Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 140803
Gene Symbol: TRPM6
TRPM6
CUI: C1865974
Disease: Hypomagnesemia 1, Intestinal
Hypomagnesemia 1, Intestinal 		0.800 GeneticVariation UNIPROT Mutations in the TRPM6 gene, encoding the epithelial Mg(2+) channel TRPM6 (transient receptor potential melastatin 6), have been proven to be the molecular cause of hypomagnesemia with secondary hypocalcemia (HSH; OMIM 602014). 23942199

2014
Entrez Id: 140803
Gene Symbol: TRPM6
TRPM6
CUI: C1865974
Disease: Hypomagnesemia 1, Intestinal
Hypomagnesemia 1, Intestinal 		0.800 GeneticVariation UNIPROT Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia. 14976260

2004
Entrez Id: 140803
Gene Symbol: TRPM6
TRPM6
CUI: C1865974
Disease: Hypomagnesemia 1, Intestinal
Hypomagnesemia 1, Intestinal 		0.800 GeneticVariation UNIPROT Using a positional candidate gene approach, we identified mutations in TRPM6 (also known as CHAK2), encoding TRPM6, in autosomal-recessive hypomagnesemia with secondary hypocalcemia (HSH, OMIM 602014), previously mapped to chromosome 9q22 (ref.3). 12032568

2002
Entrez Id: 140803
Gene Symbol: TRPM6
TRPM6
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.300 GeneticVariation UNIPROT

Entrez Id: 140803
Gene Symbol: TRPM6
TRPM6
CUI: C0345958
Disease: Large cell carcinoma of lung
Large cell carcinoma of lung 		0.300 GeneticVariation UNIPROT