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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| HFEBA-20-REGO | 20 (40 μL) | 200 μL |
|
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| HFEBA-20-REGR | 20 (40 μL) | 200 μL |
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| HFEBA-20-ORGR | 20 (40 μL) | 200 μL |
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| HFEBA-20-GOGR | 20 (40 μL) | 200 μL |
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| HFEBA-20-GRRE | 20 (40 μL) | 200 μL |
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| HFEBA-20-GROR | 20 (40 μL) | 200 μL |
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| HFEBA-20-GRGO | 20 (40 μL) | 200 μL |
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| HFEBA-20-AQOR | 20 (40 μL) | 200 μL |
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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]
Gene Symbol : HFE
Gene Name : Hemochromatosis
Chromosome : CHR 6: 260,872,80-260,962,15
Locus : 6p22.2
Alt. Genes : DHRS9
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