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]
人 CYB5A (NM_148923) cDNA克隆
| Accession: | NM_148923 |
|---|---|
| 基因名称: | CYB5A |
| 基因别名: | CYB5; MCB5 |
| 基因描述: | Homo sapiens cytochrome b5 type A (microsomal) (CYB5A), transcript variant 1, mRNA. |
| 种属: | Human |
| CDS区长度: | 405 (查看编码区序列) |
| 翻译后氨基酸长度: | 134 (查看氨基酸序列) |
| Transcript Variant: | This variant (1) represents the longest transcript and encodes the longest isoform (1). |
| 人 CYB5A (NM_148923) cDNA克隆 | transcript variant 1 |
| 人 CYB5A (NM_001914) cDNA克隆 | transcript variant 2 |
| 人 CYB5A (NM_001190807) cDNA克隆 | transcript variant 3 |
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