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RAG1 Generecombination activating gene 1 The protein encoded by this gene is involved in activation of immunoglobulin V-D-J recombination. The encoded protein is involved in recognition of the DNA substrate, but stable binding and cleavage activity also requires RAG2. Defects in this gene can be the cause of several diseases. [provided by RefSeq, Jul 2008] |
rag1 Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term rag1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
RAG1 Gene SetFrom Pathway Commons Protein-Protein Interactions interacting proteins for RAG1 from the Pathway Commons Protein-Protein Interactions dataset. |
RAG1 Gene SetFrom LINCS L1000 CMAP CRISPR Knockout Consensus Signatures genes differentially expressed following the RAG1 gene perturbation from the LINCS L1000 CMAP CRISPR Knockout Consensus Signatures dataset. |
RAG1 Gene SetFrom CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the RAG1 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas. |
RAG1-RAG2 tetramer complex Gene Setproteins in the RAG1-RAG2 tetramer complex protein complex from the CORUM Protein Complexes dataset. |
Rag1-Rag2 protein-DNA complex Gene Setproteins in the Rag1-Rag2 protein-DNA complex protein complex from the CORUM Protein Complexes dataset. |
Rag1-Rag2-Ku70-Ku80 protein-DNA complex Gene Setproteins in the Rag1-Rag2-Ku70-Ku80 protein-DNA complex protein complex from the CORUM Protein Complexes dataset. |
Combined immunodeficiency due to partial RAG1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to partial RAG1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |