Syntaxin 1b - CISMeF

Preferred Label : Syntaxin 1b;

Symbol : STX1B;

CISMeF acronym : STX1B;

Type : Gene;

Ensembl ID : ENSG00000099365;

Prefixed ID : *601485;

Details

Origin ID

601485;

UMLS CUI

C1420499;

Automatic exact mappings (from CISMeF team)
- syntaxin 1 [MeSH Descriptor]
- syntaxin 1B [ORDO Gene]
- syntaxin 1B [HGNC gene]
HGNC gene
- syntaxin 1B [HGNC gene]
NCIt concept(s)
- STX1B Gene [NCIt concept]
- STX1B wt Allele [NCIt concept]
- Syntaxin-1B [NCIt concept]
- Syntaxin-1B Isoform 2 [NCIt concept]
ORDO concept(s)
- syntaxin 1B [ORDO Gene]
Phenotypes related
- Generalized epilepsy with febrile seizures plus, type 9 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- syntaxin 1B [HGNC gene]

Keyword's position in hierarchy(ies) :

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