Homo sapiens (human): 5896 Help Entry 5896              CDS       T01001                                  Symbol RAG1, RAG-1, RNF74 Name (RefSeq) recombination activating 1   KO K10628   V(D)J recombination-activating protein 1 [EC:2.3.2.27] 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 H00093   Combined immunodeficiency H01244   T+B+Severe combined immunodeficiencies (SCIDs) H02554   Omenn syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04068 FoxO signaling pathway     5896 (RAG1)  09160 Human Diseases   09163 Immune disease    05340 Primary immunodeficiency     5896 (RAG1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    04121 Ubiquitin system [BR:hsa04121]     5896 (RAG1) Enzymes [BR:hsa01000]  2. Transferases   2.3  Acyltransferases    2.3.2  Aminoacyltransferases     2.3.2.27  RING-type E3 ubiquitin transferase      5896 (RAG1) Ubiquitin system [BR:hsa04121]  Ubiquitin ligases (E3)   Single Ring-finger type E3    Other single Ring-finger type E3     5896 (RAG1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  RAG1 RAG1_imp_bd zf-RAG1 zf-C3HC4 zf-C3HC4_2 zf-RING_6 zf-RING_2 zf-RING_10 zf-C3HC4_4 zf-RING_UBOX Motif Other DBs NCBI-GeneID:  5896 NCBI-ProteinID:  NP_000439 OMIM:  179615 HGNC:  9831 Ensembl:  ENSG00000166349 UniProt:  P15918 LinkDB All DBs Position 11:36510353..36579762 Genome browser AA seq 1043 aa AA seqDB search MAASFPPTLGLSSAPDEIQHPHIKFSEWKFKLFRVRSFEKTPEEAQKEKKDSFEGKPSLE QSPAVLDKADGQKPVPTQPLLKAHPKFSKKFHDNEKARGKAIHQANLRHLCRICGNSFRA DEHNRRYPVHGPVDGKTLGLLRKKEKRATSWPDLIAKVFRIDVKADVDSIHPTEFCHNCW SIMHRKFSSAPCEVYFPRNVTMEWHPHTPSCDICNTARRGLKRKSLQPNLQLSKKLKTVL DQARQARQHKRRAQARISSKDVMKKIANCSKIHLSTKLLAVDFPEHFVKSISCQICEHIL ADPVETNCKHVFCRVCILRCLKVMGSYCPSCRYPCFPTDLESPVKSFLSVLNSLMVKCPA KECNEEVSLEKYNHHISSHKESKEIFVHINKGGRPRQHLLSLTRRAQKHRLRELKLQVKA FADKEEGGDVKSVCMTLFLLALRARNEHRQADELEAIMQGKGSGLQPAVCLAIRVNTFLS CSQYHKMYRTVKAITGRQIFQPLHALRNAEKVLLPGYHHFEWQPPLKNVSSSTDVGIIDG LSGLSSSVDDYPVDTIAKRFRYDSALVSALMDMEEDILEGMRSQDLDDYLNGPFTVVVKE SCDGMGDVSEKHGSGPVVPEKAVRFSFTIMKITIAHSSQNVKVFEEAKPNSELCCKPLCL MLADESDHETLTAILSPLIAEREAMKSSELMLELGGILRTFKFIFRGTGYDEKLVREVEG LEASGSVYICTLCDATRLEASQNLVFHSITRSHAENLERYEVWRSNPYHESVEELRDRVK GVSAKPFIETVPSIDALHCDIGNAAEFYKIFQLEIGEVYKNPNASKEERKRWQATLDKHL RKKMNLKPIMRMNGNFARKLMTKETVDAVCELIPSEERHEALRELMDLYLKMKPVWRSSC PAKECPESLCQYSFNSQRFAELLSTKFKYRYEGKITNYFHKTLAHVPEIIERDGSIGAWA SEGNESGNKLFRRFRKMNARQSKCYEMEDVLKHHWLYTSKYLQKFMNAHNALKTSGFTMN PQASLGDPLGIEDSLESQDSMEF NT seq 3132 nt NT seq  +upstreamnt  +downstreamnt atggcagcctctttcccacccaccttgggactcagttctgccccagatgaaattcagcac ccacatattaaattttcagaatggaaatttaagctgttccgggtgagatcctttgaaaag acacctgaagaagctcaaaaggaaaagaaggattcctttgaggggaaaccctctctggag caatctccagcagtcctggacaaggctgatggtcagaagccagtcccaactcagccattg ttaaaagcccaccctaagttttcaaagaaatttcacgacaacgagaaagcaagaggcaaa gcgatccatcaagccaaccttcgacatctctgccgcatctgtgggaattcttttagagct gatgagcacaacaggagatatccagtccatggtcctgtggatggtaaaaccctaggcctt ttacgaaagaaggaaaagagagctacttcctggccggacctcattgccaaggttttccgg atcgatgtgaaggcagatgttgactcgatccaccccactgagttctgccataactgctgg agcatcatgcacaggaagtttagcagtgccccatgtgaggtttacttcccgaggaacgtg accatggagtggcacccccacacaccatcctgtgacatctgcaacactgcccgtcgggga ctcaagaggaagagtcttcagccaaacttgcagctcagcaaaaaactcaaaactgtgctt gaccaagcaagacaagcccgtcagcacaagagaagagctcaggcaaggatcagcagcaag gatgtcatgaagaagatcgccaactgcagtaagatacatcttagtaccaagctccttgca gtggacttcccagagcactttgtgaaatccatctcctgccagatctgtgaacacattctg gctgaccctgtggagaccaactgtaagcatgtcttttgccgggtctgcattctcagatgc ctcaaagtcatgggcagctattgtccctcttgccgatatccatgcttccctactgacctg gagagtccagtgaagtcctttctgagcgtcttgaattccctgatggtgaaatgtccagca aaagagtgcaatgaggaggtcagtttggaaaaatataatcaccacatctcaagtcacaag gaatcaaaagagatttttgtgcacattaataaagggggccggccccgccaacatcttctg tcgctgactcggagagctcagaagcaccggctgagggagctcaagctgcaagtcaaagcc tttgctgacaaagaagaaggtggagatgtgaagtccgtgtgcatgaccttgttcctgctg gctctgagggcgaggaatgagcacaggcaagctgatgagctggaggccatcatgcaggga aagggctctggcctgcagccagctgtttgcttggccatccgtgtcaacaccttcctcagc tgcagtcagtaccacaagatgtacaggactgtgaaagccatcacagggagacagattttt cagcctttgcatgcccttcggaatgctgagaaggtacttctgccaggctaccaccacttt gagtggcagccacctctgaagaatgtgtcttccagcactgatgttggcattattgatggg ctgtctggactatcatcctctgtggatgattacccagtggacaccattgcaaagaggttc cgctatgattcagctttggtgtctgctttgatggacatggaagaagacatcttggaaggc atgagatcccaagaccttgatgattacctgaatggccccttcactgtggtggtgaaggag tcttgtgatggaatgggagacgtgagtgagaagcatgggagtgggcctgtagttccagaa aaggcagtccgtttttcattcacaatcatgaaaattactattgcccacagctctcagaat gtgaaagtatttgaagaagccaaacctaactctgaactgtgttgcaagccattgtgcctt atgctggcagatgagtctgaccacgagacgctgactgccatcctgagtcctctcattgct gagagggaggccatgaagagcagtgaattaatgcttgagctgggaggcattctccggact ttcaagttcatcttcaggggcaccggctatgatgaaaaacttgtgcgggaagtggaaggc ctcgaggcttctggctcagtctacatttgtactctttgtgatgccacccgtctggaagcc tctcaaaatcttgtcttccactctataaccagaagccatgctgagaacctggaacgttat gaggtctggcgttccaacccttaccatgagtctgtggaagaactgcgggatcgggtgaaa ggggtctcagctaaacctttcattgagacagtcccttccatagatgcactccactgtgac attggcaatgcagctgagttctacaagatcttccagctagagataggggaagtgtataag aatcccaatgcttccaaagaggaaaggaaaaggtggcaggccacactggacaagcatctc cggaagaagatgaacctcaaaccaatcatgaggatgaatggcaactttgccaggaagctc atgaccaaagagactgtggatgcagtttgtgagttaattccttccgaggagaggcacgag gctctgagggagctgatggatctttacctgaagatgaaaccagtatggcgatcatcatgc cctgctaaagagtgcccagaatccctctgccagtacagtttcaattcacagcgttttgct gagctcctttctacgaagttcaagtataggtatgagggaaaaatcaccaattattttcac aaaaccctggcccatgttcctgaaattattgagagggatggctccattggggcatgggca agtgagggaaatgagtctggtaacaaactgtttaggcgcttccggaaaatgaatgccagg cagtccaaatgctatgagatggaagatgtcctgaaacaccactggttgtacacctccaaa tacctccagaagtttatgaatgctcataatgcattaaaaacctctgggtttaccatgaac cctcaggcaagcttaggggacccattaggcatagaggactctctggaaagccaagattca atggaattttaa

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 H00093   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_KLHDC2_KLHL20_DRC7 Kelch_3 Beta-prop_ATRN-LZTR1 Kelch_5 CHU_C PHD Motif Other DBs NCBI-GeneID:  5897 NCBI-ProteinID:  NP_000527 OMIM:  179616 HGNC:  9832 Ensembl:  ENSG00000175097 UniProt:  P55895 Structure PDBPDBj 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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