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FLVCR1

Gene

FLVCR choline and heme transporter 1

HGNCHGNC:24682EnsemblENSG00000162769NCBI Gene28982
Locus: gene with protein productLocation: 1q32.3

Also known as

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

Also known asAXPC1 · FLVCR · MFSD7B · PCA · SLC49A1
View full nomenclature history (8)
Previous symbolsAXPC1
Alias symbolsFLVCR, MFSD7B, PCA, SLC49A1
Previous namesataxia, posterior column 1, with retinitis pigmentosa, feline leukemia virus subgroup C cellular receptor 1, FLVCR heme transporter 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.

Retinitis Pigmentosa
Genetic Diseases, Inborn
Neurodegenerative Diseases
Hereditary sensory and autonomic neuropathy

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 49

Provenance

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