RNF139

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

RING finger protein 139, also known as TRC8, is a protein that in humans is encoded by the RNF139 gene.[5][6]

AliasesRNF139, HRCA1, RCA1, TRC8, ring finger protein 139
End124,488,618 bp[1]
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RNF139
Identifiers
AliasesRNF139, HRCA1, RCA1, TRC8, ring finger protein 139
External IDsOMIM: 603046; MGI: 1923091; HomoloGene: 5222; GeneCards: RNF139; OMA:RNF139 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_007218

NM_175226

RefSeq (protein)

NP_009149

NP_780435

Location (UCSC)Chr 8: 124.47 – 124.49 MbChr 15: 58.76 – 58.78 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene is a multi-membrane spanning protein containing a RING-H2 finger. This protein is located in the endoplasmic reticulum, and has been shown to possess ubiquitin ligase activity. This gene was found to be interrupted by a t(3:8) translocation in a family with hereditary renal and non-medullary thyroid cancer. Studies of the Drosophila counterpart suggested that this protein may interact with tumor suppressor protein VHL, as well as with COPS5/JAB1, a protein responsible for the degradation of tumor suppressor CDKN1B/P27KIP].[6]

References

Further reading

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