Your search for "hfe" returned 134 TaqMan® SNP Genotyping Assays
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]
HFE, HFE1, HH, HLA-H, MR2, MVCD7, TFQTL2
(Human) Q30201, (Human) B2CKL0, (Human) O75929, (Human) O75930, (Human) O75931, (Human) Q17RT0, (Human) Q96KU5, (Human) Q96KU6, (Human) Q96KU7, (Human) Q96KU8, (Human) Q9HC64, (Human) Q9HC68, (Human) Q9HC70, (Human) Q9HC83, (Mouse) P70387, (Mouse) Q14AQ5, (Mouse) Q5SZ90, (Mouse) Q9D754, (Rat) O35799, (Rat) O35175
Please enter the information below and press OK to send your cart to Core Services for purchase.