FAM20C protein, human

Preferred Label : FAM20C protein, human;

MeSH note : mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development; RefSeq NT_079592;

MeSH synonym : DMP-4 protein, human; dentin matrix protein 4, human; family with sequence similarity 20, member C protein, human;

Registry Number MeSH : EC 2.7.11.1;

Is substance : O;

UNII : EC 2.7.11.1;

Details

Origin ID

C524449;

UMLS CUI

C2001380;

MeSH term(s) associated for indexing
- casein kinase i [MeSH Descriptor]
- extracellular matrix proteins [MeSH Descriptor]
Record concept(s)
- FAM20C protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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