PROS1 protein, human

Preferred Label : PROS1 protein, human;

MeSH note : The PROS1 mutations would cause misfolding of the Protein S protein, resulting in the impairment of secretion, which is consistent with the type I PS deficiency phenotype; RefSeq NP_000313.1;

MeSH synonym : protein S, human;

Is substance : O;

Details

Origin ID

C523390;

UMLS CUI

C2002622;

MeSH term(s) associated for indexing
- blood proteins [MeSH Descriptor]
- protein S [MeSH Descriptor]
Record concept(s)
- PROS1 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Pharmacologic Substance [UMLS semantic type]
UMLS correspondences (same concept)
- Vitamin K-Dependent Protein S [NCIt concept]

Keyword's position in hierarchy(ies) :

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