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2024-04-20 02:16:42, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001113182 4807 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens bromodomain containing 2 (BRD2), transcript variant 2,
mRNA.
ACCESSION NM_001113182
VERSION NM_001113182.2 GI:313747415
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 4807)
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 4807)
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 4807)
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 4807)
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 4807)
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 4807)
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 4807)
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 4807)
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 4807)
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 4807)
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 BX648109.1, AK056504.1,
DC379337.1, AL832722.1, D42040.1 and AL645941.11.
On Dec 8, 2010 this sequence version replaced gi:164419757.
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 (2) has an alternate 5' UTR
compared to variant 1. Both variants 1 and 2 encode the same
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 :: BX648109.1 [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
1-448 BX648109.1 3-450
449-832 AK056504.1 407-790
833-841 DC379337.1 569-577
842-1947 AL832722.1 777-1882
1948-4328 D42040.1 2035-4415
4329-4807 AL645941.11 58464-58942
FEATURES Location/Qualifiers
source 1..4807
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="6"
/map="6p21.3"
gene 1..4807
/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..310
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 85
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:372863406"
variation 108..109
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:144230375"
variation 109..110
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:374442608"
variation 116
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:12173490"
variation 117
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:12173481"
variation 135
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146563954"
variation 146
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:370076653"
variation 171
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:72865875"
variation 193
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199838338"
variation 196
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:138957550"
variation 221
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:16871256"
variation 223
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:13197222"
variation 224
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:13197529"
variation 247
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:79643712"
variation 250
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:200683213"
variation 307
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201521645"
exon 311..1643
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 317
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201973858"
variation 318..319
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="gct"
/db_xref="dbSNP:370968322"
variation 321
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200600639"
variation 322
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201482654"
variation 335
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199600996"
variation 336
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200451599"
variation 337
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201226550"
variation 339
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199868873"
variation 347
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:200627256"
variation 360
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201948846"
variation 380
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150478937"
variation 386
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200949008"
variation 408
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201755026"
variation 413
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:199915030"
variation 442
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201010733"
variation 462
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201665646"
variation 465
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:372327634"
variation 477
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200120201"
variation 494
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201133050"
variation 495
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142535126"
variation 501
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200226207"
variation 534
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368867808"
variation 551
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201326064"
variation 556
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201797920"
variation 558
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:146768927"
variation 640..641
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="g"
/db_xref="dbSNP:368949163"
variation 652..653
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:34330235"
STS 660..773
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb278"
/db_xref="UniSTS:240930"
variation 679
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:73409619"
variation 692
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143541374"
variation 722
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:116880340"
variation 724
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049278"
variation 760
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:190237002"
variation 833
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:974357"
variation 957
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1803865"
variation 965
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:116415048"
variation 1014
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555087"
variation 1033
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:181742420"
variation 1081
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:11555940"
variation 1099
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:35607307"
variation 1134
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55912052"
variation 1202
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:12234140"
variation 1220
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:185537776"
variation 1241..1243
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="tcg"
/db_xref="dbSNP:150942919"
variation 1257
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1063344"
variation 1262
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:113542396"
variation 1278
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141167814"
variation 1283
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:17617655"
variation 1402
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:111483230"
variation 1406
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:369570787"
variation 1420
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:17220465"
variation 1491
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:11555088"
variation 1493
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:78280497"
variation 1528
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200590068"
variation 1529
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201899070"
variation 1543
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555089"
variation 1556
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:6916791"
variation 1560
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2071571"
variation 1571
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368022125"
variation 1578
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:370485049"
misc_feature 1585..1587
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="upstream in-frame stop codon"
variation 1605
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:373976120"
variation 1606
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:367803227"
variation 1611
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201642612"
CDS 1615..4020
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="isoform 1 is encoded by transcript variant 2;
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_001106653.1"
/db_xref="GI:164419758"
/db_xref="CCDS:CCDS4762.1"
/db_xref="GeneID:6046"
/db_xref="HGNC:1103"
/db_xref="MIM:601540"
/translation="
MLQNVTPHNKLPGEGNAGLLGLGPEAAAPGKRIRKPSLLYEGFESPTMASVPALQLTPANPPPPEVSNPKKPGRVTNQLQYLHKVVMKALWKHQFAWPFRQPVDAVKLGLPDYHKIIKQPMDMGTIKRRLENNYYWAASECMQDFNTMFTNCYIYNKPTDDIVLMAQTLEKIFLQKVASMPQEEQELVVTIPKNSHKKGAKLAALQGSVTSAHQVPAVSSVSHTALYTPPPEIPTTVLNIPHPSVISSPLLKSLHSAGPPLLAVTAAPPAQPLAKKKGVKRKADTTTPTPTAILAPGSPASPPGSLEPKAARLPPMRRESGRPIKPPRKDLPDSQQQHQSSKKGKLSEQLKHCNGILKELLSKKHAAYAWPFYKPVDASALGLHDYHDIIKHPMDLSTVKRKMENRDYRDAQEFAADVRLMFSNCYKYNPPDHDVVAMARKLQDVFEFRYAKMPDEPLEPGPLPVSTAMPPGLAKSSSESSSEESSSESSSEEEEEEDEEDEEEEESESSDSEEERAHRLAELQEQLRAVHEQLAALSQGPISKPKRKREKKEKKKKRKAEKHRGRAGADEDDKGPRAPRPPQPKKSKKASGSGGGSAALGPSGFGPSGGSGTKLPKKATKTAPPALPTGYDSEEEEESRPMSYDEKRQLSLDINKLPGEKLGRVVHIIQAREPSLRDSNPEEIEIDFETLKPSTLRELERYVLSCLRKKPRKPYTIKKPVGKTKEELALEKKRELEKRLQDVSGQLNSTKKPPKKANEKTESSSAQQVAVSRLSASSSSSDSSSSSSSSSSSDTSDSDSG
"
misc_feature 1615..1617
/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 1630..1632
/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 1723..1725
/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 1834..2154
/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(1921..1923,1942..1944,1951..1953,2068..2070,
2080..2082,2098..2100)
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="acetyllysine binding site; other site"
/db_xref="CDD:99929"
misc_feature 2506..2508
/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 2515..2517
/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 2527..2529
/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 2659..2964
/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(2740..2742,2761..2763,2770..2772,2887..2889,
2899..2901,2917..2919)
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="acetyllysine binding site; other site"
/db_xref="CDD:99930"
misc_feature 3277..3291
/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 3511..3513
/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"
variation 1626
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:147219068"
variation 1633
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:140566548"
variation 1634
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142520217"
variation 1636
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:377684930"
variation 1637
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201319601"
exon 1644..1947
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 1647
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:35974351"
variation 1669
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3752528"
variation 1682
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55650502"
variation 1685
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:368437378"
variation 1687
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:371937442"
variation 1707
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:516535"
variation 1729
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:143451360"
variation 1730
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:376209743"
variation 1733
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200307380"
variation 1734
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:148450256"
variation 1737
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:11555090"
variation 1756
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:369193752"
variation 1759
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:55669504"
variation 1760
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:3918144"
variation 1760
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="gc"
/replace="tg"
/db_xref="dbSNP:375083792"
variation 1791
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:138097363"
variation 1794
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:56109539"
variation 1805
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:146881536"
variation 1806
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199590043"
variation 1815
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:115120098"
variation 1821
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:376374651"
variation 1822
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="a"
/db_xref="dbSNP:35261809"
variation 1829
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201647382"
variation 1844
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368792346"
variation 1848
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374628062"
variation 1863
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150476702"
variation 1899
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:375791386"
variation 1902
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374599253"
variation 1928
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:138290874"
exon 1948..2085
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 1956
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:201582271"
variation 1971
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:375792679"
variation 1980
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:180909220"
variation 2001
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201754613"
variation 2010
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:9378166"
variation 2016
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:76146382"
STS 2018..2193
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="RH79050"
/db_xref="UniSTS:39777"
variation 2043
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:373853679"
variation 2056
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143509698"
exon 2086..2224
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2102
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1803864"
variation 2103
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199821934"
STS 2104..2337
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="STS-T87864"
/db_xref="UniSTS:53679"
variation 2109
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:367609858"
variation 2131
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:137960007"
variation 2134
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370287964"
STS 2144..2280
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="G67884"
/db_xref="UniSTS:225610"
variation 2158
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:200486677"
STS 2179..2254
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb741"
/db_xref="UniSTS:240935"
variation 2190
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:375469443"
variation 2196
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201572264"
variation 2197
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199497657"
exon 2225..2439
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2235
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:186277039"
STS 2237..2377
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb250"
/db_xref="UniSTS:240929"
variation 2248
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:35952031"
variation 2251
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370807550"
variation 2266
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200381760"
variation 2281
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200917553"
variation 2287..2288
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:35264453"
variation 2292
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:15912"
variation 2326
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:176250"
variation 2327
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:41270502"
variation 2340
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141377590"
variation 2393
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:35294809"
variation 2419
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:148978000"
exon 2440..2814
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2448
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:374284677"
variation 2478
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:375353506"
variation 2533
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:150794546"
variation 2548
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139156709"
variation 2556
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146092849"
variation 2562
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:369113238"
variation 2622
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200612980"
variation 2675
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:371260391"
variation 2676
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:17214085"
variation 2679
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:62407971"
variation 2697
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146801767"
variation 2750
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:140492558"
variation 2751
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:17214092"
variation 2778
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142982923"
variation 2805
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:192648574"
exon 2815..2943
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2840
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:141044200"
variation 2866
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200770939"
variation 2905
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150234115"
variation 2913
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139231674"
variation 2919
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142112689"
exon 2944..3192
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2955
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55650066"
variation 2964
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200803710"
variation 2992
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201781653"
variation 2998
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:199605967"
variation 3009
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:145849910"
variation 3018
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:138688346"
variation 3019
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201908033"
variation 3024
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200182536"
variation 3030
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200897288"
variation 3034
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:184752888"
variation 3035
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:3918143"
variation 3042
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368290193"
variation 3073
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143615833"
variation 3108
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:200663348"
variation 3109..3111
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="gag"
/db_xref="dbSNP:3918142"
variation 3111
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:200978040"
variation 3112
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:12822"
variation 3114..3115
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="gga"
/db_xref="dbSNP:41310958"
variation 3114
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201796698"
STS 3115..3240
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="SGC31960"
/db_xref="UniSTS:63641"
variation 3117
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200103856"
variation 3118
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201071191"
variation 3123
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:144872939"
variation 3126
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:148048133"
variation 3129
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55778408"
variation 3156
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201425304"
variation 3164
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:202033057"
variation 3165
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141740031"
variation 3167
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:35773608"
exon 3193..3455
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
STS 3202..3307
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb369"
/db_xref="UniSTS:240931"
variation 3213
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:191317139"
variation 3245..3246
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555938"
variation 3246
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:11037"
variation 3252
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:35845948"
variation 3254
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049369"
variation 3255
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049372"
variation 3264
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3189517"
variation 3265
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200980274"
variation 3266
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374788375"
variation 3294
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:142074834"
variation 3311
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:146321913"
variation 3318
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201989394"
variation 3319
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:34530779"
variation 3324
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1063379"
variation 3352
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:144552033"
variation 3409
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:55952113"
variation 3423
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:206781"
variation 3449
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:111308504"
exon 3456..3760
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 3456
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:141736131"
variation 3464
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:145888786"
variation 3536
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:138736016"
variation 3633
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368407034"
variation 3716
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:140400525"
exon 3761..3883
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 3815
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:375635536"
variation 3867
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:140096077"
variation 3876
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2066750"
variation 3878
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:150287231"
exon 3884..4807
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 3884
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:137898499"
variation 3885
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199954603"
STS 3889..4740
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="BRD2_3857"
/db_xref="UniSTS:462062"
variation 3896
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200578995"
variation 3899
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:149549323"
variation 3903
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201375031"
variation 3905
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200164898"
variation 3910
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:144861747"
variation 3932
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:202018564"
variation 3939
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199887337"
variation 3951
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2071876"
variation 3953
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:369127190"
variation 3966
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:202086051"
variation 3983
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200397640"
variation 3987
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3918140"
variation 4016
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:202161102"
variation 4022
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200531629"
variation 4023
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:371782351"
variation 4037
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201611634"
variation 4051
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199587809"
variation 4071
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:200408799"
variation 4073
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201062187"
variation 4075
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199866893"
variation 4102
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:147269908"
variation 4124
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201692899"
variation 4129
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:199530843"
variation 4132..4133
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201992712"
variation 4132..4133
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/replace="t"
/db_xref="dbSNP:28986268"
variation 4132
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/replace="cc"
/replace="ct"
/replace="t"
/db_xref="dbSNP:368289232"
variation 4132
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049414"
variation 4133..4134
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:373358187"
STS 4140..4252
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="D6S1894"
/db_xref="UniSTS:67698"
variation 4164
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:139189753"
STS 4175..4372
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="RH18121"
/db_xref="UniSTS:26631"
variation 4210
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:72865897"
variation 4246
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:78300601"
variation 4261
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:10829"
variation 4284
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:372641732"
variation 4329
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049526"
variation 4339
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:370640038"
variation 4370
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:201572601"
variation 4379
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555939"
variation 4383
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1803596"
variation 4420
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:185910133"
variation 4425
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:112975861"
variation 4451
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:373317674"
variation 4463..4464
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:71656056"
variation 4477
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="a"
/db_xref="dbSNP:3841159"
variation 4477
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:113758837"
variation 4479..4480
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:71645781"
STS 4482..4582
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="NIB1722"
/db_xref="UniSTS:42553"
variation 4494..4495
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="tg"
/db_xref="dbSNP:199828295"
variation 4525
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1803863"
variation 4527
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:34128205"
variation 4534
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:191209130"
variation 4556
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:115821350"
variation 4639
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:182780962"
STS 4653..4767
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="A008D22"
/db_xref="UniSTS:22045"
variation 4663
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:187202774"
variation 4677
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049639"
variation 4696
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:16871296"
variation 4720
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:60466011"
variation 4754
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:73409643"
polyA_signal 4778..4783
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
polyA_site 4807
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
ORIGIN
ggagggggagggctagtctgagccgcagccgccgcctcctccgctcgccctcctccctggcgctgaccgatggaccagccgctccgtggggaggactccggaccctggtgggggggcgggggggttctttcgcccccgtggcggagggcccctgagaggcggatacgggtgtgcctttgggggtgatgtggcgtgtggggggaaaggtccgagctcgcctggagggggagggtttttcccttaagtcatccctcccaggacttgctttttctgctctgagccggacgccggaatggagtttgaggaagagattcttcgctgctgctgccttaccgccgagaaccaccacccgccaggcgtcttgcggccacacccctggcgggttcaggcaggctacgcccacgcgacccctcccgtttccctgctttggccaatggaggagctacgaatggcacgacctgctcgagcttggcagtctccagttgggctgtgcatggaagcttgggaagactttgttggaaggggaggcggggagagagtgctggaggctctggggcgatggcttccgcacctcttccaaccaccctctttccctggagtcggcggaccacagctcagccaattggcttggagatgtggcgggttgccacttccctgtgggtctctgcggcactcttctgcctggtgactgacaccttggaaatgaagtttatgacgtcatcgttgcggctggccaatagaaaaagctcccgcggagaggtgttccttccccttcgactcagcttcttcacccgcgtgagcgagcgcgcgcgcgcggagggggtggggaaaagctcaagcagggtggcgcgcatgagcggcgaagctcctcctccccgcctatatataaagggctggcgcggggctcggcggcgccatttcgtgctggagtggagcagcctctagaacgagctggaggattctgcctaccgatacagagccttcgagtcgtccggggccgccattacaatccacctccatccgcttggaaatggccttcgtcccggcctatgactggtcccagcgggcagtacagaccccctagaagcccctggagctcccctttttcgggccccgcccaatcctcggagtctgtccaccccctctactccgccctcaagaggatttcaaagatggaggcggcggctccctaaaccacttttcgtgttcatccgcctccatccgagatcgaaacgggacctcgtcggccccgtaggggcccgacaagaagagggaatccctgcagaccaacagcgggctatattgacgacggtgtctgagatcggggaccgtcttttgaagagtcagtccctccttagttgcccgcctcagctgaggccgccgccattttcttgctgtccgccgtctgcagagcgcgccaagctgcccggagctctccgagaggccccaaagagactgctttcgtgccggccaggcagggggtttgtcgcctggaggcccaagaggaacggcctccccccaacttagcgggttatgctggaccgggcggtgaggggaaccgaggccacccggactttccgcggctgagggcagcgccggttccttgcggtcaagatgctgcaaaacgtgactccccacaataagctccctggggaagggaatgcagggttgctggggctgggcccagaagcagcagcaccagggaagaggattcgaaaaccctctctcttgtatgagggctttgagagccccacaatggcttcggtgcctgctttgcaacttacccctgccaacccaccacccccggaggtgtccaatcccaaaaagccaggacgagttaccaaccagctgcaatacctacacaaggtagtgatgaaggctctgtggaaacatcagttcgcatggccattccggcagcctgtggatgctgtcaaactgggtctaccggattatcacaaaattataaaacagcctatggacatgggtactattaagaggagacttgaaaacaattattattgggctgcttcagagtgtatgcaagattttaataccatgttcaccaactgttacatttacaacaagcccactgatgatattgtcctaatggcacaaacgctggaaaagatattcctacagaaggttgcatcaatgccacaagaagaacaagagctggtagtgaccatccctaagaacagccacaagaagggggccaagttggcagcgctccagggcagtgttaccagtgcccatcaggtgcctgccgtctcttctgtgtcacacacagccctgtatactcctccacctgagatacctaccactgtcctcaacattccccacccatcagtcatttcctctccacttctcaagtccttgcactctgctggacccccgctccttgctgttactgcagctcctccagcccagccccttgccaagaaaaaaggcgtaaagcggaaagcagatactaccacccctacacctacagccatcttggctcctggttctccagctagccctcctgggagtcttgagcctaaggcagcacggcttccccctatgcgtagagagagtggtcgccccatcaagcccccacgcaaagacttgcctgactctcagcaacaacaccagagctctaagaaaggaaagctttcagaacagttaaaacattgcaatggcattttgaaggagttactctctaagaagcatgctgcctatgcttggcctttctataaaccagtggatgcttctgcacttggcctgcatgactaccatgacatcattaagcaccccatggacctcagcactgtcaagcggaagatggagaaccgtgattaccgggatgcacaggagtttgctgctgatgtacggcttatgttctccaactgctataagtacaatcccccagatcacgatgttgtggcaatggcacgaaagctacaggatgtatttgagttccgttatgccaagatgccagatgaaccactagaaccagggcctttaccagtctctactgccatgccccctggcttggccaaatcgtcttcagagtcctccagtgaggaaagtagcagtgagagctcctctgaggaagaggaggaggaagatgaggaggacgaggaggaagaagagagtgaaagctcagactcagaggaagaaagggctcatcgcttagcagaactacaggaacagcttcgggcagtacatgaacaactggctgctctgtcccagggtccaatatccaagcccaagaggaaaagagagaaaaaagagaaaaagaagaaacggaaggcagagaagcatcgaggccgagctggggccgatgaagatgacaaggggcctagggcaccccgcccacctcaacctaagaagtccaagaaagcaagtggcagtgggggtggcagtgctgctttaggcccttctggctttggaccttctggaggaagtggcaccaagctccccaaaaaggccacaaagacagccccacctgccctgcctacaggttatgattcagaggaggaggaagagagcaggcccatgagttacgatgagaagcggcagctgagcctggacatcaacaaattacctggggagaagctgggccgagttgtgcatataatccaagccagggagccctctttacgtgattcaaacccagaagagattgagattgattttgaaacactcaagccatccacacttagagagcttgagcgctatgtcctttcctgcctacgtaagaaaccccggaagccctacaccattaagaagcctgtgggaaagacaaaggaggaactggctttggagaaaaagcgggaattagaaaagcggttacaagatgtcagcggacagctcaattctactaaaaagccccccaagaaagcgaatgagaaaacagagtcatcctctgcacagcaagtagcagtgtcacgccttagcgcttccagctccagctcagattccagctcctcctcttcctcgtcgtcgtcttcagacaccagtgattcagactcaggctaaggggtcaggccagatggggcaggaaggctccgcaggaccggacccctagaccaccctgccccacctgccccttccccctttgctgtgacacttcttcatctcacccccccccgcccccctctaggagagctggctctgcagtgggggagggatgcagggacatttactgaaggagggacatggacaaaacaacattgaattcccagccccattggggagtgatctcttggacacagagcccccattcaaaatggggcagggcaagggtgggagtgtgcaaagccctgatctggagttacctgaggccacagctgccctattcacttctaagggccctgttttgagattgtttgttctaatttattttaagctaggtaaggctggggggagggtggggccgtggtcccctcagcctccatggggagggaagaagggggagctctttttttacgttgatttttttttttctactctgttttccctttttccttccgctccatttggggccctgggggtttcagtcatctccccatttggtcccctggactgtctttgttgattctaacttgtaaataaagaaaatattattcaagttttgagttaccttaatatttgcttttgtagtgtttcaaaaggaacatcataagaattgtcttgataattttgagggaaatattactgcagtgagaaaaggcaatagctaacctataattggattgtcttaatttttaaaccagtaggcttttgctgtgtttttaataaagtaaatatgacttttgtaaattga
//
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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