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ERLIN1

Gene

ER lipid raft associated 1

HGNCHGNC:16947EnsemblENSG00000107566NCBI Gene10613
Locus: gene with protein productLocation: 10q24.31

Also known as

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

Also known asC10orf69 · SPFH1 · KE04 · Erlin-1 · SPG62
View full nomenclature history (8)
Previous symbolsC10orf69, SPFH1
Alias symbolsKE04, Erlin-1, SPG62
Previous nameschromosome 10 open reading frame 69, SPFH domain family, member 1
Alias namesBand_7 23-211 Keo4 (Interim) similar to C.elegans protein C42C1.9

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.

Spastic Paraplegia, Hereditary
Cystic Fibrosis
Intelligence
Liver Diseases
Diabetes Mellitus, Type 2
Carcinoma, Squamous Cell

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.

Small nucleolar RNA protein coding host genes

Provenance

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