ANKH

Gene

ANKH inorganic pyrophosphate transport regulator

HGNCHGNC:15492 EnsemblENSG00000154122 NCBI Gene56172

Locus: gene with protein productLocation: 5p15.2

Also known as

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

Also known asCCAL2 · CMDJ · HANK · ANK · CPPDD · SLC62A1

View full nomenclature history (11)

Previous symbolsCCAL2, CMDJ

Alias symbolsHANK, ANK, CPPDD, SLC62A1

Previous namescraniometaphyseal dysplasia, Jackson type (dominant), ankylosis, progressive (mouse) homolog, ankylosis, progressive homolog (mouse)

Alias namesMineralization regulator ANKH, solute carrier family 62, member 1

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.

Diabetes Mellitus, Type 2

Diabetic Neuropathies

Chondrocalcinosis

Alcohol drinking

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.

MicroRNA protein coding host genesSolute carrier family 62

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-07-04.

Open TargetsGene–disease associations from the Open Targets Platform.