RPGRIP1L protein, human

Preferred Label : RPGRIP1L protein, human;

MeSH note : a centrosomal protein that interacts with nephrocystin-4; mutations leads to Joubert syndrome type 7 and Meckel syndrome type 5; GenBank AB023222;

MeSH synonym : KIAA1005 protein, human; NPHP8 protein, human;

Is substance : O;

Details

Origin ID

C532826;

UMLS CUI

C2607352;

MeSH term(s) associated for indexing
- adaptor proteins, signal transducing [MeSH Descriptor]
Record concept(s)
- RPGRIP1L 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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