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2018-11-22 02:36:31, 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:

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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