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DPYSL4

Gene

dihydropyrimidinase like 4

HGNCHGNC:3016EnsemblENSG00000151640NCBI Gene10570
Locus: gene with protein productLocation: 10q26.3

Also known as

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

Also known asULIP4 · DRP-4 · CRMP3
View full nomenclature history (4)
Alias symbolsULIP4, DRP-4, CRMP3
Previous namesdihydropyrimidinase-like 4

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.

Obesity disorder
Familial focal epilepsy with variable foci
Autosomal recessive primary microcephaly
Genetic central nervous system malformation
Genetic developmental and epileptic encephalopathy

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.

M38 metallopeptidases

Provenance

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