Formin 1 - CISMeF

Preferred Label : Formin 1;

Symbol : FMN1;

CISMeF acronym : FMN1;

Type : Gene;

Alternative titles and symbols : Formin; Limb deformity, mouse, homolog of; FMN; LD;

Ensembl ID : ENSG00000248905;

Prefixed ID : *136535;

Details

Origin ID

136535;

UMLS CUI

C1539521;

Automatic exact mappings (from CISMeF team)
- EPM2A glucan phosphatase, laforin [ORDO Gene]
- FOXC2 wt Allele [NCIt concept]
- Flavin mononucleotide [LOINC component]
- Laboratory diagnosis (contextual qualifier) (qualifier value) [SNOMED CT concept]
- Left Deltoid [NCIt concept]
- Linkage Disequilibrium [NCIt concept]
- flavin mononucleotide [MeSH Descriptor]
- formin 1 [HGNC gene]
- lateral dorsal nucleus [UBERON concept]
HGNC gene
- formin 1 [HGNC gene]
See also inter- (CISMeF)
- Formins [MeSH Descriptor]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- formin 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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