Williams-Beuren syndrome chromosome region 17 homolog (human) [Mus mus - Protein

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Galnt17 loss-of-function leads to developmental delay and abnormal coordination, activity, and social interactions with cerebellar vermis pathology. [Dev Biol. 2022]
Galnt17 loss-of-function leads to developmental delay and abnormal coordination, activity, and social interactions with cerebellar vermis pathology.
Chen CY, Seward CH, Song Y, Inamdar M, Leddy AM, Zhang H, Yoo J, Kao WC, Pawlowski H, Stubbs LJ. Dev Biol. 2022 Oct; 490:155-171. Epub 2022 Aug 21.
A Mouse Mutation That Dysregulates Neighboring Galnt17 and Auts2 Genes Is Associated with Phenotypes Related to the Human AUTS2 Syndrome. [G3 (Bethesda). 2019]
A Mouse Mutation That Dysregulates Neighboring Galnt17 and Auts2 Genes Is Associated with Phenotypes Related to the Human AUTS2 Syndrome.
Weisner PA, Chen CY, Sun Y, Yoo J, Kao WC, Zhang H, Baltz ET, Troy JM, Stubbs L. G3 (Bethesda). 2019 Nov 5; 9(11):3891-3906. Epub 2019 Nov 5.
A putative polypeptide N-acetylgalactosaminyltransferase/Williams-Beuren syndrome chromosome region 17 (WBSCR17) regulates lamellipodium formation and macropinocytosis. [J Biol Chem. 2012]
A putative polypeptide N-acetylgalactosaminyltransferase/Williams-Beuren syndrome chromosome region 17 (WBSCR17) regulates lamellipodium formation and macropinocytosis.
Nakayama Y, Nakamura N, Oki S, Wakabayashi M, Ishihama Y, Miyake A, Itoh N, Kurosaka A. J Biol Chem. 2012 Sep 14; 287(38):32222-35. Epub 2012 Jul 11.

RefSeq protein isoforms
See 2 reference sequence protein isoforms for the Galnt17 gene.

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