elastin microfibril interface located protein

Preferred Label : elastin microfibril interface located protein;

MeSH note : inherited deficiency of these cpds in neutrophils causes defective neutrophil adhesion & increased susceptibility to bacterial infections; MW was thought to be 110,000, but was subsequently determined to be 180,000;

CISMeF synonym : EMILIN1 protein, human; Emilin1 protein, mouse;

MeSH synonym : emilin-1; emilin;

MeSH hyponym : elastin microfibril interfacer 1 protein, mouse; elastin microfibril interfacer 1 protein, human;

Is substance : O;

Details

Origin ID

C030340;

UMLS CUI

C0962292;

Automatic exact mappings (from CISMeF team)
- EMILIN1 Gene [NCIt concept]
- EMILIN1 wt Allele [NCIt concept]
- Elastin microfibril interfacer 1 [OMIM gene]
- elastin microfibril interfacer 1 [ORDO Gene]
Currated CISMeF NLP mapping
- EMILIN-1 [NCIt concept]
MeSH term(s) associated for indexing
- membrane glycoproteins [MeSH Descriptor]
Record concept(s)
- EMILIN1 protein, human [MeSH concept]
- Emilin1 protein, mouse [MeSH concept]
- elastin microfibril interface located protein [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]
UMLS correspondences (same concept)
- EMILIN-1 [NCIt concept]

Keyword's position in hierarchy(ies) :

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