Egl9 family hypoxia-inducible factor 1

Preferred Label : Egl9 family hypoxia-inducible factor 1;

Symbol : EGLN1;

CISMeF acronym : EGLN1;

Type : Gene;

Alternative titles and symbols : Egl9, C. elegans, homolog of, 1; Prolyl hydroxylase domain-containing protein 2; Hypoxia-inducible factor prolyl 4-hydroxylase 2; Hif prolyl 4-hydroxylase 2; Chromosome 1 open reading frame 12; Sm20, rat, homolog of; Zinc finger mynd domain-containing protein 6; PHD2; HPH2; HIFPH2; HIFP4H2; C1ORF12; SM20; ZMYND6;

Ensembl ID : ENSG00000135766;

Prefixed ID : *606425;

Details

Origin ID

606425;

UMLS CUI

C1412925;

Automatic exact mappings (from CISMeF team)
- EGLN1 Gene [NCIt concept]
- EGLN1 wt Allele [NCIt concept]
- Egl Nine Homolog 1 [NCIt concept]
- egl-9 family hypoxia inducible factor 1 [ORDO Gene]
- egl-9 family hypoxia inducible factor 1 [HGNC gene]
HGNC gene
- egl-9 family hypoxia inducible factor 1 [HGNC gene]
NCIt concept(s)
- EGLN1 Gene [NCIt concept]
- EGLN1 wt Allele [NCIt concept]
- Egl Nine Homolog 1 [NCIt concept]
ORDO concept(s)
- egl-9 family hypoxia inducible factor 1 [ORDO Gene]
Phenotypes related
- Erythrocytosis, familial, 3 [OMIM Phenotype]
- Hemoglobin, high altitude adaptation [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- EGLN1 Gene [NCIt concept]
- egl-9 family hypoxia inducible factor 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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