22473208
MIRT439784 hsa-miR-155-5p HITS-CLIP 22473208
MIRT296868 hsa-miR-20a-5p HITS-CLIP 22473208
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003684 Function Damaged DNA binding IEA
GO:0003887 Function DNA-directed DNA polymerase activity IBA 21873635
GO:0005515 Function Protein binding IPI 11485998, 22266823, 26318859
GO:0005654 Component Nucleoplasm TAS
GO:0006260 Process DNA replication TAS 10536157
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606134 14060 ENSG00000135945
Protein
UniProt ID Q9UBZ9
Protein name DNA repair protein REV1 (EC 2.7.7.-) (Alpha integrin-binding protein 80) (AIBP80) (Rev1-like terminal deoxycytidyl transferase)
Protein function Deoxycytidyl transferase involved in DNA repair. Transfers a dCMP residue from dCTP to the 3'-end of a DNA primer in a template-dependent reaction. May assist in the first step in the bypass of abasic lesions by the insertion of a nucleotide opp
PDB 2EBW , 2LSI , 2LSK , 2LSY , 2N1G , 3GQC , 3VU7 , 4BA9 , 4EXT , 4GK0 , 4GK5 , 5VZM , 6ASR , 6AXD , 6WS0 , 6WS5
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF16589 BRCT_2 45 130 BRCT domain, a BRCA1 C-terminus domain Family
PF00817 IMS 422 622 impB/mucB/samB family Family
PF11799 IMS_C 702 830 impB/mucB/samB family C-terminal domain Domain
PF14377 UBM 931 957 Ubiquitin binding region Repeat
PF14377 UBM 1009 1042 Ubiquitin binding region Repeat
PF16727 REV1_C 1167 1248 DNA repair protein REV1 C-terminal domain Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:10536157, ECO:0000269|PubMed:11278384, ECO:0000269|PubMed:11485998}.
Sequence
MRRGGWRKRAENDGWETWGGYMAAKVQKLEEQFRSDAAMQKDGTSSTIFSGVAIYVNGYT
DPSAEELRKLMMLHGGQYHVYYSRSKTTHIIATNLPNAKIKELKGEKVIRPEWIVESIKA
GRLLSYIPYQ
LYTKQSSVQKGLSFNPVCRPEDPLPGPSNIAKQLNNRVNHIVKKIETENE
VKVNGMNSWNEEDENNDFSFVDLEQTSPGRKQNGIPHPRGSTAIFNGHTPSSNGALKTQD
CLVPMVNSVASRLSPAFSQEEDKAEKSSTDFRDCTLQQLQQSTRNTDALRNPHRTNSFSL
SPLHSNTKINGAHHSTVQGPSSTKSTSSVSTFSKAAPSVPSKPSDCNFISNFYSHSRLHH
ISMWKCELTEFVNTLQRQSNGIFPGREKLKKMKTGRSALVVTDTGDMSVLNSPRHQSCIM
HVDMDCFFVSVGIRNRPDLKGKPVAVTSNRGTGRAPLRPGANPQLEWQYYQNKILKGKAA
DIPDSSLWENPDSAQANGIDSVLSRAEIASCSYEARQLGIKNGMFFGHAKQLCPNLQAVP
YDFHAYKEVAQTLYETLASYTHNIEAVSCDEALVDITEILAETKLTPDEFANAVRMEIKD
QTKCAASVGIGSNILLARMATR
KAKPDGQYHLKPEEVDDFIRGQLVTNLPGVGHSMESKL
ASLGIKTCGDLQYMTMAKLQKEFGPKTGQMLYRFCRGLDDRPVRTEKERKSVSAEINYGI
RFTQPKEAEAFLLSLSEEIQRRLEATGMKGKRLTLKIMVRKPGAPVETAKFGGHGICDNI
ARTVTLDQATDNAKIIGKAMLNMFHTMKLNISDMRGVGIHVNQLVPTNLN
PSTCPSRPSV
QSSHFPSGSYSVRDVFQVQKAKKSTEEEHKEVFRAAVDLEISSASRTCTFLPPFPAHLPT
SPDTNKAESSGKWNGLHTPVSVQSRLNLSIEVPSPSQLDQSVLEALPPDLREQVEQVCAV
QQAESHGDKKKEPVNGCNTGILPQPVGTVLLQIPEPQESNSDAGINLIALPAFSQVDPEV
FAALPAELQRELKAAYDQRQRQ
GENSTHQQSASASVPKNPLLHLKAAVKEKKRNKKKKTI
GSPKRIQSPLNNKLLNSPAKTLPGACGSPQKLIDGFLKHEGPPAEKPLEELSASTSGVPG
LSSLQSDPAGCVRPPAPNLAGAVEFNDVKTLLREWITTISDPMEEDILQVVKYCTDLIEE
KDLEKLDLVIKYMKRLMQQSVESVWNMAFDFILDNVQVVLQQTYGSTL
KVT
Sequence length 1251
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Fanconi anemia pathway   Translesion synthesis by REV1
Translesion synthesis by POLK
Translesion synthesis by POLI
Termination of translesion DNA synthesis
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Mental depression Major Depressive Disorder 22472876 ClinVar
Uterine Fibroids Uterine Fibroids GWAS
Associations from Text Mining
Disease Name Relationship Type References
Carcinogenesis Associate 26914252, 35115490
Chromosome Aberrations Inhibit 18448394
Chromosome Aberrations Associate 20028736
Colorectal Neoplasms Associate 35880088
Fanconi Anemia Associate 18448394
Inflammation Associate 23454887
Lung Neoplasms Associate 24012694
Lung Neoplasms Stimulate 35115490
Neoplasms Associate 21690293, 24167294, 37532520
Osteosarcoma Associate 25748439