Homo sapiens Rho related BTB domain containing 2 (RHOBTB2), transcript - Nucleotide

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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.

RefSeq protein product
See the reference protein sequence for rho-related BTB domain-containing protein 2 isoform 3 (NP_055993.2).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens Rho related BTB domain containing 2 (RHOBTB2), transcript variant 3...
Homo sapiens Rho related BTB domain containing 2 (RHOBTB2), transcript variant 3, mRNA
gi|1765945227|ref|NM_015178.3|

Nucleotide
Oleeae ribosomal protein L32 (rpl32) gene, partial cds; and rpl32-trnL intergeni...
Oleeae ribosomal protein L32 (rpl32) gene, partial cds; and rpl32-trnL intergenic spacer, partial sequence; chloroplast.
PopSet: 297522910

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Nucleotide