CCDC151

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
Gene location (Human)
Chr.	Chromosome 19 (human)
End	11,435,782 bp
Gene location (Mouse)
Chr.	Chromosome 9 (mouse)
End	21,913,930 bp
RNA expression pattern
	Top expressed in
	bronchial epithelial cell; ; right uterine tube; ; pituitary gland; ; anterior pituitary; ; pancreatic ductal cell; ; caudate nucleus; ; caput epididymis; ; hypothalamus; ; hippocampus proper; ; seminal vesicula;
	Top expressed in
	seminiferous tubule; ; otolith organ; ; utricle; ; spermatocyte; ; morula; ; spermatid; ; olfactory epithelium; ; primitive streak; ; lens; ; right lung lobe;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding;
Cellular component	cytoplasm; ciliary basal body; centriole; axoneme; cell projection; cilium; cytoskeleton;
Biological process	regulation of cilium assembly; determination of left/right symmetry; outer dynein arm assembly; cell projection organization; axonemal dynein complex assembly; cilium movement;
	Sources:Amigo / QuickGO
Orthologs
	115948
	77609
	ENSG00000198003
	ENSMUSG00000039632
	A5D8V7
	Q8BSN3
	NM_145045; NM_001302453; NM_001302454
	NM_001163787; NM_029939
	NP_001289382; NP_001289383; NP_659482
	NP_001157259; NP_084215
	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]

Clinical significance[edit]

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

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000198003 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000039632 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Entrez Gene: Coiled-coil domain containing 151".
^ 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.

Human CCDC151 genome location and CCDC151 gene details page in the UCSC Genome Browser.

This article on a gene on human chromosome 19 is a stub. You can help Wikipedia by expanding it.