REV1
DNA repair protein REV1
Also known as: REV1_HUMAN, REV1L
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UBZ9
- Gene
- REV1
- Ensembl
- ENSG00000135945
- Chromosome
- 2
- Canonical length
- 1251 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli
- Quaternary structure
- Homotetramer
OverviewNCBI 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 recruits DNA polymerases involved in translesion synthesis (TLS) of damaged DNA. [provided by RefSeq, Mar 2016]
Canonical amino-acid sequenceUniProt
1251 residues, UniProt reviewed canonical sequence.
>Q9UBZ9|REV1
1 MRRGGWRKRA ENDGWETWGG YMAAKVQKLE EQFRSDAAMQ KDGTSSTIFS GVAIYVNGYT
61 DPSAEELRKL MMLHGGQYHV YYSRSKTTHI IATNLPNAKI KELKGEKVIR PEWIVESIKA
121 GRLLSYIPYQ LYTKQSSVQK GLSFNPVCRP EDPLPGPSNI AKQLNNRVNH IVKKIETENE
181 VKVNGMNSWN EEDENNDFSF VDLEQTSPGR KQNGIPHPRG STAIFNGHTP SSNGALKTQD
241 CLVPMVNSVA SRLSPAFSQE EDKAEKSSTD FRDCTLQQLQ QSTRNTDALR NPHRTNSFSL
301 SPLHSNTKIN GAHHSTVQGP SSTKSTSSVS TFSKAAPSVP SKPSDCNFIS NFYSHSRLHH
361 ISMWKCELTE FVNTLQRQSN GIFPGREKLK KMKTGRSALV VTDTGDMSVL NSPRHQSCIM
421 HVDMDCFFVS VGIRNRPDLK GKPVAVTSNR GTGRAPLRPG ANPQLEWQYY QNKILKGKAA
481 DIPDSSLWEN PDSAQANGID SVLSRAEIAS CSYEARQLGI KNGMFFGHAK QLCPNLQAVP
541 YDFHAYKEVA QTLYETLASY THNIEAVSCD EALVDITEIL AETKLTPDEF ANAVRMEIKD
601 QTKCAASVGI GSNILLARMA TRKAKPDGQY HLKPEEVDDF IRGQLVTNLP GVGHSMESKL
661 ASLGIKTCGD LQYMTMAKLQ KEFGPKTGQM LYRFCRGLDD RPVRTEKERK SVSAEINYGI
721 RFTQPKEAEA FLLSLSEEIQ RRLEATGMKG KRLTLKIMVR KPGAPVETAK FGGHGICDNI
781 ARTVTLDQAT DNAKIIGKAM LNMFHTMKLN ISDMRGVGIH VNQLVPTNLN PSTCPSRPSV
841 QSSHFPSGSY SVRDVFQVQK AKKSTEEEHK EVFRAAVDLE ISSASRTCTF LPPFPAHLPT
901 SPDTNKAESS GKWNGLHTPV SVQSRLNLSI EVPSPSQLDQ SVLEALPPDL REQVEQVCAV
961 QQAESHGDKK KEPVNGCNTG ILPQPVGTVL LQIPEPQESN SDAGINLIAL PAFSQVDPEV
1021 FAALPAELQR ELKAAYDQRQ RQGENSTHQQ SASASVPKNP LLHLKAAVKE KKRNKKKKTI
1081 GSPKRIQSPL NNKLLNSPAK TLPGACGSPQ KLIDGFLKHE GPPAEKPLEE LSASTSGVPG
1141 LSSLQSDPAG CVRPPAPNLA GAVEFNDVKT LLREWITTIS DPMEEDILQV VKYCTDLIEE
1201 KDLEKLDLVI KYMKRLMQQS VESVWNMAFD FILDNVQVVL QQTYGSTLKV TLocalizationUniProt · AlphaFold · HPA
Whether an antibody against REV1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.46
- Highest tissue expression
- 22 nTPM
Expression across tissuesHPA
Tissue
- tongue: 22 nTPM
- cerebellum: 20 nTPM
- epididymis: 16 nTPM
- skeletal muscle: 15 nTPM
- endometrium: 13 nTPM
- cervix: 12 nTPM
Single-cell type
- renal collecting duct intercalated cells: 222 nCPM
- thyrotrophs: 215 nCPM
- myonuclei: 215 nCPM
- distal convoluted tubule cells: 202 nCPM
- lactotrophs: 201 nCPM
- pituicytes/fscs: 200 nCPM
Immune cell
- naive CD4 T-cell: 0.9 nTPM
- naive CD8 T-cell: 0.7 nTPM
- memory CD4 T-cell: 0.5 nTPM
- memory CD8 T-cell: 0.4 nTPM
- naive B-cell: 0.4 nTPM
- gdT-cell: 0.3 nTPM
Brain region
- cerebellum: 23 nTPM
- choroid plexus: 16 nTPM
- hypothalamus: 14 nTPM
- white matter: 13 nTPM
- cerebral cortex: 12 nTPM
- basal ganglia: 12 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.24
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.6
- DepMap mean gene effect
- -0.22
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- DNA biosynthetic process
- DNA repair
- error-free translesion synthesis
- error-prone translesion synthesis
- somatic hypermutation of immunoglobulin genes
- translesion synthesis
Molecular functions
- damaged DNA binding
- DNA binding
- DNA-(abasic site) binding
- DNA-directed DNA polymerase activity
- metal ion binding
- protein-macromolecule adaptor activity
- ubiquitin binding
- deoxycytidyl transferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- UmuC domain
- BRCT domain
- DNA polymerase, Y-family, little finger domain
- HUWE1/REV1, ubiquitin-binding motif
- BRCT domain superfamily
- DNA polymerase, Y-family, little finger domain superfamily
- Reverse transcriptase/Diguanylate cyclase domain
- DNA/RNA polymerase superfamily
- DNA polymerase IV/DNA polymerase iota-like, thumb domain
- BRCA1 C Terminus (BRCT) domain
- impB/mucB/samB family
- impB/mucB/samB family C-terminal domain
- Ubiquitin binding region
- DNA polymerase-iota, thumb domain
- DNA repair protein Rev1
- DNA repair protein Rev1, C-terminal
- Rev1, C-terminal domain superfamily
- DNA repair protein REV1, ubiquitin-binding motif 1/2
- DNA repair protein REV1 C-terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of REV1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads REV1 as an antibody target. Whether an autoantibody or antibody against REV1 could matter depends on whether native REV1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
REV1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label REV1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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