Homo sapiens (human): 5897 Help Entry 5897              CDS       T01001                                  Symbol RAG2, RAG-2 Name (RefSeq) recombination activating 2   KO K10988   recombination-activating protein 2 Organism hsa  Homo sapiens (human) Pathway hsa04068   FoxO signaling pathway hsa05340   Primary immunodeficiency Network nt06506  Double-strand break repair   Element N01467   V(D)J recombination Disease H00092   T-B-Severe combined immunodeficiency H02554   Omenn syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04068 FoxO signaling pathway     5897 (RAG2)  09160 Human Diseases   09163 Immune disease    05340 Primary immunodeficiency     5897 (RAG2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  RAG2 RAG2_PHD Kelch_3 Kelch_5 CHU_C PHD Motif Other DBs NCBI-GeneID:  5897 NCBI-ProteinID:  NP_000527 OMIM:  179616 HGNC:  9832 Ensembl:  ENSG00000175097 UniProt:  P55895 Structure PDB LinkDB All DBs Position 11:complement(36590996..36598236) Genome browser AA seq 527 aa AA seqDB search MSLQMVTVSNNIALIQPGFSLMNFDGQVFFFGQKGWPKRSCPTGVFHLDVKHNHVKLKPT IFSKDSCYLPPLRYPATCTFKGSLESEKHQYIIHGGKTPNNEVSDKIYVMSIVCKNNKKV TFRCTEKDLVGDVPEARYGHSINVVYSRGKSMGVLFGGRSYMPSTHRTTEKWNSVADCLP CVFLVDFEFGCATSYILPELQDGLSFHVSIAKNDTIYILGGHSLANNIRPANLYRIRVDL PLGSPAVNCTVLPGGISVSSAILTQTNNDEFVIVGGYQLENQKRMICNIISLEDNKIEIR EMETPDWTPDIKHSKIWFGSNMGNGTVFLGIPGDNKQVVSEGFYFYMLKCAEDDTNEEQT TFTNSQTSTEDPGDSTPFEDSEEFCFSAEANSFDGDDEFDTYNEDDEEDESETGYWITCC PTCDVDINTWVPFYSTELNKPAMIYCSHGDGHWVHAQCMDLAERTLIHLSAGSNKYYCNE HVEIARALHTPQRVLPLKKPPMKSLRKKGSGKILTPAKKSFLRRLFD NT seq 1584 nt NT seq  +upstreamnt  +downstreamnt atgtctctgcagatggtaacagtcagtaataacatagccttaattcagccaggcttctca ctgatgaattttgatggacaagttttcttctttggacaaaaaggctggcccaaaagatcc tgccccactggagttttccatctggatgtaaagcataaccatgtcaaactgaagcctaca attttctctaaggattcctgctacctccctcctcttcgctacccagccacttgcacattc aaaggcagcttggagtctgaaaagcatcaatacatcatccatggagggaaaacaccaaac aatgaggtttcagataagatttatgtcatgtctattgtttgcaagaacaacaaaaaggtt acttttcgctgcacagagaaagacttggtaggagatgttcctgaagccagatatggtcat tccattaatgtggtgtacagccgagggaaaagtatgggtgttctctttggaggacgctca tacatgccttctacccacagaaccacagaaaaatggaatagtgtagctgactgcctgccc tgtgttttcctggtggattttgaatttgggtgtgctacatcatacattcttccagaactt caggatgggctatcttttcatgtctctattgccaaaaatgacaccatctatattttagga ggacattcacttgccaataatatccggcctgccaacctgtacagaataagggttgatctt cccctgggtagcccagctgtgaattgcacagtcttgccaggaggaatctctgtctccagt gcaatcctgactcaaactaacaatgatgaatttgttattgttggtggctatcagcttgaa aatcaaaaaagaatgatctgcaacatcatctctttagaggacaacaagatagaaattcgt gagatggagaccccagattggaccccagacattaagcacagcaagatatggtttggaagc aacatgggaaatggaactgtttttcttggcataccaggagacaataaacaagttgtttca gaaggattctatttctatatgttgaaatgtgctgaagatgatactaatgaagagcagaca acattcacaaacagtcaaacatcaacagaagatccaggggattccactccctttgaagac tctgaagaattttgtttcagtgcagaagcaaatagttttgatggtgatgatgaatttgac acctataatgaagatgatgaagaagatgagtctgagacaggctactggattacatgctgc cctacttgtgatgtggatatcaacacttgggtaccattctattcaactgagctcaacaaa cccgccatgatctactgctctcatggggatgggcactgggtccatgctcagtgcatggat ctggcagaacgcacactcatccatctgtcagcaggaagcaacaagtattactgcaatgag catgtggagatagcaagagctctacacactccccaaagagtcctacccttaaaaaagcct ccaatgaaatccctccgtaaaaaaggttctggaaaaatcttgactcctgccaagaaatcc tttcttagaaggttgtttgattag

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