CCDC22

CCDC22
Identifiers
Aliases	CCDC22, CXorf37, JM1, RTSC2, coiled-coil domain containing 22
External IDs	OMIM: 300859; MGI: 1859608; HomoloGene: 8515; GeneCards: CCDC22; OMA:CCDC22 - orthologs
Gene location (Human)
Chr.	X chromosome (human)
End	49,250,520 bp
Gene location (Mouse)
Chr.	X chromosome (mouse)
End	7,471,756 bp
RNA expression pattern
	Top expressed in
	granulocyte; ; monocyte; ; mucosa of transverse colon; ; apex of heart; ; tendon of biceps brachii; ; right hemisphere of cerebellum; ; gastrocnemius muscle; ; spleen; ; blood; ; parotid gland;
	Top expressed in
	interventricular septum; ; Rostral migratory stream; ; otic vesicle; ; saccule; ; otic placode; ; internal carotid artery; ; external carotid artery; ; substantia nigra; ; fossa; ; condyle;
	More reference expression data
	n/a
Gene ontology
Molecular function	cullin family protein binding; protein binding;
Cellular component	endosome; nucleoplasm; cytosol; cellular component;
Biological process	protein transport; positive regulation of I-kappaB kinase/NF-kappaB signaling; cytoplasmic sequestering of NF-kappaB; Golgi to plasma membrane transport; positive regulation of ubiquitin-dependent protein catabolic process; negative regulation of I-kappaB kinase/NF-kappaB signaling; cellular copper ion homeostasis; post-translational protein modification; protein ubiquitination; endocytic recycling;
	Sources:Amigo / QuickGO
Orthologs
	28952
	54638
	ENSG00000101997
	ENSMUSG00000031143
	O60826
	Q9JIG7
	NM_014008
	NM_138603
	NP_054727
	NP_613069
	Wikidata
View/Edit Human	View/Edit Mouse

Coiled-coil domain containing 22 is a protein that in humans is encoded by the CCDC22 gene.