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SH2D1A

Gene

SH2 domain containing 1A

HGNCHGNC:10820EnsemblENSG00000183918NCBI Gene4068
Locus: gene with protein productLocation: Xq25

Also known as

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

Also known asIMD5 · LYP · XLP · MTCP1 · DSHP · XLPD · EBVS · SAP
View full nomenclature history (11)
Previous symbolsIMD5, LYP
Alias symbolsXLP, MTCP1, DSHP, XLPD, EBVS, SAP
Previous nameslymphoproliferative syndrome, SH2 domain protein 1A
Alias namesDuncan's disease

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.

Lymphoma
Genetic Diseases, Inborn
Neurodegenerative Diseases
Infections
Lupus Erythematosus, Systemic

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.

SH2 domain containing

Provenance

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