2024-04-25 04:36:19, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_016587 2102 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens chromobox homolog 3 (CBX3), transcript variant 2, mRNA. ACCESSION NM_016587 VERSION NM_016587.3 GI:325197147 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 2102) AUTHORS Smallwood,A., Hon,G.C., Jin,F., Henry,R.E., Espinosa,J.M. and Ren,B. TITLE CBX3 regulates efficient RNA processing genome-wide JOURNAL Genome Res. 22 (8), 1426-1436 (2012) PUBMED 22684280 REMARK GeneRIF: Loss of CBX3 results in global RNA processing defect. REFERENCE 2 (bases 1 to 2102) AUTHORS Saini,V., Hose,C.D., Monks,A., Nagashima,K., Han,B., Newton,D.L., Millione,A., Shah,J., Hollingshead,M.G., Hite,K.M., Burkett,M.W., Delosh,R.M., Silvers,T.E., Scudiero,D.A. and Shoemaker,R.H. TITLE Identification of CBX3 and ABCA5 as putative biomarkers for tumor stem cells in osteosarcoma JOURNAL PLoS ONE 7 (8), E41401 (2012) PUBMED 22870217 REMARK GeneRIF: Identification of CBX3 and ABCA5 as putative biomarkers for tumor stem cells in osteosarcoma. Erratum:[PLoS One. 2012;7(11). doi:10.1371/annotation/8c74aaee-897d-4682-b62d-d95a3506c210] REFERENCE 3 (bases 1 to 2102) AUTHORS Ruan,J., Ouyang,H., Amaya,M.F., Ravichandran,M., Loppnau,P., Min,J. and Zang,J. TITLE Structural basis of the chromodomain of Cbx3 bound to methylated peptides from histone h1 and G9a JOURNAL PLoS ONE 7 (4), E35376 (2012) PUBMED 22514736 REMARK GeneRIF: The Cbx3 chromodomain binds with comparable affinities to all of the methylated H3K9, H1K26 and G9aK185 peptides. REFERENCE 4 (bases 1 to 2102) AUTHORS Shimura,M., Toyoda,Y., Iijima,K., Kinomoto,M., Tokunaga,K., Yoda,K., Yanagida,M., Sata,T. and Ishizaka,Y. TITLE Epigenetic displacement of HP1 from heterochromatin by HIV-1 Vpr causes premature sister chromatid separation JOURNAL J. Cell Biol. 194 (5), 721-735 (2011) PUBMED 21875947 REMARK GeneRIF: HIV-1 Vpr displaces heterochromatin protein 1-alpha and heterochromatin protein 1-gamma from chromatin, resulting in premature chromatid separation. REFERENCE 5 (bases 1 to 2102) AUTHORS Canudas,S., Houghtaling,B.R., Bhanot,M., Sasa,G., Savage,S.A., Bertuch,A.A. and Smith,S. TITLE A role for heterochromatin protein 1gamma at human telomeres JOURNAL Genes Dev. 25 (17), 1807-1819 (2011) PUBMED 21865325 REMARK GeneRIF: HP1gamma localizes to telomeres in S phase, where it is required to establish/maintain cohesion REFERENCE 6 (bases 1 to 2102) AUTHORS Lehming,N., Le Saux,A., Schuller,J. and Ptashne,M. TITLE Chromatin components as part of a putative transcriptional repressing complex JOURNAL Proc. Natl. Acad. Sci. U.S.A. 95 (13), 7322-7326 (1998) PUBMED 9636147 REFERENCE 7 (bases 1 to 2102) AUTHORS Seeler,J.S., Marchio,A., Sitterlin,D., Transy,C. and Dejean,A. TITLE Interaction of SP100 with HP1 proteins: a link between the promyelocytic leukemia-associated nuclear bodies and the chromatin compartment JOURNAL Proc. Natl. Acad. Sci. U.S.A. 95 (13), 7316-7321 (1998) PUBMED 9636146 REFERENCE 8 (bases 1 to 2102) AUTHORS Lessard,J., Baban,S. and Sauvageau,G. TITLE Stage-specific expression of polycomb group genes in human bone marrow cells JOURNAL Blood 91 (4), 1216-1224 (1998) PUBMED 9454751 REFERENCE 9 (bases 1 to 2102) AUTHORS Ye,Q., Callebaut,I., Pezhman,A., Courvalin,J.C. and Worman,H.J. TITLE Domain-specific interactions of human HP1-type chromodomain proteins and inner nuclear membrane protein LBR JOURNAL J. Biol. Chem. 272 (23), 14983-14989 (1997) PUBMED 9169472 REFERENCE 10 (bases 1 to 2102) AUTHORS Ye,Q. and Worman,H.J. TITLE Interaction between an integral protein of the nuclear envelope inner membrane and human chromodomain proteins homologous to Drosophila HP1 JOURNAL J. Biol. Chem. 271 (25), 14653-14656 (1996) PUBMED 8663349 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from CD514780.1, BX648807.1 and DB565723.1. On Mar 4, 2011 this sequence version replaced gi:20544150. Summary: At the nuclear envelope, the nuclear lamina and heterochromatin are adjacent to the inner nuclear membrane. The protein encoded by this gene binds DNA and is a component of heterochromatin. This protein also can bind lamin B receptor, an integral membrane protein found in the inner nuclear membrane. The dual binding functions of the encoded protein may explain the association of heterochromatin with the inner nuclear membrane. This protein binds histone H3 tails methylated at Lys-9 sites. This protein is also recruited to sites of ultraviolet-induced DNA damage and double-strand breaks. Two transcript variants encoding the same protein but differing in the 5' UTR, have been found for this gene.[provided by RefSeq, Mar 2011]. Transcript Variant: This variant (2) contains an alternate 5' exon but encodes the same protein as transcript variant 1. 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 :: BX648807.1, AF136630.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025082 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-45 CD514780.1 12-56 46-1846 BX648807.1 2-1802 1847-2102 DB565723.1 209-464 FEATURES Location/Qualifiers source 1..2102 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="7" /map="7p15.2" gene 1..2102 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /note="chromobox homolog 3" /db_xref="GeneID:11335" /db_xref="HGNC:1553" /db_xref="HPRD:05130" /db_xref="MIM:604477" exon 1..123 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /inference="alignment:Splign:1.39.8" variation 41..42 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="tga" /db_xref="dbSNP:370625470" variation 57 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="c" /db_xref="dbSNP:200192216" exon 124..175 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /inference="alignment:Splign:1.39.8" variation 126 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:369210080" variation 135 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="c" /db_xref="dbSNP:372876793" variation 143 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:370877360" misc_feature 146..148 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /note="upstream in-frame stop codon" variation 147 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:200166027" CDS 152..703 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /note="heterochromatin protein HP1 gamma; chromobox homolog 3 (HP1 gamma homolog, Drosophila); heterochromatin-like protein 1; modifier 2 protein; heterochromatin protein 1 homolog gamma" /codon_start=1 /product="chromobox protein homolog 3" /protein_id="NP_057671.2" /db_xref="GI:20544151" /db_xref="CCDS:CCDS5398.1" /db_xref="GeneID:11335" /db_xref="HGNC:1553" /db_xref="HPRD:05130" /db_xref="MIM:604477" /translation="
MASNKTTLQKMGKKQNGKSKKVEEAEPEEFVVEKVLDRRVVNGKVEYFLKWKGFTDADNTWEPEENLDCPELIEAFLNSQKAGKEKDGTKRKSLSDSESDDSKSKKKRDAADKPRGFARGLDPERIIGATDSSGELMFLMKWKDSDEADLVLAKEANMKCPQIVIAFYEERLTWHSCPEDEAQ
" misc_feature 179..181 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="N6-acetyllysine; propagated from UniProtKB/Swiss-Prot (Q13185.4); acetylation site" misc_feature 257..385 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /note="Chromatin organization modifier (chromo) domain is a conserved region of around 50 amino acids found in a variety of chromosomal proteins, which appear to play a role in the functional organization of the eukaryotic nucleus. Experimental evidence...; Region: CHROMO; cd00024" /db_xref="CDD:237991" misc_feature 281..283 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="N6-acetyllysine; propagated from UniProtKB/Swiss-Prot (Q13185.4); acetylation site" misc_feature order(296..298,302..304,311..313,323..325,335..337, 347..352) /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /note="histone binding site; other site" /db_xref="CDD:237991" misc_feature 299..301 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="N6-acetyllysine; propagated from UniProtKB/Swiss-Prot (Q13185.4); acetylation site" misc_feature 428..430 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q13185.4); phosphorylation site" misc_feature 428..430 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 434..436 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q13185.4); phosphorylation site" misc_feature 434..436 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 440..442 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q13185.4); phosphorylation site" misc_feature 440..442 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 446..448 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q13185.4); phosphorylation site" misc_feature 446..448 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 455..457 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 518..676 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /note="Chromo Shadow Domain, found in association with N-terminal chromo (CHRromatin Organization MOdifier) domain; Chromo domains mediate the interaction of the heterochromatin with other heterochromatin proteins, thereby affecting chromatin structure (e.g; Region: ChSh; cd00034" /db_xref="CDD:237998" misc_feature order(536..538,557..559,620..622,644..646,653..655, 665..667) /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /note="dimerization interface [polypeptide binding]; other site" /db_xref="CDD:237998" misc_feature order(644..646,653..655) /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /note="potential binding pit; other site" /db_xref="CDD:237998" misc_feature 668..670 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 677..679 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q13185.4); phosphorylation site" misc_feature 677..679 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" exon 176..318 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /inference="alignment:Splign:1.39.8" variation 215 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:371590498" variation 310 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:192881539" exon 319..481 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /inference="alignment:Splign:1.39.8" variation 368 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:199646600" variation 404 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:11554895" variation 412 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:148438009" variation 445 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:142550836" variation 454 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:372035189" exon 482..576 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /inference="alignment:Splign:1.39.8" STS 489..686 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /standard_name="CBX3" /db_xref="UniSTS:503620" variation 505 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:376630956" variation 538 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:200410047" variation 568 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:200791010" exon 577..2102 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /inference="alignment:Splign:1.39.8" variation 623 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:372760990" variation 625 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:372183110" variation 653 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="t" /db_xref="dbSNP:151101852" variation 686..687 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="a" /db_xref="dbSNP:34210465" variation 718 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:9768418" variation 735 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:191976883" variation 746 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="t" /db_xref="dbSNP:145395285" variation 795 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="c" /db_xref="dbSNP:184267440" variation 842 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:376832373" variation 933 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:189467571" variation 1038 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:182369741" variation 1041 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:9768454" variation 1073..1074 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="tt" /db_xref="dbSNP:368752748" variation 1074..1079 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="tttgtgtg" /db_xref="dbSNP:150882395" variation 1074..1077 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="tttgtg" /db_xref="dbSNP:150158222" variation 1075..1088 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="ttgtgtgtgtgtgtgt" /db_xref="dbSNP:56362406" variation 1076..1081 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="tgtgtgtg" /db_xref="dbSNP:199895382" variation 1076..1077 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="tgt" /db_xref="dbSNP:78265643" variation 1076..1077 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="tgtg" /db_xref="dbSNP:202216295" variation 1076 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="tg" /db_xref="dbSNP:200992022" variation 1077 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:9769357" variation 1078..1080 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="gtgt" /db_xref="dbSNP:70943279" variation 1079 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="g" /replace="t" /db_xref="dbSNP:12532361" variation 1081 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="g" /replace="t" /db_xref="dbSNP:200128779" variation 1087 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="g" /replace="t" /db_xref="dbSNP:201652043" variation 1089 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="g" /replace="t" /db_xref="dbSNP:201093455" variation 1140 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:111871239" variation 1198 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:184550155" variation 1257 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:10156063" variation 1332 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:3735554" variation 1391 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="g" /db_xref="dbSNP:189258793" variation 1487 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:374505442" variation 1544 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:11554894" STS 1572..1815 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /standard_name="RH24974" /db_xref="UniSTS:85612" STS 1643..1823 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /standard_name="HSC11F052" /db_xref="UniSTS:60487" STS 1649..1750 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /standard_name="D7S2103E" /db_xref="UniSTS:151124" variation 1664 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="g" /db_xref="dbSNP:375726042" variation 1677 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:7186" variation 1751 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="t" /db_xref="dbSNP:78619479" variation 1808..1810 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="tgg" /db_xref="dbSNP:144437057" variation 1810..1812 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="" /replace="gtg" /db_xref="dbSNP:377589440" variation 1834 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="t" /db_xref="dbSNP:13247806" variation 1841 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:28407029" variation 1846 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="c" /db_xref="dbSNP:142267744" variation 1852 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="g" /replace="t" /db_xref="dbSNP:373262978" variation 1860 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="c" /replace="t" /db_xref="dbSNP:181300726" variation 1880 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="g" /db_xref="dbSNP:369134863" variation 1943 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="a" /replace="t" /db_xref="dbSNP:111891412" variation 1944 /gene="CBX3" /gene_synonym="HECH; HP1-GAMMA; HP1Hs-gamma" /replace="g" /replace="t" /db_xref="dbSNP:115829318" ORIGIN
tccccccggcggccccgcgcgcagctcccggctccctcccccttcggatgtggcttgagctgtaggcgcggagggccggagacgctgcagacccgcgacccggagcagctcggaggcggtgaataatagctcttcaagtctgcaataaaaaatggcctccaacaaaactacattgcaaaaaatgggaaaaaaacagaatggaaagagtaaaaaagttgaagaggcagagcctgaagaatttgtcgtggaaaaagtactagatcgacgtgtagtgaatgggaaagtggaatatttcctgaagtggaagggatttacagatgctgacaatacttgggaacctgaagaaaatttagattgtccagaattgattgaagcgtttcttaactctcagaaagctggcaaagaaaaagatggtacaaaaagaaaatctttatctgacagtgaatctgatgacagcaaatcaaagaagaaaagagatgctgctgacaaaccaagaggatttgccagaggtcttgatcctgaaagaataattggtgccacagacagcagtggagaattgatgtttctcatgaaatggaaagattcagatgaggcagacttggtgctggcgaaagaggcaaatatgaagtgtcctcaaattgtaattgctttttatgaagagagactaacttggcattcttgtccagaagatgaagctcaataattgttcacattgttcttttatatatatttatatatatatataaaaattgggtcttagattttgatttactagtgtgacaaaataactacatcctaatgaaaatcaagtttgatatgtttgttttgaaagtagcgttggaagagttgttgggggttttttgcatccatagcactggttactttgaacaaataaataaaagctttctgtagttgcttcctttatcagaaaagaacatttgataccatggtatatcatttcctcttcattaaagaacagcttttctaaatgttgggggaaatgtccatagtcattactcagtcaaaacttgtgttctcatgagcctaaggaccattctagatttattacgtgttttttgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtatccataaaatgcatatgtaaatttttttttgtttttaagcattcacccaaacaaaaaaatcacaggtaaacccatgtttctgagatgccattattccaagcaaaataagagataatcccttcaagttaaattgaaaattttcctgaaaccatacatttcaagtgaaataagtaattctagataggacaatttaaattggataattttaaagtgtctataattgcagtggtttatttgcaaaattcctaaaaggaaaaattttatcactgccatcacagcaggtttcctcatccagatgaggaaactagacaaatgctagtgtgttttaactagctaaacaaaactaagttaaatgaacatttaaaagtttccctagcgggccattccttagcaaaatgttggaatccctgttgctacattgactaaaaggtcatgatgaatggaatatgtaagacttggctcatagaaacctaatcagatggttagaggtgttggcagtttaggacctgctgtcataaatgtgtgaacaaccttttgtaacctaacctattgacctgcatgttttttctttaccccaattcattacatggaggctcaatcttgagtttgctttactggttcagcaaaagccaggaagaacaactttgtagtaatcaaaatgttatccaactgtatattgtttactttattgtaaatactggtgaacagtggttaataaatagttttatattcctttatgcaattattagacttttttctttatttgatatgcctttacagtagaaatagaaatgcccacactcattggattatctttgtttataagttagatgataccagtaaggcattacagtacatatcctagatcttttgagcttacgagttttaaacttgaatatgtatttccacaggaatgtttccacagttgggaaataaaagtttcatgtgatgcctagggtcaattgtctcattaaaatgaggttttaaattctg
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:11335 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:11335 -> Molecular function: GO:0019899 [enzyme binding] evidence: IPI GeneID:11335 -> Molecular function: GO:0019904 [protein domain specific binding] evidence: IPI GeneID:11335 -> Molecular function: GO:0042802 [identical protein binding] evidence: IPI GeneID:11335 -> Biological process: GO:0006338 [chromatin remodeling] evidence: NAS GeneID:11335 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA GeneID:11335 -> Biological process: GO:0045892 [negative regulation of transcription, DNA-dependent] evidence: IDA GeneID:11335 -> Biological process: GO:0045892 [negative regulation of transcription, DNA-dependent] evidence: IMP GeneID:11335 -> Cellular component: GO:0000779 [condensed chromosome, centromeric region] evidence: ISS GeneID:11335 -> Cellular component: GO:0000785 [chromatin] evidence: IDA GeneID:11335 -> Cellular component: GO:0005634 [nucleus] evidence: IDA GeneID:11335 -> Cellular component: GO:0005635 [nuclear envelope] evidence: ISS GeneID:11335 -> Cellular component: GO:0005637 [nuclear inner membrane] evidence: NAS GeneID:11335 -> Cellular component: GO:0005719 [nuclear euchromatin] evidence: IDA GeneID:11335 -> Cellular component: GO:0005720 [nuclear heterochromatin] evidence: IDA GeneID:11335 -> Cellular component: GO:0005819 [spindle] evidence: IDA GeneID:11335 -> Cellular component: GO:0031618 [nuclear centromeric heterochromatin] evidence: ISS
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