Homeobox c13 - CISMeF

Preferred Label : Homeobox c13;

Symbol : HOXC13;

CISMeF acronym : HOXC13;

Type : Gene;

Alternative titles and symbols : Homeobox 3g; HOX3G;

Included titles and symbols : Hoxc13/nup98 fusion gene;

Ensembl ID : ENSG00000123364;

Prefixed ID : *142976;

Details

Origin ID

142976;

UMLS CUI

C1415677;

Automatic exact mappings (from CISMeF team)
- HOXC13 Gene [NCIt concept]
- HOXC13 wt Allele [NCIt concept]
- Homeobox Protein Hox-C13 [NCIt concept]
- NUP98/HOXC13 Fusion Gene [NCIt concept]
- homeobox C13 [ORDO Gene]
- homeobox C13 [HGNC gene]
HGNC gene
- homeobox C13 [HGNC gene]
NCIt concept(s)
- HOXC13 Gene [NCIt concept]
- HOXC13 wt Allele [NCIt concept]
- Homeobox Protein Hox-C13 [NCIt concept]
ORDO concept(s)
- homeobox C13 [ORDO Gene]
Phenotypes related
- Ectodermal dysplasia 9, hair/nail type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HOXC13 Gene [NCIt concept]
- homeobox C13 [HGNC gene]

Keyword's position in hierarchy(ies) :

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