REPIN1
DNA-binding protein REPIN1
Also known as: AP4, H_DJ0584D14.12, REPI1_HUMAN, RIP60, Zfp464, ZNF464
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BWE0
- Gene
- REPIN1
- Ensembl
- ENSG00000214022
- Chromosome
- 7
- Canonical length
- 567 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables sequence-specific DNA binding activity. Predicted to be involved in regulation of fatty acid transport and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within positive regulation of D-glucose import. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
567 residues, UniProt reviewed canonical sequence.
>Q9BWE0|REPIN1
1 MLERRCRGPL AMGLAQPRLL SGPSQESPQT LGKESRGLRQ QGTSVAQSGA QAPGRAHRCA
61 HCRRHFPGWV ALWLHTRRCQ ARLPLPCPEC GRRFRHAPFL ALHRQVHAAA TPDLGFACHL
121 CGQSFRGWVA LVLHLRAHSA AKRPIACPKC ERRFWRRKQL RAHLRRCHPP APEARPFICG
181 NCGRSFAQWD QLVAHKRVHV AEALEEAAAK ALGPRPRGRP AVTAPRPGGD AVDRPFQCAC
241 CGKRFRHKPN LIAHRRVHTG ERPHQCPECG KRFTNKPYLT SHRRIHTGEK PYPCKECGRR
301 FRHKPNLLSH SKIHKRSEGS AQAAPGPGSP QLPAGPQESA AEPTPAVPLK PAQEPPPGAP
361 PEHPQDPIEA PPSLYSCDDC GRSFRLERFL RAHQRQHTGE RPFTCAECGK NFGKKTHLVA
421 HSRVHSGERP FACEECGRRF SQGSHLAAHR RDHAPDRPFV CPDCGKAFRH KPYLAAHRRI
481 HTGEKPYVCP DCGKAFSQKS NLVSHRRIHT GERPYACPDC DRSFSQKSNL ITHRKSHIRD
541 GAFCCAICGQ TFDDEERLLA HQKKHDVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against REPIN1 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)
- 0.48
- Highest tissue expression
- 126 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 126 nTPM
- liver: 83 nTPM
- adrenal gland: 72 nTPM
- pituitary gland: 65 nTPM
- pancreas: 64 nTPM
- colon: 63 nTPM
Single-cell type
- adipocytes: 5.1 nCPM
- cardiomyocytes: 2.7 nCPM
- granulosa cells: 0.8 nCPM
- thymocytes: 0.8 nCPM
- enterocytes: 0.7 nCPM
- late spermatids: 0.7 nCPM
Immune cell
- plasmacytoid DC: 7.8 nTPM
- eosinophil: 2.7 nTPM
- memory B-cell: 2.5 nTPM
- naive B-cell: 2.4 nTPM
- naive CD4 T-cell: 2.3 nTPM
- myeloid DC: 2.2 nTPM
Brain region
- choroid plexus: 97 nTPM
- medulla oblongata: 91 nTPM
- thalamus: 85 nTPM
- midbrain: 79 nTPM
- cerebral cortex: 77 nTPM
- pons: 77 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)
- 0.54
- gnomAD pLI
- 0.09
- gnomAD missense Z
- 2.43
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of REPIN1 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 REPIN1 as an antibody target. Whether an autoantibody or antibody against REPIN1 could matter depends on whether native REPIN1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
REPIN1 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 REPIN1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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