Synaptojanin 1

Preferred Label : Synaptojanin 1;

Symbol : SYNJ1;

CISMeF acronym : SYNJ1;

Type : Gene;

Ensembl ID : ENSG00000159082;

Prefixed ID : *604297;

Details

Origin ID

604297;

UMLS CUI

C1420552;

Automatic exact mappings (from CISMeF team)
- SYNJ1 Gene [NCIt concept]
- Synaptojanin-1 [NCIt concept]
- synaptojanin 1 [ORDO Gene]
- synaptojanin 1 [HGNC gene]
HGNC gene
- synaptojanin 1 [HGNC gene]
NCIt concept(s)
- SYNJ1 Gene [NCIt concept]
- SYNJ1 wt Allele [NCIt concept]
- Synaptojanin-1 [NCIt concept]
ORDO concept(s)
- synaptojanin 1 [ORDO Gene]
Phenotypes related
- Developmental and epileptic encephalopathy 53 [OMIM Phenotype]
- Parkinson disease 20, early-onset [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SYNJ1 Gene [NCIt concept]
- synaptojanin 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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