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2024-04-25 18:54:42, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_005104 4907 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens bromodomain containing 2 (BRD2), transcript variant 1,
mRNA.
ACCESSION NM_005104
VERSION NM_005104.3 GI:164419756
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 4907)
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 4907)
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 4907)
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 4907)
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 4907)
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 4907)
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 4907)
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 4907)
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 4907)
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 4907)
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 D42040.1, DA127395.1,
BP271262.1, DC379337.1, AL832722.1, AI983495.1 and H11588.1.
On Jan 2, 2008 this sequence version replaced gi:12408641.
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 (1) and variant 2 encode the same
predominant isoform (1).
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: D42040.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025082 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-258 D42040.1 1-258
259-605 DA127395.1 30-376
606-919 BP271262.1 270-583
920-928 DC379337.1 569-577
929-1794 AL832722.1 777-1642
1795-4415 D42040.1 1795-4415
4416-4699 AI983495.1 2-285 c
4700-4907 H11588.1 1-208 c
FEATURES Location/Qualifiers
source 1..4907
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="6"
/map="6p21.3"
gene 1..4907
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="bromodomain containing 2"
/db_xref="GeneID:6046"
/db_xref="HGNC:1103"
/db_xref="HPRD:03326"
/db_xref="MIM:601540"
exon 1..397
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 5
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:9276935"
variation 29
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:370700605"
variation 102
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="g"
/db_xref="dbSNP:144708781"
variation 112
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:111227999"
variation 119
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:192593423"
variation 140
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:113472313"
variation 171
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:114383918"
variation 216..218
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="acg"
/replace="ggc"
/db_xref="dbSNP:34854167"
variation 243
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370095948"
variation 288
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:3135331"
variation 313
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="g"
/db_xref="dbSNP:368750193"
variation 375
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:143892329"
exon 398..1730
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 404
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201973858"
variation 405..406
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="gct"
/db_xref="dbSNP:370968322"
variation 408
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200600639"
variation 409
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201482654"
variation 422
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199600996"
variation 423
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200451599"
variation 424
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201226550"
variation 426
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199868873"
variation 434
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:200627256"
variation 447
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201948846"
variation 467
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150478937"
variation 473
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200949008"
variation 495
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201755026"
variation 500
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:199915030"
variation 529
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201010733"
variation 549
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201665646"
variation 552
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:372327634"
variation 564
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200120201"
variation 581
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201133050"
variation 582
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142535126"
variation 588
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200226207"
variation 621
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368867808"
variation 638
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201326064"
variation 643
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201797920"
variation 645
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:146768927"
variation 727..728
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="g"
/db_xref="dbSNP:368949163"
variation 739..740
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:34330235"
STS 747..860
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb278"
/db_xref="UniSTS:240930"
variation 766
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:73409619"
variation 779
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143541374"
variation 809
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:116880340"
variation 811
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049278"
variation 847
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:190237002"
variation 920
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:974357"
variation 1044
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1803865"
variation 1052
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:116415048"
variation 1101
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555087"
variation 1120
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:181742420"
variation 1168
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:11555940"
variation 1186
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:35607307"
variation 1221
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55912052"
variation 1289
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:12234140"
variation 1307
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:185537776"
variation 1328..1330
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="tcg"
/db_xref="dbSNP:150942919"
variation 1344
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1063344"
variation 1349
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:113542396"
variation 1365
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141167814"
variation 1370
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:17617655"
variation 1489
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:111483230"
variation 1493
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:369570787"
variation 1507
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:17220465"
variation 1578
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:11555088"
variation 1580
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:78280497"
variation 1615
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200590068"
variation 1616
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201899070"
variation 1630
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555089"
variation 1643
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:6916791"
variation 1647
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2071571"
variation 1658
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368022125"
variation 1665
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:370485049"
misc_feature 1672..1674
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="upstream in-frame stop codon"
variation 1692
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:373976120"
variation 1693
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:367803227"
variation 1698
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201642612"
CDS 1702..4107
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="isoform 1 is encoded by transcript variant 1;
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 1"
/protein_id="NP_005095.1"
/db_xref="GI:4826806"
/db_xref="CCDS:CCDS4762.1"
/db_xref="GeneID:6046"
/db_xref="HGNC:1103"
/db_xref="HPRD:03326"
/db_xref="MIM:601540"
/translation="
MLQNVTPHNKLPGEGNAGLLGLGPEAAAPGKRIRKPSLLYEGFESPTMASVPALQLTPANPPPPEVSNPKKPGRVTNQLQYLHKVVMKALWKHQFAWPFRQPVDAVKLGLPDYHKIIKQPMDMGTIKRRLENNYYWAASECMQDFNTMFTNCYIYNKPTDDIVLMAQTLEKIFLQKVASMPQEEQELVVTIPKNSHKKGAKLAALQGSVTSAHQVPAVSSVSHTALYTPPPEIPTTVLNIPHPSVISSPLLKSLHSAGPPLLAVTAAPPAQPLAKKKGVKRKADTTTPTPTAILAPGSPASPPGSLEPKAARLPPMRRESGRPIKPPRKDLPDSQQQHQSSKKGKLSEQLKHCNGILKELLSKKHAAYAWPFYKPVDASALGLHDYHDIIKHPMDLSTVKRKMENRDYRDAQEFAADVRLMFSNCYKYNPPDHDVVAMARKLQDVFEFRYAKMPDEPLEPGPLPVSTAMPPGLAKSSSESSSEESSSESSSEEEEEEDEEDEEEEESESSDSEEERAHRLAELQEQLRAVHEQLAALSQGPISKPKRKREKKEKKKKRKAEKHRGRAGADEDDKGPRAPRPPQPKKSKKASGSGGGSAALGPSGFGPSGGSGTKLPKKATKTAPPALPTGYDSEEEEESRPMSYDEKRQLSLDINKLPGEKLGRVVHIIQAREPSLRDSNPEEIEIDFETLKPSTLRELERYVLSCLRKKPRKPYTIKKPVGKTKEELALEKKRELEKRLQDVSGQLNSTKKPPKKANEKTESSSAQQVAVSRLSASSSSSDSSSSSSSSSSSDTSDSDSG
"
misc_feature 1702..1704
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/experiment="experimental evidence, no additional details
recorded"
/note="N-acetylmethionine; propagated from
UniProtKB/Swiss-Prot (P25440.2); acetylation site"
misc_feature 1717..1719
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P25440.2); phosphorylation site"
misc_feature 1810..1812
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P25440.2); phosphorylation site"
misc_feature 1921..2241
/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(2008..2010,2029..2031,2038..2040,2155..2157,
2167..2169,2185..2187)
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="acetyllysine binding site; other site"
/db_xref="CDD:99929"
misc_feature 2593..2595
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P25440.2); phosphorylation site"
misc_feature 2593..2595
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2602..2604
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P25440.2); phosphorylation site"
misc_feature 2602..2604
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2614..2616
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P25440.2); phosphorylation site"
misc_feature 2614..2616
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2746..3051
/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(2827..2829,2848..2850,2857..2859,2974..2976,
2986..2988,3004..3006)
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="acetyllysine binding site; other site"
/db_xref="CDD:99930"
misc_feature 3364..3378
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (P25440.2);
Region: Nuclear localization signal (Potential)"
misc_feature 3598..3600
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P25440.2); phosphorylation site"
misc_feature 3871..3873
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
variation 1713
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:147219068"
variation 1720
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:140566548"
variation 1721
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142520217"
variation 1723
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:377684930"
variation 1724
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201319601"
exon 1731..2034
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 1734
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:35974351"
variation 1756
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3752528"
variation 1769
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55650502"
variation 1772
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:368437378"
variation 1774
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:371937442"
variation 1794
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:516535"
variation 1816
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:143451360"
variation 1817
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:376209743"
variation 1820
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200307380"
variation 1821
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:148450256"
variation 1824
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:11555090"
variation 1843
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:369193752"
variation 1846
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:55669504"
variation 1847
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:3918144"
variation 1847
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="gc"
/replace="tg"
/db_xref="dbSNP:375083792"
variation 1878
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:138097363"
variation 1881
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:56109539"
variation 1892
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:146881536"
variation 1893
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199590043"
variation 1902
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:115120098"
variation 1908
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:376374651"
variation 1909
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="a"
/db_xref="dbSNP:35261809"
variation 1916
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201647382"
variation 1931
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368792346"
variation 1935
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374628062"
variation 1950
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150476702"
variation 1986
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:375791386"
variation 1989
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374599253"
variation 2015
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:138290874"
exon 2035..2172
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2043
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:201582271"
variation 2058
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:375792679"
variation 2067
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:180909220"
variation 2088
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201754613"
variation 2097
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:9378166"
variation 2103
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:76146382"
STS 2105..2280
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="RH79050"
/db_xref="UniSTS:39777"
variation 2130
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:373853679"
variation 2143
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143509698"
exon 2173..2311
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2189
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1803864"
variation 2190
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199821934"
STS 2191..2424
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="STS-T87864"
/db_xref="UniSTS:53679"
variation 2196
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:367609858"
variation 2218
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:137960007"
variation 2221
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370287964"
STS 2231..2367
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="G67884"
/db_xref="UniSTS:225610"
variation 2245
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:200486677"
STS 2266..2341
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb741"
/db_xref="UniSTS:240935"
variation 2277
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:375469443"
variation 2283
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201572264"
variation 2284
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199497657"
exon 2312..2526
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2322
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:186277039"
STS 2324..2464
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb250"
/db_xref="UniSTS:240929"
variation 2335
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:35952031"
variation 2338
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370807550"
variation 2353
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200381760"
variation 2368
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200917553"
variation 2374..2375
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:35264453"
variation 2379
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:15912"
variation 2413
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:176250"
variation 2414
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:41270502"
variation 2427
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141377590"
variation 2480
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:35294809"
variation 2506
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:148978000"
exon 2527..2901
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2535
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:374284677"
variation 2565
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:375353506"
variation 2620
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:150794546"
variation 2635
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139156709"
variation 2643
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146092849"
variation 2649
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:369113238"
variation 2709
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200612980"
variation 2762
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:371260391"
variation 2763
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:17214085"
variation 2766
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:62407971"
variation 2784
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146801767"
variation 2837
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:140492558"
variation 2838
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:17214092"
variation 2865
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142982923"
variation 2892
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:192648574"
exon 2902..3030
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2927
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:141044200"
variation 2953
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200770939"
variation 2992
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150234115"
variation 3000
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139231674"
variation 3006
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142112689"
exon 3031..3279
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 3042
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55650066"
variation 3051
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200803710"
variation 3079
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201781653"
variation 3085
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:199605967"
variation 3096
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:145849910"
variation 3105
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:138688346"
variation 3106
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201908033"
variation 3111
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200182536"
variation 3117
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200897288"
variation 3121
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:184752888"
variation 3122
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:3918143"
variation 3129
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368290193"
variation 3160
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143615833"
variation 3195
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:200663348"
variation 3196..3198
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="gag"
/db_xref="dbSNP:3918142"
variation 3198
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:200978040"
variation 3199
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:12822"
variation 3201..3202
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="gga"
/db_xref="dbSNP:41310958"
variation 3201
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201796698"
STS 3202..3327
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="SGC31960"
/db_xref="UniSTS:63641"
variation 3204
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200103856"
variation 3205
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201071191"
variation 3210
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:144872939"
variation 3213
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:148048133"
variation 3216
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55778408"
variation 3243
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201425304"
variation 3251
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:202033057"
variation 3252
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141740031"
variation 3254
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:35773608"
exon 3280..3542
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
STS 3289..3394
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb369"
/db_xref="UniSTS:240931"
variation 3300
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:191317139"
variation 3332..3333
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555938"
variation 3333
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:11037"
variation 3339
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:35845948"
variation 3341
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049369"
variation 3342
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049372"
variation 3351
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3189517"
variation 3352
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200980274"
variation 3353
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374788375"
variation 3381
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:142074834"
variation 3398
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:146321913"
variation 3405
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201989394"
variation 3406
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:34530779"
variation 3411
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1063379"
variation 3439
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:144552033"
variation 3496
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:55952113"
variation 3510
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:206781"
variation 3536
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:111308504"
exon 3543..3847
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 3543
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:141736131"
variation 3551
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:145888786"
variation 3623
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:138736016"
variation 3720
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368407034"
variation 3803
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:140400525"
exon 3848..3970
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 3902
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:375635536"
variation 3954
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:140096077"
variation 3963
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2066750"
variation 3965
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:150287231"
exon 3971..4894
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 3971
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:137898499"
variation 3972
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199954603"
STS 3976..4827
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="BRD2_3857"
/db_xref="UniSTS:462062"
variation 3983
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200578995"
variation 3986
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:149549323"
variation 3990
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201375031"
variation 3992
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200164898"
variation 3997
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:144861747"
variation 4019
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:202018564"
variation 4026
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199887337"
variation 4038
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2071876"
variation 4040
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:369127190"
variation 4053
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:202086051"
variation 4070
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200397640"
variation 4074
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3918140"
variation 4103
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:202161102"
variation 4109
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200531629"
variation 4110
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:371782351"
variation 4124
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201611634"
variation 4138
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199587809"
variation 4158
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:200408799"
variation 4160
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201062187"
variation 4162
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199866893"
variation 4189
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:147269908"
variation 4211
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201692899"
variation 4216
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:199530843"
variation 4219..4220
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201992712"
variation 4219..4220
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/replace="t"
/db_xref="dbSNP:28986268"
variation 4219
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/replace="cc"
/replace="ct"
/replace="t"
/db_xref="dbSNP:368289232"
variation 4219
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049414"
variation 4220..4221
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:373358187"
STS 4227..4339
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="D6S1894"
/db_xref="UniSTS:67698"
variation 4251
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:139189753"
STS 4262..4459
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="RH18121"
/db_xref="UniSTS:26631"
variation 4297
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:72865897"
variation 4333
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:78300601"
variation 4348
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:10829"
variation 4371
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:372641732"
variation 4416
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049526"
variation 4426
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:370640038"
variation 4457
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:201572601"
variation 4466
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555939"
variation 4470
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1803596"
variation 4507
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:185910133"
variation 4512
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:112975861"
variation 4538
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:373317674"
variation 4550..4551
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:71656056"
variation 4564
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="a"
/db_xref="dbSNP:3841159"
variation 4564
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:113758837"
variation 4566..4567
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:71645781"
STS 4569..4669
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="NIB1722"
/db_xref="UniSTS:42553"
variation 4581..4582
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="tg"
/db_xref="dbSNP:199828295"
variation 4612
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1803863"
variation 4614
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:34128205"
variation 4621
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:191209130"
variation 4643
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:115821350"
polyA_signal 4679..4684
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
polyA_site 4699
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
variation 4726
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:182780962"
STS 4740..4854
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="A008D22"
/db_xref="UniSTS:22045"
variation 4750
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:187202774"
variation 4764
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049639"
variation 4783
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:16871296"
variation 4807
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:60466011"
variation 4841
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:73409643"
polyA_signal 4865..4870
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
polyA_site 4894
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
ORIGIN
ggactgcgggataggaagctggggatatggacaagcagcagcgttatagcgctctgggtttcgggacataggcctgggccatgcggcccccttggccccttggcgcgacccccaggaacgttcggaaagctggtcctcgtggctgggggaaaggcggggggtgggggggaagcgggcacgtgaccccggtcagccaatctgggtgctgctgacgtggccgcgcggccccgatgctctccccacccccccagcccgttcgggaagggaggggctgggggctacgccccctcccccagcacggcttcgttttctgggggggggttgacaccccggattacataccccgtaccaagccgagggcaactttggaggccccctggaaggctttaggatccagattcttcgctgctgctgccttaccgccgagaaccaccacccgccaggcgtcttgcggccacacccctggcgggttcaggcaggctacgcccacgcgacccctcccgtttccctgctttggccaatggaggagctacgaatggcacgacctgctcgagcttggcagtctccagttgggctgtgcatggaagcttgggaagactttgttggaaggggaggcggggagagagtgctggaggctctggggcgatggcttccgcacctcttccaaccaccctctttccctggagtcggcggaccacagctcagccaattggcttggagatgtggcgggttgccacttccctgtgggtctctgcggcactcttctgcctggtgactgacaccttggaaatgaagtttatgacgtcatcgttgcggctggccaatagaaaaagctcccgcggagaggtgttccttccccttcgactcagcttcttcacccgcgtgagcgagcgcgcgcgcgcggagggggtggggaaaagctcaagcagggtggcgcgcatgagcggcgaagctcctcctccccgcctatatataaagggctggcgcggggctcggcggcgccatttcgtgctggagtggagcagcctctagaacgagctggaggattctgcctaccgatacagagccttcgagtcgtccggggccgccattacaatccacctccatccgcttggaaatggccttcgtcccggcctatgactggtcccagcgggcagtacagaccccctagaagcccctggagctcccctttttcgggccccgcccaatcctcggagtctgtccaccccctctactccgccctcaagaggatttcaaagatggaggcggcggctccctaaaccacttttcgtgttcatccgcctccatccgagatcgaaacgggacctcgtcggccccgtaggggcccgacaagaagagggaatccctgcagaccaacagcgggctatattgacgacggtgtctgagatcggggaccgtcttttgaagagtcagtccctccttagttgcccgcctcagctgaggccgccgccattttcttgctgtccgccgtctgcagagcgcgccaagctgcccggagctctccgagaggccccaaagagactgctttcgtgccggccaggcagggggtttgtcgcctggaggcccaagaggaacggcctccccccaacttagcgggttatgctggaccgggcggtgaggggaaccgaggccacccggactttccgcggctgagggcagcgccggttccttgcggtcaagatgctgcaaaacgtgactccccacaataagctccctggggaagggaatgcagggttgctggggctgggcccagaagcagcagcaccagggaagaggattcgaaaaccctctctcttgtatgagggctttgagagccccacaatggcttcggtgcctgctttgcaacttacccctgccaacccaccacccccggaggtgtccaatcccaaaaagccaggacgagttaccaaccagctgcaatacctacacaaggtagtgatgaaggctctgtggaaacatcagttcgcatggccattccggcagcctgtggatgctgtcaaactgggtctaccggattatcacaaaattataaaacagcctatggacatgggtactattaagaggagacttgaaaacaattattattgggctgcttcagagtgtatgcaagattttaataccatgttcaccaactgttacatttacaacaagcccactgatgatattgtcctaatggcacaaacgctggaaaagatattcctacagaaggttgcatcaatgccacaagaagaacaagagctggtagtgaccatccctaagaacagccacaagaagggggccaagttggcagcgctccagggcagtgttaccagtgcccatcaggtgcctgccgtctcttctgtgtcacacacagccctgtatactcctccacctgagatacctaccactgtcctcaacattccccacccatcagtcatttcctctccacttctcaagtccttgcactctgctggacccccgctccttgctgttactgcagctcctccagcccagccccttgccaagaaaaaaggcgtaaagcggaaagcagatactaccacccctacacctacagccatcttggctcctggttctccagctagccctcctgggagtcttgagcctaaggcagcacggcttccccctatgcgtagagagagtggtcgccccatcaagcccccacgcaaagacttgcctgactctcagcaacaacaccagagctctaagaaaggaaagctttcagaacagttaaaacattgcaatggcattttgaaggagttactctctaagaagcatgctgcctatgcttggcctttctataaaccagtggatgcttctgcacttggcctgcatgactaccatgacatcattaagcaccccatggacctcagcactgtcaagcggaagatggagaaccgtgattaccgggatgcacaggagtttgctgctgatgtacggcttatgttctccaactgctataagtacaatcccccagatcacgatgttgtggcaatggcacgaaagctacaggatgtatttgagttccgttatgccaagatgccagatgaaccactagaaccagggcctttaccagtctctactgccatgccccctggcttggccaaatcgtcttcagagtcctccagtgaggaaagtagcagtgagagctcctctgaggaagaggaggaggaagatgaggaggacgaggaggaagaagagagtgaaagctcagactcagaggaagaaagggctcatcgcttagcagaactacaggaacagcttcgggcagtacatgaacaactggctgctctgtcccagggtccaatatccaagcccaagaggaaaagagagaaaaaagagaaaaagaagaaacggaaggcagagaagcatcgaggccgagctggggccgatgaagatgacaaggggcctagggcaccccgcccacctcaacctaagaagtccaagaaagcaagtggcagtgggggtggcagtgctgctttaggcccttctggctttggaccttctggaggaagtggcaccaagctccccaaaaaggccacaaagacagccccacctgccctgcctacaggttatgattcagaggaggaggaagagagcaggcccatgagttacgatgagaagcggcagctgagcctggacatcaacaaattacctggggagaagctgggccgagttgtgcatataatccaagccagggagccctctttacgtgattcaaacccagaagagattgagattgattttgaaacactcaagccatccacacttagagagcttgagcgctatgtcctttcctgcctacgtaagaaaccccggaagccctacaccattaagaagcctgtgggaaagacaaaggaggaactggctttggagaaaaagcgggaattagaaaagcggttacaagatgtcagcggacagctcaattctactaaaaagccccccaagaaagcgaatgagaaaacagagtcatcctctgcacagcaagtagcagtgtcacgccttagcgcttccagctccagctcagattccagctcctcctcttcctcgtcgtcgtcttcagacaccagtgattcagactcaggctaaggggtcaggccagatggggcaggaaggctccgcaggaccggacccctagaccaccctgccccacctgccccttccccctttgctgtgacacttcttcatctcacccccccccgcccccctctaggagagctggctctgcagtgggggagggatgcagggacatttactgaaggagggacatggacaaaacaacattgaattcccagccccattggggagtgatctcttggacacagagcccccattcaaaatggggcagggcaagggtgggagtgtgcaaagccctgatctggagttacctgaggccacagctgccctattcacttctaagggccctgttttgagattgtttgttctaatttattttaagctaggtaaggctggggggagggtggggccgtggtcccctcagcctccatggggagggaagaagggggagctctttttttacgttgatttttttttttctactctgttttccctttttccttccgctccatttggggccctgggggtttcagtcatctccccatttggtcccctggactgtctttgttgattctaacttgtaaataaagaaaatattattcaagttttgagttaccttaatatttgcttttgtagtgtttcaaaaggaacatcataagaattgtcttgataattttgagggaaatattactgcagtgagaaaaggcaatagctaacctataattggattgtcttaatttttaaaccagtaggcttttgctgtgtttttaataaagtaaatatgacttttgtaaattgaaaaaaaaaaaaaa
//
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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