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2024-04-19 23:37:12, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001193426 2608 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens suppressor of variegation 3-9 homolog 2 (Drosophila)
(SUV39H2), transcript variant 4, mRNA.
ACCESSION NM_001193426
VERSION NM_001193426.1 GI:301171604
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 2608)
AUTHORS Syreeni,A., El-Osta,A., Forsblom,C., Sandholm,N., Parkkonen,M.,
Tarnow,L., Parving,H.H., McKnight,A.J., Maxwell,A.P., Cooper,M.E.
and Groop,P.H.
CONSRTM FinnDiane Study Group
TITLE Genetic examination of SETD7 and SUV39H1/H2 methyltransferases and
the risk of diabetes complications in patients with type 1 diabetes
JOURNAL Diabetes 60 (11), 3073-3080 (2011)
PUBMED 21896933
REMARK GeneRIF: genetic association studies in a Finnish population with
type I diabetes: The minor T allele of exonic SNP rs17353856 in
SUV39H2 is associated with diabetic retinopathy (in a larger
meta-analysis); thus an genetic variation may be protective.
REFERENCE 2 (bases 1 to 2608)
AUTHORS Benlhabib,H. and Mendelson,C.R.
TITLE Epigenetic regulation of surfactant protein A gene (SP-A)
expression in fetal lung reveals a critical role for Suv39h
methyltransferases during development and hypoxia
JOURNAL Mol. Cell. Biol. 31 (10), 1949-1958 (2011)
PUBMED 21402781
REMARK GeneRIF: findings suggest that Suv39H1 and Suv39H2 are key
hypoxia-induced methyltransferases; their decline in fetal lung
during late gestation is critical for epigenetic changes resulting
in the developmental induction of SP-A
REFERENCE 3 (bases 1 to 2608)
AUTHORS Sun,X.J., Xu,P.F., Zhou,T., Hu,M., Fu,C.T., Zhang,Y., Jin,Y.,
Chen,Y., Chen,S.J., Huang,Q.H., Liu,T.X. and Chen,Z.
TITLE Genome-wide survey and developmental expression mapping of
zebrafish SET domain-containing genes
JOURNAL PLoS ONE 3 (1), E1499 (2008)
PUBMED 18231586
REMARK GeneRIF: The SUV39H2 gene is found in tetrapods (e.g., human, mouse
and frog) but not in zebrafish, suggesting that this gene is
generated by a tetrapod lineage-specific gene duplication event.
Publication Status: Online-Only
REFERENCE 4 (bases 1 to 2608)
AUTHORS Wu,C., Ma,M.H., Brown,K.R., Geisler,M., Li,L., Tzeng,E., Jia,C.Y.,
Jurisica,I. and Li,S.S.
TITLE Systematic identification of SH3 domain-mediated human
protein-protein interactions by peptide array target screening
JOURNAL Proteomics 7 (11), 1775-1785 (2007)
PUBMED 17474147
REFERENCE 5 (bases 1 to 2608)
AUTHORS Yoon,K.A., Hwangbo,B., Kim,I.J., Park,S., Kim,H.S., Kee,H.J.,
Lee,J.E., Jang,Y.K., Park,J.G. and Lee,J.S.
TITLE Novel polymorphisms in the SUV39H2 histone methyltransferase and
the risk of lung cancer
JOURNAL Carcinogenesis 27 (11), 2217-2222 (2006)
PUBMED 16774942
REMARK GeneRIF: a novel SUV39H2 polymorphism may have a role in lung
cancer susceptibility for smokers
GeneRIF: Observational study of gene-disease association and
gene-environment interaction. (HuGE Navigator)
REFERENCE 6 (bases 1 to 2608)
AUTHORS Frontelo,P., Leader,J.E., Yoo,N., Potocki,A.C., Crawford,M.,
Kulik,M. and Lechleider,R.J.
TITLE Suv39h histone methyltransferases interact with Smads and cooperate
in BMP-induced repression
JOURNAL Oncogene 23 (30), 5242-5251 (2004)
PUBMED 15107829
REFERENCE 7 (bases 1 to 2608)
AUTHORS Deloukas,P., Earthrowl,M.E., Grafham,D.V., Rubenfield,M.,
French,L., Steward,C.A., Sims,S.K., Jones,M.C., Searle,S.,
Scott,C., Howe,K., Hunt,S.E., Andrews,T.D., Gilbert,J.G.,
Swarbreck,D., Ashurst,J.L., Taylor,A., Battles,J., Bird,C.P.,
Ainscough,R., Almeida,J.P., Ashwell,R.I., Ambrose,K.D.,
Babbage,A.K., Bagguley,C.L., Bailey,J., Banerjee,R., Bates,K.,
Beasley,H., Bray-Allen,S., Brown,A.J., Brown,J.Y., Burford,D.C.,
Burrill,W., Burton,J., Cahill,P., Camire,D., Carter,N.P.,
Chapman,J.C., Clark,S.Y., Clarke,G., Clee,C.M., Clegg,S., Corby,N.,
Coulson,A., Dhami,P., Dutta,I., Dunn,M., Faulkner,L., Frankish,A.,
Frankland,J.A., Garner,P., Garnett,J., Gribble,S., Griffiths,C.,
Grocock,R., Gustafson,E., Hammond,S., Harley,J.L., Hart,E.,
Heath,P.D., Ho,T.P., Hopkins,B., Horne,J., Howden,P.J., Huckle,E.,
Hynds,C., Johnson,C., Johnson,D., Kana,A., Kay,M., Kimberley,A.M.,
Kershaw,J.K., Kokkinaki,M., Laird,G.K., Lawlor,S., Lee,H.M.,
Leongamornlert,D.A., Laird,G., Lloyd,C., Lloyd,D.M., Loveland,J.,
Lovell,J., McLaren,S., McLay,K.E., McMurray,A.,
Mashreghi-Mohammadi,M., Matthews,L., Milne,S., Nickerson,T.,
Nguyen,M., Overton-Larty,E., Palmer,S.A., Pearce,A.V., Peck,A.I.,
Pelan,S., Phillimore,B., Porter,K., Rice,C.M., Rogosin,A.,
Ross,M.T., Sarafidou,T., Sehra,H.K., Shownkeen,R., Skuce,C.D.,
Smith,M., Standring,L., Sycamore,N., Tester,J., Thorpe,A.,
Torcasso,W., Tracey,A., Tromans,A., Tsolas,J., Wall,M., Walsh,J.,
Wang,H., Weinstock,K., West,A.P., Willey,D.L., Whitehead,S.L.,
Wilming,L., Wray,P.W., Young,L., Chen,Y., Lovering,R.C.,
Moschonas,N.K., Siebert,R., Fechtel,K., Bentley,D., Durbin,R.,
Hubbard,T., Doucette-Stamm,L., Beck,S., Smith,D.R. and Rogers,J.
TITLE The DNA sequence and comparative analysis of human chromosome 10
JOURNAL Nature 429 (6990), 375-381 (2004)
PUBMED 15164054
REFERENCE 8 (bases 1 to 2608)
AUTHORS Ait-Si-Ali,S., Guasconi,V., Fritsch,L., Yahi,H., Sekhri,R.,
Naguibneva,I., Robin,P., Cabon,F., Polesskaya,A. and
Harel-Bellan,A.
TITLE A Suv39h-dependent mechanism for silencing S-phase genes in
differentiating but not in cycling cells
JOURNAL EMBO J. 23 (3), 605-615 (2004)
PUBMED 14765126
REFERENCE 9 (bases 1 to 2608)
AUTHORS O'Carroll,D., Scherthan,H., Peters,A.H., Opravil,S., Haynes,A.R.,
Laible,G., Rea,S., Schmid,M., Lebersorger,A., Jerratsch,M.,
Sattler,L., Mattei,M.G., Denny,P., Brown,S.D., Schweizer,D. and
Jenuwein,T.
TITLE Isolation and characterization of Suv39h2, a second histone H3
methyltransferase gene that displays testis-specific expression
JOURNAL Mol. Cell. Biol. 20 (24), 9423-9433 (2000)
PUBMED 11094092
REFERENCE 10 (bases 1 to 2608)
AUTHORS Rea,S., Eisenhaber,F., O'Carroll,D., Strahl,B.D., Sun,Z.W.,
Schmid,M., Opravil,S., Mechtler,K., Ponting,C.P., Allis,C.D. and
Jenuwein,T.
TITLE Regulation of chromatin structure by site-specific histone H3
methyltransferases
JOURNAL Nature 406 (6796), 593-599 (2000)
PUBMED 10949293
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
DB040298.1, BC029360.1 and BC007754.2.
Transcript Variant: This variant (4) uses an alternate donor splice
site at an internal coding exon compared to variant 1, maintaining
the reading frame, and resulting in a shorter isoform (3) missing
an internal protein segment compared compared to isoform 1.
##Evidence-Data-START##
Transcript exon combination :: BC029360.1, BG501493.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025085 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-80 DB040298.1 1-80
81-1366 BC029360.1 1-1286
1367-2608 BC007754.2 1852-3093
FEATURES Location/Qualifiers
source 1..2608
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10p13"
gene 1..2608
/gene="SUV39H2"
/gene_synonym="KMT1B"
/note="suppressor of variegation 3-9 homolog 2
(Drosophila)"
/db_xref="GeneID:79723"
/db_xref="HGNC:17287"
/db_xref="MIM:606503"
exon 1..137
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="alignment:Splign:1.39.8"
misc_feature 92..94
/gene="SUV39H2"
/gene_synonym="KMT1B"
/note="upstream in-frame stop codon"
variation 102
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:375333545"
CDS 107..799
/gene="SUV39H2"
/gene_synonym="KMT1B"
/EC_number="2.1.1.43"
/note="isoform 3 is encoded by transcript variant 4;
histone-lysine N-methyltransferase SUV39H2; H3-K9-HMTase
2; su(var)3-9 homolog 2; lysine N-methyltransferase 1B;
histone H3-K9 methyltransferase 2"
/codon_start=1
/product="histone-lysine N-methyltransferase SUV39H2
isoform 3"
/protein_id="NP_001180355.1"
/db_xref="GI:301171605"
/db_xref="CCDS:CCDS53493.1"
/db_xref="GeneID:79723"
/db_xref="HGNC:17287"
/db_xref="MIM:606503"
/translation="
MAAVGAEARGAWCVPCLVSLDTLQELCRKEKLTCKSIGITKRNLNNYEVEYLCDYKVVKDMEYYLVKWKGWPDSTNTWEPLQNLKCPLLLQQFSNDKHNYLSQVITSEEAERRGQFYDNKGITYLFDLDYESDEFTVDAARYGNVSHFVNHSCDPNLQVFNVFIDNLDTRLPRIALFSTRTINAGEELTFDYQMKGSGDISSDSIDHSPAKKRVRTVCKCGAVTCRGYLN
"
misc_feature 245..385
/gene="SUV39H2"
/gene_synonym="KMT1B"
/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:28908"
misc_feature order(245..247,302..304,308..310,317..319,329..331,
341..343,353..358)
/gene="SUV39H2"
/gene_synonym="KMT1B"
/note="histone binding site; other site"
/db_xref="CDD:28908"
misc_feature <404..685
/gene="SUV39H2"
/gene_synonym="KMT1B"
/note="SET (Su(var)3-9, Enhancer-of-zeste, Trithorax)
domain; Region: SET; smart00317"
/db_xref="CDD:197649"
exon 138..283
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="alignment:Splign:1.39.8"
variation 214
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:369200305"
variation 225
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="c"
/db_xref="dbSNP:373386573"
exon 284..415
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="alignment:Splign:1.39.8"
variation 373
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:148153307"
variation 394
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:376764262"
variation 396
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:140852434"
exon 416..562
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="alignment:Splign:1.39.8"
variation 475
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:190174096"
variation 487
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:183140822"
variation 488
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:148667087"
variation 532
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:17353856"
variation 538
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:369186882"
variation 553
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:147278353"
exon 563..692
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="alignment:Splign:1.39.8"
variation 607
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="g"
/db_xref="dbSNP:61730323"
variation 632
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:369793867"
exon 693..2602
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="alignment:Splign:1.39.8"
variation 768
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:199727444"
variation 778
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:144605484"
variation 794
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:201395473"
variation 818
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="g"
/db_xref="dbSNP:375126181"
variation 854
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:368830300"
variation 890
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:113301024"
variation 911
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:373511332"
variation 926
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="c"
/db_xref="dbSNP:11547181"
variation 947
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:373567048"
variation 958
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="c"
/db_xref="dbSNP:180989547"
variation 962
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace=""
/replace="g"
/db_xref="dbSNP:375028927"
STS 1081..1202
/gene="SUV39H2"
/gene_synonym="KMT1B"
/standard_name="RH48597"
/db_xref="UniSTS:71892"
variation 1139
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="g"
/db_xref="dbSNP:116910335"
variation 1152
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="c"
/db_xref="dbSNP:75420442"
polyA_signal 1314..1319
/gene="SUV39H2"
/gene_synonym="KMT1B"
variation 1333..1335
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace=""
/replace="aat"
/db_xref="dbSNP:367684066"
polyA_site 1334
/gene="SUV39H2"
/gene_synonym="KMT1B"
polyA_site 1350
/gene="SUV39H2"
/gene_synonym="KMT1B"
polyA_signal 1359..1364
/gene="SUV39H2"
/gene_synonym="KMT1B"
variation 1371..1374
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace=""
/replace="aatt"
/db_xref="dbSNP:371874353"
polyA_site 1376
/gene="SUV39H2"
/gene_synonym="KMT1B"
polyA_site 1387
/gene="SUV39H2"
/gene_synonym="KMT1B"
variation 1484
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:142967205"
variation 1541
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:185218421"
variation 1603
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:41284455"
variation 1694
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:11594111"
variation 1765
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:190438184"
variation 1881
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:181251834"
variation 2019
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:61843036"
variation 2156
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:75516757"
variation 2178
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:376829730"
variation 2236
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:150828159"
variation 2361
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:139176971"
variation 2425
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:11259385"
STS 2464..2546
/gene="SUV39H2"
/gene_synonym="KMT1B"
/standard_name="L18426"
/db_xref="UniSTS:34648"
STS 2465..2544
/gene="SUV39H2"
/gene_synonym="KMT1B"
/standard_name="D5S1597E"
/db_xref="UniSTS:151019"
STS 2466..2568
/gene="SUV39H2"
/gene_synonym="KMT1B"
/standard_name="D11S2921"
/db_xref="UniSTS:152074"
STS 2468..2537
/gene="SUV39H2"
/gene_synonym="KMT1B"
/standard_name="D1S1423"
/db_xref="UniSTS:149619"
variation 2505
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:186353154"
variation 2523
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:191603474"
variation 2524
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:371491790"
variation 2543
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="g"
/db_xref="dbSNP:183557434"
variation 2591
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="t"
/db_xref="dbSNP:79193913"
ORIGIN
aacaagccccggcccccaagtcccgcgcgggccggccaggggcggggcgtcgggccagctgagctatcccgtcagaccgcgccagtttgaatgaaagctctacaagatggcggcggtcggggccgaggcgcgaggagcttggtgtgtgccttgcctagtttcacttgatactcttcaggaattatgtagaaaagaaaagctcacatgtaaatcgattggaatcaccaaaaggaatctaaacaattatgaggtggaatacttgtgtgactacaaggtagtaaaggatatggaatattatcttgtaaaatggaaaggatggccagattctacaaatacttgggaacctttgcaaaatctgaagtgcccgttactgcttcagcaattctctaatgacaagcataattatttatctcaggtaatcacaagtgaagaagctgaaagacgaggacagttctatgacaacaagggaatcacgtatctctttgatctggactatgagtctgatgaattcacagtggatgcggctcgatacggcaatgtgtctcattttgtgaatcacagctgtgacccaaatcttcaggtgttcaatgttttcattgataacctcgatactcgtcttccccgaatagcattgttttccacaagaaccataaatgctggagaagagctgacttttgattatcaaatgaaaggttctggagatatatcttcagattctattgaccacagcccagccaaaaagagggtcagaacagtatgtaaatgtggagctgtgacttgcagaggttacctcaactgaactttttcaggaaatagagctgatgattataatatttttttcctaatgttaacatttttaaaaatacatatttgggactcttattatcaaggttctacctatgttaatttacaattcatgtttcaagacatttgccaaatgtattaccgatgcctctgaaaagggggtcactgggtctcatagactgatatgaagtcgacatatttatagtgcttagagaccaaactaatggaaggcagactatttacagcttagtatatgtgtacttaagtctatgtgaacagagaaatgcctcccgtagtgtttgaaagcgttaagctgataatgtaattaacaactgctgagagatcaaagattcaacttgccatacacctcaaattcggagaaacagttaatttgggcaaatctacagttctgtttttgctactctattgtcattcctgtttaatactcactgtacttgtatttgagacaaataggtgatactgaattttatactgttttctacttttccattaaaacattggcacctcaatgataaagaaatttaaggtataaaattaaatgtaaaaattaatttcagcttcatttcgtatttcgaagcaatctagactgttgtgatgagtgtatgtctgaacctgtaattcttaaaagacttcttaatcttctagaagaaaaatctccgaagagctctctctagaagtccaaaatggctagccattatgcttctttgaaaggacatgataatgggaccaggatggttttttggagtaccaagcaaggggaatggagcactttaagggcgcctgttagtaacatgaattggaaatctgtgtcgagtacctctgatctaaacggtaaaacaagctgcctggagagcagctgtacctaacaatactgtaatgtacattaacattacagcctctcaatttcaggcaggtgtaacagttcctttccaccagatttaatatttttatacttcctgcaggttcttcttaaaaagtaatctatatttttgaactgatacttgttttatacataaattttttttagatgtgataaagctaaacttggccaaagtgtgtgcctgaattattagacctttttattagtcaacctacgaagactaaaatagaatatattagttttcaagggagtgggaggcttccaacatagtattgaatctcaggaaaaactattctttcatgtctgattctgagatttctaattgtgttgtgaaaatgataaatgcagcaaatctagctttcagtattcctaatttttacctaagctcattgctccaggctttgattacctaaaataagcttggataaaattgaaccaacttcaagaatgcagcacttcttaatctttagctctttcttgggagaagctagactttattcattatattgctatgacaacttcactctttcataatatataggataaattgtttacatgattggaccctcagattctgttaaccaaaattgcagaatggggggccaggcctgtgtggtggctcacacctgtgatcccagcactttgggaggctgaggtaggaggatcacgtgaggtcgggagttcaagaccagcctggccatcatggtgaaaccctgtctctactgaaaatacaaaaattagccgggcgtggtggcacacgcctgtagtcccagctactcaggaggctgaggcaggagaatcacttgaattcaggaggcggaggttgcagtgagccaagatcataccactgcactgcagcctgagtgacacagtaagactgtctccaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:79723 -> Molecular function: GO:0003682 [chromatin binding] evidence: IEA
GeneID:79723 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:79723 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA
GeneID:79723 -> Molecular function: GO:0046974 [histone methyltransferase activity (H3-K9 specific)] evidence: IDA
GeneID:79723 -> Biological process: GO:0006333 [chromatin assembly or disassembly] evidence: IMP
GeneID:79723 -> Biological process: GO:0006338 [chromatin remodeling] evidence: IDA
GeneID:79723 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
GeneID:79723 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: IEA
GeneID:79723 -> Biological process: GO:0007140 [male meiosis] evidence: IEA
GeneID:79723 -> Biological process: GO:0030154 [cell differentiation] evidence: IEA
GeneID:79723 -> Cellular component: GO:0000775 [chromosome, centromeric region] evidence: IEA
GeneID:79723 -> Cellular component: GO:0000785 [chromatin] evidence: IDA
GeneID:79723 -> Cellular component: GO:0005720 [nuclear heterochromatin] evidence: IEA
ANNOTATIONS from NCBI Entrez Gene (20130726):
NP_001180355 -> EC 2.1.1.43
by
@meso_cacase at
DBCLS
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