C9orf72 protein, human

Preferred Label : C9orf72 protein, human;

MeSH note : mutation leads to both chromsome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia; GenBank BC020851;

MeSH synonym : chromosome 9 open reading frame 72 protein, human; MGC23980 protein, human;

Is substance : O;

Details

Origin ID

C568651;

UMLS CUI

C3252868;

MeSH term(s) associated for indexing
- C9orf72 Protein [MeSH Descriptor]
- proteins [MeSH Descriptor]
Record concept(s)
- C9orf72 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]
UMLS correspondences (same concept)
- Guanine Nucleotide Exchange Factor C9orf72 [NCIt concept]

Keyword's position in hierarchy(ies) :

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