Transient receptor potential cation channel, subfamily M, member 7

This TRPM7 gene resembles TRPM6 in its ability to channel divalent cations including magnesium, so it might play a role magnesium homeostasis. Genetic variations are associated with amyotrophic lateral sclerosis, too.

Genetests:

Clinic	Method	Massive parallel sequencing
	Turnaround	25 days
	Specimen type	genomic DNA

Research	Method	Genomic sequencing of the entire coding region
	Turnaround	25 days
	Specimen type	genomic DNA

Related Diseases:

Hypomagnesemia
	EGFR
	Gitelman syndrome
		SLC12A3
	Hereditary myokymia type 1
		KCNA1
	Hypomagnesemia with hypercalciuria and nephrocalcinosis
		CLDN16
	Hypomagnesemia with hypercalciuria and nephrocalcinosis with ocular involvement
		CLDN19
	Hypomagnesemia with normocalciuria
		EGF
	Intestinal hypomagnesemia with secondary hypocalcemia
		TRPM6
	Isolated dominant hypomagnesemia
		FXYD2
	Renal cysts and diabetes (RCAD)
		HNF1B
	Renal hypomagnesemia 6
		CNNM2
	TRPM7

Update:

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