CCDC177

CCDC177
Identifiers
Aliases	CCDC177, C14orf162, PLPL, coiled-coil domain containing 177
External IDs	MGI: 2686414; HomoloGene: 128326; GeneCards: CCDC177; OMA:CCDC177 - orthologs
Gene location (Human)
Chr.	Chromosome 14 (human)
End	69,574,871 bp
Gene location (Mouse)
Chr.	Chromosome 12 (mouse)
End	80,807,461 bp
RNA expression pattern
	Top expressed in
	secondary oocyte; ; ganglionic eminence; ; ventricular zone; ; testicle; ; Cerebellum; ; cerebellar cortex; ; cerebellar hemisphere; ; right hemisphere of cerebellum; ; prefrontal cortex; ; postcentral gyrus;
	Top expressed in
	Rostral migratory stream; ; substantia nigra; ; fossa; ; trigeminal ganglion; ; supraoptic nucleus; ; lateral septal nucleus; ; ganglionic eminence; ; ventromedial nucleus; ; lumbar subsegment of spinal cord; ; retina;
	More reference expression data
	n/a
Orthologs
	56936
	380768
	ENSG00000267909
	ENSMUSG00000062961
	Q9NQR7
	Q3UHB8
	NM_001271507; NM_020181
	NM_001008423
	NP_001258436
	NP_001008423
	Wikidata
View/Edit Human	View/Edit Mouse

Coiled-Coil Domain Containing 177 (CCDC177) is a protein, which in humans, is encoded by the gene CCDC177. It is composed of a coiled helical domain that spans half of the protein. CCDC177 deletions are associated with intellectual disability and congenital heart defects.