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TRPM6

Gene

transient receptor potential cation channel subfamily M member 6

HGNCHGNC:17995EnsemblENSG00000119121NCBI Gene140803
Locus: gene with protein productLocation: 9q21.13

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asHOMG · HSH · CHAK2 · FLJ22628
View full nomenclature history (6)
Previous symbolsHOMG, HSH
Alias symbolsCHAK2, FLJ22628
Previous nameshypomagnesemia, secondary hypocalcemia, transient receptor potential cation channel, subfamily M, member 6

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Genetic Diseases, Inborn
Nephrolithiasis
Bladder calculus
Alcohol drinking
Neurodegenerative Diseases
Dementia, Vascular

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Transient receptor potential cation channelsAlpha kinases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.