Pre-b-cell leukemia transcription factor 1

Preferred Label : Pre-b-cell leukemia transcription factor 1;

Symbol : PBX1;

CISMeF acronym : PBX1;

Type : Gene;

Included titles and symbols : Pre-b-cell leukemia transcription factor pseudogene 1; Pbx1/e2a fusion gene; PBXP1;

Ensembl ID : ENSG00000185630;

Prefixed ID : *176310;

Details

Origin ID

176310;

UMLS CUI

C1418285;

Automatic exact mappings (from CISMeF team)
- PBX homeobox 1 [HGNC gene]
- PBX homeobox 1 [ORDO Gene]
- PBX1 Gene [NCIt concept]
- Pre-B-Cell Leukemia Transcription Factor 1 [MeSH Descriptor]
- Pre-B-Cell Leukemia Transcription Factor 1 [NCIt concept]
- TCF3/PBX1 Fusion Gene [NCIt concept]
HGNC gene
- PBX homeobox 1 [HGNC gene]
NCIt concept(s)
- PBX1 Gene [NCIt concept]
- PBX1 wt Allele [NCIt concept]
- Pre-B-Cell Leukemia Transcription Factor 1 [NCIt concept]
ORDO concept(s)
- PBX homeobox 1 [ORDO Gene]
Phenotypes related
- Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PBX homeobox 1 [HGNC gene]
- PBX1 Gene [NCIt concept]

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