Homeobox b1 - CISMeF

Preferred Label : Homeobox b1;

Symbol : HOXB1;

CISMeF acronym : HOXB1;

Type : Gene;

Alternative titles and symbols : Homeobox 2i; Hox-2.9, mouse, homolog of; HOX2I;

Ensembl ID : ENSG00000120094;

Prefixed ID : *142968;

Details

Origin ID

142968;

UMLS CUI

C1415663;

Automatic exact mappings (from CISMeF team)
- HOXB1 Gene [NCIt concept]
- HOXB1 wt Allele [NCIt concept]
- Homeobox Protein Hox-B1 [NCIt concept]
- homeobox B1 [ORDO Gene]
- homeobox B1 [HGNC gene]
HGNC gene
- homeobox B1 [HGNC gene]
NCIt concept(s)
- HOXB1 Gene [NCIt concept]
- HOXB1 wt Allele [NCIt concept]
- Homeobox Protein Hox-B1 [NCIt concept]
ORDO concept(s)
- homeobox B1 [ORDO Gene]
Phenotypes related
- Facial paresis, hereditary congenital, 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HOXB1 Gene [NCIt concept]
- homeobox B1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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