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RPGRIP1L protein, human MeSH Supplementary Concept Data 2025


MeSH Supplementary
RPGRIP1L protein, human
Unique ID
C532826
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C532826
Entry Term(s)
KIAA1005 protein, human
NPHP8 protein, human
Registry Numbers
0
Heading Mapped to
*Adaptor Proteins, Signal Transducing
Frequency
42
Note
a centrosomal protein that interacts with nephrocystin-4; mutations leads to Joubert syndrome type 7 and Meckel syndrome type 5; GenBank AB023222
Source
Nat Genet 2007 Jul;39(7):882-8
Date of Entry
2008/11/09
Revision Date
2016/02/29
RPGRIP1L protein, human Preferred
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