2024-03-28 19:07:12, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001759 6531 bp mRNA linear PRI 07-JUL-2013 DEFINITION Homo sapiens cyclin D2 (CCND2), mRNA. ACCESSION NM_001759 VERSION NM_001759.3 GI:209969683 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 6531) AUTHORS Zhang,L., Liu,X., Jin,H., Guo,X., Xia,L., Chen,Z., Bai,M., Liu,J., Shang,X., Wu,K., Pan,Y. and Fan,D. TITLE miR-206 inhibits gastric cancer proliferation in part by repressing cyclinD2 JOURNAL Cancer Lett. 332 (1), 94-101 (2013) PUBMED 23348698 REMARK GeneRIF: miR-206 could suppress gastric carcinoma cell proliferation at least partially through targeting cyclinD2 expression. REFERENCE 2 (bases 1 to 6531) AUTHORS Zhou,J., Tian,Y., Li,J., Lu,B., Sun,M., Zou,Y., Kong,R., Luo,Y., Shi,Y., Wang,K. and Ji,G. TITLE miR-206 is down-regulated in breast cancer and inhibits cell proliferation through the up-regulation of cyclinD2 JOURNAL Biochem. Biophys. Res. Commun. 433 (2), 207-212 (2013) PUBMED 23466356 REMARK GeneRIF: Cyclin D2 is a direct target of miR-206 in breast cancer cells REFERENCE 3 (bases 1 to 6531) AUTHORS Peters U, Jiao S, Schumacher FR, Hutter CM, Aragaki AK, Baron JA, Berndt SI, Bezieau S, Brenner H, Butterbach K, Caan BJ, Campbell PT, Carlson CS, Casey G, Chan AT, Chang-Claude J, Chanock SJ, Chen LS, Coetzee GA, Coetzee SG, Conti DV, Curtis KR, Duggan D, Edwards T, Fuchs CS, Gallinger S, Giovannucci EL, Gogarten SM, Gruber SB, Haile RW, Harrison TA, Hayes RB, Henderson BE, Hoffmeister M, Hopper JL, Hudson TJ, Hunter DJ, Jackson RD, Jee SH, Jenkins MA, Jia WH, Kolonel LN, Kooperberg C, Kury S, Lacroix AZ, Laurie CC, Laurie CA, Le Marchand L, Lemire M, Levine D, Lindor NM, Liu Y, Ma J, Makar KW, Matsuo K, Newcomb PA, Potter JD, Prentice RL, Qu C, Rohan T, Rosse SA, Schoen RE, Seminara D, Shrubsole M, Shu XO, Slattery ML, Taverna D, Thibodeau SN, Ulrich CM, White E, Xiang Y, Zanke BW, Zeng YX, Zhang B, Zheng W and Hsu L. CONSRTM Colon Cancer Family Registry and the Genetics and Epidemiology of Colorectal Cancer Consortium TITLE Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis JOURNAL Gastroenterology 144 (4), 799-807 (2013) PUBMED 23266556 REMARK GeneRIF: CCND2 gene polymorphism is associated in the pathogenesis of colorectal cancers. Review article REFERENCE 4 (bases 1 to 6531) AUTHORS Avery,C.L., Sitlani,C.M., Arking,D.E., Arnett,D.K., Bis,J.C., Boerwinkle,E., Buckley,B.M., Ida Chen,Y.D., de Craen,A.J., Eijgelsheim,M., Enquobahrie,D., Evans,D.S., Ford,I., Garcia,M.E., Gudnason,V., Harris,T.B., Heckbert,S.R., Hochner,H., Hofman,A., Hsueh,W.C., Isaacs,A., Jukema,J.W., Knekt,P., Kors,J.A., Krijthe,B.P., Kristiansson,K., Laaksonen,M., Liu,Y., Li,X., Macfarlane,P.W., Newton-Cheh,C., Nieminen,M.S., Oostra,B.A., Peloso,G.M., Porthan,K., Rice,K., Rivadeneira,F.F., Rotter,J.I., Salomaa,V., Sattar,N., Siscovick,D.S., Slagboom,P.E., Smith,A.V., Sotoodehnia,N., Stott,D.J., Stricker,B.H., Sturmer,T., Trompet,S., Uitterlinden,A.G., van Duijn,C., Westendorp,R.G., Witteman,J.C., Whitsel,E.A. and Psaty,B.M. TITLE Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval JOURNAL Pharmacogenomics J. (2013) In press PUBMED 23459443 REMARK Publication Status: Available-Online prior to print REFERENCE 5 (bases 1 to 6531) CONSRTM GENDEP Investigators; MARS Investigators; STAR*D Investigators TITLE Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies JOURNAL Am J Psychiatry 170 (2), 207-217 (2013) PUBMED 23377640 REFERENCE 6 (bases 1 to 6531) AUTHORS Hirai,H., Roussel,M.F., Kato,J.Y., Ashmun,R.A. and Sherr,C.J. TITLE Novel INK4 proteins, p19 and p18, are specific inhibitors of the cyclin D-dependent kinases CDK4 and CDK6 JOURNAL Mol. Cell. Biol. 15 (5), 2672-2681 (1995) PUBMED 7739547 REFERENCE 7 (bases 1 to 6531) AUTHORS Meyerson,M. and Harlow,E. TITLE Identification of G1 kinase activity for cdk6, a novel cyclin D partner JOURNAL Mol. Cell. Biol. 14 (3), 2077-2086 (1994) PUBMED 8114739 REFERENCE 8 (bases 1 to 6531) AUTHORS Ewen,M.E., Sluss,H.K., Sherr,C.J., Matsushime,H., Kato,J. and Livingston,D.M. TITLE Functional interactions of the retinoblastoma protein with mammalian D-type cyclins JOURNAL Cell 73 (3), 487-497 (1993) PUBMED 8343202 REFERENCE 9 (bases 1 to 6531) AUTHORS Xiong,Y., Menninger,J., Beach,D. and Ward,D.C. TITLE Molecular cloning and chromosomal mapping of CCND genes encoding human D-type cyclins JOURNAL Genomics 13 (3), 575-584 (1992) PUBMED 1386336 REFERENCE 10 (bases 1 to 6531) AUTHORS Inaba,T., Matsushime,H., Valentine,M., Roussel,M.F., Sherr,C.J. and Look,A.T. TITLE Genomic organization, chromosomal localization, and independent expression of human cyclin D genes JOURNAL Genomics 13 (3), 565-574 (1992) PUBMED 1386335 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BX476896.1, BC089384.1, AC006122.24 and AI055922.1. On Oct 25, 2008 this sequence version replaced gi:16950656. Summary: The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with and functions as a regulatory subunit of CDK4 or CDK6, whose activity is required for cell cycle G1/S transition. This protein has been shown to interact with and be involved in the phosphorylation of tumor suppressor protein Rb. Knockout studies of the homologous gene in mouse suggest the essential roles of this gene in ovarian granulosa and germ cell proliferation. High level expression of this gene was observed in ovarian and testicular tumors. [provided by RefSeq, Oct 2008]. Sequence Note: The RefSeq transcript and protein were derived from transcript and genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: D13639.1, M90813.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025082 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: full length. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-48 BX476896.1 2-49 49-1279 BC089384.1 1-1231 1280-6195 AC006122.24 31204-36119 c 6196-6531 AI055922.1 1-336 c FEATURES Location/Qualifiers source 1..6531 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="12" /map="12p13" gene 1..6531 /gene="CCND2" /gene_synonym="KIAK0002" /note="cyclin D2" /db_xref="GeneID:894" /db_xref="HGNC:1583" /db_xref="HPRD:00451" /db_xref="MIM:123833" exon 1..500 /gene="CCND2" /gene_synonym="KIAK0002" /inference="alignment:Splign:1.39.8" variation 24 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:114606068" variation 85 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:71583750" variation 105 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:117697711" variation 129 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:149580434" variation 135 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:1049606" variation 257 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:3217786" variation 270 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:3217787" variation 272 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:3217788" CDS 306..1175 /gene="CCND2" /gene_synonym="KIAK0002" /note="G1/S-specific cyclin D2" /codon_start=1 /product="G1/S-specific cyclin-D2" /protein_id="NP_001750.1" /db_xref="GI:4502617" /db_xref="CCDS:CCDS8524.1" /db_xref="GeneID:894" /db_xref="HGNC:1583" /db_xref="HPRD:00451" /db_xref="MIM:123833" /translation="
MELLCHEVDPVRRAVRDRNLLRDDRVLQNLLTIEERYLPQCSYFKCVQKDIQPYMRRMVATWMLEVCEEQKCEEEVFPLAMNYLDRFLAGVPTPKSHLQLLGAVCMFLASKLKETSPLTAEKLCIYTDNSIKPQELLEWELVVLGKLKWNLAAVTPHDFIEHILRKLPQQREKLSLIRKHAQTFIALCATDFKFAMYPPSMIATGSVGAAICGLQQDEEVSSLTCDALTELLAKITNTDVDCLKACQEQIEAVLLNSLQQYRQDQRDGSKSEDELDQASTPTDVRDIDL
" misc_feature 468..737 /gene="CCND2" /gene_synonym="KIAK0002" /note="Cyclin box fold. Protein binding domain functioning in cell-cycle and transcription control. Present in cyclins, TFIIB and Retinoblastoma (RB).The cyclins consist of 8 classes of cell cycle regulators that regulate cyclin dependent kinases (CDKs). TFIIB...; Region: CYCLIN; cd00043" /db_xref="CDD:28924" misc_feature order(468..473,489..494,498..503,567..569,597..602) /gene="CCND2" /gene_synonym="KIAK0002" /note="binding site 1" /db_xref="CDD:28924" misc_feature order(624..626,636..638,657..659,711..713,720..725) /gene="CCND2" /gene_synonym="KIAK0002" /note="binding site 2" /db_xref="CDD:28924" misc_feature 765..1103 /gene="CCND2" /gene_synonym="KIAK0002" /note="Cyclin, C-terminal domain; Region: Cyclin_C; pfam02984" /db_xref="CDD:202499" variation 327 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:370617608" variation 334 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:200897111" variation 338 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:371641860" variation 341 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:374125669" variation 419 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:146122734" variation 474 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:61731957" exon 501..716 /gene="CCND2" /gene_synonym="KIAK0002" /inference="alignment:Splign:1.39.8" variation 599 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:200880354" variation 686 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:184590007" variation 711 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="g" /db_xref="dbSNP:368616285" STS 716..876 /gene="CCND2" /gene_synonym="KIAK0002" /standard_name="CCND2" /db_xref="UniSTS:503952" exon 717..876 /gene="CCND2" /gene_synonym="KIAK0002" /inference="alignment:Splign:1.39.8" variation 725 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:202080680" variation 755 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:140100329" variation 760 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="c" /db_xref="dbSNP:199719393" variation 783 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:182823354" variation 809 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:201241721" variation 817 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:367874736" variation 829 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="g" /db_xref="dbSNP:143681287" variation 875 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="g" /db_xref="dbSNP:3217805" exon 877..1025 /gene="CCND2" /gene_synonym="KIAK0002" /inference="alignment:Splign:1.39.8" variation 911 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:199552192" variation 915 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:61755286" variation 933 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:202056442" variation 939 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:199882809" variation 992 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:375356578" variation 1007 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:139239250" variation 1023 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:373099767" exon 1026..6522 /gene="CCND2" /gene_synonym="KIAK0002" /inference="alignment:Splign:1.39.8" variation 1052 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:149961693" STS 1059..1183 /gene="CCND2" /gene_synonym="KIAK0002" /standard_name="RH70876" /db_xref="UniSTS:49452" variation 1061 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:145050894" variation 1065 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="g" /db_xref="dbSNP:76269597" variation 1090 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:142170178" variation 1106 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="g" /db_xref="dbSNP:199959738" variation 1107 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:3217921" variation 1118 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:147821686" variation 1184 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="g" /db_xref="dbSNP:375075998" variation 1192 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:201029184" variation 1202..1203 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="ga" /db_xref="dbSNP:71534272" variation 1204 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:372914898" variation 1206 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:149455238" variation 1207 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:182223310" variation 1211 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="c" /db_xref="dbSNP:369380641" variation 1271 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="a" /db_xref="dbSNP:202049688" STS 1283..1394 /gene="CCND2" /gene_synonym="KIAK0002" /standard_name="D12S1880" /db_xref="UniSTS:38416" variation 1346 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:143104448" variation 1471 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:370162310" STS 1498..2288 /gene="CCND2" /gene_synonym="KIAK0002" /standard_name="CCND2_91" /db_xref="UniSTS:276169" variation 1639 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:187268980" variation 1898 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:10849029" variation 1923 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:114807534" variation 1944 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:117673615" variation 1972 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:190921478" variation 2241 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:3217922" variation 2244 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:373098535" variation 2309 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="c" /db_xref="dbSNP:148214337" variation 2519 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /db_xref="dbSNP:34524099" variation 2520 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /db_xref="dbSNP:56048189" variation 2520 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /db_xref="dbSNP:140621197" variation 2530..2532 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="ttt" /db_xref="dbSNP:75211979" variation 2532..2533 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /replace="tt" /db_xref="dbSNP:200860740" variation 2532 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /replace="tt" /db_xref="dbSNP:56044137" variation 2536 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="c" /db_xref="dbSNP:200982928" variation 2540 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:35155154" variation 2543 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:34997979" variation 2550 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:141278429" variation 2781..2782 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /db_xref="dbSNP:150151031" variation 2829 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="c" /db_xref="dbSNP:3217923" variation 2851 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:77471844" variation 2851 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /db_xref="dbSNP:66494535" variation 2865..2866 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /db_xref="dbSNP:34569142" variation 2865 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /replace="tt" /db_xref="dbSNP:34609911" variation 2866 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="c" /db_xref="dbSNP:199786641" variation 2876 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:4466913" variation 3027 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:182684983" variation 3078..3079 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="gtt" /db_xref="dbSNP:147082841" variation 3094 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:201420580" variation 3101..3110 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="ggttttttgg" /db_xref="dbSNP:375128557" variation 3121..3122 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /db_xref="dbSNP:71756035" variation 3257 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:74786417" variation 3262 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:370634757" variation 3324 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:139789164" variation 3348 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /db_xref="dbSNP:35604856" variation 3365 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:185406911" variation 3381 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:190269104" variation 3557 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:3217924" variation 3639 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:3217925" variation 3683 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:3217926" variation 3703 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:79512920" variation 3768 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:182883448" variation 3804 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:3217927" variation 3821 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:199619940" variation 3824 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:375898612" variation 3844 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:3217928" variation 3849 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:147247521" variation 3851 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:3217929" variation 3874 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:12580778" variation 3886..3887 /gene="CCND2" /gene_synonym="KIAK0002" /replace="cg" /replace="tt" /db_xref="dbSNP:34007392" variation 3886 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:12581036" variation 3887 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:12581037" variation 3933 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:187218956" variation 3942 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:192927564" variation 4039 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:1049610" variation 4102 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="c" /db_xref="dbSNP:28364775" variation 4159 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:1049611" variation 4271 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:374274472" variation 4295 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:3217930" variation 4301 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:368190451" variation 4344 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:3217931" variation 4387 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:371955525" variation 4406 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:183927620" variation 4409..4410 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="g" /db_xref="dbSNP:377098479" variation 4458 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="c" /db_xref="dbSNP:3217932" variation 4468 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:188877509" variation 4533 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="g" /db_xref="dbSNP:192655661" variation 4538 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:140753367" variation 4641 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:369495045" variation 4663 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:183933121" variation 4718 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:149766775" variation 4735 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="t" /db_xref="dbSNP:55944753" variation 4762 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:1049612" variation 4813 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:145781080" variation 4987 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:188655271" variation 5000 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:3217933" variation 5091..5093 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="gag" /db_xref="dbSNP:77970983" variation 5119 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:191621202" variation 5128..5129 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="c" /db_xref="dbSNP:35080571" variation 5166 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:148525558" variation 5538 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="g" /db_xref="dbSNP:115254226" variation 5563 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:184203728" variation 5599..5600 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="ag" /db_xref="dbSNP:374023888" variation 5646 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:71579230" variation 5711 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:181806646" variation 5808 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:187282643" variation 5920 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="g" /db_xref="dbSNP:190523603" variation 5975 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="t" /db_xref="dbSNP:146593405" variation 6043 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="g" /db_xref="dbSNP:180860278" variation 6126 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:4765775" variation 6145 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /db_xref="dbSNP:67603280" variation 6166 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:200404720" variation 6167 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="t" /db_xref="dbSNP:61152953" variation 6176 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="tt" /db_xref="dbSNP:71766856" variation 6211 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:3217934" variation 6213 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:141438670" variation 6236 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:189733699" variation 6240 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:3210008" variation 6272 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:1049651" STS 6304..6495 /gene="CCND2" /gene_synonym="KIAK0002" /standard_name="EST16F6" /db_xref="UniSTS:263148" variation 6306 /gene="CCND2" /gene_synonym="KIAK0002" /replace="a" /replace="g" /db_xref="dbSNP:182399319" variation 6310 /gene="CCND2" /gene_synonym="KIAK0002" /replace="" /replace="aa" /db_xref="dbSNP:71787105" variation 6324 /gene="CCND2" /gene_synonym="KIAK0002" /replace="c" /replace="t" /db_xref="dbSNP:185544647" STS 6370..6502 /gene="CCND2" /gene_synonym="KIAK0002" /standard_name="RH68283" /db_xref="UniSTS:77452" variation 6398 /gene="CCND2" /gene_synonym="KIAK0002" /replace="g" /replace="t" /db_xref="dbSNP:11549724" ORIGIN
gcccagccagcttgcgtcaccgcttcagagcggagaagagcgagcaggggagagcgagaccagttttaaggggaggaccggtgcgagtgaggcagccccgaggctctgctcgcccaccacccaatcctcgcctcccttctgctccaccttctctctctgccctcacctctcccccgaaaaccccctatttagccaaaggaaggaggtcaggggaacgctctcccctccccttccaaaaaacaaaaacagaaaaacccttttccaggccggggaaagcaggagggagaggggccgccgggctggccatggagctgctgtgccacgaggtggacccggtccgcagggccgtgcgggaccgcaacctgctccgagacgaccgcgtcctgcagaacctgctcaccatcgaggagcgctaccttccgcagtgctcctacttcaagtgcgtgcagaaggacatccaaccctacatgcgcagaatggtggccacctggatgctggaggtctgtgaggaacagaagtgcgaagaagaggtcttccctctggccatgaattacctggaccgtttcttggctggggtcccgactccgaagtcccatctgcaactcctgggtgctgtctgcatgttcctggcctccaaactcaaagagaccagcccgctgaccgcggagaagctgtgcatttacaccgacaactccatcaagcctcaggagctgctggagtgggaactggtggtgctggggaagttgaagtggaacctggcagctgtcactcctcatgacttcattgagcacatcttgcgcaagctgccccagcagcgggagaagctgtctctgatccgcaagcatgctcagaccttcattgctctgtgtgccaccgactttaagtttgccatgtacccaccgtcgatgatcgcaactggaagtgtgggagcagccatctgtgggctccagcaggatgaggaagtgagctcgctcacttgtgatgccctgactgagctgctggctaagatcaccaacacagacgtggattgtctcaaagcttgccaggagcagattgaggcggtgctcctcaatagcctgcagcagtaccgtcaggaccaacgtgacggatccaagtcggaggatgaactggaccaagccagcacccctacagacgtgcgggatatcgacctgtgaggatgccagttgggccgaaagagagagacgcgtccataatctggtctcttcttctttctggttgtttttgttctttgtgttttagggtgaaacttaaaaaaaaaattctgcccccacctagatcatatttaaagatcttttagaagtgagagaaaaaggtcctacgaaaacggaataataaaaagcatttggtgcctatttgaagtacagcataagggaatcccttgtatatgcgaacagttattgtttgattatgtaaaagtaatagtaaaatgcttacaggaaaacctgcagagtagttagagaatatgtatgcctgcaatatgggaacaaattagaggagacttttttttttcatgttatgagctagcacatacacccccttgtagtataatttcaaggaactgtgtacgccatttatggcatgattagattgcaaagcaatgaactcaagaaggaattgaaataaggagggacatgatggggaaggagtacaaaacaatctctcaacatgattgaaccatttgggatggagaagcacctttgctctcagccacctgttactaagtcaggagtgtagttggatctctacattaatgtcctcttgctgtctacagtagctgctacctaaaaaaagatgttttattttgccagttggacacaggtgattggctcctgggtttcatgttctgtgacatcctgcttcttcttccaaatgcagttcattgcagacaccaccatattgctatctaatggggaaatgtagctatgggccataaccaaaactcacatgaaacggaggcagatggagaccaagggtgggatccagaatggagtcttttctgttattgtatttaaaagggtaatgtggccttggcatttcttcttagaaaaaaactaatttttggtgctgattggcatgtctggttcacagtttagcattgttataaaccattccattcgaaaagcactttgaaaaattgttcccgagcgatagatgggatggtttatgcaagtcatgctgaatactcctcccctcttctcttttgccccctcccttcctgcccccagtctgggttactcttcgcttctggtatctggcgttctttggtacacagttctggtgttcctaccaggactcaagagacaccccttcctgctgacattcccatcacaacattcctcagacaagcctgtaaactaaaatctgttaccattctgatggcacagaaggatcttaattcccatctctatacttctcctttggacatggaaagaaaagttattgctggtgcaaagatagatggctgaacatcagggtgtggcattttgttcccttttccgtttttttttttttattgttgttgttaattttattgcaaagttgtattcagcgtacttgaatttttcttcctctccacttcttagaggcattcagttagcaaagaggttggagcaacaacttttttttttttttttgcacaattgtaattgacaggtaatgaagctatttgttaaaatatttgcctttttaagtaaaaaagaaaaatcagaacagggctatttgaagaattattttatacacagattctgccttgtttcatagtatgagggttgaagacggaaaacaatctaagggtctctcatttttttaattttgttttgttcagtttggtttttttttttttttgcgctgctaagaagctaaagtcatccatccttattcacgttgacagtacctagctgtaatgtttcacagagtgtgctgctattttataaacatttttataatatattattttactgcttaaattccaagtcctgaagtagatggttgagatatgagttcttcgtactggaaaagcccttccgtagtttgttttcttctggtagcatattcatggttgtttttttttttcttttttggttttttggttttttttttttcctctgatcacattcttcaaagacggagtattctttacctcaggtttactggacaaaatcaataactacaaaaggcaatgattcacgcttttgttttcataatacctcacaaccgtacagtttctgcttgggagcccattcgcatgaggaatacagaagcagtgtgagcagggctgactccctctcaggtggaaggcagggcggtctcactcccagggacctttttggtcatggaggccatcgggctcccagttagaccctggtatcctcatcatgatggaaaaaatacattgaaccaagggatcctccctccccttcaaggcagacgttcagtacaaacatttatgcggtaggctcagatgtcgtaatttgcacttaggtaccaggtgtcaggaaacagactaaaaagaattccaccaggctgtttggagatcctcatcttggagctttttcaaaagcggggcttcatctgcaaagggccctttcatcttgaagtttttcccctccgtctttcccctcccctggcatggacaccttgtgtttaggatcatctctgcaggtttcctaggtctgaatctgcgagtagatgaacctgcagcaagcagcgtttatggtgcttccttctccctcctctgtctcaaactgcgcaggcaagcactatgcaagcccaggccctctgctgagcggtactaaacggtcgggttttcaatcacactgaattggcaggataagaaaaataggtcagataagtatgggatgatagttgaagggaggtgaagaggctgcttctctacagaggtgaaattccagatgagtcagtctcttgggaagtgtgtttagaagggttcaggactttgtgagttagcatgaccctaaaattctaggggatttctggtgggacaatgggtggtgaattctgaagttttggagagggaagtggagcagccagcaagtaagctagccagagttttctcaagagccagctttgctcagcacactctcctgggccccaaggagtcccacggaatggggaaagcgggaaccctggagttcttgggaatcttggagcctaaagagaaaccgaggtgcaaattcatttcatggtgactgacccttgagcttaaacagaagcagcaaatgaaagaaccggacaaataaggaagggcacaagcctacccgactctatttacagtctgtaactttccactcttcctgtagtcccgaggcccctgggtccttctagcttttctctttcccatccttggggccttgtgtgatgatgggtgtggggctgccgatgggaaagtcgggggttgttaggcttttctgcctgctcctgcttaaacacaagaaggaatcctggattttgccctctccttagctcttagtctctttggtaggagttttgttccagaggagctctcccccttggatttgaacttgctctttttgttgttgttgttctttctcttctttttcttacctcccactaaaggggttccaaattatcctggtctttttctaccttgttgtgtttctatctcgtctttacttccatctgtttgtttttttctccatcagtgggggccgagttgttcccccagcctgccaaattttgatccttcccctcttttggccaaatcctagggggaagaaatcctagtatgccaaaaatatatgctaagcataattaaactccatgcgggtccataacagccaagaagcctgcaggagaaagccaagggcagttccctccgcagaacaccccatgcgtgctgagaggcgagctccttgaagaaggggctgttcttccaggaggccttattttgaactgcctcaggaccccactggagagcacagcatgccttactactgggtcatccttggtctatgtgctctgtactggaggctctgttctgcctcttatcagccaggtcaggggcacacatggcttaagtgacaaagccagaggagaagacaaccctgacagcatcacgctgcatcccattgctagcaggattggcaactcttcagacggagctgcgcttccctgcagtctagcacctctagggcctctccagactgtgccctgggagctctgggactgaaaggttaagaacataaggcaggatcagatgactctctccaagagggcaggggaattttctctccatgggccacaggggacagggctgggagaagaaatagacttgcaccttatgtcatgtaaataattgattttctagttcaagaagataatattggtagtgtgggaattggaggtaggaaggggaggaagtctgagtaagccagttggcttctaagccaaaaggattcctctttgtttatctctgagacagtccaaccttgagaatagctttaaaagggaaattaatgctgagatgataaagtccccttaagccaacaaaccctctgtagctatagaatgagtgcaggtttctattggtgtggactcagagcaatttacaagagctgttcatgcagccatccatttgtgcaaaatagggtaagaagattcaagaggatatttattacttcctcataccacatggcttttgatgattctggattctaaacaacccagaatggtcatttcaggcacaacgatactacattcgtgtgtgtctgcttttaaacttggctgggctatcagaccctattctcggctcaggttttgagaagccatcagcaaatgtgtacgtgcatgctgtagctgcagcctgcatcccttcgcctgcagcctactttggggaaataaagtgccttactgactgtagccattacagtatccaatgtcttttgacaggtgcctgtccttgaaaaacaaagtttctatttttatttttaattggtttagttcttaactgctggccaactcttacatccccagcaaatcatcgggccattggattttttccattatgttcatcacccttatatcatgtacctcagatctctctctctctcctctctctcagttatgtagtttcttgtcttggacttttttttttcttttctttttctttttttttttgctttaaaacaagtgtgatgccatatcaagtccatgttattctctcacagtgtactctataagaggtgtgggtgtctgtttggtcaggatgttagaaagtgctgataagtagcatgatcagtgtatgcgaaaaggtttttaggaagtatggcaaaaatgttgtattggctatgatggtgacatgatatagtcagctgccttttaagaggtcttatctgttcagtgttaagtgatttaaaaaaataataacctgttttctgactagtttaaagatggatttgaaaatggttttgaatgcaattaggttatgctatttggacaataaactcaccttgacctaaattaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:894 -> Molecular function: GO:0019901 [protein kinase binding] evidence: IPI GeneID:894 -> Biological process: GO:0001934 [positive regulation of protein phosphorylation] evidence: IDA GeneID:894 -> Biological process: GO:0007049 [cell cycle] evidence: IEA GeneID:894 -> Biological process: GO:0045737 [positive regulation of cyclin-dependent protein kinase activity] evidence: IDA GeneID:894 -> Biological process: GO:0051301 [cell division] evidence: IEA GeneID:894 -> Cellular component: GO:0000307 [cyclin-dependent protein kinase holoenzyme complex] evidence: IDA GeneID:894 -> Cellular component: GO:0000785 [chromatin] evidence: IDA GeneID:894 -> Cellular component: GO:0005634 [nucleus] evidence: IDA GeneID:894 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA GeneID:894 -> Cellular component: GO:0005829 [cytosol] evidence: IDA GeneID:894 -> Cellular component: GO:0031965 [nuclear membrane] evidence: IDA
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@meso_cacase at
DBCLS
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