人 HFE (NM_000410) cDNA克隆

基本信息

Accession: NM_000410
基因名称: HFE
基因别名: HH; HFE1; HLA-H; MVCD7; TFQTL2
基因描述: Homo sapiens hemochromatosis (HFE), transcript variant 1, mRNA.
种属: Human
CDS区长度: 1047 (查看编码区序列)
翻译后氨基酸长度: 348 (查看氨基酸序列)
Transcript Variant: This variant (1) encodes the longest isoform.

订购信息

产品编号 产品名称 载体 规格 价格
G122113 人 HFE (NM_000410) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 HFE (NM_000410) cDNA克隆 transcript variant 1
人 HFE (NM_139010) cDNA克隆 transcript variant 10
人 HFE (NM_139011) cDNA克隆 transcript variant 11
人 HFE (NM_139003) cDNA克隆 transcript variant 3
人 HFE (NM_139004) cDNA克隆 transcript variant 4
人 HFE (NM_139006) cDNA克隆 transcript variant 6
人 HFE (NM_139007) cDNA克隆 transcript variant 7
人 HFE (NM_139008) cDNA克隆 transcript variant 8
人 HFE (NM_139009) cDNA克隆 transcript variant 9

基因简介

The protein encoded by this gene is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M). It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in this gene. At least nine alternatively spliced variants have been described for this gene. Additional variants have been found but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]

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