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2024-04-24 05:29:14, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_017667 5713 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens coiled-coil domain containing 132 (CCDC132),
transcript variant 1, mRNA.
ACCESSION NM_017667
VERSION NM_017667.3 GI:384229075
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 5713)
AUTHORS Bailey,S.D., Xie,C., Do,R., Montpetit,A., Diaz,R., Mohan,V.,
Keavney,B., Yusuf,S., Gerstein,H.C., Engert,J.C. and Anand,S.
CONSRTM DREAM investigators
TITLE Variation at the NFATC2 locus increases the risk of
thiazolidinedione-induced edema in the Diabetes REduction
Assessment with ramipril and rosiglitazone Medication (DREAM) study
JOURNAL Diabetes Care 33 (10), 2250-2253 (2010)
PUBMED 20628086
REMARK GeneRIF: Observational study of gene-disease association,
gene-environment interaction, and pharmacogenomic / toxicogenomic.
(HuGE Navigator)
REFERENCE 2 (bases 1 to 5713)
AUTHORS Matsumoto,Y., Imai,Y., Sugita,Y., Tanaka,T., Tsujimoto,G., Saito,H.
and Oshida,T.
TITLE CCDC132 is highly expressed in atopic dermatitis T cells
JOURNAL Mol Med Rep 3 (1), 83-87 (2010)
PUBMED 21472204
REFERENCE 3 (bases 1 to 5713)
AUTHORS Talmud,P.J., Drenos,F., Shah,S., Shah,T., Palmen,J., Verzilli,C.,
Gaunt,T.R., Pallas,J., Lovering,R., Li,K., Casas,J.P., Sofat,R.,
Kumari,M., Rodriguez,S., Johnson,T., Newhouse,S.J., Dominiczak,A.,
Samani,N.J., Caulfield,M., Sever,P., Stanton,A., Shields,D.C.,
Padmanabhan,S., Melander,O., Hastie,C., Delles,C., Ebrahim,S.,
Marmot,M.G., Smith,G.D., Lawlor,D.A., Munroe,P.B., Day,I.N.,
Kivimaki,M., Whittaker,J., Humphries,S.E. and Hingorani,A.D.
CONSRTM ASCOT investigators; NORDIL investigators; BRIGHT Consortium
TITLE Gene-centric association signals for lipids and apolipoproteins
identified via the HumanCVD BeadChip
JOURNAL Am. J. Hum. Genet. 85 (5), 628-642 (2009)
PUBMED 19913121
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 4 (bases 1 to 5713)
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
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
BC017888.1, AB100163.1, BC035984.1, AC002379.1 and BE671517.1.
On Apr 13, 2012 this sequence version replaced gi:62865870.
Transcript Variant: This variant (1) encodes the longest isoform
(a).
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
##Evidence-Data-START##
Transcript exon combination :: AB100163.1, BC152424.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025083, ERS025084 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-43 BC017888.1 1-43
44-2294 AB100163.1 1-2251
2295-3613 BC035984.1 298-1616
3614-5703 AC002379.1 86323-88412
5704-5713 BE671517.1 1-10 c
FEATURES Location/Qualifiers
source 1..5713
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="7"
/map="7q21.3"
gene 1..5713
/gene="CCDC132"
/note="coiled-coil domain containing 132"
/db_xref="GeneID:55610"
/db_xref="HGNC:25956"
exon 1..161
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 9
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:76810131"
variation 38
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:115505401"
variation 64
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:376190032"
variation 74
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:370533330"
misc_feature 90..92
/gene="CCDC132"
/note="upstream in-frame stop codon"
variation 112
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:369703869"
CDS 129..3023
/gene="CCDC132"
/note="isoform a is encoded by transcript variant 1;
coiled-coil domain-containing protein 132"
/codon_start=1
/product="coiled-coil domain-containing protein 132
isoform a"
/protein_id="NP_060137.2"
/db_xref="GI:62865871"
/db_xref="CCDS:CCDS43617.1"
/db_xref="GeneID:55610"
/db_xref="HGNC:25956"
/translation="
MQKIKSLMTRQGLKSPQESLSDLGAIESLRVPGKEEFRELREQPSDPQAEQELINSIEQVYFSVDSFDIVKYELEKLPPVLNLQELEAYRDKLKQQQAAVSKKVADLILEKQPAYVKELERVTSLQTGLQLAAVICTNGRRHLNIAKEGFTQASLGLLANQRKRQLLIGLLKSLRTIKTLQRTDVRLSEMLEEEDYPGAIQLCLECQKAASTFKHYSCISELNSKLQDTLEQIEEQLDVALSKICKNFDINHYTKVQQAYRLLGKTQTAMDQLHMHFTQAIHNTVFQVVLGYVELCAGNTDTKFQKLQYKDLCTHVTPDSYIPCLADLCKALWEVMLSYYRTMEWHEKHDNEDTASASEGSNMIGTEETNFDRGYIKKKLEHGLTRIWQDVQLKVKTYLLGTDLSIFKYDDFIFVLDIISRLMQVGEEFCGSKSEVLQESIRKQSVNYFKNYHRTRLDELRMFLENETWELCPVKSNFSILQLHEFKFMEQSRSPSVSPSKQPVSTSSKTVTLFEQYCSGGNPFEIQANHKDEETEDVLASNGYESDEQEKSAYQEYDSDSDVPEELKRDYVDEQTGDGPVKSVSRETLKSRKKSDYSLNKVNAPILTNTTLNVIRLVGKYMQMMNILKPIAFDVIHFMSQLFDYYLYAIYTFFGRNDSLESTGLGLSSSRLRTTLNRIQESLIDLEVSADPTATLTAAEERKEKVPSPHLSHLVVLTSGDTLYGLAERVVATESLVFLAEQFEFLQPHLDAVMPAVKKPFLQQFYSQTVSTASELRKPIYWIVAGKALDYEQMLLLMANVKWDVKEIMSQHNIYVDALLKEFEQFNRRLNEVSKRVRIPLPVSNILWEHCIRLANRTIVEGYANVKKCSNEGRALMQLDFQQFLMKLEKLTDIRPIPDKEFVETYIKAYYLTENDMERWIKEHREYSTKQLTNLVNVCLGSHINKKARQKLLAAIDDIDRPKR
"
misc_feature 171..173
/gene="CCDC132"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q96JG6.3); phosphorylation site"
misc_feature 288..1163
/gene="CCDC132"
/note="Protein of unknown function N-terminal domain
(DUF2450); Region: DUF2450; pfam10475"
/db_xref="CDD:151041"
misc_feature 1602..1604
/gene="CCDC132"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1608..1610
/gene="CCDC132"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q96JG6.3); phosphorylation site"
misc_feature 1608..1610
/gene="CCDC132"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1620..1622
/gene="CCDC132"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q96JG6.3); phosphorylation site"
misc_feature 1620..1622
/gene="CCDC132"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1803..1805
/gene="CCDC132"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q96JG6.3); phosphorylation site"
misc_feature 1809..1811
/gene="CCDC132"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q96JG6.3); phosphorylation site"
misc_feature 2295..3002
/gene="CCDC132"
/note="Protein of unknown function C-terminus (DUF2451);
Region: DUF2451; pfam10474"
/db_xref="CDD:151040"
variation 138
/gene="CCDC132"
/replace="a"
/replace="t"
/db_xref="dbSNP:372814646"
exon 162..230
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 163
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:377215860"
variation 188
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:143665286"
variation 221
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:146829042"
exon 231..353
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 249
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:368989470"
variation 261
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:371874797"
variation 284
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:372697126"
exon 354..425
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 391
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:185236240"
variation 422
/gene="CCDC132"
/replace="a"
/replace="t"
/db_xref="dbSNP:367996589"
exon 426..479
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 457
/gene="CCDC132"
/replace="a"
/replace="t"
/db_xref="dbSNP:146490784"
exon 480..550
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 485
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:17851579"
variation 501
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:140993533"
variation 519
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:111678071"
exon 551..668
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 557
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:375674244"
variation 579
/gene="CCDC132"
/replace="a"
/replace="c"
/db_xref="dbSNP:143512538"
variation 580
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:370247072"
variation 618
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:374485392"
variation 619
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:201400427"
exon 669..704
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 684
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:145621721"
exon 705..787
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 725
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:200949909"
variation 777
/gene="CCDC132"
/replace="a"
/replace="c"
/db_xref="dbSNP:372089506"
exon 788..830
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 812
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:375400119"
exon 831..929
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 842
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:377185723"
variation 861
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:148835608"
variation 910
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:370126178"
exon 930..1070
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 950
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:202242070"
variation 980
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:375006121"
variation 994
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:368851885"
variation 1034
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:200883111"
exon 1071..1203
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 1106
/gene="CCDC132"
/replace="a"
/replace="c"
/db_xref="dbSNP:188742733"
variation 1134
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:200944614"
variation 1160
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:138784387"
variation 1182
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:369737684"
variation 1188
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:202155789"
variation 1195
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:199896068"
exon 1204..1295
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 1218
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:377270059"
variation 1232
/gene="CCDC132"
/replace="a"
/replace="c"
/db_xref="dbSNP:199714930"
variation 1238
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:200187082"
variation 1246
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:371166383"
variation 1271
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:373817251"
variation 1287
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:375780858"
variation 1294..1295
/gene="CCDC132"
/replace=""
/replace="g"
/db_xref="dbSNP:140810598"
exon 1296..1390
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 1299
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:201054996"
variation 1319
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:200434482"
variation 1344
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:374290264"
variation 1387
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:368241812"
exon 1391..1489
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 1412
/gene="CCDC132"
/replace="a"
/replace="c"
/db_xref="dbSNP:371633008"
variation 1440
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:376939967"
variation 1443
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:369316514"
variation 1489
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:11540025"
exon 1490..1580
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 1530
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:137879844"
variation 1564
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:200751674"
variation 1574
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:369067607"
exon 1581..1757
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 1606
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:146809545"
variation 1713
/gene="CCDC132"
/replace="a"
/replace="t"
/db_xref="dbSNP:200076275"
variation 1720
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:371073974"
exon 1758..1876
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 1841
/gene="CCDC132"
/replace="a"
/replace="t"
/db_xref="dbSNP:368505711"
variation 1856
/gene="CCDC132"
/replace="a"
/replace="c"
/db_xref="dbSNP:141252888"
exon 1877..1983
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 1923
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:374860561"
exon 1984..2105
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 2015
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:367596092"
variation 2019
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:199629360"
variation 2066
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:371808024"
exon 2106..2186
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 2117
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:375083734"
exon 2187..2335
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 2224
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:373349963"
variation 2293
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:376216197"
variation 2294
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:200975765"
variation 2295
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:2106432"
variation 2316
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:377166540"
exon 2336..2432
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 2360
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:371325624"
variation 2378
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:376064331"
exon 2433..2591
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 2445
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:191341151"
variation 2501
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:377259320"
variation 2575
/gene="CCDC132"
/replace="a"
/replace="t"
/db_xref="dbSNP:368046857"
exon 2592..2713
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 2675
/gene="CCDC132"
/replace="a"
/replace="c"
/db_xref="dbSNP:373044128"
exon 2714..2903
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 2719
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:200136574"
variation 2722
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:61741161"
variation 2763
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:2374639"
variation 2805
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:377675568"
variation 2816
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:3764799"
variation 2858
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:148888740"
variation 2877
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:377485014"
variation 2883
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:200300253"
exon 2904..5710
/gene="CCDC132"
/inference="alignment:Splign:1.39.8"
variation 2914
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:61745719"
variation 2948
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:370500282"
variation 2991
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:373958295"
variation 3000
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:368407161"
variation 3028
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:371906960"
variation 3046
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:144266211"
variation 3048
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:192787205"
variation 3058
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:368865634"
variation 3062
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:372156123"
variation 3071
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:146571220"
variation 3091
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:184288073"
variation 3093
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:140043089"
variation 3095
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:142268872"
variation 3109
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:151222457"
variation 3134
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:140358038"
variation 3180
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:75758985"
variation 3221..3222
/gene="CCDC132"
/replace=""
/replace="g"
/db_xref="dbSNP:34521532"
variation 3252
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:370407683"
variation 3274
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:17165292"
variation 3311
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:372037711"
variation 3312
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:189188031"
variation 3339
/gene="CCDC132"
/replace="a"
/replace="t"
/db_xref="dbSNP:182276909"
variation 3348
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:77206719"
STS 3358..3471
/gene="CCDC132"
/standard_name="RH44310"
/db_xref="UniSTS:81088"
variation 3491
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:11540024"
variation 3508
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:186327200"
variation 3653
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:142147490"
variation 3673
/gene="CCDC132"
/replace="a"
/replace="c"
/db_xref="dbSNP:3735650"
variation 3744
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:145899579"
variation 3751
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:111634740"
variation 3819
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:2285506"
variation 4001
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:17165299"
variation 4051
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:138716693"
variation 4132
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:142722832"
variation 4134
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:376781675"
variation 4170
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:58383093"
variation 4225
/gene="CCDC132"
/replace="a"
/replace="c"
/db_xref="dbSNP:114980211"
variation 4244
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:143421699"
variation 4262
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:148379408"
variation 4339
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:116637828"
variation 4359
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:77226429"
variation 4394
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:189459808"
variation 4414
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:141557557"
variation 4454
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:181458400"
variation 4489
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:186046386"
variation 4503
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:2285507"
variation 4525
/gene="CCDC132"
/replace="c"
/replace="g"
/db_xref="dbSNP:191376387"
variation 4572
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:118115946"
variation 4632
/gene="CCDC132"
/replace="a"
/replace="c"
/db_xref="dbSNP:150883928"
variation 4653
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:183038785"
variation 4690
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:375123175"
variation 4783
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:74713513"
variation 4793
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:374654008"
variation 4995..4996
/gene="CCDC132"
/replace=""
/replace="t"
/replace="tt"
/db_xref="dbSNP:35020495"
variation 4995
/gene="CCDC132"
/replace=""
/replace="ttt"
/db_xref="dbSNP:200289887"
variation 5004
/gene="CCDC132"
/replace=""
/replace="tt"
/db_xref="dbSNP:10546852"
variation 5016
/gene="CCDC132"
/replace="a"
/replace="t"
/db_xref="dbSNP:10238215"
variation 5184
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:17165300"
variation 5193
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:142943490"
variation 5370
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:17165301"
variation 5376
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:146104663"
variation 5398
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:376377612"
variation 5402
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:201022056"
variation 5472
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:117491408"
variation 5529
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:185887518"
variation 5536
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:73712852"
variation 5566
/gene="CCDC132"
/replace="a"
/replace="g"
/db_xref="dbSNP:73219929"
variation 5601
/gene="CCDC132"
/replace="g"
/replace="t"
/db_xref="dbSNP:369169965"
variation 5706
/gene="CCDC132"
/replace="c"
/replace="t"
/db_xref="dbSNP:190856711"
ORIGIN
aggataccctgggtcggctcctccacgtgaccacccactatggcttcctagtgtcagggccagctgtgtagtggctcggtgtgatttgttagctctttgaggcagggtaccctcctcaggatttcgatatgcaaaaaatcaaatctctcatgacccgacagggtctgaaaagccctcaagaaagcctcagtgatcttggtgccatagagagtctccgggtccctggaaaggaagaattcagggaacttcgagaacagccaagtgaccctcaagctgaacaagagcttattaatagtattgaacaagtatatttttctgtggattcatttgatattgttaaatatgagctggagaagcttccacctgttctcaatttgcaagaattagaggcgtatagagacaaattgaaacaacagcaagctgcagtatctaaaaaagtggcagatttaatccttgaaaaacagcctgcttatgtaaaggaacttgaaagagttacctcattgcagacaggtcttcaattagctgctgttatctgtacaaatgggagaagacacttgaatattgcaaaggaaggttttactcaagctagtttaggccttcttgcaaatcaaaggaaacgtcagttgctgattggacttctgaaatctctgagaactataaaaacattgcaaagaacagatgtacggttaagtgaaatgctggaggaggaagattatccaggagctattcagttgtgccttgaatgtcaaaaagctgccagcacttttaaacattacagttgtataagtgaactgaattcaaagctgcaagatactttggaacagattgaggaacagctggacgtagctctttccaaaatctgcaagaattttgacattaaccattataccaaggttcaacaagcttatcgacttcttggaaaaacacagacagcaatggatcaacttcatatgcacttcacccaagccattcacaacaccgtgtttcaagttgttcttggttatgtggaactatgtgcaggaaacacagacacaaaattccaaaagctgcaatataaggatctctgtacacatgttacaccagacagctatattccatgccttgcagacctgtgcaaagcactatgggaagttatgctcagctattataggactatggaatggcatgaaaagcatgacaatgaggatactgcttcagcttctgaagggagtaatatgataggtactgaagaaactaattttgatcgtggctacataaaaaagaaattagaacatggacttacacgaatatggcaggatgttcagctaaaagtaaaaacctacttgcttggaactgatttgtctatattcaaatatgatgatttcatctttgttttggatataatcagcaggttgatgcaagttggagaagaattttgtggtagcaagtctgaagttttacaggaatctattagaaaacaaagtgtcaattatttcaagaattaccatagaacacggctcgatgaactgagaatgttcttagagaatgagacttgggaactttgtcctgttaagtcaaatttcagcatcttgcaacttcatgaatttaaattcatggaacagtctcgctccccatcagtttcacctagtaaacagccagtctcaacttcttcaaaaacagtgaccttgtttgagcagtactgtagtggtgggaatccatttgaaattcaggccaaccacaaagatgaagaaacagaagatgtcttagcttctaatgggtatgaatctgatgaacaagaaaagagtgcctatcaagagtatgacagtgacagtgatgttcctgaggaactcaaacgagactatgtggatgagcagacaggagatggtcctgtgaaaagtgtttctcgggaaactctaaaaagcaggaagaaatcagattacagtctaaataaagtgaatgcacctatcttaacaaatacaacattgaacgtcataagacttgttggaaaatatatgcagatgatgaacattcttaagccaattgcctttgatgttattcatttcatgtctcaactatttgattattacttgtatgcaatatataccttttttggtcggaatgattcattggaatcaactggactcggccttagtagtagtagactaagaacaactctaaacagaatacaagaaagccttattgatctagaagtttcagctgatcctactgccacactcacagcagcagaagaaagaaaggagaaggtgccaagtccacacctcagtcacctagtggttttgacatctggggatacgctgtatgggttggcagaaagagtggtagccacggaatccttggtattcttggctgaacagtttgagttccttcagccacatctggatgctgtgatgcctgcagtcaaaaagccctttcttcagcagttctattctcagacagtctcaaccgccagtgaactacggaaaccaatttactggattgtagctggtaaagcccttgattatgaacagatgctgcttctcatggctaatgtgaaatgggatgtaaaagaaattatgtcacagcacaacatatatgtagatgcactattaaaggaatttgagcagtttaacaggaggctaaatgaagtttctaagagagttcgcatacccttgcctgtgtctaatatactttgggaacattgtatacgattggctaatcgaactattgtagaaggatatgccaatgtcaagaaatgcagtaatgagggtcgtgccctgatgcaattggattttcaacagtttttaatgaaacttgaaaaactaacagatattagacccattcctgataaagaatttgtagaaacttatattaaagcttattacctaactgagaatgacatggaacggtggatcaaagagcacagggaatattcaacgaagcagctgaccaatctggtgaatgtttgcctgggatcccatatcaataagaaagcaagacaaaaacttctagcagctatagatgatatagacagacctaaaagataatgaacacagctctctttcctcaatggcattgatcctcactcaacatatatgacctgaaagccagtttttttatgcacttctgacaactatctgctaagaaaactttgtgcatgtttttttgactggaaagtggaaaatattgaaatgtgtgtggtgttctcatgacttttatatgctgtggtctcttcaacttttggtctcatttgttgtaatctgaaatgatgttgccgccttgtcataacaatggttatgtgactacagttatacattttacagaagaatgtaccataagtatataattagaagaacagtggcttaatatatgtatgggaagtttatggaaaatgaagttggcacttttctaccctctgagcttggttcttaataagcataatgtgagggtgaatatgtagtatctcctaattatgagcactgcatgagaattaaaaaacacatgtaagtaaaatagttgaaaaatcagtatgttctctgtttttaaaatgtcaaagtttatgtcagggttaatttagttataacaaagtgatcataatggtgaaatttaataaatatactctagtatgatcagcctatgtgagactacattttgattttttgtgtggcatgcagatgtcatgaactatagtgcagcttttagtgtgttctaattttaattgttttatatcctgaaaccaatggtgaaaagtaatttcattgagggtaccttttcaatgcctgagtagcatacagaatcatgattatgagactttcttttatctttctttataaaaatatgtggtttttttgttgaaagttttggtctctttaaattcagattttgtcttaggacagtaaaacccaggttgactgactcaggaaacagttgtctgctagtcactcataaatgtacggtcatatgttcactcttcttaaatatccaccttttataacacaaatgtaaaatagtatcagtctagccaatgatgaactctggaatccacttagtcttcagtaagtatgtgctgttcctctaaactttgccctgaagccagggatcttctcctaatgtatgtgacataaaaatccattttccatgtactcttgccaactgtctgataaggaattttgtgtgtgttctttctgactggagagtggaggacatctaagcttgtgtggcattggtccaatgattgccatgcatgacctgtaacatcaacagctcacagaatcctaaggaatcatgtgagaaacaggccttgggtcttatgagtcttctgggacctaaggtgataaaatggatggcacagaatggcatgtgatcaagcatggaggtgataaggaaacaattgctactctgtgtccatcagtccctgcgatgtctgtaaatgcacagtgtaatgtgaagcactttcagaatatgtttgtgtgtgtctgtatgctgagtgttttcttttcatcctctcatgtcggagttcatttactgtcaatttaaaactttcctcttgtaaaaaggtatgagtttggtgccattatgatttggttgtggctagattatatacttgtgaagtagattctgcctgtagccattatttatatgcagccacttgaagaaaacaaacatgagataagcttggtccttgagtttaaatggcatatttagctgggcacataaagagctaatcaatcttttaaaatttgcagttgatgaagagctgcttatttttctcttctacatggattttatagttggtttcctttaatttctactttagttggccctagataatatgaacaggaatcacctgcctggtagagcccagtgttttccaaggtaataggaattgatacaaaagaattacttatcttgttagagactcgaccatgcaatctgacagaccttttaacctacccttactttgctttctccatcttcaaaatgaaatggtggatctttttaatgctttttgaaaaaggttttttttttttttttttttcattaaaaggtagcttaataagtgctagctagcatcaaaacagtaacaggaggtttgagtcatgaagttacctaatcacaagagagttaccagacatttctcaaatactttatacagtaatattgagttataaccatgtaacattttatgaaactaattttcagataaatacaattgaaaagctgagaatgtaaatggaattatacgtgttccaaaaactatcattaccaaaaatttattatttttgagtctaaactttccttaactttgacattttccatgaaagtttcctgtagaatttaccatgggagcatggtaaattagcattccctgagaaagaatgatcatttctacaaatacattgtcttgcatttaaaaatgctaggggggcacatagcaattcaaatgaactagtttgctttggtttataaaaccaacagagattttgtaagttcactttaactaataaactcatttacacaacttattaaatgaatttctcttgaaaccagggccatatggtattttatcatatctttaaataaaatttcgaaatttctatttagctgagtgctaaagtgaaactttgttagattaaatagctttttcttaactcaccaaaaagtagtaaaaggcttgtaattcaattcaccttgtaagcatagttgtcttttgtaataaaaaactagatctgaaaaa
//
by
@meso_cacase at
DBCLS
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