Homo sapiens recombination activating protein 2 (RAG2) gene, partial c - Nucleotide

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From variant of uncertain significance to likely pathogenic in two siblings with atypical RAG2 Deficiency: a case report and review of the literature. [BMC Pediatr. 2024]
From variant of uncertain significance to likely pathogenic in two siblings with atypical RAG2 Deficiency: a case report and review of the literature.
Taghizadeh Mortezaei N, Mohammadi S, Abolhassani H, Shokri S, Nabavi M, Fallahpour M, Bemanian MH. BMC Pediatr. 2024 Feb 13; 24(1):116. Epub 2024 Feb 13.
Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre. [Clin Exp Immunol. 2024]
Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre.
Karaatmaca B, Cagdas D, Esenboga S, Erman B, Tan C, Turul Ozgur T, Boztug K, van der Burg M, Sanal O, Tezcan I. Clin Exp Immunol. 2024 Feb 7; 215(2):160-176.
A novel loss of function mutation in the PHD domain of the RAG2 gene, affecting zinc-binding affinity. [Mol Biol Rep. 2023]
A novel loss of function mutation in the PHD domain of the RAG2 gene, affecting zinc-binding affinity.
Jabbarpour N, Bonyadi M, Sadeghi L. Mol Biol Rep. 2023 Oct; 50(10):8771-8775. Epub 2023 Aug 13.

RefSeq alternative splicing
See 6 reference mRNA sequence splice variants for the RAG2 gene.

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Nucleotide