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SLC67A2

Gene

solute carrier family 67 member 2

HGNCHGNC:28158EnsemblENSG00000135953NCBI Gene84804
Locus: gene with protein productLocation: 2q12.1

Also known as

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

Also known asMFSD9 · MGC11332
View full nomenclature history (3)
Previous symbolsMFSD9
Alias symbolsMGC11332
Previous namesmajor facilitator superfamily domain containing 9

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.

Pulmonary Emphysema
Musculoskeletal Diseases
Pulmonary Disease, Chronic Obstructive
Eosinophilic Esophagitis
Ovarian neoplasm
Pre-Eclampsia

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 67

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-07-09.
Open TargetsGene–disease associations from the Open Targets Platform.