Seroatlas · Human Serome Atlas

ERVV-1

Endogenous retrovirus group V member 1 Env polyprotein

Also known as: ENVV1, ERVV1_HUMAN, FLJ32214, HERV-V1

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
B6SEH8
Gene
ERVV-1
Ensembl
ENSG00000269526
Chromosome
19
Canonical length
477 aa
Protein class
Predicted membrane proteins
Subcellular location
Centrosome,Cytosol

OverviewNCBI Gene

Many different human endogenous retrovirus (HERV) families are expressed in normal placental tissue at high levels, suggesting that HERVs are functionally important in reproduction. This gene is part of an HERV provirus on human chromosome 19 that has inactivating mutations in the gag and pol genes. The gene's envelope protein is expressed in the human placenta but is truncated at its C-terminus. [provided by RefSeq, Oct 2015]

Canonical amino-acid sequenceUniProt

477 residues, UniProt reviewed canonical sequence.

>B6SEH8|ERVV-1
     1  MTEKFLFLYL SLLPMPLLSQ AQWNENSLVS FSKIIASGNH LSNCWICHNF ITRSSSYQYI
    61  LVRNFSLNLT FGSGIPEGQH KSVPLQVSLA NSAHQVPCLD LTPPFNQSSK TSFYFYNCSS
   121  LNQTCCPCPE GHCDRKNTSE EGFPSPTIHP MSFSPAGCHP NLTHWCPAKQ MNDYRDKSPQ
   181  NRCAAWEGKE LITWRVLYLL PKAHTVPTWP KSTVPLGGPL SPACNQTIPA GWKSQLHKWF
   241  DSHIPRWACT PPGYVFLCGP QKNKLPFDGS PKITYSTPPV ANLYTCINNI QHTGECAVGL
   301  LGPRGIGVTI YNTTQPRQKR ALGLILAGMG AAIGMIAPWG GFTYHDVTLR NLSRQIDNIA
   361  KSTRDSISKL KASIDSLANV VMNNRLALDY LLAEQGGVCA VISKSCCIYV NNSGAIEEDI
   421  KKIYDEVTWL HNFGKGDSAG SIWEAVKSAL PSLTWFVPLL GPAALNSLLS PLWPLSL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against ERVV-1 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
Unknown
Secreted
No
Transmembrane segments
1
Mean surface accessibility (rSASA)
0.5
Highest tissue expression
15 nTPM

Expression across tissuesHPA

Tissue

  • placenta: 15 nTPM
  • cerebellum: 1 nTPM
  • kidney: 0.8 nTPM
  • vagina: 0.4 nTPM
  • cervix: 0.2 nTPM
  • prostate: 0.2 nTPM

Single-cell type

  • syncytiotrophoblasts: 386 nCPM
  • cytotrophoblasts: 8.4 nCPM
  • migrating cytotrophoblasts: 6.2 nCPM
  • breast lactating cells: 1.5 nCPM
  • extravillous trophoblasts: 1.3 nCPM
  • retinal amacrine cells: 0.7 nCPM

Immune cell

  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM
  • intermediate monocyte: 0 nTPM
  • MAIT T-cell: 0 nTPM

Brain region

  • cerebellum: 1.3 nTPM
  • basal ganglia: 0.8 nTPM
  • cerebral cortex: 0.8 nTPM
  • hippocampal formation: 0.6 nTPM
  • pons: 0.6 nTPM
  • hypothalamus: 0.5 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 missense Z
1.24

OntologyGO

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads ERVV-1 as an antibody target. Whether an autoantibody or antibody against ERVV-1 could matter depends on whether native ERVV-1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

ERVV-1 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 ERVV-1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/ERVV-1. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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