CCDC151

Last updated
ODAD3
Identifiers
Aliases ODAD3 , CILD30, coiled-coil domain containing 151, ODA10, CCDC151, outer dynein arm docking complex subunit 3
External IDs OMIM: 615956 MGI: 1924859 HomoloGene: 16533 GeneCards: ODAD3
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_145045
NM_001302453
NM_001302454

NM_001163787
NM_029939

RefSeq (protein)

NP_001289382
NP_001289383
NP_659482

NP_001157259
NP_084215

Location (UCSC) Chr 19: 11.42 – 11.44 Mb Chr 9: 21.9 – 21.91 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Coiled-coil domain containing 151 is a protein that in humans is encoded by the CCDC151 gene. [5]

Contents

Clinical significance

Mutations in CCDC151 are associated to Primary ciliary dyskinesia. [6]

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References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000198003 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000039632 - 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 151".
  6. Alsaadi MM, Erzurumluoglu AM, Rodriguez S, Guthrie PA, Gaunt TR, Omar HZ, Mubarak M, Alharbi KK, Al-Rikabi AC, Day IN (December 2014). "Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia". Human Mutation. 35 (12): 1446–8. doi:10.1002/humu.22698. PMC   4489323 . PMID   25224326.

Further reading