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SLC10A7

Gene

solute carrier family 10 member 7

HGNCHGNC:23088EnsemblENSG00000120519NCBI Gene84068
Locus: gene with protein productLocation: 4q31.22

Also known as

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

Also known asC4orf13 · MGC25043 · DKFZp566M114 · DKFZp313H0531 · DKFZp779O2438
View full nomenclature history (7)
Previous symbolsC4orf13
Alias symbolsMGC25043, DKFZp566M114, DKFZp313H0531, DKFZp779O2438
Previous nameschromosome 4 open reading frame 13, solute carrier family 10, member 7

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.

Scoliosis
Smoking initiation
Alcohol drinking
Communicable Diseases

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.

Solute carrier family 10

Provenance

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