Paired box gene 3

Preferred Label : Paired box gene 3;

Symbol : PAX3;

CISMeF acronym : PAX3;

Type : Gene;

Alternative titles and symbols : Paired domain gene hup2; HUP2;

Included titles and symbols : Pax3/fkhr fusion gene;

Ensembl ID : ENSG00000135903;

Prefixed ID : *606597;

Details

Origin ID

606597;

UMLS CUI

C1335192;

Automatic exact mappings (from CISMeF team)
- FOXO1/PAX3 Fusion Gene [NCIt concept]
- PAX3 Gene [NCIt concept]
- PAX3 gene [LOINC component]
- PAX3 wt Allele [NCIt concept]
- PAX3/FOXO1 Fusion Gene [NCIt concept]
- Paired Box Protein Pax-3 [NCIt concept]
- paired box 3 [ORDO Gene]
- paired box 3 [HGNC gene]
HGNC gene
- paired box 3 [HGNC gene]
NCIt concept(s)
- PAX3 Gene [NCIt concept]
- PAX3 wt Allele [NCIt concept]
- Paired Box Protein Pax-3 [NCIt concept]
ORDO concept(s)
- paired box 3 [ORDO Gene]
Phenotypes related
- Craniofacial-deafness-hand syndrome [OMIM Phenotype]
- Rhabdomyosarcoma 2 [OMIM Phenotype]
- Waardenburg syndrome, type 1 [OMIM Phenotype]
- Waardenburg syndrome, type 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PAX3 Gene [NCIt concept]
- PAX3 gene [LOINC component]
- paired box 3 [HGNC gene]

Keyword's position in hierarchy(ies) :

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