COX10

URI: https://gptkb.org/entity/COX10
GPTKB entity
Statements (18)
Predicate Object
gptkbp:instanceOf gptkb:gene
gptkbp:alternativeName gptkb:protoheme_IX_farnesyltransferase
gptkbp:associatedWith gptkb:mitochondrial_complex_IV_deficiency
gptkbp:encodes gptkb:cytochrome_c_oxidase_assembly_protein_COX10_homolog,_mitochondrial
gptkbp:expressedIn mitochondria
gptkbp:function heme A biosynthesis
gptkbp:geneType protein-coding
gptkbp:HGNC_ID 2296
https://www.w3.org/2000/01/rdf-schema#label COX10
gptkbp:involvedIn oxidative phosphorylation
gptkbp:locatedOnChromosome gptkb:17p12
gptkbp:mutationAssociatedWith gptkb:Leigh_syndrome
gptkb:mitochondrial_encephalopathy
gptkbp:OMIM 602125
gptkbp:orthologInMouse gptkb:Cox10
gptkbp:UniProtID gptkb:Q12887
gptkbp:bfsParent gptkb:Leigh_syndrome
gptkbp:bfsLayer 7