TRPM7/CYP19A1 Fusion Gene

A fusion gene that results from a complex chromosomal rearrangement of the q arm of chromosome 15 where exon 1 of the TRPM7 gene is fused with exon 2 of the CYP19A1 gene. This fused gene causes increased expression of the CYP19A1 gene and is associated with aromatase excess syndrome. (NCI Thesaurus)

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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…

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.