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2020-10-26 19:47:37, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001010895            4666 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens excision repair cross-complementing rodent repair
            deficiency, complementation group 6-like 2 (ERCC6L2), mRNA.
ACCESSION   NM_001010895 XM_088578
VERSION     NM_001010895.2  GI:157364962
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 4666)
  AUTHORS   Lamesch,P., Li,N., Milstein,S., Fan,C., Hao,T., Szabo,G., Hu,Z.,
            Venkatesan,K., Bethel,G., Martin,P., Rogers,J., Lawlor,S.,
            McLaren,S., Dricot,A., Borick,H., Cusick,M.E., Vandenhaute,J.,
            Dunham,I., Hill,D.E. and Vidal,M.
  TITLE     hORFeome v3.1: a resource of human open reading frames representing
            over 10,000 human genes
  JOURNAL   Genomics 89 (3), 307-315 (2007)
   PUBMED   17207965
REFERENCE   2  (bases 1 to 4666)
  AUTHORS   Venter,J.C., Adams,M.D., Myers,E.W., Li,P.W., Mural,R.J.,
            Sutton,G.G., Smith,H.O., Yandell,M., Evans,C.A., Holt,R.A.,
            Gocayne,J.D., Amanatides,P., Ballew,R.M., Huson,D.H., Wortman,J.R.,
            Zhang,Q., Kodira,C.D., Zheng,X.H., Chen,L., Skupski,M.,
            Subramanian,G., Thomas,P.D., Zhang,J., Gabor Miklos,G.L.,
            Nelson,C., Broder,S., Clark,A.G., Nadeau,J., McKusick,V.A.,
            Zinder,N., Levine,A.J., Roberts,R.J., Simon,M., Slayman,C.,
            Hunkapiller,M., Bolanos,R., Delcher,A., Dew,I., Fasulo,D.,
            Flanigan,M., Florea,L., Halpern,A., Hannenhalli,S., Kravitz,S.,
            Levy,S., Mobarry,C., Reinert,K., Remington,K., Abu-Threideh,J.,
            Beasley,E., Biddick,K., Bonazzi,V., Brandon,R., Cargill,M.,
            Chandramouliswaran,I., Charlab,R., Chaturvedi,K., Deng,Z., Di
            Francesco,V., Dunn,P., Eilbeck,K., Evangelista,C., Gabrielian,A.E.,
            Gan,W., Ge,W., Gong,F., Gu,Z., Guan,P., Heiman,T.J., Higgins,M.E.,
            Ji,R.R., Ke,Z., Ketchum,K.A., Lai,Z., Lei,Y., Li,Z., Li,J.,
            Liang,Y., Lin,X., Lu,F., Merkulov,G.V., Milshina,N., Moore,H.M.,
            Naik,A.K., Narayan,V.A., Neelam,B., Nusskern,D., Rusch,D.B.,
            Salzberg,S., Shao,W., Shue,B., Sun,J., Wang,Z., Wang,A., Wang,X.,
            Wang,J., Wei,M., Wides,R., Xiao,C., Yan,C., Yao,A., Ye,J., Zhan,M.,
            Zhang,W., Zhang,H., Zhao,Q., Zheng,L., Zhong,F., Zhong,W., Zhu,S.,
            Zhao,S., Gilbert,D., Baumhueter,S., Spier,G., Carter,C.,
            Cravchik,A., Woodage,T., Ali,F., An,H., Awe,A., Baldwin,D.,
            Baden,H., Barnstead,M., Barrow,I., Beeson,K., Busam,D., Carver,A.,
            Center,A., Cheng,M.L., Curry,L., Danaher,S., Davenport,L.,
            Desilets,R., Dietz,S., Dodson,K., Doup,L., Ferriera,S., Garg,N.,
            Gluecksmann,A., Hart,B., Haynes,J., Haynes,C., Heiner,C.,
            Hladun,S., Hostin,D., Houck,J., Howland,T., Ibegwam,C., Johnson,J.,
            Kalush,F., Kline,L., Koduru,S., Love,A., Mann,F., May,D.,
            McCawley,S., McIntosh,T., McMullen,I., Moy,M., Moy,L., Murphy,B.,
            Nelson,K., Pfannkoch,C., Pratts,E., Puri,V., Qureshi,H.,
            Reardon,M., Rodriguez,R., Rogers,Y.H., Romblad,D., Ruhfel,B.,
            Scott,R., Sitter,C., Smallwood,M., Stewart,E., Strong,R., Suh,E.,
            Thomas,R., Tint,N.N., Tse,S., Vech,C., Wang,G., Wetter,J.,
            Williams,S., Williams,M., Windsor,S., Winn-Deen,E., Wolfe,K.,
            Zaveri,J., Zaveri,K., Abril,J.F., Guigo,R., Campbell,M.J.,
            Sjolander,K.V., Karlak,B., Kejariwal,A., Mi,H., Lazareva,B.,
            Hatton,T., Narechania,A., Diemer,K., Muruganujan,A., Guo,N.,
            Sato,S., Bafna,V., Istrail,S., Lippert,R., Schwartz,R., Walenz,B.,
            Yooseph,S., Allen,D., Basu,A., Baxendale,J., Blick,L., Caminha,M.,
            Carnes-Stine,J., Caulk,P., Chiang,Y.H., Coyne,M., Dahlke,C.,
            Mays,A., Dombroski,M., Donnelly,M., Ely,D., Esparham,S., Fosler,C.,
            Gire,H., Glanowski,S., Glasser,K., Glodek,A., Gorokhov,M.,
            Graham,K., Gropman,B., Harris,M., Heil,J., Henderson,S., Hoover,J.,
            Jennings,D., Jordan,C., Jordan,J., Kasha,J., Kagan,L., Kraft,C.,
            Levitsky,A., Lewis,M., Liu,X., Lopez,J., Ma,D., Majoros,W.,
            McDaniel,J., Murphy,S., Newman,M., Nguyen,T., Nguyen,N., Nodell,M.,
            Pan,S., Peck,J., Peterson,M., Rowe,W., Sanders,R., Scott,J.,
            Simpson,M., Smith,T., Sprague,A., Stockwell,T., Turner,R.,
            Venter,E., Wang,M., Wen,M., Wu,D., Wu,M., Xia,A., Zandieh,A. and
            Zhu,X.
  TITLE     The sequence of the human genome
  JOURNAL   Science 291 (5507), 1304-1351 (2001)
   PUBMED   11181995
  REMARK    Erratum:[Science 2001 Jun 5;292(5523):1838]
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            DB153432.1, AL161454.10 and BC075860.1.
            On Sep 19, 2007 this sequence version replaced gi:58219007.
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC140702.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025086, ERS025091 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-567               DB153432.1         3-569
            568-759             AL161454.10        90344-90535         c
            760-3846            BC075860.1         1-3087
            3847-3848           AL161454.10        3463-3464           c
            3849-4666           BC075860.1         3090-3907
FEATURES             Location/Qualifiers
     source          1..4666
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="9"
                     /map="9q22.32"
     gene            1..4666
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="excision repair cross-complementing rodent repair
                     deficiency, complementation group 6-like 2"
                     /db_xref="GeneID:375748"
                     /db_xref="HGNC:26922"
                     /db_xref="HPRD:17362"
     exon            1..467
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       23
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186000728"
     variation       64
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147324037"
     variation       79
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112083815"
     variation       93
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202197538"
     variation       121
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:199917784"
     misc_feature    152..154
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="upstream in-frame stop codon"
     variation       235
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191249511"
     variation       242
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373338065"
     variation       305
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112412135"
     variation       343
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141071823"
     variation       357
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75475951"
     CDS             389..2527
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="stretch responsive protein 278; RAD26L hypothetical
                     protein; putative repair and recombination helicase
                     RAD26L"
                     /codon_start=1
                     /product="putative DNA repair and recombination protein
                     RAD26-like"
                     /protein_id="NP_001010895.1"
                     /db_xref="GI:58219008"
                     /db_xref="CCDS:CCDS35072.1"
                     /db_xref="GeneID:375748"
                     /db_xref="HGNC:26922"
                     /db_xref="HPRD:17362"
                     /translation="
MQPGSAPPPGRMDPSAPQPRAETSGKDIWHPGERCLAPSPDNGKLCEASIKSITVDENGKSFAVVLYADFQERKIPLKQLQEVKFVKDCPRNLIFDDEDLEKPYFPNRKFPSSSVAFKLSDNGDSIPYTINRYLRDYQREGTRFLYGHYIHGGGCILGDDMGLGKTVQVISFLAAVLHKKGTREDIENNMPEFLLRSMKKEPLSSTAKKMFLIVAPLSVLYNWKDELDTWGYFRVTVLHGNRKDNELIRVKQRKCEIALTTYETLRLCLDELNSLEWSAVIVDEAHRIKNPKARVTEVMKALKCNVRIGLTGTILQNNMKELWCVMDWAVPGLLGSGTYFKKQFSDPVEHGQRHTATKRELATGRKAMQRLAKKMSGWFLRRTKTLIKDQLPKKEDRMVYCSLTDFQKAVYQTVLETEDVTLILQSSEPCTCRSGQKRRNCCYKTNSHGETVKTLYLSYLTVLQKVANHVALLQAASTSKQQETLIKRICDQVFSRFPDFVQKSKDAAFETLSDPKYSGKMKVLQQLLNHCRKNRDKVLLFSFSTKLLDVLQQYCMASGLDYRRLDGSTKSEERLKIVKEFNSTQDVNICLVSTMAGGLGLNFVGANVVVLFDPTWNPANDLQAIDRAYRIGQCRDVKVLRLISLGTVEEIMYLRQIYKQQLHCVVVGSENAKRYFEAVQGSKEHQGELFGIHNLFKFRSQGSCLTKDILEV
"
     misc_feature    482..634
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="Tudor domains are found in many eukaryotic
                     organisms and have been implicated in protein-protein
                     interactions in which methylated protein substrates bind
                     to these domains. For example, the Tudor domain of
                     Survival of Motor Neuron (SMN) binds to...; Region: TUDOR;
                     cd04508"
                     /db_xref="CDD:119391"
     misc_feature    order(503..505,518..520,524..526,593..595,599..601)
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="dimethylated arginine/lysine binding site [chemical
                     binding]; other site"
                     /db_xref="CDD:119391"
     misc_feature    797..1807
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="SNF2 family N-terminal domain; Region: SNF2_N;
                     pfam00176"
                     /db_xref="CDD:201060"
     misc_feature    848..1330
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="DEAD-like helicases superfamily. A diverse family
                     of proteins involved in ATP-dependent RNA or DNA
                     unwinding. This domain contains the ATP-binding region;
                     Region: DEXDc; cd00046"
                     /db_xref="CDD:28927"
     misc_feature    872..886
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="ATP binding site [chemical binding]; other site"
                     /db_xref="CDD:28927"
     misc_feature    1235..1246
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q5T890.1);
                     Region: DEAH box"
     misc_feature    1235..1246
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="putative Mg++ binding site [ion binding]; other
                     site"
                     /db_xref="CDD:28927"
     misc_feature    1913..2308
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="Helicase superfamily c-terminal domain; associated
                     with DEXDc-, DEAD-, and DEAH-box proteins, yeast
                     initiation factor 4A, Ski2p, and Hepatitis C virus NS3
                     helicases; this domain is found in a wide variety of
                     helicases and helicase related proteins; may...; Region:
                     HELICc; cd00079"
                     /db_xref="CDD:28960"
     misc_feature    order(2015..2026,2084..2089,2168..2176)
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="nucleotide binding region [chemical binding]; other
                     site"
                     /db_xref="CDD:28960"
     misc_feature    order(2192..2194,2255..2257,2267..2269,2276..2278)
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /note="ATP-binding site [chemical binding]; other site"
                     /db_xref="CDD:28960"
     variation       389
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:690528"
     variation       390
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:10986795"
     variation       407
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:56108623"
     variation       409
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:202222262"
     variation       410
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201393222"
     variation       413
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371970239"
     variation       414
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:78293324"
     variation       429
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:151308487"
     variation       433
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371776172"
     variation       442..443
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:35504182"
     variation       442
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:139286981"
     exon            468..892
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       538
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374932786"
     variation       581
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148041136"
     variation       584
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141719745"
     variation       611
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146034461"
     variation       656
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184611791"
     variation       657
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367785775"
     variation       704
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138730206"
     variation       709
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201848920"
     variation       723
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200286500"
     variation       795
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201929399"
     variation       796
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:61746533"
     variation       800
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146075543"
     variation       808
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370249357"
     variation       817
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375681798"
     variation       828
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61740729"
     variation       840
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368518723"
     variation       845
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372469673"
     exon            893..1015
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       921
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200568420"
     variation       935
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149385968"
     variation       956
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:77857685"
     variation       961
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371706944"
     variation       1007
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374911552"
     exon            1016..1209
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       1020
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61748989"
     variation       1051
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369055167"
     variation       1060
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148565931"
     variation       1071
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:182659090"
     variation       1116
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372604415"
     variation       1123
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376740581"
     variation       1134
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142906169"
     variation       1146
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200549063"
     variation       1147
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147747872"
     variation       1163
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:690086"
     variation       1184
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201243110"
     variation       1185
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369782292"
     exon            1210..1371
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       1213
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181919944"
     variation       1268
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377624956"
     variation       1283
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370912243"
     exon            1372..1579
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       1406
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377544589"
     variation       1426
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:140978745"
     variation       1437
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370407012"
     variation       1453
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144924790"
     variation       1487
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186390247"
     variation       1516
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147782697"
     variation       1518
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140078259"
     variation       1520
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200807189"
     variation       1533
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373574073"
     variation       1561
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:150328847"
     variation       1564
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368880452"
     variation       1569
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:79398697"
     exon            1580..1720
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       1616
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142685145"
     variation       1645
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147361064"
     variation       1646
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371003658"
     variation       1668
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138517503"
     variation       1673
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:59765732"
     variation       1679
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138666484"
     variation       1717
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374484016"
     exon            1721..1834
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       1725
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141894834"
     variation       1766
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:202143780"
     variation       1771
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371892712"
     variation       1794
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375051537"
     variation       1796
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:146551545"
     variation       1799
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200558009"
     variation       1800
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201546231"
     variation       1801
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201406110"
     variation       1827
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200888020"
     variation       1831
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371832920"
     exon            1835..1954
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       1899
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148305949"
     variation       1931
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374831913"
     exon            1955..2026
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     STS             1975..2092
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /standard_name="MARC_14930-14931:1032547547:3"
                     /db_xref="UniSTS:267775"
     variation       1996
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141400231"
     variation       2003
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150855705"
     variation       2008
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200839216"
     variation       2011
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139285024"
     variation       2013
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:377215343"
     exon            2027..2172
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       2035
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143996230"
     variation       2036
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200688685"
     variation       2044
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139587179"
     variation       2059
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376256925"
     variation       2065
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140913718"
     variation       2140
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201825396"
     variation       2163
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2274654"
     exon            2173..2268
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       2201
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368747018"
     variation       2237
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:376428556"
     variation       2247
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200972525"
     exon            2269..2368
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       2344
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:182252007"
     variation       2351
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147948835"
     variation       2357
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147984545"
     exon            2369..4647
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /inference="alignment:Splign:1.39.8"
     variation       2390
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:76938369"
     variation       2396
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201361900"
     variation       2406
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371620653"
     variation       2442
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374654068"
     variation       2464
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148406466"
     variation       2470
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367848303"
     variation       2476
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371776270"
     variation       2506
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368998957"
     variation       2515
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374108634"
     variation       2525
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369776234"
     variation       2553
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201831168"
     variation       2602
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:187477905"
     variation       2692..2696
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace=""
                     /replace="ctaaa"
                     /db_xref="dbSNP:374403172"
     variation       2713
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:589362"
     variation       2750
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:192286402"
     variation       2831
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184817706"
     variation       2853
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:189136620"
     variation       2907
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:686048"
     variation       2993
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371067527"
     variation       3050
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:73656590"
     variation       3175
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192189557"
     variation       3185
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184510556"
     variation       3223
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189383832"
     variation       3236
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:377612173"
     variation       3294
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115920293"
     variation       3351
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:372373092"
     variation       3364
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:78604771"
     variation       3426
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:10988835"
     variation       3468
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181166341"
     variation       3486
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111436235"
     variation       3502
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374238723"
     variation       3534
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146769771"
     variation       3711
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148876661"
     variation       3721
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:113126324"
     variation       3852
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143565798"
     variation       3895
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184114131"
     variation       3940
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188856651"
     variation       4024
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116087401"
     variation       4033
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150953610"
     variation       4042
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140785832"
     variation       4158
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:145739109"
     variation       4280
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181611790"
     variation       4335
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138668640"
     variation       4369
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376277806"
     variation       4466
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:187057336"
     variation       4555
                     /gene="ERCC6L2"
                     /gene_synonym="C9orf102; RAD26L; SR278"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192338239"
ORIGIN      
caattcgggagcccgttctcgcgggattttccaagaccgggttggaatttgcgggggttaggagacggaagtcagagcctaggaagatttgggggtcgccttgccggcctcctgtcctcctccggcggcggcggagcccgagagaactaggtgaacaccgctttgccagcctcacacagcgtcccctggctctgccgccgctccggacgtcgccctcccgttctgcttgggtccccttagtcgctacctttgctgggatccccctcctccatcctgtggcttcgggttgccgaagagcgatgctcggagggcggccggaagtggcgttggccgccattggcctgccggccagccaccttgctgtcctccgccgccttccgggtgttacatgcagccgggctcggcccctccccctggccggatggatccgtcggcgccacagccccgcgcggaaacctcaggcaaagacatatggcatccaggagaaagatgtcttgccccttctccagataatggaaaactttgtgaagcaagcataaaatctatcacagtggatgaaaatggcaagtcatttgcagtcgtcttatatgcagattttcaagaaaggaaaatacctcttaaacagcttcaagaagtgaaatttgttaaagattgccctaggaatcttatatttgatgatgaagatttagaaaaaccttatttcccaaaccgaaaatttccatcatcttctgttgcttttaaattatctgacaatggagactctattccttataccatcaataggtatttgagagactaccaaagagaaggaacccggtttctttatggacactacatccatggaggagggtgcattctgggtgatgacatgggacttggaaaaacagtacaggttatttcatttctggctgcagttttgcataaaaagggaactcgtgaggatattgaaaataacatgccagagtttttactaagaagtatgaaaaaggaacccctttcttctacagcaaaaaagatgttcttaatagttgctcctctttctgtcctctacaactggaaggatgaattggacacctggggatatttcagagtcactgttttacatggaaacagaaaagataatgaattaattcgtgtaaagcagaggaaatgtgaaattgctctaacaacttatgaaacactacgcttatgcctggatgaacttaacagtttggaatggtcagctgtcattgtggatgaagctcatagaatcaagaatccaaaagctagagtaacagaagttatgaaagctttgaaatgtaatgtccgcattggcctcactggaaccatccttcagaacaacatgaaggaactgtggtgtgttatggactgggctgtgccaggccttttagggagtgggacctacttcaagaagcagttttctgacccagtagaacatggtcagagacacacggcaacaaagagagaactagccactggccgaaaggccatgcaaagacttgccaaaaagatgtctggctggtttctcaggcgcaccaagactcttatcaaggatcagttgcctaagaaggaagaccggatggtgtattgttctttgacagatttccagaaagctgtctatcaaacagtgttagaaacagaggacgtgactttgatacttcaatcttctgagccttgtacctgtaggagtggccaaaaaaggagaaattgttgttataagaccaattctcatggtgaaacagtgaaaaccttgtatctcagttaccttacagtccttcagaaggtagctaaccatgtcgcgctactgcaagctgctagtacttccaaacaacaggaaacacttatcaaaaggatatgtgatcaggtattttccagattcccagattttgtgcagaaaagcaaagatgcagcctttgaaacactttctgaccctaaatacagtggaaaaatgaaggtccttcagcagcttttaaatcattgcaggaaaaacagagataaagttcttctcttttctttttccaccaagttgcttgacgtgctacagcagtactgtatggcgtctgggcttgattaccgacgacttgatggaagtacaaaatcagaggaaagactcaagattgtaaaagagttcaacagtacacaagatgttaacatttgccttgtctctacaatggctggtggactaggcctcaattttgtcggtgccaatgttgttgtattatttgatcctacttggaatccagccaatgatcttcaagccattgacagagcatataggattggacaatgtagagatgtcaaagtgcttaggctgatatccttgggaactgtggaggaaatcatgtatttacgacagatatacaagcagcaacttcactgtgtggtggttggaagtgaaaatgccaaacgatattttgaagcagttcaaggatctaaagagcatcaaggagagctttttgggatccataacctcttcaaatttaggtcccaagggtcttgtcttacgaaggacatcctggaggtgtgaacttcttctctgaccttttcaataatattttaaatacagtttttcttcctcaggaaatctgaaatacaattgctgttgccttttcagagaaacttttggttttctttatcaaaaatgccttggaatttttacttttagagaataagaaatgaattattgtacctctaaactaagattttcccatgcataattacaaataatgcacacacacaaatgtatatgctgggtagtatgaactccaaggcaattttaaataggcagagagaagtttatagttttgaaaacagctgctgaagtcaggaactaaaaaaagaggttttcctaaataaacaaaaatataaaatgtgttttaattaaaagttaccaaatactccctgagatgtactctcatgtctcatggagatttttgttttctgttcccaataaaaattccacaccagtattttaaactctccctgttgtgttcatcctcagcatacagatgtttcttattcctcaaacaaaatattttatatccttttttaaaaaaatctttaagttcttttatataccggaatactaaggatattaacctattttctaattgatattcatataggtatcataaaatcctggagtatcatctttttcaacctcctcatggtatagatgaggaaactgagtcttagagaacttcaggatatttctcttgacttccaggactttgtagtaaaatcttaatgtacttcatttattcagtaagtaccataaaggcagttcaaggagcaattggttcctgtccttgaggaacttaaaccatcttgaccggaggtggaagagaacgtttacataataaccatgcaatgtcaggaatcgtatgctgaacaagttaaacagtagaccatggatggctgggggagaggaaggtatatattatttgaatcctataaatgttgttactattatacagtttctgatatatactgctgagtttctattttatagtaactatatttgattctgaattcagtggcccatttggagtcctactttttggggttttttccccttgctttttaaatacgctgtttctttcatgaatttgttctttccagtttcccttttcatatcaataactttgtttgccctccagctcccaaacccagctgctacctccatctcagagtactacttgacatgcctatattgatgttaaagtcaattgtctataaaaatattagcattttattatttatcctgttttctgtcatatatgacatagttacctgtttttatcagaataaccacctatttctttgttaaacaagtgttatataagacatatcaggatgacaggttattaagtagaaaaagttcccttgtttatcgtgccactgcactccagcctggggaacaaagcaagagacttgtctcaaaaacaaaaaacaaaaacaaaaaaaagttctcttgttcactggttattctaagaatatcttgtttcaccttcagaagtgtttattaatgacaggaccatccatgtcttacattttcttttttaaaaatatcttttaagttctttaatataccagaacactaagaatattaacctattttctaattgatattaataaggggtgacaaggccatccatgccctacatttgtcttgctaggcatatcattggcacttgattattaagttaaattttgaattaaaattactcatttgtcatcaatcagaatgtaaatttattcaggattggttagattcatgctgctttgggccaaaaggtgcttctaaatattattattagccccatataatgggagtacctatcataaagtaaaaggagtatttcacttcatgtgagacatttttaatttttaaaggttgtataaaatctcttttaaaatgttttaagatgtaaaaatttgaatatttacacttataatcttatgatttctgggcaatttcattctgttttgcattgactttccattatctatattatggtttctcttcaaagatagatattgagagttcattttacaagtatttgttgagcatctgctaaatgtcaggtactgttcatagagctttgcatacataaaagaacaaaataaacaaaacgatcctgtctaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:375748 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA
            GeneID:375748 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA
            GeneID:375748 -> Molecular function: GO:0008026 [ATP-dependent helicase activity] evidence: IEA
            GeneID:375748 -> Biological process: GO:0006281 [DNA repair] evidence: IEA
            GeneID:375748 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
            GeneID:375748 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA
            GeneID:375748 -> Cellular component: GO:0005815 [microtubule organizing center] evidence: IEA

by @meso_cacase at DBCLS
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