CCDC151

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Coiled-coil domain containing 151 is a protein that in humans is encoded by the CCDC151 gene. [1]

Clinical significance

Mutations in CCDC151 are associated to Primary ciliary dyskinesia .[2]

References

  1. ↑ "Entrez Gene: Coiled-coil domain containing 151". Retrieved 2014-09-17.
  2. ↑ Alsaadi, M. M.; Erzurumluoglu, A. M.; Rodriguez, S; Guthrie, P. A.; Gaunt, T. R.; Omar, H. Z.; Mubarak, M; Alharbi, K. K.; Al-Rikabi, A. C.; Day, I. N. (2014). "Nonsense mutation in coiled coil domain containing 151 gene (CCDC151) causes Primary ciliary dyskinesia". Human Mutation. 35: 1446–8. doi:10.1002/humu.22698. PMC 4489323. PMID 25224326.

External links

Further reading

  • Jerber, J; Baas, D; Soulavie, F; Chhin, B; Cortier, E; Vesque, C; Thomas, J; Durand, B (2014). "The coiled-coil domain containing protein CCDC151 is required for the function of IFT-dependent motile cilia in animals". Human Molecular Genetics. 23 (3): 563–77. doi:10.1093/hmg/ddt445. PMID 24067530.


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