small vasohibin-binding protein isoform b [Rattus norvegicus]

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Defective tubulin detyrosination causes structural brain abnormalities with cognitive deficiency in humans and mice. [Hum Mol Genet. 2019]
Defective tubulin detyrosination causes structural brain abnormalities with cognitive deficiency in humans and mice.
Pagnamenta AT, Heemeryck P, Martin HC, Bosc C, Peris L, Uszynski I, Gory-Fauré S, Couly S, Deshpande C, Siddiqui A, et al. Hum Mol Genet. 2019 Oct 15; 28(20):3391-3405.
Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia. [Genet Med. 2019]
Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia.
Iqbal Z, Tawamie H, Ba W, Reis A, Halak BA, Sticht H, Uebe S, Kasri NN, Riazuddin S, van Bokhoven H, et al. Genet Med. 2019 Aug; 21(8):1790-1796. Epub 2019 Jan 4.
Crystal structure of the tubulin tyrosine carboxypeptidase complex VASH1-SVBP. [Nat Struct Mol Biol. 2019]
Crystal structure of the tubulin tyrosine carboxypeptidase complex VASH1-SVBP.
Adamopoulos A, Landskron L, Heidebrecht T, Tsakou F, Bleijerveld OB, Altelaar M, Nieuwenhuis J, Celie PHN, Brummelkamp TR, Perrakis A. Nat Struct Mol Biol. 2019 Jul; 26(7):567-570. Epub 2019 Jul 1.

RefSeq mRNA
See reference mRNA sequence for the Svbp gene (NM_001038992.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the Svbp gene.

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Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
Transcript/Protein Information [PANTHER Classification System]
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PANTHER Classification System

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