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2024-04-26 14:30:52, GGRNA : RefSeq release 60 (20130726)
LOCUS NR_034181 3002 bp RNA linear PRI 16-JUL-2013
DEFINITION Homo sapiens suppressor of variegation 3-9 homolog 2 (Drosophila)
(SUV39H2), transcript variant 6, non-coding RNA.
ACCESSION NR_034181
VERSION NR_034181.1 GI:301171620
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 3002)
AUTHORS Syreeni A, El-Osta A, Forsblom C, Sandholm N, Parkkonen M, Tarnow
L, Parving HH, McKnight AJ, Maxwell AP, Cooper ME and Groop PH.
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 3002)
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 3002)
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 3002)
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 3002)
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 3002)
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 3002)
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 3002)
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 3002)
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 3002)
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, AK225369.1 and BC007754.2.
Transcript Variant: This variant (6) is missing an internal exon
compared to variant 1. It is represented as non-coding because the
use of the 5'-most supported translational start codon as used in
variant 1, renders the transcript a candidate for nonsense-mediated
mRNA decay (NMD).
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-101 DB040298.1 1-101
102-1679 AK225369.1 1-1578
1680-3002 BC007754.2 1771-3093
FEATURES Location/Qualifiers
source 1..3002
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10p13"
gene 1..3002
/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"
misc_RNA 1..3002
/gene="SUV39H2"
/gene_synonym="KMT1B"
/product="suppressor of variegation 3-9 homolog 2
(Drosophila), transcript variant 6"
/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"
variation 102
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:375333545"
misc_feature 107..244
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="COORDINATES: ab initio prediction:ORF Finder"
/note="upstream ORF has strong Kozak sequence and overlaps
primary ORF; nonsense-mediated decay (NMD) candidate"
exon 138..809
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="alignment:Splign:1.39.8"
misc_feature 141..1193
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="COORDINATES:
alignment:Blast2seq::RefSeq|NM_001193424.1"
/note="primary ORF"
variation 227
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:148153307"
variation 248
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:376764262"
variation 250
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:140852434"
variation 304
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:144521316"
variation 308
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:3740112"
variation 322..323
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace=""
/replace="c"
/db_xref="dbSNP:35348245"
variation 327
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:372163934"
variation 339
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:201043867"
variation 352
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="g"
/db_xref="dbSNP:138508980"
variation 360
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="c"
/db_xref="dbSNP:45473500"
variation 368
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:150726093"
variation 479
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:138078553"
variation 505
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="g"
/db_xref="dbSNP:149546848"
variation 515
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:200539708"
variation 522
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="c"
/db_xref="dbSNP:376480219"
variation 713
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:368991744"
variation 741
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:375736366"
variation 743
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:199654065"
variation 779
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:144034230"
exon 810..956
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="alignment:Splign:1.39.8"
variation 869
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:190174096"
variation 881
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:183140822"
variation 882
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:148667087"
variation 926
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:17353856"
variation 932
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:369186882"
variation 947
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:147278353"
exon 957..1086
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="alignment:Splign:1.39.8"
variation 1001
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="g"
/db_xref="dbSNP:61730323"
variation 1026
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:369793867"
exon 1087..2996
/gene="SUV39H2"
/gene_synonym="KMT1B"
/inference="alignment:Splign:1.39.8"
variation 1162
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:199727444"
variation 1172
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:144605484"
variation 1188
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:201395473"
variation 1212
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="g"
/db_xref="dbSNP:375126181"
variation 1248
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:368830300"
variation 1284
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:113301024"
variation 1305
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:373511332"
variation 1320
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="c"
/db_xref="dbSNP:11547181"
variation 1341
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:373567048"
variation 1352
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="c"
/db_xref="dbSNP:180989547"
variation 1356
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace=""
/replace="g"
/db_xref="dbSNP:375028927"
variation 1533
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="g"
/db_xref="dbSNP:116910335"
variation 1546
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="c"
/db_xref="dbSNP:75420442"
polyA_signal 1708..1713
/gene="SUV39H2"
/gene_synonym="KMT1B"
variation 1727..1729
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace=""
/replace="aat"
/db_xref="dbSNP:367684066"
polyA_site 1728
/gene="SUV39H2"
/gene_synonym="KMT1B"
polyA_site 1744
/gene="SUV39H2"
/gene_synonym="KMT1B"
polyA_signal 1753..1758
/gene="SUV39H2"
/gene_synonym="KMT1B"
variation 1765..1768
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace=""
/replace="aatt"
/db_xref="dbSNP:371874353"
polyA_site 1770
/gene="SUV39H2"
/gene_synonym="KMT1B"
polyA_site 1781
/gene="SUV39H2"
/gene_synonym="KMT1B"
variation 1878
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:142967205"
variation 1935
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:185218421"
variation 1997
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:41284455"
variation 2088
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:11594111"
variation 2159
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:190438184"
variation 2275
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:181251834"
variation 2413
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:61843036"
variation 2550
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:75516757"
variation 2572
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:376829730"
variation 2630
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:150828159"
variation 2755
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:139176971"
variation 2819
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:11259385"
variation 2899
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="g"
/replace="t"
/db_xref="dbSNP:186353154"
variation 2917
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="t"
/db_xref="dbSNP:191603474"
variation 2918
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="g"
/db_xref="dbSNP:371491790"
variation 2937
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="c"
/replace="g"
/db_xref="dbSNP:183557434"
variation 2985
/gene="SUV39H2"
/gene_synonym="KMT1B"
/replace="a"
/replace="t"
/db_xref="dbSNP:79193913"
ORIGIN
aacaagccccggcccccaagtcccgcgcgggccggccaggggcggggcgtcgggccagctgagctatcccgtcagaccgcgccagtttgaatgaaagctctacaagatggcggcggtcggggccgaggcgcgaggaggatatggaatattatcttgtaaaatggaaaggatggccagattctacaaatacttgggaacctttgcaaaatctgaagtgcccgttactgcttcagcaattctctaatgacaagcataattatttatctcaggtaaagaaaggcaaagcaataactccaaaagacaataacaaaactttgaaacctgccattgctgagtacattgtgaagaaggctaaacaaaggatagctctgcagagatggcaagatgaactcaacagaagaaagaatcataaaggaatgatatttgttgaaaatactgttgatttagagggcccaccttcagacttctattacattaacgaatacaaaccagctcctggaatcagcttagtcaatgaagctacctttggttgttcatgcacagattgcttctttcaaaaatgttgtcctgctgaagctggagttcttttggcttataataaaaaccaacaaattaaaatcccacctggtactcccatctatgaatgcaactcaaggtgtcagtgtggtcctgattgtcccaataggattgtacaaaaaggcacacagtattcgctttgcatctttcgaactagcaatggacgtggctggggtgtaaagacccttgtgaagattaaaagaatgagttttgtcatggaatatgttggagaggtaatcacaagtgaagaagctgaaagacgaggacagttctatgacaacaagggaatcacgtatctctttgatctggactatgagtctgatgaattcacagtggatgcggctcgatacggcaatgtgtctcattttgtgaatcacagctgtgacccaaatcttcaggtgttcaatgttttcattgataacctcgatactcgtcttccccgaatagcattgttttccacaagaaccataaatgctggagaagagctgacttttgattatcaaatgaaaggttctggagatatatcttcagattctattgaccacagcccagccaaaaagagggtcagaacagtatgtaaatgtggagctgtgacttgcagaggttacctcaactgaactttttcaggaaatagagctgatgattataatatttttttcctaatgttaacatttttaaaaatacatatttgggactcttattatcaaggttctacctatgttaatttacaattcatgtttcaagacatttgccaaatgtattaccgatgcctctgaaaagggggtcactgggtctcatagactgatatgaagtcgacatatttatagtgcttagagaccaaactaatggaaggcagactatttacagcttagtatatgtgtacttaagtctatgtgaacagagaaatgcctcccgtagtgtttgaaagcgttaagctgataatgtaattaacaactgctgagagatcaaagattcaacttgccatacacctcaaattcggagaaacagttaatttgggcaaatctacagttctgtttttgctactctattgtcattcctgtttaatactcactgtacttgtatttgagacaaataggtgatactgaattttatactgttttctacttttccattaaaacattggcacctcaatgataaagaaatttaaggtataaaattaaatgtaaaaattaatttcagcttcatttcgtatttcgaagcaatctagactgttgtgatgagtgtatgtctgaacctgtaattcttaaaagacttcttaatcttctagaagaaaaatctccgaagagctctctctagaagtccaaaatggctagccattatgcttctttgaaaggacatgataatgggaccaggatggttttttggagtaccaagcaaggggaatggagcactttaagggcgcctgttagtaacatgaattggaaatctgtgtcgagtacctctgatctaaacggtaaaacaagctgcctggagagcagctgtacctaacaatactgtaatgtacattaacattacagcctctcaatttcaggcaggtgtaacagttcctttccaccagatttaatatttttatacttcctgcaggttcttcttaaaaagtaatctatatttttgaactgatacttgttttatacataaattttttttagatgtgataaagctaaacttggccaaagtgtgtgcctgaattattagacctttttattagtcaacctacgaagactaaaatagaatatattagttttcaagggagtgggaggcttccaacatagtattgaatctcaggaaaaactattctttcatgtctgattctgagatttctaattgtgttgtgaaaatgataaatgcagcaaatctagctttcagtattcctaatttttacctaagctcattgctccaggctttgattacctaaaataagcttggataaaattgaaccaacttcaagaatgcagcacttcttaatctttagctctttcttgggagaagctagactttattcattatattgctatgacaacttcactctttcataatatataggataaattgtttacatgattggaccctcagattctgttaaccaaaattgcagaatggggggccaggcctgtgtggtggctcacacctgtgatcccagcactttgggaggctgaggtaggaggatcacgtgaggtcgggagttcaagaccagcctggccatcatggtgaaaccctgtctctactgaaaatacaaaaattagccgggcgtggtggcacacgcctgtagtcccagctactcaggaggctgaggcaggagaatcacttgaattcaggaggcggaggttgcagtgagccaagatcataccactgcactgcagcctgagtgacacagtaagactgtctccaaaaaaaaaaaaaaaaaa
//
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
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