Homo sapiens (human): 80010 Help Entry 80010             CDS       T01001                                  Symbol RMI1, BLAP75, C9orf76, FAAP75 Name (RefSeq) RecQ mediated genome instability 1   KO K10990   RecQ-mediated genome instability protein 1 Organism hsa  Homo sapiens (human) Pathway hsa03460   Fanconi anemia pathway Network nt06506  Double-strand break repair   Element N01447   Double Holliday junction dissolution Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09124 Replication and repair    03460 Fanconi anemia pathway     80010 (RMI1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03400 DNA repair and recombination proteins [BR:hsa03400]     80010 (RMI1) DNA repair and recombination proteins [BR:hsa03400]  Eukaryotic type   DSBR (double strand breaks repair)    HR (homologous recombination)     Bloom's syndrome complex (BTR)      80010 (RMI1)    FA (Fanconi anemia) pathway      80010 (RMI1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  RMI1_C RMI1_N_C RMI1_N_N DUF4672 Rbx_binding Motif Other DBs NCBI-GeneID:  80010 NCBI-ProteinID:  NP_001345220 OMIM:  610404 HGNC:  25764 Ensembl:  ENSG00000178966 UniProt:  Q9H9A7 Structure PDBPDBj LinkDB All DBs Position 9:83980359..84004074 Genome browser AA seq 625 aa AA seqDB search MNVTSIALRAETWLLAAWHVKVPPMWLEACINWIQEENNNVNLSQAQMNKQVFEQWLLTD LRDLEHPLLPDGILEIPKGELNGFYALQINSLVDVSQPAYSQIQKLRGKNTTNDLVTAEA QVTPKPWEAKPSRMLMLQLTDGIVQIQGMEYQPIPILHSDLPPGTKILIYGNISFRLGVL LLKPENVKVLGGEVDALLEEYAQEKVLARLIGEPDLVVSVIPNNSNENIPRVTDVLDPAL GPSDEELLASLDENDELTANNDTSSERCFTTGSSSNTIPTRQSSFEPEFVISPRPKEEPS NLSIHVMDGELDDFSLEEALLLEETVQKEQMETKELQPLTFNRNADRSIERFSHNPNTTN NFSLTCKNGNNNWSEKNVSEQMTNEDKSFGCPSVRDQNRSIFSVHCNVPLAHDFTNKEKN LETDNKIKQTSSSDSHSLNNKILNREVVNYVQKRNSQISNENDCNLQSCSLRSSENSINL SIAMDLYSPPFVYLSVLMASKPKEVTTVKVKAFIVTLTGNLSSSGGIWSITAKVSDGTAY LDVDFVDEILTSLIGFSVPEMKQSKKDPLQYQKFLEGLQKCQRDLIDLCCLMTISFNPSL SKAMVLALQDVNMEHLENLKKRLNK NT seq 1878 nt NT seq  +upstreamnt  +downstreamnt atgaatgtgactagtattgcattaagagctgaaacttggcttttagctgcatggcatgtt aaagtacctccgatgtggctggaagcttgtattaactggattcaagaagaaaataataat gttaacttgagtcaggcccaaatgaataaacaagtgtttgagcagtggctccttactgat ctgagggatttggagcatcctcttttacccgatggcattttagaaattccaaaaggagaa ttaaatggattttatgctctgcagattaattccttggttgatgtaagtcagcctgcatac tcccagatacagaagttgagaggaaagaatacaacaaatgatctagttacagctgaagca caagtaaccccaaaaccttgggaagcaaagccttcacgaatgttgatgctgcagctaact gatggaatcgtacaaatacagggaatggaatatcagcctattccaattcttcatagtgat cttcctccaggtacaaaaattttgatttatggaaatatatctttccgtcttggtgttctc ttattgaaaccagaaaacgtgaaagtgttaggaggtgaagtagatgctcttttagaagaa tatgcccaagaaaaagtacttgcaagattaataggggaacctgatcttgtagtttcagtc ataccaaacaattctaacgaaaacattcccagagttacagatgttctagatcctgcatta ggtccttctgatgaagaactcttggcaagtcttgatgaaaatgatgagcttacagcaaat aatgacacttcctcagaacgatgtttcaccacaggtagttcctcaaataccattcccaca agacagtcaagttttgagccagaatttgttatttctccaagaccaaaagaggaaccatca aacctatctatacatgtaatggatggagaattagatgacttttcactggaggaggccttg cttttagaagaaactgtccagaaagaacagatggaaactaaggaattgcaaccattgact tttaacagaaatgccgatcgaagtatagagagattttcacataatcctaatactacgaat aacttttctttgacttgcaaaaatggaaacaataattggagtgaaaaaaatgtatctgaa caaatgactaatgaagacaaatcatttggttgtccatctgttagagaccaaaacaggagt attttttcagttcattgtaatgtacccttagcccatgattttacaaataaagaaaagaac ttagagacagataataaaataaaacaaaccagcagttcagatagccattccttaaataat aaaatattaaatagagaggtggtcaactatgtacagaaaaggaattcacaaatttctaat gaaaatgattgtaatttacagagttgttctttaagatcatcagagaatagcattaatctt tctattgccatggatttgtattctccaccctttgtctatttgtctgttctaatggccagc aaaccaaaggaagttacaacagtgaaagtgaaagcatttattgtaaccttaactggaaat ctctcaagttctggtggtatttggagtataactgcaaaggtgtctgatggtactgcatat ctagatgtagactttgtggatgaaatacttactagcttgatagggttctcagtaccagaa atgaaacagtcaaaaaaggatcctcttcaataccaaaagttcctggaagggttgcagaaa tgtcaaagagatctaatagatttgtgctgtctaatgactatttcatttaatccttccttg tctaaagcaatggtactggcattacaagatgttaatatggaacaccttgagaatctaaag aagcggttaaataaataa

Homo sapiens (human): 116028 Help Entry 116028            CDS       T01001                                  Symbol RMI2, BLAP18, C16orf75 Name (RefSeq) RecQ mediated genome instability 2   KO K15365   RecQ-mediated genome instability protein 2 Organism hsa  Homo sapiens (human) Pathway hsa03460   Fanconi anemia pathway Network nt06506  Double-strand break repair   Element N01447   Double Holliday junction dissolution Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09124 Replication and repair    03460 Fanconi anemia pathway     116028 (RMI2)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03400 DNA repair and recombination proteins [BR:hsa03400]     116028 (RMI2) DNA repair and recombination proteins [BR:hsa03400]  Eukaryotic type   DSBR (double strand breaks repair)    HR (homologous recombination)     Bloom's syndrome complex (BTR)      116028 (RMI2)    FA (Fanconi anemia) pathway      116028 (RMI2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  RMI2 Motif Other DBs NCBI-GeneID:  116028 NCBI-ProteinID:  NP_689521 OMIM:  612426 HGNC:  28349 Ensembl:  ENSG00000175643 UniProt:  Q96E14 Structure PDBPDBj LinkDB All DBs Position 16:11345459..11351760 Genome browser AA seq 147 aa AA seqDB search MAAAADSFSGGPAGVRLPRSPPLKVLAEQLRRDAEGGPGAWRLSRAAAGRGPLDLAAVWM QGRVVMADRGEARLRDPSGDFSVRGLERVPRGRPCLVPGKYVMVMGVVQACSPEPCLQAV KMTDLSDNPIHESMWELEVEDLHRNIP NT seq 444 nt NT seq  +upstreamnt  +downstreamnt atggcggcggctgcggactcgttctcaggcggccccgcgggggtgcggcttccgaggtcg ccgccactcaaggtgctggcggagcagctgcggcgcgacgcggagggcggcccgggcgcg tggcggctgtcacgggcggcggcgggccgcgggccgctggacctggcggccgtgtggatg cagggcagggtagtgatggcggaccgcggcgaggctcggctgagggacccgagcggggac ttctcggtccgcggcctggagcgggtgccgcgcgggcggccctgtctagtcccaggaaag tatgtgatggtgatgggagtggttcaggcctgcagccctgagccctgcctgcaggctgtg aagatgacagacctttctgataatcccatccatgaaagtatgtgggaactggaggtagaa gatttacacaggaatattccttag

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