Your search for "trpm1" returned 780 TaqMan® SNP Genotyping Assays
transient receptor potential cation channel subfamily M member 1
This gene encodes a member of the transient receptor potential melastatin subfamily of transient receptor potential ion channels. The encoded protein is a calcium permeable cation channel that is expressed in melanocytes and may play a role in melanin synthesis. Specific mutations in this gene are the cause autosomal recessive complete congenital stationary night blindness-1C. The expression of this protein is inversely correlated with melanoma aggressiveness and as such it is used as a prognostic marker for melanoma metastasis. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2011]
4732499L03RIK, AI606771, CSNB1C, LTRPC1, MLSN1, TRPM1
(Human) Q7Z4N2, (Human) D9IDV2, (Human) D9IDV3, (Human) F8W865, (Human) H0YN37, (Human) O75560, (Human) Q6PE48, (Human) Q7Z4N1, (Human) Q7Z4N3, (Human) Q7Z4N4, (Human) Q7Z4N5, (Mouse) Q2TV84, (Mouse) O70334, (Mouse) Q2WEA6, (Mouse) Q3TPG5, (Mouse) Q3UEW7, (Mouse) Q3UFV6, (Mouse) Q3UFW1, (Mouse) Q3UG69, (Mouse) Q5U4B3, (Mouse) Q640P5, (Rat) Q2WEA5, (Rat) Q2WEA4
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