cytochrome b5 type A (microsomal)

Symbol

CYB5A (may also be known as: None)

Organism

Human

Description

The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]

Orthologs

SymbolSpecies
cyb5a Danio rerio
Cyb5a Mus musculus
Cyb5a Rattus norvegicus
CYB5 Saccharomyces cerevisiae
oca8 Schizosaccharomyces pombe

Links to external resources

Changes associated with this gene

GO Terms

GO IDGO TermGO Category
GO:0006766 vitamin metabolic process biological_process
GO:0006767 water-soluble vitamin metabolic process biological_process
GO:0006810 transport biological_process
GO:0019852 L-ascorbic acid metabolic process biological_process
GO:0022900 electron transport chain biological_process
GO:0044281 small molecule metabolic process biological_process
GO:0005737 cytoplasm cellular_component
GO:0005739 mitochondrion cellular_component
GO:0005741 mitochondrial outer membrane cellular_component
GO:0005783 endoplasmic reticulum cellular_component
GO:0005789 endoplasmic reticulum membrane cellular_component
GO:0005792 microsome cellular_component
GO:0016020 membrane cellular_component
GO:0016021 integral to membrane cellular_component
GO:0004033 aldo-keto reductase (NADP) activity molecular_function
GO:0004129 cytochrome-c oxidase activity molecular_function
GO:0019899 enzyme binding molecular_function
GO:0020037 heme binding molecular_function
GO:0046872 metal ion binding molecular_function