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// Workers AI · dad joke modeWhat did CCDC8 say to its date? "You're a great cell-ebration match

From Wikipedia, the free encyclopedia

CCDC8
Identifiers
AliasesCCDC8, 3M3, PPP1R20, p90, coiled-coil domain containing 8
External IDsOMIM: 614145; MGI: 3612184; GeneCards: CCDC8
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_032040

NM_001101535

RefSeq (protein)

NP_114429

NP_001095005

Location (UCSC)Chr 19: 46.41 – 46.41 MbChr 7: 16.73 – 16.73 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Coiled-coil domain containing 8 is a protein that in humans is encoded by the CCDC8 gene.[5]

Function

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This gene encodes a coiled coil domain-containing protein. The encoded protein functions as a cofactor required for p53-mediated apoptosis following DNA damage, and may also play a role in growth through interactions with the cytoskeletal adaptor protein obscurin-like 1.

Clinical relevance

[edit]

Mutations in this gene have been shown to cause 3-M syndrome.[6]

References

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  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000169515 – Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000041117 – Ensembl, May 2017
  3. ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ↑ "Entrez Gene: Coiled-coil domain containing 8". Retrieved 2011-12-30.
  6. ↑ Hanson D, Murray PG, O'Sullivan J, Urquhart J, Daly S, Bhaskar SS, et al. (July 2011). "Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth". American Journal of Human Genetics. 89 (1): 148–153. doi:10.1016/j.ajhg.2011.05.028. PMC 3135816. PMID 21737058.
[edit]

This article incorporates text from the United States National Library of Medicine, which is in the public domain.