NPHP3 (Entrez ID: 27031)

Entrez Gene ID 27031
Official Gene Symbol NPHP3 (GeneCards)
Full name nephrocystin 3
Location 3q22.1
Other ids Vega : OTTHUMG00000159713
MIM : 608002
HGNC : HGNC:7907
Ensembl : ENSG00000113971
Other names MKS7, NPH3, RHPD, RHPD1, SLSN3, CFAP31
Summary This gene encodes a protein containing a coiled-coil (CC) domain, a tubulin-tyrosine ligase (TTL) domain, and a tetratrico peptide repeat (TPR) domain. The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development. Mutations in this gene are associated with nephronophthisis type 3, and also with renal-hepatic-pancreatic dysplasia, and Meckel syndrome type 7. Naturally occurring read-through transcripts exist between this gene and the downstream ACAD11 (acyl-CoA dehydrogenase family, member 11) gene. [provided by RefSeq, Feb 2011]

Variants

Found 1 variant in this database.