signal-induced proliferation-associated 1-like protein 3 isoform X2 [M - Protein

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A 16.7 kb deletion in Sipa1l3 is associated with juvenile cataract in mice. [Mamm Genome. 2017]
A 16.7 kb deletion in Sipa1l3 is associated with juvenile cataract in mice.
Walker LR, Tosky ER, Sutton KM, Griess R, Abebe MD, Barnes SY, Cunnigham T, Kachman SD, Nielsen MK, Ciobanu DC. Mamm Genome. 2017 Dec; 28(11-12):515-519. Epub 2017 Sep 26.
Mutations in SIPA1L3 cause eye defects through disruption of cell polarity and cytoskeleton organization. [Hum Mol Genet. 2015]
Mutations in SIPA1L3 cause eye defects through disruption of cell polarity and cytoskeleton organization.
Greenlees R, Mihelec M, Yousoof S, Speidel D, Wu SK, Rinkwitz S, Prokudin I, Perveen R, Cheng A, Ma A, et al. Hum Mol Genet. 2015 Oct 15; 24(20):5789-804. Epub 2015 Jul 30.
iSyTE: integrated Systems Tool for Eye gene discovery. [Invest Ophthalmol Vis Sci. 2012]
iSyTE: integrated Systems Tool for Eye gene discovery.
Lachke SA, Ho JW, Kryukov GV, O'Connell DJ, Aboukhalil A, Bulyk ML, Park PJ, Maas RL. Invest Ophthalmol Vis Sci. 2012 Mar; 53(3):1617-27. Epub 2012 Mar 21.

RefSeq mRNA
See reference mRNA sequence for the Sipa1l3 gene (XM_006540404.5).
RefSeq protein isoforms
See 16 reference sequence protein isoforms for the Sipa1l3 gene.

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Protein