EMILIN1 wt Allele

Preferred Label : EMILIN1 wt Allele;

NCIt synonyms : EMILIN wt Allele; EMILIN; DKFZP586M121; EMILIN-1; EMILIN1; Elastin Microfibril Interfacer 1 wt Allele; Elastin Microfibril Interface Located Gene; gp115; EMI;

NCIt definition : Human EMILIN1 wild-type allele is located within 2p23.3 and is approximately 8 kb in length. This allele, which encodes EMILIN-1 protein, plays a role in the regulation of both blood vessel structure and transforming growth factor beta signaling.;

GenBank Accession Number : NM_007046;

Details

Origin ID

C52483;

UMLS CUI

C1705457;

OMIM relation
- Elastin microfibril interfacer 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_has_physical_location
- 2: 27213585-27220914 [NCIt concept]
gene_in_chromosomal_location
- 2p23.3 [NCIt concept]
gene_plays_role_in_process
- Cell Adhesion Process [NCIt concept]
- Cell Growth [NCIt concept]
- Cell Movement [NCIt concept]
- Morphogenesis [NCIt concept]
- Organogenesis [NCIt concept]
- Wound Repair [NCIt concept]

Keyword's position in hierarchy(ies) :

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