TRPM7 wt Allele

Human TRPM7 wild-type allele is located in the vicinity of 15q21 and is approximately 130 kb in length. This allele, which encodes transient receptor potential cation channel subfamily M member 7 protein, is involved in the mediation of both protein phosphorylation and ion transport. Mutation of the gene is associated with amyotrophic lateral sclerosis-parkinsonism/dementia complex type 1. A chromosomal rearrangement of this gene and the CYP19A1 gene is associated with aromatase excess syndrome. (NCI Thesaurus)

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TRPM7 Gene

This gene plays a role in both ion transport and protein phosphorylation.

TRPM5 wt Allele

Human TRPM5 wild-type allele is located in the vicinity of 11p15.5 and is approximately 19 kb in length. This allele, which encodes…

TRPM5 Gene

This gene is involved in the regulation of cellular calcium flux.

TRPC4 wt Allele

Human TRPC4 wild-type allele is located in the vicinity of 13q13.3 and is approximately 234 kb in length. This allele, which encodes…

TRPC4 Gene

This gene plays a role in calcium ion transport.

TRPC2 Gene

Human TRPC2 gene is located within 11p15.4-p15.3 and is approximately 28 kb in length. This gene is a pseudogene that has no…