Sequence Detail

ID/Version

Q7TNH6 Q69Z39 E9QN29 D6RHB4 E9Q5X1 Q8C7Z3 Q9D6D1 Q8C798 (UniProt | EBI)

Last sequence update: 2012-02-22
Last annotation update: 2024-05-29

Sequence description from provider

RecName: Full=Nephrocystin-3;

Provider

SWISS-PROT

Sequence

Polypeptide 1325 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Nphp3	nephronophthisis 3 (adolescent)	54	98	3	7

Sequence references in MGI

J:91453 Olbrich H, et al., Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis. Nat Genet. 2003 Aug;34(4):455-9
J:92575 Okazaki N, et al., Prediction of the coding sequences of mouse homologues of KIAA gene: IV. The complete nucleotide sequences of 500 mouse KIAA-homologous cDNAs identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries. DNA Res. 2004 Jun 30;11(3):205-18
J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:139258 Bergmann C, et al., Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. Am J Hum Genet. 2008 Apr;82(4):959-70