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2024-04-17 01:43:14, 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 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
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