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TRPM6 - transient receptor potential cation channel subfamily M member 6
- Synonym(s) : CHAK2, FLJ22628
- Previous symbols and names : HOMG, HSH, hypomagnesemia, secondary hypocalcemia, transient receptor potential cation channel, subfamily M, member 6
- Type : gene with protein product
- Chromosomal location : 9q21.13
- OMIM: 607009
- HGNC: 17995
- UniProtKB: Q9BX84
- Genatlas: TRPM6
- GenCC: TRPM6
- Ensembl: ENSG00000119121
- IUPHAR-DB: 498
- Reactome: Q9BX84
- LOVD: TRPM6
Diseases list
- Disease-causing germline mutation(s) in Primary hypomagnesemia with secondary hypocalcemia
ORPHA:30924

Additional information
Patient-centred resources for this gene
Research activities on this gene
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