small vasohibin-binding protein isoform X1 [Homo sapiens]

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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.
Vasohibin 2 is transcriptionally activated and promotes angiogenesis in hepatocellular carcinoma. [Oncogene. 2013]
Vasohibin 2 is transcriptionally activated and promotes angiogenesis in hepatocellular carcinoma.
Xue X, Gao W, Sun B, Xu Y, Han B, Wang F, Zhang Y, Sun J, Wei J, Lu Z, et al. Oncogene. 2013 Mar 28; 32(13):1724-34. Epub 2012 May 21.

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Protein