Ammecr1 protein, mouse

Preferred Label : Ammecr1 protein, mouse;

MeSH note : AMMECR1 - Alport syndrome, mental retardation, midface hypolplasia, and elliptocytosis chromosomal region gene 1; may be a regulatory factor involved in development of above syndrome; RefSeq NM_019496;

MeSH synonym : Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 homolog (human) protein, mouse;

Is substance : O;

Details

Origin ID

C485590;

UMLS CUI

C1313773;

MeSH term(s) associated for indexing
- proteins [MeSH Descriptor]
Record concept(s)
- Ammecr1 protein, mouse [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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