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SDE2

Gene

spliceosome associated SDE2

HGNCHGNC:26643EnsemblENSG00000143751NCBI Gene163859
Locus: gene with protein productLocation: 1q42.12

Also known as

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

Also known asC1orf55 · FLJ35382
View full nomenclature history (5)
Previous symbolsC1orf55
Alias symbolsFLJ35382
Previous namesSDE2 telomere maintenance homolog, chromosome 1 open reading frame 55, SDE2 telomere maintenance homolog (S. pombe)

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.

Neurodegenerative Diseases
Nephritis
Myasthenia Gravis
Vascular Diseases
Toxoplasmosis
Miyoshi myopathy
Prostatic Neoplasms

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.

Spliceosomal C complexSpliceosomal P complex

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-07-02.
Open TargetsGene–disease associations from the Open Targets Platform.