C9orf78

C9orf78
Identifiers
Aliases	C9orf78, HCA59, HSPC220, bA409K20.3, chromosome 9 open reading frame 78, CSU2, TLS1
External IDs	MGI: 2385132; HomoloGene: 9551; GeneCards: C9orf78; OMA:C9orf78 - orthologs
Gene location (Human)
Chr.	Chromosome 9 (human)
End	129,835,863 bp
Gene location (Mouse)
Chr.	Chromosome 2 (mouse)
End	30,872,213 bp
RNA expression pattern
	Top expressed in
	monocyte; ; Achilles tendon; ; C1 segment; ; gastrocnemius muscle; ; anterior cingulate cortex; ; tibial arteries; ; Descending thoracic aorta; ; gonad; ; stromal cell of endometrium; ; gastric mucosa;
	Top expressed in
	neural layer of retina; ; dentate gyrus of hippocampal formation granule cell; ; Cerebellum; ; Hypothalamus; ; olfactory bulb; ; tail of embryo; ; cerebellar cortex; ; granulocyte; ; ovary; ; superior frontal gyrus;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	protein binding;
Cellular component	nucleoplasm; cytosol; nucleus; spliceosomal complex;
Biological process	regulation of mRNA splicing, via spliceosome;
	Sources:Amigo / QuickGO
Orthologs
	51759
	227707
	ENSG00000136819
	ENSMUSG00000026851
	Q9NZ63
	Q3TQI7
	NM_016520
	NM_144885
	NP_057604
	NP_659134
	Wikidata
View/Edit Human	View/Edit Mouse

Uncharacterized protein C9orf78 is a protein that in humans is encoded by the C9orf78 gene.