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CYB5A / Cytochrome b5 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.
|Gene Name:||cytochrome b5 type A (microsomal)|
|Synonyms:||CYB5A, CYB5, Cytochrome b5 (microsomal), MCB5, Type 1 cyt-b5, Cytochrome b-5, Cytochrome b5|
|Target Sequences:||NM_001914 NP_001905.1 P00167|
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