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Homo sapiens KIAA0717 mRNA for KIAA0717 protein

GenBank: AB018260.2

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Articles about the RHOBTB2 gene

Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders. [Genet Med. 2023]
Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders.
Langhammer F, Maroofian R, Badar R, Gregor A, Rochman M, Ratliff JB, Koopmans M, Herget T, Hempel M, Kortüm F, et al. Genet Med. 2023 Aug; 25(8):100885. Epub 2023 May 8.
Mild head trauma: Acute encephalopathy trigger in children with RHOBTB2 de novo mutation. [Neurologia (Engl Ed). 2022]
Mild head trauma: Acute encephalopathy trigger in children with RHOBTB2 de novo mutation.
Jové Blanco A, Lorente Romero J, Barredo Valderrama E, Castro de Castro P. Neurologia (Engl Ed). 2022 Oct; 37(8):702-703.
Identification of RHOBTB2 aberration as an independent prognostic indicator in acute myeloid leukemia. [Aging (Albany NY). 2021]
Identification of RHOBTB2 aberration as an independent prognostic indicator in acute myeloid leukemia.
Liu P, Ma Q, Chen H, Zhang L, Zhang X. Aging (Albany NY). 2021 Jun 1; 13(11):15269-15284. Epub 2021 Jun 1.

Reference sequence information

RefSeq alternative splicing
See 14 reference mRNA sequence splice variants for the RHOBTB2 gene.

More about the RHOBTB2 gene

The protein encoded by this gene is a small Rho GTPase and a candidate tumor suppressor. The encoded protein interacts with the cullin-3 pro...
Also Known As: DBC2, DEE64, EIEE64, p83

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Protein
Protein sequence from Nucleotide coding region
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reagents [ExactAntigen/Labome]
reagents
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