Homo sapiens (human): 2175 Help Entry 2175              CDS       T01001                                  Symbol FANCA, FA, FA-H, FA1, FAA, FACA, FAH, FANCH Name (RefSeq) FA complementation group A   KO K10888   fanconi anemia group A protein Organism hsa  Homo sapiens (human) Pathway hsa03460   Fanconi anemia pathway Network nt06508  Interstrand crosslink repair   Element N01464   Fanconi anemia pathway Disease H00238   Fanconi anemia Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09124 Replication and repair    03460 Fanconi anemia pathway     2175 (FANCA)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03400 DNA repair and recombination proteins [BR:hsa03400]     2175 (FANCA) DNA repair and recombination proteins [BR:hsa03400]  Eukaryotic type   DSBR (double strand breaks repair)    FA (Fanconi anemia) pathway     FA core complex      2175 (FANCA) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Fanconi_A_N FANCA_CTD FANCA_arcN FANCA_helical Motif Other DBs NCBI-GeneID:  2175 NCBI-ProteinID:  NP_000126 OMIM:  607139 HGNC:  3582 Ensembl:  ENSG00000187741 UniProt:  O15360 Structure PDBPDBj LinkDB All DBs Position 16:complement(89737549..89816647) Genome browser AA seq 1455 aa AA seqDB search MSDSWVPNSASGQDPGGRRRAWAELLAGRVKREKYNPERAQKLKESAVRLLRSHQDLNAL LLEVEGPLCKKLSLSKVIDCDSSEAYANHSSSFIGSALQDQASRLGVPVGILSAGMVASS VGQICTAPAETSHPVLLTVEQRKKLSSLLEFAQYLLAHSMFSRLSFCQELWKIQSSLLLE AVWHLHVQGIVSLQELLESHPDMHAVGSWLFRNLCCLCEQMEASCQHADVARAMLSDFVQ MFVLRGFQKNSDLRRTVEPEKMPQVTVDVLQRMLIFALDALAAGVQEESSTHKIVRCWFG VFSGHTLGSVISTDPLKRFFSHTLTQILTHSPVLKASDAVQMQREWSFARTHPLLTSLYR RLFVMLSAEELVGHLQEVLETQEVHWQRVLSFVSALVVCFPEAQQLLEDWVARLMAQAFE SCQLDSMVTAFLVVRQAALEGPSAFLSYADWFKASFGSTRGYHGCSKKALVFLFTFLSEL VPFESPRYLQVHILHPPLVPGKYRSLLTDYISLAKTRLADLKVSIENMGLYEDLSSAGDI TEPHSQALQDVEKAIMVFEHTGNIPVTVMEASIFRRPYYVSHFLPALLTPRVLPKVPDSR VAFIESLKRADKIPPSLYSTYCQACSAAEEKPEDAALGVRAEPNSAEEPLGQLTAALGEL RASMTDPSQRDVISAQVAVISERLRAVLGHNEDDSSVEISKIQLSINTPRLEPREHMAVD LLLTSFCQNLMAASSVAPPERQGPWAALFVRTMCGRVLPAVLTRLCQLLRHQGPSLSAPH VLGLAALAVHLGESRSALPEVDVGPPAPGAGLPVPALFDSLLTCRTRDSLFFCLKFCTAA ISYSLCKFSSQSRDTLCSCLSPGLIKKFQFLMFRLFSEARQPLSEEDVASLSWRPLHLPS ADWQRAALSLWTHRTFREVLKEEDVHLTYQDWLHLELEIQPEADALSDTERQDFHQWAIH EHFLPESSASGGCDGDLQAACTILVNALMDFHQSSRSYDHSENSDLVFGGRTGNEDIISR LQEMVADLELQQDLIVPLGHTPSQEHFLFEIFRRRLQALTSGWSVAASLQRQRELLMYKR ILLRLPSSVLCGSSFQAEQPITARCEQFFHLVNSEMRNFCSHGGALTQDITAHFFRGLLN ACLRSRDPSLMVDFILAKCQTKCPLILTSALVWWPSLEPVLLCRWRRHCQSPLPRELQKL QEGRQFASDFLSPEAASPAPNPDWLSAAALHFAIQQVREENIRKQLKKLDCEREELLVFL FFFSLMGLLSSHLTSNSTTDLPKAFHVCAAILECLEKRKISWLALFQLTESDLRLGRLLL RVAPDQHTRLLPFAFYSLLSYFHEDAAIREEAFLHVAVDMYLKLVQLFVAGDTSTVSPPA GRSLELKGQGNPVELITKARLFLLQLIPRCPKKSFSHVAELLADRGDCDPEVSAALQSRQ QAAPDADLSQEPHLF NT seq 4368 nt NT seq  +upstreamnt  +downstreamnt atgtccgactcgtgggtcccgaactccgcctcgggccaggacccagggggccgccggagg gcctgggccgagctgctggcgggaagggtcaagagggaaaaatataatcctgaaagggca cagaaattaaaggaatcagctgtgcgcctcctgcgaagccatcaggacctgaatgccctt ttgcttgaggtagaaggtccactgtgtaaaaaattgtctctcagcaaagtgattgactgt gacagttctgaggcctatgctaatcattctagttcatttataggctctgctttgcaggat caagcctcaaggctgggggttcccgtgggtattctctcagccgggatggttgcctctagc gtgggacagatctgcacggctccagcggagaccagtcaccctgtgctgctgactgtggag cagagaaagaagctgtcttccctgttagagtttgctcagtatttattggcacacagtatg ttctcccgtctttccttctgtcaagaattatggaaaatacagagttctttgttgcttgaa gcggtgtggcatcttcacgtacaaggcattgtgagcctgcaagagctgctggaaagccat cccgacatgcatgctgtgggatcgtggctcttcaggaatctgtgctgcctttgtgaacag atggaagcatcctgccagcatgctgacgtcgccagggccatgctttctgattttgttcaa atgtttgttttgaggggatttcagaaaaactcagatctgagaagaactgtggagcctgaa aaaatgccgcaggtcacggttgatgtactgcagagaatgctgatttttgcacttgacgct ttggctgctggagtacaggaggagtcctccactcacaagatcgtgaggtgctggttcgga gtgttcagtggacacacgcttggcagtgtaatttccacagatcctctgaagaggttcttc agtcataccctgactcagatactcactcacagccctgtgctgaaagcatctgatgctgtt cagatgcagagagagtggagctttgcgcggacacaccctctgctcacctcactgtaccgc aggctctttgtgatgctgagtgcagaggagttggttggccatttgcaagaagttctggaa acgcaggaggttcactggcagagagtgctctcctttgtgtctgccctggttgtctgcttt ccagaagcgcagcagctgcttgaagactgggtggcgcgtttgatggcccaggcattcgag agctgccagctggacagcatggtcactgcgttcctggttgtgcgccaggcagcactggag ggcccctctgcgttcctgtcatatgcagactggttcaaggcctcctttgggagcacacga ggctaccatggctgcagcaagaaggccctggtcttcctgtttacgttcttgtcagaactc gtgccttttgagtctccccggtacctgcaggtgcacattctccacccacccctggttccc ggcaagtaccgctccctcctcacagactacatctcattggccaagacacggctggccgac ctcaaggtttctatagaaaacatgggactctacgaggatttgtcatcagctggggacatt actgagccccacagccaagctcttcaggatgttgaaaaggccatcatggtgtttgagcat acggggaacatcccagtcaccgtcatggaggccagcatattcaggaggccttactacgtg tcccacttcctccccgccctgctcacacctcgagtgctccccaaagtccctgactcccgt gtggcgtttatagagtctctgaagagagcagataaaatccccccatctctgtactccacc tactgccaggcctgctctgctgctgaagagaagccagaagatgcagccctgggagtgagg gcagaacccaactctgctgaggagcccctgggacagctcacagctgcactgggagagctg agagcctccatgacagaccccagccagcgtgatgttatatcggcacaggtggcagtgatt tctgaaagactgagggctgtcctgggccacaatgaggatgacagcagcgttgagatatca aagattcagctcagcatcaacacgccgagactggagccacgggaacacatggctgtggac ctcctgctgacgtctttctgtcagaacctgatggctgcctccagtgtcgctcccccggag aggcagggtccctgggctgccctcttcgtgaggaccatgtgtggacgtgtgctccctgca gtgctcacccggctctgccagctgctccgtcaccagggcccgagcctgagtgccccacat gtgctggggttggctgccctggccgtgcacctgggtgagtccaggtctgcgctcccagag gtggatgtgggtcctcctgcacctggtgctggccttcctgtccctgcgctctttgacagc ctcctgacctgtaggacgagggattccttgttcttctgcctgaaattttgtacagcagca atttcttactctctctgcaagttttcttcccagtcacgagatactttgtgcagctgctta tctccaggccttattaaaaagtttcagttcctcatgttcagattgttctcagaggcccga cagcctctttctgaggaggacgtagccagcctttcctggagacccttgcaccttccttct gcagactggcagagagctgccctctctctctggacacacagaaccttccgagaggtgttg aaagaggaagatgttcacttaacttaccaagactggttacacctggagctggaaattcaa cctgaagctgatgctctttcagatactgaacggcaggacttccaccagtgggcgatccat gagcactttctccctgagtcctcggcttcagggggctgtgacggagacctgcaggctgcg tgtaccattcttgtcaacgcactgatggatttccaccaaagctcaaggagttatgaccac tcagaaaattctgatttggtctttggtggccgcacaggaaatgaggatattatttccaga ttgcaggagatggtagctgacctggagctgcagcaagacctcatagtgcctctcggccac accccttcccaggagcacttcctctttgagattttccgcagacggctccaggctctgaca agcgggtggagcgtggctgccagccttcagagacagagggagctgctaatgtacaaacgg atcctcctccgcctgccttcgtctgtcctctgcggcagcagcttccaggcagaacagccc atcactgccagatgcgagcagttcttccacttggtcaactctgagatgagaaacttctgc tcccacggaggtgccctgacacaggacatcactgcccacttcttcaggggcctcctgaac gcctgtctgcggagcagagacccctccctgatggtcgacttcatactggccaagtgccag acgaaatgccccttaattttgacctctgctctggtgtggtggccgagcctggagcctgtg ctgctctgccggtggaggagacactgccagagcccgctgccccgggaactgcagaagcta caagaaggccggcagtttgccagcgatttcctctcccctgaggctgcctccccagcaccc aacccggactggctctcagctgctgcactgcactttgcgattcaacaagtcagggaagaa aacatcaggaagcagctaaagaagctggactgcgagagagaggagctattggttttcctt ttcttcttctccttgatgggcctgctgtcgtcacatctgacctcaaatagcaccacagac ctgccaaaggctttccacgtttgtgcagcaatcctcgagtgtttagagaagaggaagata tcctggctggcactctttcagttgacagagagtgacctcaggctggggcggctcctcctc cgtgtggccccggatcagcacaccaggctgctgcctttcgctttttacagtcttctctcc tacttccatgaagacgcggccatcagggaagaggccttcctgcatgttgctgtggacatg tacttgaagctggtccagctcttcgtggctggggatacaagcacagtttcacctccagct ggcaggagcctggagctcaagggtcagggcaaccccgtggaactgataacaaaagctcgt ctttttctgctgcagttaatacctcggtgcccgaaaaagagcttctcacacgtggcagag ctgctggctgatcgtggggactgcgacccagaggtgagcgccgccctccagagcagacag caggctgcccctgacgctgacctgtcccaggagcctcatctcttctga

Homo sapiens (human): 2187 Help Entry 2187              CDS       T01001                                  Symbol FANCB, FA2, FAAP90, FAAP95, FAB, FACB Name (RefSeq) FA complementation group B   KO K10889   fanconi anemia group B protein Organism hsa  Homo sapiens (human) Pathway hsa03460   Fanconi anemia pathway Network nt06508  Interstrand crosslink repair   Element N01464   Fanconi anemia pathway Disease H00238   Fanconi anemia Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09124 Replication and repair    03460 Fanconi anemia pathway     2187 (FANCB)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03400 DNA repair and recombination proteins [BR:hsa03400]     2187 (FANCB) DNA repair and recombination proteins [BR:hsa03400]  Eukaryotic type   DSBR (double strand breaks repair)    FA (Fanconi anemia) pathway     FA core complex      2187 (FANCB) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  DP Motif Other DBs NCBI-GeneID:  2187 NCBI-ProteinID:  NP_001018123 OMIM:  300515 HGNC:  3583 Ensembl:  ENSG00000181544 UniProt:  Q8NB91 Structure PDBPDBj LinkDB All DBs Position X:complement(14689524..14873069) Genome browser AA seq 859 aa AA seqDB search MTSKQAMSSNEQERLLCYNGEVLVFQLSKGNFADKEPTKTPILHVRRMVFDRGTKVFVQK STGFFTIKEENSHLKIMCCNCVSDFRTGINLPYIVIEKNKKNNVFEYFLLILHSTNKFEM RLSFKLGYEMKDGLRVLNGPLILWRHVKAFFFISSQTGKVVSVSGNFSSIQWAGEIENLG MVLLGLKECCLSEEECTQEPSKSDYAIWNTKFCVYSLESQEVLSDIYIIPPAYSSVVTYV HICATEIIKNQLRISLIALTRKNQLISFQNGTPKNVCQLPFGDPCAVQLMDSGGGNLFFV VSFISNNACAVWKESFQVAAKWEKLSLVLIDDFIGSGTEQVLLLFKDSLNSDCLTSFKIT DLGKINYSSEPSDCNEDDLFEDKQENRYLVVPPLETGLKVCFSSFRELRQHLLLKEKIIS KSYKALINLVQGKDDNTSSAEEKECLVPLCGEEENSVHILDEKLSDNFQDSEQLVEKIWY RVIDDSLVVGVKTTSSLKLSLNDVTLSLLMDQAHDSRFRLLKCQNRVIKLSTNPFPAPYL MPCEIGLEAKRVTLTPDSKKEESFVCEHPSKKECVQIITAVTSLSPLLTFSKFCCTVLLQ IMERESGNCPKDRYVVCGRVFLSLEDLSTGKYLLTFPKKKPIEHMEDLFALLAAFHKSCF QITSPGYALNSMKVWLLEHMKCEIIKEFPEVYFCERPGSFYGTLFTWKQRTPFEGILIIY SRNQTVMFQCLHNLIRILPINCFLKNLKSGSENFLIDNMAFTLEKELVTLSSLSSAIAKH ESNFMQRCEVSKGKSSVVAAALSDRRENIHPYRKELQREKKKMLQTNLKVSGALYREITL KVAEVQLKSDFAAQKLSNL NT seq 2580 nt NT seq  +upstreamnt  +downstreamnt atgactagcaaacaagcaatgtcatctaacgaacaagaaaggctcttgtgttataatggg gaagtccttgttttccagttgtctaaaggaaattttgcagataaagagcctacaaaaaca cccatattacatgtcagaagaatggtatttgacagaggaacaaaagtatttgttcagaag tccactggattttttaccataaaggaagaaaactctcatttaaaaatcatgtgttgcaac tgtgtgtcagatttcagaactggaattaacctcccttacattgtgatagaaaaaaataaa aagaataatgtttttgaatattttttactaatccttcacagtactaataaatttgaaatg cgtttgagttttaaactaggctatgagatgaaggatggcctaagggtccttaatggccct ttaattttatggaggcatgtcaaagcattcttctttatctcttctcaaactggcaaagtt gttagtgtgtcaggtaacttttcctctattcagtgggcaggggagattgaaaatttaggt atggttttattgggactaaaggaatgttgtttatctgaggaagaatgtactcaagagcct tcaaaatcagattatgcaatttggaataccaaattttgtgtatattctcttgaaagtcaa gaagtattaagtgatatatacattattcctcctgcttacagcagtgtggtgacttatgta catatttgtgcaactgagatcatcaaaaaccagttaagaatatctctcattgcccttact cgaaagaatcagctgatttcatttcagaatggaactcctaaaaatgtgtgccagcttcca tttggagatccttgtgcagttcaacttatggattcaggtggaggaaacctctttttcgtt gtatcctttatatccaataatgcttgtgctgtatggaaagagagctttcaggttgctgct aaatgggaaaaacttagcttagtactgatagatgactttattggaagtggaactgaacaa gtactcctactttttaaggactccttgaactcagactgcctgacttcatttaaaataacg gatcttggaaaaataaactattcgagtgaaccatcagattgcaatgaagatgacttattt gaagacaaacaagagaatcgttacctggtggttccacctctagaaacaggactgaaagtt tgtttttcttcttttcgggaattacggcagcatctgttgcttaaggaaaaaattatttca aaatcttacaaagctttaataaacctagttcaaggaaaagatgataatacgtcaagtgca gaggagaaggaatgtcttgttcctctttgtggtgaagaagaaaattctgtccatatctta gatgaaaagttatcagacaattttcaagattcagaacagctagtagagaagatatggtat cgtgtaatagatgatagcttggttgttggagtgaaaactacatcttctttgaagctgtcc ctgaatgatgtgactttatcattgttaatggatcaagcccatgactccagatttcggctt ctaaagtgtcaaaatagggtgattaagttgagtacaaatcctttcccagcaccatacttg atgccatgtgaaataggattggaagcaaaaagggtcacgttgacccctgatagcaagaaa gaggaaagctttgtttgtgaacacccatctaagaaagagtgtgtacagataattactgct gtaacatctctttcaccacttttaacattcagtaaattttgttgcactgtactgctacaa attatggagagagaaagtggtaactgtcctaaagatcgttatgttgtgtgtggcagagtt tttttaagtctagaagatctttcaactgggaagtacctactgacatttccaaagaagaaa cctatagagcacatggaagatctttttgcacttcttgcagcattccataaatcttgtttt caaatcacatcacccggctatgccctgaattcaatgaaggtgtggctcttagaacatatg aaatgtgaaataatcaaagaatttccagaagtgtacttttgtgaaagaccgggaagtttc tatgggacactcttcacttggaaacagagaacaccattcgaagggattttaataatctat tccaggaatcaaacagttatgttccagtgccttcataatctcatcagaattctccctata aactgtttcctcaaaaatctaaaatcaggaagtgagaatttcctaattgataatatggca tttactttggagaaggaactagtcacccttagttctctttcttctgccatagctaaacat gaaagcaattttatgcagaggtgtgaagtgagcaaaggaaagagtagtgtcgtcgcggct gctttatcagacagaagggaaaatatccatccctacagaaaagaacttcagagagaaaag aagaaaatgttgcaaacgaacctaaaagtgagtggtgccctttacagagaaataactttg aaagtagctgaggttcagttgaaatcagactttgctgcacagaaactgagtaatttataa

Homo sapiens (human): 2176 Help Entry 2176              CDS       T01001                                  Symbol FANCC, FA3, FAC, FACC Name (RefSeq) FA complementation group C   KO K10890   fanconi anemia group C protein Organism hsa  Homo sapiens (human) Pathway hsa03460   Fanconi anemia pathway Network nt06508  Interstrand crosslink repair   Element N01464   Fanconi anemia pathway Disease H00238   Fanconi anemia Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09124 Replication and repair    03460 Fanconi anemia pathway     2176 (FANCC)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03400 DNA repair and recombination proteins [BR:hsa03400]     2176 (FANCC) DNA repair and recombination proteins [BR:hsa03400]  Eukaryotic type   DSBR (double strand breaks repair)    FA (Fanconi anemia) pathway     FA core complex      2176 (FANCC) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Fanconi_C EF-hand_2 Motif Other DBs NCBI-GeneID:  2176 NCBI-ProteinID:  NP_000127 OMIM:  613899 HGNC:  3584 Ensembl:  ENSG00000158169 UniProt:  Q00597 A0A024R9N2 Structure PDBPDBj LinkDB All DBs Position 9:complement(95099054..95317709) Genome browser AA seq 558 aa AA seqDB search MAQDSVDLSCDYQFWMQKLSVWDQASTLETQQDTCLHVAQFQEFLRKMYEALKEMDSNTV IERFPTIGQLLAKACWNPFILAYDESQKILIWCLCCLINKEPQNSGQSKLNSWIQGVLSH ILSALRFDKEVALFTQGLGYAPIDYYPGLLKNMVLSLASELRENHLNGFNTQRRMAPERV ASLSRVCVPLITLTDVDPLVEALLICHGREPQEILQPEFFEAVNEAILLKKISLPMSAVV CLWLRHLPSLEKAMLHLFEKLISSERNCLRRIECFIKDSSLPQAACHPAIFRVVDEMFRC ALLETDGALEIIATIQVFTQCFVEALEKASKQLRFALKTYFPYTSPSLAMVLLQDPQDIP RGHWLQTLKHISELLREAVEDQTHGSCGGPFESWFLFIHFGGWAEMVAEQLLMSAAEPPT ALLWLLAFYYGPRDGRQQRAQTMVQVKAVLGHLLAMSRSSSLSAQDLQTVAGQGTDTDLR APAQQLIRHLLLNFLLWAPGGHTIAWDVITLMAHTAEITHEIIGFLDQTLYRWNRLGIES PRSEKLARELLKELRTQV NT seq 1677 nt NT seq  +upstreamnt  +downstreamnt atggctcaagattcagtagatctttcttgtgattatcagttttggatgcagaagctttct gtatgggatcaggcttccactttggaaacccagcaagacacctgtcttcacgtggctcag ttccaggagttcctaaggaagatgtatgaagccttgaaagagatggattctaatacagtc attgaaagattccccacaattggtcaactgttggcaaaagcttgttggaatccttttatt ttagcatatgatgaaagccaaaaaattctaatatggtgcttatgttgtctaattaacaaa gaaccacagaattctggacaatcaaaacttaactcctggatacagggtgtattatctcat atactttcagcactcagatttgataaagaagttgctcttttcactcaaggtcttgggtat gcacctatagattactatcctggtttgcttaaaaatatggttttatcattagcgtctgaa ctcagagagaatcatcttaatggatttaacactcaaaggcgaatggctcccgagcgagtg gcgtccctgtcacgagtttgtgtcccacttattaccctgacagatgttgaccccctggtg gaggctctcctcatctgtcatggacgtgaacctcaggaaatcctccagccagagttcttt gaggctgtaaacgaggccattttgctgaagaagatttctctccccatgtcagctgtagtc tgcctctggcttcggcaccttcccagccttgaaaaagcaatgctgcatctttttgaaaag ctaatctccagtgagagaaattgtctgagaaggatcgaatgctttataaaagattcatcg ctgcctcaagcagcctgccaccctgccatattccgggttgttgatgagatgttcaggtgt gcactcctggaaaccgatggggccctggaaatcatagccactattcaggtgtttacgcag tgctttgtagaagctctggagaaagcaagcaagcagctgcggtttgcactcaagacctac tttccttacacttctccatctcttgccatggtgctgctgcaagaccctcaagatatccct cggggacactggctccagacactgaagcatatttctgaactgctcagagaagcagttgaa gaccagactcatgggtcctgcggaggtccctttgagagctggttcctgttcattcacttc ggaggatgggctgagatggtggcagagcaattactgatgtcggcagccgaaccccccacg gccctgctgtggctcttggccttctactacggcccccgtgatgggaggcagcagagagca cagactatggtccaggtgaaggccgtgctgggccacctcctggcaatgtccagaagcagc agcctctcagcccaggacctgcagacggtagcaggacagggcacagacacagacctcaga gctcctgcacaacagctgatcaggcaccttctcctcaacttcctgctctgggctcctgga ggccacacgatcgcctgggatgtcatcaccctgatggctcacactgctgagataactcac gagatcattggctttcttgaccagaccttgtacagatggaatcgtcttggcattgaaagc cctagatcagaaaaactggcccgagagctccttaaagagctgcgaactcaagtctag

Homo sapiens (human): 2178 Help Entry 2178              CDS       T01001                                  Symbol FANCE, FACE, FAE Name (RefSeq) FA complementation group E   KO K10892   fanconi anemia group E protein Organism hsa  Homo sapiens (human) Pathway hsa03460   Fanconi anemia pathway Network nt06508  Interstrand crosslink repair   Element N01464   Fanconi anemia pathway Disease H00238   Fanconi anemia Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09124 Replication and repair    03460 Fanconi anemia pathway     2178 (FANCE)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03400 DNA repair and recombination proteins [BR:hsa03400]     2178 (FANCE) DNA repair and recombination proteins [BR:hsa03400]  Eukaryotic type   DSBR (double strand breaks repair)    FA (Fanconi anemia) pathway     FA core complex      2178 (FANCE) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  FA_FANCE Motif Other DBs NCBI-GeneID:  2178 NCBI-ProteinID:  NP_068741 OMIM:  613976 HGNC:  3586 Ensembl:  ENSG00000112039 UniProt:  Q9HB96 Structure PDBPDBj LinkDB All DBs Position 6:35452338..35467102 Genome browser AA seq 536 aa AA seqDB search MATPDAGLPGAEGVEPAPWAQLEAPARLLLQALQAGPEGARRGLGVLRALGSRGWEPFDW GRLLEALCREEPVVQGPDGRLELKPLLLRLPRICQRNLMSLLMAVRPSLPESGLLSVLQI AQQDLAPDPDAWLRALGELLRRDLGVGTSMEGASPLSERCQRQLQSLCRGLGLGGRRLKS PQAPDPEEEENRDSQQPGKRRKDSEEEAASPEGKRVPKRLRCWEEEEDHEKERPEHKSLE SLADGGSASPIKDQPVMAVKTGEDGSNLDDAKGLAESLELPKAIQDQLPRLQQLLKTLEE GLEGLEDAPPVELQLLHECSPSQMDLLCAQLQLPQLSDLGLLRLCTWLLALSPDLSLSNA TVLTRSLFLGRILSLTSSASRLLTTALTSFCAKYTYPVCSALLDPVLQAPGTGPAQTELL CCLVKMESLEPDAQVLMLGQILELPWKEETFLVLQSLLERQVEMTPEKFSVLMEKLCKKG LAATTSMAYAKLMLTVMTKYQANITETQRLGLAMALEPNTTFLRKSLKAALKHLGP NT seq 1611 nt NT seq  +upstreamnt  +downstreamnt atggcgacaccggacgcggggctccctggggctgagggcgtggagccggcgccctgggcg cagctggaggcccccgcccgcctcctgctgcaggcgctgcaggcggggcctgagggggcg cggcgcggcctgggggtgctccgggcgctgggcagccgcggctgggagcccttcgactgg ggtcgcttgctcgaggccctgtgccgggaggagccggtcgtgcaggggcctgacggccgt ctggagctgaaaccactgttgctgcgattgccccggatatgccagaggaacctgatgtcc ctgctgatggccgttcggccatcgctgccggaaagtgggctcctctctgtgctgcagatt gcccagcaggacctagcccctgacccagatgcctggctccgtgccctgggggaattgctg cgaagggatttgggggtggggacctccatggagggagcttctccactgtctgaaagatgc cagagacagctccaaagtctatgtagggggctgggcctggggggcaggaggttgaaatcc ccccaggctccagaccctgaagaagaggagaacagggactcccagcagcctgggaaacgc agaaaggactcagaggaagaggctgccagtcctgaggggaagagggtccccaaaagatta cggtgttgggaagaggaagaagatcatgagaaggagagacccgaacataagtcactggaa tccctggcagatggaggaagtgcatctcctattaaggaccagcctgtcatggcagttaag actggcgaggacggttcgaatctggatgatgctaaaggtctggctgagagtttggagttg cccaaagctatccaggaccagcttcccaggctgcagcagctgctgaagaccttggaggag gggttagagggattggaggatgcccccccagttgagctacagcttcttcacgaatgtagt cccagccagatggacttgctgtgtgcccagctgcagctccctcagctctcagacctcggt ctcctgcggctctgcacctggctgctggccctttcacctgatctcagcctcagcaatgct actgtgctgaccagaagcctctttcttggacggatcctctccttgacttcctcagcctcc cgcctgcttacaactgccctgacctccttctgtgccaaatatacataccctgtctgcagc gccctccttgaccctgtgctccaggccccaggcacaggtcctgctcaaacagagttactg tgttgccttgtgaagatggagtccctggagccagatgcacaggttctaatgctgggacag atcttggagctgccctggaaggaggaaactttcttggtgttgcagtcactcctagagcgg caggtggagatgacccctgagaagttcagtgtcttaatggagaagctctgtaaaaagggg ctggcagccaccacctccatggcctatgccaagctcatgctgacagtgatgaccaagtat caggctaacatcactgagacccagaggctgggcctggctatggccctagaacctaacacc accttcctgaggaagtccctgaaggccgccttgaaacatttgggcccctga

Homo sapiens (human): 2188 Help Entry 2188              CDS       T01001                                  Symbol FANCF, FAF Name (RefSeq) FA complementation group F   KO K10893   fanconi anemia group F protein Organism hsa  Homo sapiens (human) Pathway hsa03460   Fanconi anemia pathway Network nt06508  Interstrand crosslink repair   Element N01464   Fanconi anemia pathway Disease H00238   Fanconi anemia Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09124 Replication and repair    03460 Fanconi anemia pathway     2188 (FANCF)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03400 DNA repair and recombination proteins [BR:hsa03400]     2188 (FANCF) DNA repair and recombination proteins [BR:hsa03400]  Eukaryotic type   DSBR (double strand breaks repair)    FA (Fanconi anemia) pathway     FA core complex      2188 (FANCF) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  FANCF DUF5753 Motif Other DBs NCBI-GeneID:  2188 NCBI-ProteinID:  NP_073562 OMIM:  613897 HGNC:  3587 Ensembl:  ENSG00000183161 UniProt:  Q9NPI8 A3KME0 Structure PDBPDBj LinkDB All DBs Position 11:complement(22622533..22625823) Genome browser AA seq 374 aa AA seqDB search MESLLQHLDRFSELLAVSSTTYVSTWDPATVRRALQWARYLRHIHRRFGRHGPIRTALER RLHNQWRQEGGFGRGPVPGLANFQALGHCDVLLSLRLLENRALGDAARYHLVQQLFPGPG VRDADEETLQESLARLARRRSAVHMLRFNGYRENPNLQEDSLMKTQAELLLERLQEVGKA EAERPARFLSSLWERLPQNNFLKVIAVALLQPPLSRRPQEELEPGIHKSPGEGSQVLVHW LLGNSEVFAAFCRALPAGLLTLVTSRHPALSPVYLGLLTDWGQRLHYDLQKGIWVGTESQ DVPWEELHNRFQSLCQAPPPLKDKVLTALETCKAQDGDFEVPGLSIWTDLLLALRSGAFR KRQVLGLSAGLSSV NT seq 1125 nt NT seq  +upstreamnt  +downstreamnt atggaatcccttctgcagcacctggatcgcttttccgagcttctggcggtctcaagcact acctacgtcagcacctgggaccccgccaccgtgcgccgggccttgcagtgggcgcgctac ctgcgccacatccatcggcgctttggtcggcatggccccattcgcacggctctggagcgg cggctgcacaaccagtggaggcaagagggcggctttgggcggggtccagttccgggatta gcgaacttccaggccctcggtcactgtgacgtcctgctctctctgcgcctgctggagaac cgggccctcggggatgcagctcgttaccacctggtgcagcaactctttcccggcccgggc gtccgggacgccgatgaggagacactccaagagagcctggcccgccttgcccgccggcgg tctgcggtgcacatgctgcgcttcaatggctatagagagaacccaaatctccaggaggac tctctgatgaagacccaggcggagctgctgctggagcgtctgcaggaggtggggaaggcc gaagcggagcgtcccgccaggtttctcagcagcctgtgggagcgcttgcctcagaacaac ttcctgaaggtgatagcggtggcgctgttgcagccgcctttgtctcgtcggccccaagaa gagttggaacccggcatccacaaatcacctggagaggggagccaagtgctagtccactgg cttctggggaattcggaagtctttgctgccttttgtcgcgccctcccagccgggcttttg actttagtgactagccgccacccagcgctgtctcctgtctatctgggtctgctaacagac tggggtcaacgtttgcactatgaccttcagaaaggcatttgggttggaactgagtcccaa gatgtgccctgggaggagttgcacaataggtttcaaagcctctgtcaggcccctccacct ctgaaagataaagttctaactgccctggagacctgtaaagcgcaggatggagattttgaa gtacctggtcttagcatctggacagacctcttattagctcttcgtagtggtgcatttagg aaaagacaagttttgggtctcagcgcaggcctcagttctgtatag

Homo sapiens (human): 2189 Help Entry 2189              CDS       T01001                                  Symbol FANCG, FAG, XRCC9 Name (RefSeq) FA complementation group G   KO K10894   fanconi anemia group G protein Organism hsa  Homo sapiens (human) Pathway hsa03460   Fanconi anemia pathway Network nt06508  Interstrand crosslink repair   Element N01464   Fanconi anemia pathway Disease H00238   Fanconi anemia Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09124 Replication and repair    03460 Fanconi anemia pathway     2189 (FANCG)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03400 DNA repair and recombination proteins [BR:hsa03400]     2189 (FANCG) DNA repair and recombination proteins [BR:hsa03400]  Eukaryotic type   DSBR (double strand breaks repair)    FA (Fanconi anemia) pathway     FA core complex      2189 (FANCG) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  TPR_2 TPR_8 TPR_1 TPR_7 TPR_12 Hpt Motif Other DBs NCBI-GeneID:  2189 NCBI-ProteinID:  NP_004620 OMIM:  602956 HGNC:  3588 Ensembl:  ENSG00000221829 UniProt:  O15287 Q53XM5 Structure PDBPDBj LinkDB All DBs Position 9:complement(35073839..35079942) Genome browser AA seq 622 aa AA seqDB search MSRQTTSVGSSCLDLWREKNDRLVRQAKVAQNSGLTLRRQQLAQDALEGLRGLLHSLQGL PAAVPVLPLELTVTCNFIILRASLAQGFTEDQAQDIQRSLERVLETQEQQGPRLEQGLRE LWDSVLRASCLLPELLSALHRLVGLQAALWLSADRLGDLALLLETLNGSQSGASKDLLLL LKTWSPPAEELDAPLTLQDAQGLKDVLLTAFAYRQGLQELITGNPDKALSSLHEAASGLC PRPVLVQVYTALGSCHRKMGNPQRALLYLVAALKEGSAWGPPLLEASRLYQQLGDTTAEL ESLELLVEALNVPCSSKAPQFLIEVELLLPPPDLASPLHCGTQSQTKHILASRCLQTGRA GDAAEHYLDLLALLLDSSEPRFSPPPSPPGPCMPEVFLEAAVALIQAGRAQDALTLCEEL LSRTSSLLPKMSRLWEDARKGTKELPYCPLWVSATHLLQGQAWVQLGAQKVAISEFSRCL ELLFRATPEEKEQGAAFNCEQGCKSDAALQQLRAAALISRGLEWVASGQDTKALQDFLLS VQMCPGNRDTYFHLLQTLKRLDRRDEATALWWRLEAQTKGSHEDALWSLPLYLESYLSWI RPSDRDAFLEEFRTSLPKSCDL NT seq 1869 nt NT seq  +upstreamnt  +downstreamnt atgtcccgccagaccacctctgtgggctccagctgcctggacctgtggagggaaaagaat gaccggctcgttcgacaggccaaggtggctcagaactccggtctgactctgaggcgacag cagttggctcaggatgcactggaagggctcagagggctcctccatagtctgcaagggctc cctgcagctgttcctgttcttcccttggagctgactgtcacctgcaacttcattatcctg agggcaagcttggcccagggtttcacagaggatcaggcccaggatatccagcggagccta gagagagtgctggagacacaggagcagcaggggcccaggttggaacaggggctcagggag ctgtgggactctgtccttcgtgcttcctgccttctgccggagctgctgtctgccctgcac cgcctggttggcctgcaggctgccctctggttgagtgctgaccgtcttggggacctggcc ttgttactagagaccctgaatggcagccagagtggagcctctaaggatctgctgttactt ctgaaaacttggagtcccccagctgaggaattagatgctccattgaccctgcaggatgcc cagggattgaaggatgtcctcctgacagcatttgcctaccgccaaggtctccaggagctg atcacagggaacccagacaaggcactaagcagccttcatgaagcggcctcaggcctgtgt ccacggcctgtgttggtccaggtgtacacagcactggggtcctgtcaccgtaagatggga aatccacagagagcactgttgtacttggttgcagccctgaaagagggatcagcctggggt cctccacttctggaggcctctaggctctatcagcaactgggggacacaacagcagagctg gagagtctggagctgctagttgaggccttgaatgtcccatgcagttccaaagccccgcag tttctcattgaggtagaattactactgccaccacctgacctagcctcaccccttcattgt ggcactcagagccagaccaagcacatactagcaagcaggtgcctacagacggggagggca ggagacgctgcagagcattacttggacctgctggccctgttgctggatagctcggagcca aggttctccccacccccctcccctccagggccctgtatgcctgaggtgtttttggaggca gcggtagcactgatccaggcaggcagagcccaagatgccttgactctatgtgaggagttg ctcagccgcacatcatctctgctacccaagatgtcccggctgtgggaagatgccagaaaa ggaaccaaggaactgccatactgcccactctgggtctctgccacccacctgcttcagggc caggcctgggttcaactgggtgcccaaaaagtggcaattagtgaatttagcaggtgcctc gagctgctcttccgggccacacctgaggaaaaagaacaaggggcagctttcaactgtgag cagggatgtaagtcagatgcggcactgcagcagcttcgggcagccgccctaattagtcgt ggactggaatgggtagccagcggccaggataccaaagccttacaggacttcctcctcagt gtgcagatgtgcccaggtaatcgagacacttactttcacctgcttcagactctgaagagg ctagatcggagggatgaggccactgcactctggtggaggctggaggcccaaactaagggg tcacatgaagatgctctgtggtctctccccctgtacctagaaagctatttgagctggatc cgtccctctgatcgtgacgccttccttgaagaatttcggacatctctgccaaagtcttgt gacctgtag

Homo sapiens (human): 199990 Help Entry 199990            CDS       T01001                                  Symbol FAAP20, C1orf86, FP7162 Name (RefSeq) FA core complex associated protein 20 Organism hsa  Homo sapiens (human) Network nt06508  Interstrand crosslink repair   Element N01464   Fanconi anemia pathway SSDB OrthologParalogGene clusterGFIT Motif Pfam:  FANCA_interact UBZ_FAAP20 Zn-C2H2_12 Motif Other DBs NCBI-GeneID:  199990 NCBI-ProteinID:  NP_872339 OMIM:  615183 HGNC:  26428 Ensembl:  ENSG00000162585 UniProt:  Q6NZ36 Structure PDBPDBj LinkDB All DBs Position 1:complement(2184477..2212720) Genome browser AA seq 180 aa AA seqDB search MEAARRPRLGLSRRRPRPAGGPSGGRPWFLLGGDERERLWAELLRTVSPELILDHEVPSL PAFPGQEPRCGPEPTEVFTVGPKTFSWTPFPPDLWGPGRSYRLLHGAGGHLESPARSLPQ RPAPDPCRAPRVEQQPSVEGAAALRSCPMCQKEFAPRLTQLDVDSHLAQCLAESTEDVTW NT seq 543 nt NT seq  +upstreamnt  +downstreamnt atggaggcggcgcggaggccgcggctggggttgagccgccggaggccgcgcccggcgggc gggccttctggcggccgcccctggtttctcctggggggtgatgagcgggagcggctctgg gccgagctactgcgcacggtgagcccggagctgatcctggatcacgaggtgccttcactg cccgccttcccaggacaggagcccaggtgcggcccggagcccactgaagtcttcactgtc ggacccaagaccttttcctggacaccctttccgccggacctgtggggcccgggccgttcc taccggctgcttcacggggcaggagggcacctggaatcccccgccaggtccctgccccag cgcccggcacctgatccctgcagggcccccagggtggagcagcagccgtctgtggagggt gccgcggccctgcgcagctgccccatgtgccagaaggagttcgcccccaggctgacccag ctggatgttgacagccacctggcccagtgcttggccgaaagcacagaagacgtgacgtgg tga

Homo sapiens (human): 80233 Help Entry 80233             CDS       T01001                                  Symbol FAAP100, C17orf70, FANCX Name (RefSeq) FA core complex associated protein 100   KO K10993   fanconi anemia core complex 100 kDa subunit Organism hsa  Homo sapiens (human) Pathway hsa03460   Fanconi anemia pathway Network nt06508  Interstrand crosslink repair   Element N01464   Fanconi anemia pathway Disease H00238   Fanconi anemia Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09124 Replication and repair    03460 Fanconi anemia pathway     80233 (FAAP100)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03400 DNA repair and recombination proteins [BR:hsa03400]     80233 (FAAP100) DNA repair and recombination proteins [BR:hsa03400]  Eukaryotic type   DSBR (double strand breaks repair)    FA (Fanconi anemia) pathway     FA core complex      80233 (FAAP100) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  FANCAA Motif Other DBs NCBI-GeneID:  80233 NCBI-ProteinID:  NP_079437 OMIM:  611301 HGNC:  26171 Ensembl:  ENSG00000185504 UniProt:  Q0VG06 A4ZI32 Structure PDBPDBj LinkDB All DBs Position 17:complement(81539891..81553133) Genome browser AA seq 881 aa AA seqDB search MAGAAPRVRYLAGFCCPLGGLAAGKPRVLCHEAEVFLSTGSELVYVYDQEGGLLTAAFRF PDQVWHLELLAPRRLLYALCARRGLYCLSLDHPGRSRSTSQDDRDSEDGDQPSPVIPVDP DACILPDAALCAFTLLDSVLVTLVQGPARWKMQLFEQPCPGEDPRPGGQIGEVELSSYTP PAGVPGKPAAPHFLPVLCSVSPSGSRVPHDLLGGSGGFTLEDALFGLLFGADATLLQSPV VLCGLPDGQLCCVILKALVTSRSAPGDPNALVKILHHLEEPVIFIGALKTEPQAAEAAEN FLPDEDVHCDCLVAFGHHGRMLAIKASWDESGKLVPELREYCLPGPVLCAACGGGGRVYH STPSDLCVVDLSRGSTPLGPEQPEEGPGGLPPMLCPASLNICSVVSLSASPRTHEGGTKL LALSAKGRLMTCSLDLDSEMPGPARMTTESAGQKIKELLSGIGNISERVSFLKKAVDQRN KALTSLNEAMNVSCALLSSGTGPRPISCTTSTTWSRLQTQDVLMATCVLENSSSFSLDQG WTLCIQVLTSSCALDLDSACSAITYTIPVDQLGPGARREVTLPLGPGENGGLDLPVTVSC TLFYSLREVVGGALAPSDSEDPFLDECPSDVLPEQEGVCLPLSRHTVDMLQCLRFPGLAP PHTRAPSPLGPTRDPVATFLETCREPGSQPAGPASLRAEYLPPSVASIKVSAELLRAALK DGHSGVPLCCATLQWLLAENAAVDVVRARALSSIQGVAPDGANVHLIVREVAMTDLCPAG PIQAVEIQVESSSLADICRAHHAVVGRMQTMVTEQATQGSSAPDLRVQYLRQIHANHETL LREVQTLRDRLCTEDEASSCATAQRLLQVYRQLRHPSLILL NT seq 2646 nt NT seq  +upstreamnt  +downstreamnt atggccggcgccgcgccgcgggtccgctacctggcgggcttctgctgccctctcgggggc ctggcggcgggcaagccccgcgtgctgtgccatgaggcagaggtcttcctgtccaccggg agcgagctcgtctacgtgtacgaccaggagggcgggctgctgaccgcggcgttccggttc cccgaccaggtgtggcacctggagctgctggcgccgcgcaggttgctgtacgcgctgtgc gcccggaggggcctctactgcctgtcgctggaccacccgggcaggagcaggtctacgagc caggatgacagggacagcgaggacggtgaccagccttcccccgtgatccctgtggacccc gatgcctgcatccttcccgatgctgcgctgtgcgcgttcaccttgctggacagtgtgctg gtcaccctggtgcagggccctgcccgatggaagatgcagctgtttgagcagccctgtcct ggggaggacccccggccaggaggccagatcggtgaggtggagctgtcctcctacacgccc ccagccggggtcccaggaaagcctgcagccccccacttccttccagtgctgtgctctgtg tcaccatcaggctccagggtcccgcacgacctcctcgggggctccgggggcttcacgctg gaggacgccctcttcgggctcctctttggagctgatgccaccctcctgcagtcacctgtg gtcctctgtggtctccctgatggccagctctgctgtgtgatcctgaaggccctggtcacc tccaggtcagcccctggtgacccaaatgcccttgtcaagatcctccatcacctggaggag cccgtcatcttcataggggccttgaagacagagccacaggctgcagaagctgcagagaat tttctgcctgacgaggatgtgcactgtgactgcctggtggcctttggtcaccacggccgg atgctggccatcaaggccagctgggatgagtccgggaagctggtgcccgagctgcgggag tactgcctcccaggccctgtgctctgcgctgcctgtggcgggggtggccgcgtgtaccac agcaccccttctgacctctgtgtggtggatctgtctcggggaagcaccccgctgggccct gagcagcccgaagaaggcccgggaggcctgccccccatgctgtgcccagccagcctgaac atctgcagtgtcgtctcgctgtccgcgtctcccaggacgcatgaaggtggcaccaagctc ctggccctgtccgccaaaggccgcctgatgacctgcagcctggacctggactctgagatg cctggcccagccaggatgaccacagagagtgcaggtcagaaaataaaggagctgctgtct ggaattggcaacatctctgagagagtgtcttttctaaagaaggcggttgaccagcggaac aaggcactgacaagcctcaacgaggccatgaacgtgagctgtgcactgctgtcaagcggc acgggccccagacccatctcctgcaccaccagcaccacctggagccgcctgcagacacag gatgtgctcatggccacctgcgtgctagagaacagcagcagcttcagcctggaccagggg tggaccctgtgcatccaggtgctcaccagctcctgtgctctcgacctggactcggcctgc tccgccatcacctacaccatccccgtggaccagctcggccccggtgctcggcgggaggtg acgctacccctgggccctggtgagaacggcgggctcgacctgcccgtgaccgtgtcctgc acgctgttctacagtctcagggaggtggtgggcggggcccttgccccctcagactctgag gacccctttctggatgagtgcccctccgacgtcctgcccgagcaagagggtgtttgcctg cccctgagcaggcacacagtggacatgctgcagtgtctgcgcttccctggcctggccccg ccacacacacgggccccctccccactcggccccacccgagaccctgtggccacttttctg gaaacttgtcgggagcctggcagccagccagcaggacccgcctccctgcgggccgagtac ctgcccccatctgtggcttccatcaaggtgtcggcggagctgctcagagctgccttgaag gacggccactcaggcgtgcccctgtgctgtgccaccctgcagtggctccttgctgagaat gctgctgtggacgtcgtgagggcccgagcactatcttccatccagggagtggcccctgat ggcgccaacgttcacctcatcgtccgagaggtggccatgactgacctgtgcccagcaggg cccatccaggccgtggagattcaagtggaaagctcctctctggccgacatttgcagggcg caccatgccgttgtcgggcgcatgcagacgatggtgacagagcaggccacccagggctcc agcgctcctgatctccgtgtgcagtacctccgccagatccacgccaaccacgagacactg ctgcgggaggtgcagaccctgcgcgaccggctctgcacggaggatgaggccagctcctgt gccaccgcccagaggctgctacaggtgtaccggcagctgcgccaccccagcctcatcctg ctgtga

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