Tbc1 domain family, member 2b

Preferred Label : Tbc1 domain family, member 2b;

Symbol : TBC1D2B;

Type : Gene;

Alternative titles and symbols : KIAA1055;

Ensembl ID : ENSG00000167202;

Prefixed ID : *619152;

Details

Origin ID

619152;

UMLS CUI

C1823230;

Automatic exact mappings (from CISMeF team)
- TBC1 Domain Family Member 2B [NCIt concept]
Currated CISMeF NLP mapping
- TBC1 domain family member 2B [HGNC gene]
- TBC1D2B Gene [NCIt concept]
HGNC gene
- TBC1 domain family member 2B [HGNC gene]
NCIt concept(s)
- TBC1 Domain Family Member 2B [NCIt concept]
- TBC1D2B Gene [NCIt concept]
- TBC1D2B wt Allele [NCIt concept]
Phenotypes related
- Neurodevelopmental disorder with seizures and gingival overgrowth [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- TBC1 domain family member 2B [HGNC gene]
- TBC1D2B Gene [NCIt concept]
Validated automatic mappings to BTNT
- TBC1D2B wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

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