RIKEN cDNA 1110020C03 [Mus musculus]

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Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice. [JCI Insight. 2023]
Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice.
Ma A, Zhou J, Ali H, Abbas T, Ali I, Muhammad Z, Dil S, Chen J, Huang X, Ma H, et al. JCI Insight. 2023 Feb 8; 8(3). Epub 2023 Feb 8.
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome. [Am J Med Genet A. 2011]
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome.
Rorick NK, Kinoshita A, Weirather JL, Peyrard-Janvid M, de Lima RL, Dunnwald M, Shanske AL, Moretti-Ferreira D, Koillinen H, Kere J, et al. Am J Med Genet A. 2011 Jun; 155A(6):1314-21. Epub 2011 May 13.
Szt2, a novel gene for seizure threshold in mice. [Genes Brain Behav. 2009]
Szt2, a novel gene for seizure threshold in mice.
Frankel WN, Yang Y, Mahaffey CL, Beyer BJ, O'Brien TP. Genes Brain Behav. 2009 Jul; 8(5):568-76.

RefSeq protein isoforms
See 4 reference sequence protein isoforms for the Cfap57 gene.

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Protein