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2024-04-27 11:08:48, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001199455 4602 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens bromodomain containing 2 (BRD2), transcript variant 3,
mRNA.
ACCESSION NM_001199455
VERSION NM_001199455.1 GI:313747416
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 4602)
AUTHORS Tang,X., Peng,R., Ren,Y., Apparsundaram,S., Deguzman,J.,
Bauer,C.M., Hoffman,A.F., Hamilton,S., Liang,Z., Zeng,H.,
Fuentes,M.E., Demartino,J.A., Kitson,C., Stevenson,C.S. and
Budd,D.C.
TITLE BET bromodomain proteins mediate downstream signaling events
following growth factor stimulation in human lung fibroblasts and
are involved in bleomycin-induced pulmonary fibrosis
JOURNAL Mol. Pharmacol. 83 (1), 283-293 (2013)
PUBMED 23115324
REMARK GeneRIF: Brd2 and Brd4 proteins mediatE the responses of LFs after
growth factor stimulation and drivE the induction of lung fibrosis
in mice in response to bleomycin challenge.
REFERENCE 2 (bases 1 to 4602)
AUTHORS Yavuz,E.N., Ozdemir,O., Catal,S., Bebek,N., Ozbek,U. and Baykan,B.
TITLE Bromodomain-containing protein 2 gene in photosensitive epilepsy
JOURNAL Seizure 21 (8), 646-648 (2012)
PUBMED 22766109
REMARK GeneRIF: Our study did not confirm the presence of the genetic
variants previously found to link the BRD2 gene to the idiopathic
form of photosensitive epilepsy.
REFERENCE 3 (bases 1 to 4602)
AUTHORS Barda,S., Paz,G., Yogev,L., Yavetz,H., Lehavi,O., Hauser,R.,
Botchan,A., Breitbart,H. and Kleiman,S.E.
TITLE Expression of BET genes in testis of men with different
spermatogenic impairments
JOURNAL Fertil. Steril. 97 (1), 46-52 (2012)
PUBMED 22035730
REMARK GeneRIF: The BRDT gene was not expressed in testicular tissue from
patients with Sertoli cells only, whereas the other three genes of
the BET family retained expression in all the sperm pathologies.
REFERENCE 4 (bases 1 to 4602)
AUTHORS Shang,E., Cui,Q., Wang,X., Beseler,C., Greenberg,D.A. and
Wolgemuth,D.J.
TITLE The bromodomain-containing gene BRD2 is regulated at transcription,
splicing, and translation levels
JOURNAL J. Cell. Biochem. 112 (10), 2784-2793 (2011)
PUBMED 21608014
REMARK GeneRIF: The bromodomain-containing gene BRD2 is regulated at
transcription, splicing, and translation levels.
REFERENCE 5 (bases 1 to 4602)
AUTHORS Umehara,T., Nakamura,Y., Wakamori,M., Ozato,K., Yokoyama,S. and
Padmanabhan,B.
TITLE Structural implications for K5/K12-di-acetylated histone H4
recognition by the second bromodomain of BRD2
JOURNAL FEBS Lett. 584 (18), 3901-3908 (2010)
PUBMED 20709061
REMARK GeneRIF: the crystal structure of the second bromodomain of BRD2
(BRD2-BD2) in complex with the di-acetylated histone H4 tail
(H4K5ac/K12ac) was shown.
REFERENCE 6 (bases 1 to 4602)
AUTHORS Denis,G.V. and Green,M.R.
TITLE A novel, mitogen-activated nuclear kinase is related to a
Drosophila developmental regulator
JOURNAL Genes Dev. 10 (3), 261-271 (1996)
PUBMED 8595877
REMARK GeneRIF: The BRD2 gene is homologous to the mammalian cell cycle
regulator TAFII250 and the Drosophila trithorax group gene female
sterile homeotic; the gene encodes a nuclear-localized kinase with
signal transduction activity.
REFERENCE 7 (bases 1 to 4602)
AUTHORS Thorpe,K.L., Abdulla,S., Kaufman,J., Trowsdale,J. and Beck,S.
TITLE Phylogeny and structure of the RING3 gene
JOURNAL Immunogenetics 44 (5), 391-396 (1996)
PUBMED 8781126
REFERENCE 8 (bases 1 to 4602)
AUTHORS Haynes,S.R., Dollard,C., Winston,F., Beck,S., Trowsdale,J. and
Dawid,I.B.
TITLE The bromodomain: a conserved sequence found in human, Drosophila
and yeast proteins
JOURNAL Nucleic Acids Res. 20 (10), 2603 (1992)
PUBMED 1350857
REFERENCE 9 (bases 1 to 4602)
AUTHORS Beck,S., Hanson,I., Kelly,A., Pappin,D.J. and Trowsdale,J.
TITLE A homologue of the Drosophila female sterile homeotic (fsh) gene in
the class II region of the human MHC
JOURNAL DNA Seq. 2 (4), 203-210 (1992)
PUBMED 1352711
REFERENCE 10 (bases 1 to 4602)
AUTHORS Okamoto,N., Ando,A., Kawai,J., Yoshiwara,T., Tsuji,K. and Inoko,H.
TITLE Orientation of HLA-DNA gene and identification of a CpG
island-associated gene adjacent to DNA in human major
histocompatibility complex class II region
JOURNAL Hum. Immunol. 32 (3), 221-228 (1991)
PUBMED 1663500
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from CN398334.1, DC379337.1,
AL832722.1, BC063840.1 and AL645941.11.
Summary: This gene encodes a transcriptional regulator that belongs
to the BET (bromodomains and extra terminal domain) family of
proteins. This protein associates with transcription complexes and
with acetylated chromatin during mitosis, and it selectively binds
to the acetylated lysine-12 residue of histone H4 via its two
bromodomains. The gene maps to the major histocompatability complex
(MHC) class II region on chromosome 6p21.3, but sequence comparison
suggests that the protein is not involved in the immune response.
This gene has been implicated in juvenile myoclonic epilepsy, a
common form of epilepsy that becomes apparent in adolescence.
Multiple alternatively spliced variants have been described for
this gene. [provided by RefSeq, Dec 2010].
Transcript Variant: This variant (3) has an additional in-frame
exon in the CDS compared to variant 1. The resulting isoform (2) is
longer than isoform 1.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript 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 :: BC063840.1 [ECO:0000332]
RNAseq introns :: mixed/partial sample support
ERS025081, ERS025082 [ECO:0000350]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-522 CN398334.1 6-527
523-531 DC379337.1 569-577
532-1397 AL832722.1 777-1642
1398-4123 BC063840.1 263-2988
4124-4602 AL645941.11 58464-58942
FEATURES Location/Qualifiers
source 1..4602
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="6"
/map="6p21.3"
gene 1..4602
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="bromodomain containing 2"
/db_xref="GeneID:6046"
/db_xref="HGNC:1103"
/db_xref="MIM:601540"
exon 1..1333
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 7
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201973858"
variation 8..9
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="gct"
/db_xref="dbSNP:370968322"
variation 11
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200600639"
variation 12
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201482654"
variation 25
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199600996"
variation 26
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200451599"
variation 27
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201226550"
variation 29
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199868873"
variation 37
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:200627256"
variation 50
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201948846"
variation 70
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150478937"
variation 76
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200949008"
variation 98
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201755026"
variation 103
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:199915030"
variation 132
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201010733"
variation 152
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201665646"
variation 155
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:372327634"
variation 167
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200120201"
variation 184
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201133050"
variation 185
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142535126"
variation 191
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200226207"
variation 224
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368867808"
variation 241
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201326064"
variation 246
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201797920"
variation 248
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:146768927"
variation 330..331
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="g"
/db_xref="dbSNP:368949163"
variation 342..343
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:34330235"
STS 350..463
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb278"
/db_xref="UniSTS:240930"
variation 369
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:73409619"
variation 382
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143541374"
variation 412
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:116880340"
variation 414
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049278"
variation 450
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:190237002"
variation 523
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:974357"
variation 647
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1803865"
variation 655
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:116415048"
variation 704
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555087"
variation 723
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:181742420"
variation 771
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:11555940"
variation 789
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:35607307"
variation 824
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55912052"
variation 892
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:12234140"
variation 910
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:185537776"
variation 931..933
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="tcg"
/db_xref="dbSNP:150942919"
variation 947
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1063344"
variation 952
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:113542396"
variation 968
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141167814"
variation 973
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:17617655"
variation 1092
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:111483230"
variation 1096
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:369570787"
variation 1110
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:17220465"
variation 1181
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:11555088"
variation 1183
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:78280497"
variation 1218
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200590068"
variation 1219
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201899070"
variation 1233
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555089"
variation 1246
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:6916791"
variation 1250
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2071571"
variation 1261
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368022125"
variation 1268
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:370485049"
misc_feature 1275..1277
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="upstream in-frame stop codon"
variation 1295
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:373976120"
variation 1296
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:367803227"
variation 1301
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201642612"
CDS 1305..3815
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="isoform 2 is encoded by transcript variant 3;
female sterile homeotic-related gene 1;
bromodomain-containing 2; bromodomain-containing protein
2; O27.1.1; really interesting new gene 3 protein"
/codon_start=1
/product="bromodomain-containing protein 2 isoform 2"
/protein_id="NP_001186384.1"
/db_xref="GI:313747417"
/db_xref="CCDS:CCDS56420.1"
/db_xref="GeneID:6046"
/db_xref="HGNC:1103"
/db_xref="MIM:601540"
/translation="
MLQNVTPHNKLPGEGNAGLLGLGPEAAAPGKRIRKPSLLYEGFESPTMASVPALQLTPANPPPPEVSNPKKPGRVTNQLQYLHKVVMKALWKHQFAWPFRQPVDAVKLGLPDYHKIIKQPMDMGTIKRRLENNYYWAASECMQDFNTMFTNCYIYNKPTDDIVLMAQTLEKIFLQKVASMPQEEQELVVTIPKNSHKKGAKLAALQGSVTSAHQVPAVSSVSHTALYTPPPEIPTTVLNIPHPSVISSPLLKSLHSAGPPLLAVTAAPPAQPLAKKKGVKRKADTTTPTPTAILAPGSPASPPGSLEPKAARLPPMRRESGRPIKPPRKDLPDSQQQHQSSKKGKLSEQLKHCNGILKELLSKKHAAYAWPFYKPVDASALGLHDYHDIIKHPMDLSTVKRKMENRDYRDAQEFAADVRLMFSNCYKYNPPDHDVVAMARKLQDVFEFRYAKMPDEPLEPGPLPVSTAMPPGLAKSSSESSSEESSSESSSEEEEEEDEEDEEEEESESSDSEEERAHRLAELQEQLRAVHEQLAALSQGPISKPKRKREKKEKKKKRKAEKHRGRAGADEDDKGPRAPRPPQPKKSKKASGSGGGSAALGPSGFGPSGGSGTKLQAGVQWRDLGLLQPPLLGFKRFSCLSLPSSQDYRLPKKATKTAPPALPTGYDSEEEEESRPMSYDEKRQLSLDINKLPGEKLGRVVHIIQAREPSLRDSNPEEIEIDFETLKPSTLRELERYVLSCLRKKPRKPYTIKKPVGKTKEELALEKKRELEKRLQDVSGQLNSTKKPPKKANEKTESSSAQQVAVSRLSASSSSSDSSSSSSSSSSSDTSDSDSG
"
misc_feature 1524..1844
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="Bromodomain, Brdt_like subfamily, repeat I. Human
Brdt is a testis-specific member of the BET subfamily of
bromodomain proteins; the first bromodomain in Brdt has
been shown to be essential for male germ cell
differentiation. Bromodomains are 110 amino...; Region:
Bromo_Brdt_I_like; cd05497"
/db_xref="CDD:99929"
misc_feature order(1611..1613,1632..1634,1641..1643,1758..1760,
1770..1772,1788..1790)
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="acetyllysine binding site; other site"
/db_xref="CDD:99929"
misc_feature 2349..2654
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="Bromodomain, Brdt_like subfamily, repeat II. Human
Brdt is a testis-specific member of the BET subfamily of
bromodomain proteins; the first bromodomain in Brdt has
been shown to be essential for male germ cell
differentiation. Bromodomains are 110 amino...; Region:
Bromo_Brdt_II_like; cd05498"
/db_xref="CDD:99930"
misc_feature order(2430..2432,2451..2453,2460..2462,2577..2579,
2589..2591,2607..2609)
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="acetyllysine binding site; other site"
/db_xref="CDD:99930"
misc_feature 3150..>3257
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="Putative binding domain; Region: GVQW; pfam13900"
/db_xref="CDD:206071"
variation 1316
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:147219068"
variation 1323
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:140566548"
variation 1324
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142520217"
variation 1326
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:377684930"
variation 1327
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201319601"
exon 1334..1637
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 1337
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:35974351"
variation 1359
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3752528"
variation 1372
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55650502"
variation 1375
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:368437378"
variation 1377
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:371937442"
variation 1397
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:516535"
variation 1419
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:143451360"
variation 1420
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:376209743"
variation 1423
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200307380"
variation 1424
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:148450256"
variation 1427
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:11555090"
variation 1446
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:369193752"
variation 1449
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:55669504"
variation 1450
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:3918144"
variation 1450
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="gc"
/replace="tg"
/db_xref="dbSNP:375083792"
variation 1481
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:138097363"
variation 1484
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:56109539"
variation 1495
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:146881536"
variation 1496
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199590043"
variation 1505
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:115120098"
variation 1511
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:376374651"
variation 1512
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="a"
/db_xref="dbSNP:35261809"
variation 1519
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201647382"
variation 1534
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368792346"
variation 1538
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374628062"
variation 1553
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150476702"
variation 1589
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:375791386"
variation 1592
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374599253"
variation 1618
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:138290874"
exon 1638..1775
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 1646
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:201582271"
variation 1661
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:375792679"
variation 1670
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:180909220"
variation 1691
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201754613"
variation 1700
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:9378166"
variation 1706
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:76146382"
STS 1708..1883
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="RH79050"
/db_xref="UniSTS:39777"
variation 1733
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:373853679"
variation 1746
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143509698"
exon 1776..1914
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 1792
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1803864"
variation 1793
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199821934"
STS 1794..2027
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="STS-T87864"
/db_xref="UniSTS:53679"
variation 1799
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:367609858"
variation 1821
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:137960007"
variation 1824
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370287964"
STS 1834..1970
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="G67884"
/db_xref="UniSTS:225610"
variation 1848
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:200486677"
STS 1869..1944
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb741"
/db_xref="UniSTS:240935"
variation 1880
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:375469443"
variation 1886
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201572264"
variation 1887
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199497657"
exon 1915..2129
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 1925
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:186277039"
STS 1927..2067
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb250"
/db_xref="UniSTS:240929"
variation 1938
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:35952031"
variation 1941
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370807550"
variation 1956
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200381760"
variation 1971
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200917553"
variation 1977..1978
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:35264453"
variation 1982
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:15912"
variation 2016
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:176250"
variation 2017
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:41270502"
variation 2030
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141377590"
variation 2083
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:35294809"
variation 2109
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:148978000"
exon 2130..2504
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2138
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:374284677"
variation 2168
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:375353506"
variation 2223
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:150794546"
variation 2238
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139156709"
variation 2246
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146092849"
variation 2252
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:369113238"
variation 2312
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200612980"
variation 2365
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:371260391"
variation 2366
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:17214085"
variation 2369
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:62407971"
variation 2387
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146801767"
variation 2440
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:140492558"
variation 2441
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:17214092"
variation 2468
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142982923"
variation 2495
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:192648574"
exon 2505..2633
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2530
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:141044200"
variation 2556
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200770939"
variation 2595
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150234115"
variation 2603
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139231674"
variation 2609
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142112689"
exon 2634..2882
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2645
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55650066"
variation 2654
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200803710"
variation 2682
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201781653"
variation 2688
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:199605967"
variation 2699
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:145849910"
variation 2708
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:138688346"
variation 2709
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201908033"
variation 2714
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200182536"
variation 2720
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200897288"
variation 2724
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:184752888"
variation 2725
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:3918143"
variation 2732
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368290193"
variation 2763
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143615833"
variation 2798
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:200663348"
variation 2799..2801
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="gag"
/db_xref="dbSNP:3918142"
variation 2801
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:200978040"
variation 2802
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:12822"
variation 2804..2805
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="gga"
/db_xref="dbSNP:41310958"
variation 2804
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201796698"
STS 2805..2930
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="SGC31960"
/db_xref="UniSTS:63641"
variation 2807
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200103856"
variation 2808
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201071191"
variation 2813
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:144872939"
variation 2816
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:148048133"
variation 2819
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55778408"
variation 2846
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201425304"
variation 2854
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:202033057"
variation 2855
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141740031"
variation 2857
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:35773608"
exon 2883..3145
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
STS 2892..2997
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb369"
/db_xref="UniSTS:240931"
variation 2903
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:191317139"
variation 2935..2936
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555938"
variation 2936
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:11037"
variation 2942
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:35845948"
variation 2944
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049369"
variation 2945
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049372"
variation 2954
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3189517"
variation 2955
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200980274"
variation 2956
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374788375"
variation 2984
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:142074834"
variation 3001
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:146321913"
variation 3008
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201989394"
variation 3009
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:34530779"
variation 3014
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1063379"
variation 3042
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:144552033"
variation 3099
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:55952113"
variation 3113
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:206781"
variation 3139
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:111308504"
exon 3146..3250
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 3166
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:188765357"
variation 3200
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:112616809"
variation 3210
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370604802"
variation 3243
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:206778"
exon 3251..3555
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 3251
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:141736131"
variation 3259
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:145888786"
variation 3331
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:138736016"
variation 3428
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368407034"
variation 3511
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:140400525"
exon 3556..3678
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 3610
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:375635536"
variation 3662
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:140096077"
variation 3671
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2066750"
variation 3673
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:150287231"
exon 3679..4602
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 3679
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:137898499"
variation 3680
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199954603"
STS 3684..4535
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="BRD2_3857"
/db_xref="UniSTS:462062"
variation 3691
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200578995"
variation 3694
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:149549323"
variation 3698
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201375031"
variation 3700
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200164898"
variation 3705
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:144861747"
variation 3727
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:202018564"
variation 3734
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199887337"
variation 3746
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2071876"
variation 3748
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:369127190"
variation 3761
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:202086051"
variation 3778
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200397640"
variation 3782
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3918140"
variation 3811
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:202161102"
variation 3817
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200531629"
variation 3818
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:371782351"
variation 3832
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201611634"
variation 3846
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199587809"
variation 3866
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:200408799"
variation 3868
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201062187"
variation 3870
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199866893"
variation 3897
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:147269908"
variation 3919
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201692899"
variation 3924
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:199530843"
variation 3927..3928
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201992712"
variation 3927..3928
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/replace="t"
/db_xref="dbSNP:28986268"
variation 3927
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/replace="cc"
/replace="ct"
/replace="t"
/db_xref="dbSNP:368289232"
variation 3927
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049414"
variation 3928..3929
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:373358187"
STS 3935..4047
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="D6S1894"
/db_xref="UniSTS:67698"
variation 3959
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:139189753"
STS 3970..4167
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="RH18121"
/db_xref="UniSTS:26631"
variation 4005
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:72865897"
variation 4041
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:78300601"
variation 4056
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:10829"
variation 4079
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:372641732"
variation 4124
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049526"
variation 4134
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:370640038"
variation 4165
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:201572601"
variation 4174
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555939"
variation 4178
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1803596"
variation 4215
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:185910133"
variation 4220
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:112975861"
variation 4246
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:373317674"
variation 4258..4259
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:71656056"
variation 4272
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="a"
/db_xref="dbSNP:3841159"
variation 4272
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:113758837"
variation 4274..4275
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:71645781"
STS 4277..4377
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="NIB1722"
/db_xref="UniSTS:42553"
variation 4289..4290
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="tg"
/db_xref="dbSNP:199828295"
variation 4320
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1803863"
variation 4322
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:34128205"
variation 4329
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:191209130"
variation 4351
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:115821350"
variation 4434
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:182780962"
STS 4448..4562
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="A008D22"
/db_xref="UniSTS:22045"
variation 4458
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:187202774"
variation 4472
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049639"
variation 4491
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:16871296"
variation 4515
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:60466011"
variation 4549
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:73409643"
polyA_signal 4573..4578
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
polyA_site 4602
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
ORIGIN
attcttcgctgctgctgccttaccgccgagaaccaccacccgccaggcgtcttgcggccacacccctggcgggttcaggcaggctacgcccacgcgacccctcccgtttccctgctttggccaatggaggagctacgaatggcacgacctgctcgagcttggcagtctccagttgggctgtgcatggaagcttgggaagactttgttggaaggggaggcggggagagagtgctggaggctctggggcgatggcttccgcacctcttccaaccaccctctttccctggagtcggcggaccacagctcagccaattggcttggagatgtggcgggttgccacttccctgtgggtctctgcggcactcttctgcctggtgactgacaccttggaaatgaagtttatgacgtcatcgttgcggctggccaatagaaaaagctcccgcggagaggtgttccttccccttcgactcagcttcttcacccgcgtgagcgagcgcgcgcgcgcggagggggtggggaaaagctcaagcagggtggcgcgcatgagcggcgaagctcctcctccccgcctatatataaagggctggcgcggggctcggcggcgccatttcgtgctggagtggagcagcctctagaacgagctggaggattctgcctaccgatacagagccttcgagtcgtccggggccgccattacaatccacctccatccgcttggaaatggccttcgtcccggcctatgactggtcccagcgggcagtacagaccccctagaagcccctggagctcccctttttcgggccccgcccaatcctcggagtctgtccaccccctctactccgccctcaagaggatttcaaagatggaggcggcggctccctaaaccacttttcgtgttcatccgcctccatccgagatcgaaacgggacctcgtcggccccgtaggggcccgacaagaagagggaatccctgcagaccaacagcgggctatattgacgacggtgtctgagatcggggaccgtcttttgaagagtcagtccctccttagttgcccgcctcagctgaggccgccgccattttcttgctgtccgccgtctgcagagcgcgccaagctgcccggagctctccgagaggccccaaagagactgctttcgtgccggccaggcagggggtttgtcgcctggaggcccaagaggaacggcctccccccaacttagcgggttatgctggaccgggcggtgaggggaaccgaggccacccggactttccgcggctgagggcagcgccggttccttgcggtcaagatgctgcaaaacgtgactccccacaataagctccctggggaagggaatgcagggttgctggggctgggcccagaagcagcagcaccagggaagaggattcgaaaaccctctctcttgtatgagggctttgagagccccacaatggcttcggtgcctgctttgcaacttacccctgccaacccaccacccccggaggtgtccaatcccaaaaagccaggacgagttaccaaccagctgcaatacctacacaaggtagtgatgaaggctctgtggaaacatcagttcgcatggccattccggcagcctgtggatgctgtcaaactgggtctaccggattatcacaaaattataaaacagcctatggacatgggtactattaagaggagacttgaaaacaattattattgggctgcttcagagtgtatgcaagattttaataccatgttcaccaactgttacatttacaacaagcccactgatgatattgtcctaatggcacaaacgctggaaaagatattcctacagaaggttgcatcaatgccacaagaagaacaagagctggtagtgaccatccctaagaacagccacaagaagggggccaagttggcagcgctccagggcagtgttaccagtgcccatcaggtgcctgccgtctcttctgtgtcacacacagccctgtatactcctccacctgagatacctaccactgtcctcaacattccccacccatcagtcatttcctctccacttctcaagtccttgcactctgctggacccccgctccttgctgttactgcagctcctccagcccagccccttgccaagaaaaaaggcgtaaagcggaaagcagatactaccacccctacacctacagccatcttggctcctggttctccagctagccctcctgggagtcttgagcctaaggcagcacggcttccccctatgcgtagagagagtggtcgccccatcaagcccccacgcaaagacttgcctgactctcagcaacaacaccagagctctaagaaaggaaagctttcagaacagttaaaacattgcaatggcattttgaaggagttactctctaagaagcatgctgcctatgcttggcctttctataaaccagtggatgcttctgcacttggcctgcatgactaccatgacatcattaagcaccccatggacctcagcactgtcaagcggaagatggagaaccgtgattaccgggatgcacaggagtttgctgctgatgtacggcttatgttctccaactgctataagtacaatcccccagatcacgatgttgtggcaatggcacgaaagctacaggatgtatttgagttccgttatgccaagatgccagatgaaccactagaaccagggcctttaccagtctctactgccatgccccctggcttggccaaatcgtcttcagagtcctccagtgaggaaagtagcagtgagagctcctctgaggaagaggaggaggaagatgaggaggacgaggaggaagaagagagtgaaagctcagactcagaggaagaaagggctcatcgcttagcagaactacaggaacagcttcgggcagtacatgaacaactggctgctctgtcccagggtccaatatccaagcccaagaggaaaagagagaaaaaagagaaaaagaagaaacggaaggcagagaagcatcgaggccgagctggggccgatgaagatgacaaggggcctagggcaccccgcccacctcaacctaagaagtccaagaaagcaagtggcagtgggggtggcagtgctgctttaggcccttctggctttggaccttctggaggaagtggcaccaaactccaggctggagtgcagtggcgtgatctcggcttactgcaacctccacttctcgggttcaagcgattctcctgcctcagcctcccaagtagccaggattacaggctccccaaaaaggccacaaagacagccccacctgccctgcctacaggttatgattcagaggaggaggaagagagcaggcccatgagttacgatgagaagcggcagctgagcctggacatcaacaaattacctggggagaagctgggccgagttgtgcatataatccaagccagggagccctctttacgtgattcaaacccagaagagattgagattgattttgaaacactcaagccatccacacttagagagcttgagcgctatgtcctttcctgcctacgtaagaaaccccggaagccctacaccattaagaagcctgtgggaaagacaaaggaggaactggctttggagaaaaagcgggaattagaaaagcggttacaagatgtcagcggacagctcaattctactaaaaagccccccaagaaagcgaatgagaaaacagagtcatcctctgcacagcaagtagcagtgtcacgccttagcgcttccagctccagctcagattccagctcctcctcttcctcgtcgtcgtcttcagacaccagtgattcagactcaggctaaggggtcaggccagatggggcaggaaggctccgcaggaccggacccctagaccaccctgccccacctgccccttccccctttgctgtgacacttcttcatctcacccccccccgcccccctctaggagagctggctctgcagtgggggagggatgcagggacatttactgaaggagggacatggacaaaacaacattgaattcccagccccattggggagtgatctcttggacacagagcccccattcaaaatggggcagggcaagggtgggagtgtgcaaagccctgatctggagttacctgaggccacagctgccctattcacttctaagggccctgttttgagattgtttgttctaatttattttaagctaggtaaggctggggggagggtggggccgtggtcccctcagcctccatggggagggaagaagggggagctctttttttacgttgatttttttttttctactctgttttccctttttccttccgctccatttggggccctgggggtttcagtcatctccccatttggtcccctggactgtctttgttgattctaacttgtaaataaagaaaatattattcaagttttgagttaccttaatatttgcttttgtagtgtttcaaaaggaacatcataagaattgtcttgataattttgagggaaatattactgcagtgagaaaaggcaatagctaacctataattggattgtcttaatttttaaaccagtaggcttttgctgtgtttttaataaagtaaatatgacttttgtaaattga
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:6046 -> Molecular function: GO:0003682 [chromatin binding] evidence: IDA
GeneID:6046 -> Molecular function: GO:0070577 [histone acetyl-lysine binding] evidence: IDA
GeneID:6046 -> Biological process: GO:0006334 [nucleosome assembly] evidence: IMP
GeneID:6046 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
GeneID:6046 -> Biological process: GO:0006357 [regulation of transcription from RNA polymerase II promoter] evidence: IDA
GeneID:6046 -> Biological process: GO:0007283 [spermatogenesis] evidence: TAS
GeneID:6046 -> Biological process: GO:0016568 [chromatin modification] evidence: IEA
GeneID:6046 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
GeneID:6046 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA
by
@meso_cacase at
DBCLS
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