Inverted formin 2

Preferred Label : Inverted formin 2;

Symbol : INF2;

CISMeF acronym : INF2;

Type : Gene;

Alternative titles and symbols : Formin, inverted, 2; Chromosome 14 open reading frame 173; C14ORF173;

Ensembl ID : ENSG00000203485;

Prefixed ID : *610982;

Details

Origin ID

610982;

UMLS CUI

C1539048;

Automatic exact mappings (from CISMeF team)
- inverted formin 2 [HGNC gene]
- inverted formin, FH2 and WH2 domain containing [ORDO Gene]
HGNC gene
- inverted formin 2 [HGNC gene]
NCIt concept(s)
- INF2 Gene [NCIt concept]
- INF2 wt Allele [NCIt concept]
- Inverted Formin-2 [NCIt concept]
ORDO concept(s)
- inverted formin, FH2 and WH2 domain containing [ORDO Gene]
Phenotypes related
- Charcot-marie-tooth disease, dominant intermediate e [OMIM Phenotype]
- Focal segmental glomerulosclerosis 5 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- INF2 Gene [NCIt concept]
- inverted formin 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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