HCCS (gene)

HCCS
Identifiers
Aliases	HCCS, CCHL, MCOPS7, MLS, LSDMCA1, holocytochrome c synthase
External IDs	OMIM: 300056; MGI: 106911; HomoloGene: 3897; GeneCards: HCCS; OMA:HCCS - orthologs
Gene location (Human)
Chr.	X chromosome (human)
End	11,123,086 bp
Gene location (Mouse)
Chr.	X chromosome (mouse)
End	168,103,368 bp
RNA expression pattern
	Top expressed in
	Skeletal muscle tissue of biceps brachii; ; gastrocnemius muscle; ; muscle of thigh; ; right ventricle; ; mucosa of transverse colon; ; Skeletal muscle tissue of rectus abdominis; ; vastus lateralis muscle; ; left ventricle; ; deltoid muscle; ; gonad;
	Top expressed in
	right ventricle; ; digastric muscle; ; atrioventricular valve; ; myocardium of ventricle; ; sternocleidomastoid muscle; ; interventricular septum; ; temporal muscle; ; soleus muscle; ; intercostal muscle; ; cumulus cell;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	metal ion binding; lyase activity; holocytochrome-c synthase activity;
Cellular component	mitochondrion; mitochondrial inner membrane; membrane;
Biological process	animal organ morphogenesis; cytochrome c-heme linkage;
	Sources:Amigo / QuickGO
Orthologs
	3052
	15159
	ENSG00000004961
	ENSMUSG00000031352
	P53701
	P53702
	NM_005333; NM_001122608; NM_001171991
	NM_008222; NM_001331049; NM_001331050
	NP_001116080; NP_001165462; NP_005324
	NP_001317978; NP_001317979; NP_032248
	Wikidata
View/Edit Human	View/Edit Mouse

Cytochrome c-type heme lyase is an enzyme that in humans is encoded by the HCCS gene on chromosome X.