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2024-04-19 17:13:05, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_014653 4650 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens WSC domain containing 2 (WSCD2), mRNA.
ACCESSION NM_014653 XM_033113
VERSION NM_014653.2 GI:55749666
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 4650)
AUTHORS Greenwood,T.A., Akiskal,H.S., Akiskal,K.K. and Kelsoe,J.R.
CONSRTM Bipolar Genome Study
TITLE Genome-wide association study of temperament in bipolar disorder
reveals significant associations with three novel Loci
JOURNAL Biol. Psychiatry 72 (4), 303-310 (2012)
PUBMED 22365631
REFERENCE 2 (bases 1 to 4650)
AUTHORS Kato,N., Miyata,T., Tabara,Y., Katsuya,T., Yanai,K., Hanada,H.,
Kamide,K., Nakura,J., Kohara,K., Takeuchi,F., Mano,H., Yasunami,M.,
Kimura,A., Kita,Y., Ueshima,H., Nakayama,T., Soma,M., Hata,A.,
Fujioka,A., Kawano,Y., Nakao,K., Sekine,A., Yoshida,T.,
Nakamura,Y., Saruta,T., Ogihara,T., Sugano,S., Miki,T. and
Tomoike,H.
TITLE High-density association study and nomination of susceptibility
genes for hypertension in the Japanese National Project
JOURNAL Hum. Mol. Genet. 17 (4), 617-627 (2008)
PUBMED 18003638
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AB018332.2, BX488602.1, BM511109.1, AK098069.1 and BX647283.1.
On or before Nov 22, 2004 this sequence version replaced
gi:42659913, gi:7662305.
##Evidence-Data-START##
Transcript exon combination :: AB018332.2, BC110330.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025091 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-2721 AB018332.2 1-2721
2722-2722 BX488602.1 345-345
2723-3378 AB018332.2 2723-3378
3379-3468 BM511109.1 475-564
3469-4217 AK098069.1 1264-2012
4218-4298 BX647283.1 4263-4343
4299-4650 BX647283.1 4350-4701
FEATURES Location/Qualifiers
source 1..4650
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12q23.3"
gene 1..4650
/gene="WSCD2"
/note="WSC domain containing 2"
/db_xref="GeneID:9671"
/db_xref="HGNC:29117"
/db_xref="HPRD:17196"
exon 1..193
/gene="WSCD2"
/inference="alignment:Splign:1.39.8"
variation 11
/gene="WSCD2"
/replace="g"
/replace="t"
/db_xref="dbSNP:41314111"
variation 13
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:377660517"
variation 102
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:191178226"
variation 158
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:3751212"
exon 194..1126
/gene="WSCD2"
/inference="alignment:Splign:1.39.8"
variation 464
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:114900718"
variation 498
/gene="WSCD2"
/replace="c"
/replace="g"
/db_xref="dbSNP:191168534"
variation 508
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141308427"
variation 549
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371884561"
misc_feature 577..579
/gene="WSCD2"
/note="upstream in-frame stop codon"
variation 596
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145067987"
variation 703
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:182957037"
CDS 745..2442
/gene="WSCD2"
/codon_start=1
/product="WSC domain-containing protein 2"
/protein_id="NP_055468.2"
/db_xref="GI:55749667"
/db_xref="CCDS:CCDS41828.1"
/db_xref="GeneID:9671"
/db_xref="HGNC:29117"
/db_xref="HPRD:17196"
/translation="
MAKLWFKFQRYFRRKPVRFFTFLALYLTAGSLVFLHSGFVGQPAVSGNQANPAAAGGPAEGAELSFLGDMHLGRGFRDTGEASSIARRYGPWFKGKDGNERAKLGDYGGAWSRALKGRVVREKEEERAKYIGCYLDDTQSRALRGVSFFDYKKMTIFRCQDNCAERGYLYGGLEFGAECYCGHKIQATNVSEAECDMECKGERGSVCGGANRLSVYRLQLAQESARRYGSAVFRGCFRRPDNLSLALPVTAAMLNMSVDKCVDFCTEKEYPLAALAGTACHCGFPTTRFPLHDREDEQLCAQKCSAEEFESCGTPSYFIVYQTQVQDNRCMDRRFLPGKSKQLIALASFPGAGNTWARHLIELATGFYTGSYYFDGSLYNKGFKGERDHWRSGRTICIKTHESGQKEIEAFDAAILLIRNPYKALMAEFNRKYGGHIGFAAHAHWKGKEWPEFVRNYAPWWATHTLDWLKFGKKVLVVHFEDLKQDLFVQLGRMVSLLGVAVREDRLLCVESQKDGNFKRSGLRKLEYDPYTADMQKTISAYIKMVDAALKGRNLTGVPDDYYPR
"
misc_feature 799..867
/gene="WSCD2"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q2TBF2.2);
transmembrane region"
misc_feature 1126..1401
/gene="WSCD2"
/note="present in yeast cell wall integrity and stress
response component proteins; Region: WSC; smart00321"
/db_xref="CDD:128616"
misc_feature 1432..1716
/gene="WSCD2"
/note="present in yeast cell wall integrity and stress
response component proteins; Region: WSC; smart00321"
/db_xref="CDD:128616"
variation 797
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199708893"
variation 816
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:200435102"
variation 843
/gene="WSCD2"
/replace="c"
/replace="g"
/db_xref="dbSNP:370666613"
variation 893
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:61737703"
variation 894
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367680277"
variation 900
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371557089"
variation 908
/gene="WSCD2"
/replace="c"
/replace="g"
/db_xref="dbSNP:375448975"
variation 973
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200708985"
variation 991
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368781045"
variation 1004
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371817011"
variation 1011
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375207995"
variation 1046
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199742201"
variation 1055
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369086967"
variation 1066
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371652885"
variation 1082
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:187550758"
variation 1100
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1426355"
variation 1105
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199556088"
variation 1106
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201631606"
variation 1118
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:369077410"
exon 1127..1241
/gene="WSCD2"
/inference="alignment:Splign:1.39.8"
variation 1146
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:186969165"
variation 1217
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:191412045"
variation 1241
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371095870"
exon 1242..1426
/gene="WSCD2"
/inference="alignment:Splign:1.39.8"
variation 1272
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141128245"
variation 1275
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368739228"
variation 1276
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372232788"
variation 1287
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200772431"
variation 1304
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368311688"
variation 1305
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372067181"
variation 1312
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368726337"
variation 1336..1337
/gene="WSCD2"
/replace=""
/replace="a"
/db_xref="dbSNP:35731310"
variation 1347
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:79029951"
variation 1352
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:187377943"
variation 1415
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:137898269"
variation 1416
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371716560"
variation 1421
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374953285"
exon 1427..1548
/gene="WSCD2"
/inference="alignment:Splign:1.39.8"
variation 1444
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201882028"
variation 1457
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139768498"
variation 1464
/gene="WSCD2"
/replace="c"
/replace="g"
/db_xref="dbSNP:199888315"
variation 1465
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:183614363"
variation 1478
/gene="WSCD2"
/replace="a"
/replace="t"
/db_xref="dbSNP:201886947"
variation 1523
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:61739295"
variation 1527
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:724832"
variation 1529
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375714840"
variation 1541
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:3764002"
exon 1549..1723
/gene="WSCD2"
/inference="alignment:Splign:1.39.8"
variation 1552
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371020572"
variation 1553
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374336162"
variation 1576
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:76277633"
variation 1578
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:367855700"
variation 1601
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:188653401"
variation 1613
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371724221"
variation 1660
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:7138767"
variation 1662
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367674517"
variation 1665
/gene="WSCD2"
/replace="c"
/replace="g"
/db_xref="dbSNP:180963117"
variation 1681
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371743603"
exon 1724..1888
/gene="WSCD2"
/inference="alignment:Splign:1.39.8"
variation 1730
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370079769"
variation 1809
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372566704"
variation 1814
/gene="WSCD2"
/replace="c"
/replace="g"
/db_xref="dbSNP:138948518"
variation 1831
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376376643"
variation 1866
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371103273"
exon 1889..2089
/gene="WSCD2"
/inference="alignment:Splign:1.39.8"
variation 1906
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371344222"
variation 1907
/gene="WSCD2"
/replace="a"
/replace="t"
/db_xref="dbSNP:375154761"
variation 1920
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368092771"
variation 1952
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371514918"
variation 1955
/gene="WSCD2"
/replace="g"
/replace="t"
/db_xref="dbSNP:201146972"
variation 1956
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:202097270"
variation 1982
/gene="WSCD2"
/replace="c"
/replace="g"
/db_xref="dbSNP:376643141"
variation 1998
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200630899"
variation 2016
/gene="WSCD2"
/replace="c"
/replace="g"
/db_xref="dbSNP:372334494"
exon 2090..4636
/gene="WSCD2"
/inference="alignment:Splign:1.39.8"
variation 2107
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201772868"
variation 2121
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144706841"
variation 2139
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373411891"
variation 2178
/gene="WSCD2"
/replace="g"
/replace="t"
/db_xref="dbSNP:200611217"
variation 2222
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:377538937"
variation 2241
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138523163"
variation 2242
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:41314115"
variation 2248
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:202152897"
variation 2298
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:370666947"
variation 2303
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199889302"
variation 2314
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374705143"
variation 2343
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367689597"
variation 2380
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:185274692"
variation 2401
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371932635"
variation 2402
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374517422"
variation 2412
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368931933"
variation 2422
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371843593"
variation 2445
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375174623"
variation 2446
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:191068644"
variation 2456
/gene="WSCD2"
/replace="g"
/replace="t"
/db_xref="dbSNP:140259524"
variation 2487
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:181768524"
variation 2547
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372116411"
variation 2575
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:377200318"
variation 2633
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145510893"
variation 2722
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:12819456"
variation 2875
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138142123"
variation 2887
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:187047527"
variation 2888
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:191435377"
variation 2895
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:41314117"
variation 2920
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:183590538"
variation 2984
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141720882"
variation 2989
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:188079823"
variation 3003
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368808534"
variation 3057
/gene="WSCD2"
/replace="c"
/replace="g"
/db_xref="dbSNP:150556800"
variation 3087
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:190081175"
variation 3145
/gene="WSCD2"
/replace="c"
/replace="g"
/db_xref="dbSNP:201256887"
variation 3158
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:182241252"
variation 3200
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:186476008"
variation 3212
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:201623847"
variation 3215..3216
/gene="WSCD2"
/replace=""
/replace="ca"
/db_xref="dbSNP:142388442"
variation 3236
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:11113782"
variation 3237
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:192600498"
variation 3320
/gene="WSCD2"
/replace="c"
/replace="g"
/db_xref="dbSNP:11113783"
variation 3379
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:11113784"
variation 3394
/gene="WSCD2"
/replace="g"
/replace="t"
/db_xref="dbSNP:74450755"
variation 3438
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138609887"
variation 3486
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:185423887"
variation 3499
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:60500216"
variation 3562
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376089621"
variation 3589
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:188995965"
variation 3641
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369429969"
variation 3677
/gene="WSCD2"
/replace="g"
/replace="t"
/db_xref="dbSNP:149586635"
variation 3727
/gene="WSCD2"
/replace="g"
/replace="t"
/db_xref="dbSNP:192960245"
variation 3740
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:147285498"
variation 3788
/gene="WSCD2"
/replace="g"
/replace="t"
/db_xref="dbSNP:185273359"
variation 3875
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043649"
variation 3912..3913
/gene="WSCD2"
/replace=""
/replace="g"
/db_xref="dbSNP:34095608"
STS 4035..4202
/gene="WSCD2"
/standard_name="NIB1630"
/db_xref="UniSTS:10225"
variation 4101
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:188834791"
polyA_signal 4190..4195
/gene="WSCD2"
polyA_site 4213
/gene="WSCD2"
polyA_site 4218
/gene="WSCD2"
/experiment="experimental evidence, no additional details
recorded"
variation 4228
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144630498"
variation 4252
/gene="WSCD2"
/replace="a"
/replace="c"
/db_xref="dbSNP:181115770"
variation 4270..4273
/gene="WSCD2"
/replace=""
/replace="gtgtgt"
/db_xref="dbSNP:372802789"
variation 4271..4272
/gene="WSCD2"
/replace=""
/replace="gt"
/replace="gtgtgtgtgt"
/db_xref="dbSNP:72108827"
variation 4280..4281
/gene="WSCD2"
/replace=""
/replace="tgtgtgtgtg"
/db_xref="dbSNP:72348982"
variation 4288..4289
/gene="WSCD2"
/replace=""
/replace="tgtg"
/db_xref="dbSNP:72099370"
variation 4291..4292
/gene="WSCD2"
/replace=""
/replace="gtgt"
/replace="gtgtgtgt"
/db_xref="dbSNP:67445287"
variation 4299..4300
/gene="WSCD2"
/replace=""
/replace="gt"
/replace="gtgtgtgtgt"
/db_xref="dbSNP:35004904"
variation 4299
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:60876553"
variation 4301
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200903688"
variation 4302..4303
/gene="WSCD2"
/replace=""
/replace="t"
/db_xref="dbSNP:72328922"
variation 4302
/gene="WSCD2"
/replace="a"
/replace="t"
/db_xref="dbSNP:202024042"
variation 4303..4304
/gene="WSCD2"
/replace=""
/replace="ga"
/replace="t"
/db_xref="dbSNP:34755138"
variation 4304
/gene="WSCD2"
/replace="a"
/replace="t"
/db_xref="dbSNP:371503612"
variation 4345
/gene="WSCD2"
/replace="a"
/replace="g"
/db_xref="dbSNP:147526788"
variation 4421
/gene="WSCD2"
/replace="a"
/replace="t"
/db_xref="dbSNP:371213432"
variation 4511
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:9739493"
variation 4544
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148590942"
variation 4575
/gene="WSCD2"
/replace="c"
/replace="t"
/db_xref="dbSNP:56167194"
polyA_site 4636
/gene="WSCD2"
ORIGIN
cccagggcccggcaggaggagccttggtggcgagaaaggaaatccaggctcccctttccttaaagccactgcagcagctgggaaggcgcccacagagcgggcgcgccaagcgggacgcgggagtcgcagagagggaccccgggcgcctgctgagctcagctggcagagtttgcaagtggcggagacccttcaggtggcatccctgagtcctgatgcctgactggatggaggcccaccagcttctgttcccatgaggtagaaaggccaagcttggtcttcagctggggaagaggccagaaacaaggcccccagtgaaataacccagatccattggcctgaggagcagagaaagggcaagaagtgaactgcagctgctggtaaccctcagaaaccttctccaagtgctattctcacagttctttaggaacactctgaagtgaagaacaatatgtaggaaaatgggaccaacttatgtgtgttctgagcctcaaaacccccttgttggcccaaagaagctcaccttcagtttgggagggctggtaagctccatcctttctcatggcctcagccaagcattgaacttgccctccccttctggccttggtgatcactttttcaggaagagtgagactgaggacccccaagtgttccatccctaaggaaagcttgggaaaccaagccccttccatcctctcccaagcaccccagccaagccccagagagccagtccggaatgatcccactatggccaagctctggttcaaattccagcggtacttccgccggaaacctgtgcgcttctttaccttcctggcactctacctgactgctgggagccttgtcttccttcactctggctttgtgggccagcccgctgtctcggggaaccaggcgaaccccgctgctgcaggaggcccagctgagggtgctgagctgtccttcttgggtgacatgcatctgggcagaggtttccgggacacaggtgaagcctcaagcattgctcgcaggtacggaccctggttcaagggcaaggatgggaatgagagagccaagcttggcgactacggtggagcctggagccgagccctcaaggggagggttgtccgggagaaggaggaagagcgagccaagtacatcggctgctacctggatgacacccagagtcgggcccttcgaggagtgtccttttttgactacaaaaagatgaccatcttccgttgccaggacaactgtgctgaacggggttacctgtatggcgggctggagttcggcgccgagtgctactgcggccacaagatccaggcgacgaacgtgagcgaggcagagtgcgacatggagtgcaagggcgagcgaggcagcgtgtgcggcggcgccaaccgcctctctgtctaccggctgcagctggcccaggagtcggcccgcaggtatggaagtgcagtgttccggggctgcttccgcaggcccgacaacctttccctggccttacccgtgacagctgccatgctgaacatgtctgtggacaaatgcgtggacttctgcactgagaaggagtacccgctggcagctcttgcaggcaccgcctgccactgtgggtttcccaccacccgattcccgctccatgacagagaggatgagcagctctgtgcccagaagtgcagcgcggaggagtttgagagctgcgggactcctagttacttcattgtgtaccagacacaagtccaagacaaccgttgcatggacagaaggttcctgccaggcaagtccaagcagctcattgctttggccagcttcccaggtgctggcaacacgtgggctcgccacctcattgaattggccacaggcttctacactggcagctactacttcgatggctccctctacaacaaagggtttaaaggtgagcgggaccactggcgcagcggacggaccatctgcatcaagacgcacgaaagcggccagaaagagatcgaggccttcgacgccgccatcctgctcatccgcaacccctacaaagccctcatggctgagttcaaccgcaagtacggcggccacataggctttgctgcgcatgcccactggaagggcaaagagtggccagagttcgtgaggaactatgccccgtggtgggccactcacacactggactggctcaagtttggcaagaaggtgctggtggtgcactttgaggacctgaagcaggacctctttgtccagctgggccggatggtcagcctgctgggcgtggctgtcagggaggaccggctgctctgtgtggagagccagaaggatggcaacttcaagcgctcagggctccggaagctcgagtatgacccctatactgcggacatgcagaagaccatctctgcctacatcaagatggtggatgcagccctcaaagggcggaacctaacgggtgtccccgatgactactacccaagatgatgcgtccacacagggggagggtagactgggagtcctgaccacgcaggccctggggactcaagacccctggttacccccactcatctgtcctctctttggtctggggacaatccccttggctgctctttgccttcaatgagtttcctgcatgacagaggaggctcaagggaagagattgcccaggcactaccactctgctcacatgttccccccttggcaatgtggggcatcttgtttagggggttctagttacatggactcttttctgtctcctgggtccctgcccccaccactctgggttccatttgtgggagggagggctcatccacatcatggagacttgctggatgccccatggcaattgtcaaggctcttgatgcaagagcccagggggctattgtaaaaacttggccccagatgcttgtcccttctgggctgagatttcgcagcccccttctcatctccacccaagaagtgctggcaccgatgtttaactcaggccaccttctgttctaaagaaagattgctgggaagtttctccgtggccttaggtttctgacatcctggatagtgtggggaggtaatggtgctcacagtaggttaattggagacaccatgtggggccattggtgttatgagccccccaggccacactgcttctcagaaatgagctgcttgcctttccacctccagggcatgaaccctgcccctttctatccatgctgtgtccaggaggtgaccttgagatcctgataccaccttcaaggaacctcaggcaccaacagtgagcccacgaggatggtcacatgccatgtgcagaatttgacttaagagagagccccagtgacacatctctccatggtgggctccagtcagtcttacactgcccttctgacccctacaaatgggtcctttgctatccaggtgagacagcaagagtgttcttaatcagatggaaccacacccaaaatggacccccactaccttcccagaccatatatctccccttgatcatagtccaacagggccagcttcccttgggggccctttaaggaatggggtgaatgaaattgtgtcatttctatacaaacactgctctcttgatgctgaaatgccaaaccgaaggatttctgaggacctaaatcacggagcatcaatcttacaaagtgttggtccagagtcccatctcttccccaaccctggataccagtagcttcccacccagtccaaacctgcaccatccatcattatgtagatgaaaaagccataggtcatagcctctttgctattctattggagtagcctccctaggcagtccctctgaagccttggagtgcaggtaaatgctcattcccaagtagcaaagagaccatggagaaggtgcgtgtaaagagatatatttttgtaagaggaatatgattaatacattccgccccttggaacctggccatgcaaagcaagggcacagggattagacctgtggcacacttccccaattccctcatctgtaggatttgggctgccccaggcccacccagggggctctgaatgtattttgtaccgtgtttctttcccccaggagaatttttagtcttctttcatgaagcagtggaggggttggcctcccttctactgggaggttgactctctctgggagactcttggtccaagacctgggtcagttctttgctggtggtcccctctgaccacaagcttctgcctgaagattcctcaggtcaacaccatcattaaatgcgagttttgttgatgattctaccatgtggtagagtgttgtgtaagacaggttcacaaatgggatgttttcctagtgtgtgtgtgtgtgtgtgtgtgtgtgtatgagagagagagagagagacaacagagacagagagaggcagagaggcatagagagacagagagagagacaagaaacagagatagacagaaaatgttcggggtggcaggcgggttggtgtataactgctttgtgcctgtgtgactctggcatagctgctcagggagaattacgtgcctctgtgtgtaaaattgcctttgtgttctcctgcctctctatgttttgaaactgtatcccacaagttgccggtatgaccatcttatttgtaatgagtctgtgcaggtccttgtgtatggaattgcacccgtgtaaaggaggaaatggtcagtgtgcatgaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:9671 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
by
@meso_cacase at
DBCLS
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