full name
COX10, heme A:farnesyltransferase cytochrome c oxidase assembly factor

synonyms
COX10, ENSG00000006695

HGNC
HGNC:2260

Entrez Gene
Gene:1352

ENSEMBL
ENSG00000006695

location
chr: 17
start: 13972719
stop: 14111996
strand: +

OMIM
OMIM:602125: COX10 (Autosomal recessive inheritance,Heterogeneous,Mitochondrial inheritance)
OMIM:256000: Leigh syndrome due to mitochondrial COX4 deficiency
OMIM:220110: Mitochondrial complex IV deficiency

transcripts
NM_001303.3

pathways
Heme biosynthesis [NCBI:1270187] [REACTOME:R-HSA-189451] [PUBMED:16839620] [PUBMED:10522552]
Metabolic pathways [NCBI:132956] [KEGG:hsa01100]
Metabolism [NCBI:1269956] [REACTOME:R-HSA-1430728]
Metabolism of porphyrins [NCBI:1270186] [REACTOME:R-HSA-189445]
Oxidative phosphorylation [NCBI:82942] [KEGG:hsa00190] [PUBMED:16584177] [PUBMED:16469879]
Porphyrin and chlorophyll metabolism [NCBI:83021] [KEGG:hsa00860] [PUBMED:12195810] [PUBMED:11283349] [PUBMED:10217486] [PUBMED:11007789] [PUBMED:10518530] [PUBMED:12055304] [PUBMED:12196148] [PUBMED:17506685] [PUBMED:16245042] [PUBMED:23922391] [PUBMED:23042036] [PUBMED:9461500]