VITO1 protein [Homo sapiens]

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A Molecular Study of Pediatric Spindle and Sclerosing Rhabdomyosarcoma: Identification of Novel and Recurrent VGLL2-related Fusions in Infantile Cases. [Am J Surg Pathol. 2016]
A Molecular Study of Pediatric Spindle and Sclerosing Rhabdomyosarcoma: Identification of Novel and Recurrent VGLL2-related Fusions in Infantile Cases.
Alaggio R, Zhang L, Sung YS, Huang SC, Chen CL, Bisogno G, Zin A, Agaram NP, LaQuaglia MP, Wexler LH, et al. Am J Surg Pathol. 2016 Feb; 40(2):224-35.
Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases. [Neurogenetics. 2012]
Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases.
Rosenfeld JA, Amrom D, Andermann E, Andermann F, Veilleux M, Curry C, Fisher J, Deputy S, Aylsworth AS, Powell CM, et al. Neurogenetics. 2012 Feb; 13(1):31-47. Epub 2012 Jan 5.
VITO-1, a novel vestigial related protein is predominantly expressed in the skeletal muscle lineage. [Mech Dev. 2002]
VITO-1, a novel vestigial related protein is predominantly expressed in the skeletal muscle lineage.
Mielcarek M, Günther S, Krüger M, Braun T. Mech Dev. 2002 Dec; 119 Suppl 1:S269-74.

RefSeq protein isoforms
See 4 reference sequence protein isoforms for the VGLL2 gene.

Nucleotide
Nucleotide sequence from coding region
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Transcript/Protein Information [PANTHER Classification System]
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reagents [ExactAntigen/Labome]
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ExactAntigen/Labome

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Protein