Nuclear factor I/x

Preferred Label : Nuclear factor I/x;

Symbol : NFIX;

CISMeF acronym : NFIX;

Type : Gene;

Alternative titles and symbols : Nuclear factor I, X-type; Ccaat-binding transcription factor; NF1A;

Ensembl ID : ENSG00000008441;

Prefixed ID : *164005;

Details

Origin ID

164005;

UMLS CUI

C1417707;

Automatic exact mappings (from CISMeF team)
- NFIX Gene [NCIt concept]
- NFIX wt Allele [NCIt concept]
- Nuclear Factor 1 A-Type [NCIt concept]
- Nuclear Factor 1 C-Type [NCIt concept]
- Nuclear Factor 1 X-Type [NCIt concept]
- Nuclear Factor-I [NCIt concept]
- ccaat-binding factor [MeSH Descriptor]
- nfi transcription factors [MeSH Descriptor]
- nuclear factor I C [HGNC gene]
- nuclear factor I X [ORDO Gene]
- nuclear factor I X [HGNC gene]
HGNC gene
- nuclear factor I X [HGNC gene]
NCIt concept(s)
- NFIX Gene [NCIt concept]
- NFIX wt Allele [NCIt concept]
- Nuclear Factor 1 X-Type [NCIt concept]
ORDO concept(s)
- nuclear factor I X [ORDO Gene]
Phenotypes related
- Malan syndrome [OMIM Phenotype]
- Marshall-smith syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NFIX Gene [NCIt concept]
- nuclear factor I X [HGNC gene]

Keyword's position in hierarchy(ies) :

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