COX7B

COX7B
Identifiers
AliasesCOX7B, APLCC, LSDMCA2, cytochrome c oxidase subunit 7B
External IDsOMIM: 300885; MGI: 1913392; HomoloGene: 1406; GeneCards: COX7B; OMA:COX7B - orthologs
Orthologs
SpeciesHumanMouse
Entrez

1349

66142

Ensembl

ENSG00000131174

ENSMUSG00000031231

UniProt

P24311

P56393

RefSeq (mRNA)

NM_001866

NM_025379

RefSeq (protein)

NP_001857

NP_079655

Location (UCSC)Chr X: 77.9 – 77.91 MbChr X: 105.06 – 105.07 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Cytochrome c oxidase subunit 7B, mitochondrial (COX7B) is an enzyme that in humans is encoded by the COX7B gene. COX7B is a nuclear-encoded subunit of cytochrome c oxidase (COX). Cytochrome c oxidase (complex IV) is a multi-subunit enzyme complex that couples the transfer of electrons from cytochrome c to molecular oxygen and contributes to a proton electrochemical gradient across the inner mitochondrial membrane, acting as the terminal enzyme of the mitochondrial respiratory chain. Work with Oryzias latices has linked disruptions in COX7B with microphthalmia with linear skin lesions (MLS), microcephaly, and mitochondrial disease. Clinically, mutations in COX7B have been associated with linear skin defects with multiple congenital anomalies.