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2024-04-20 22:59:15, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001199456 3210 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens bromodomain containing 2 (BRD2), transcript variant 4,
mRNA.
ACCESSION NM_001199456
VERSION NM_001199456.1 GI:313747418
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 3210)
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 3210)
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 3210)
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 3210)
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 3210)
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 3210)
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 3210)
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 3210)
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 3210)
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 3210)
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 BX647233.1, D42040.1 and
AL645941.11.
Summary: This gene encodes a transcriptional regulator that belongs
to the BET (bromodomains and extra terminal domain) family of
proteins. This protein associates with transcription complexes and
with acetylated chromatin during mitosis, and it selectively binds
to the acetylated lysine-12 residue of histone H4 via its two
bromodomains. The gene maps to the major histocompatability complex
(MHC) class II region on chromosome 6p21.3, but sequence comparison
suggests that the protein is not involved in the immune response.
This gene has been implicated in juvenile myoclonic epilepsy, a
common form of epilepsy that becomes apparent in adolescence.
Multiple alternatively spliced variants have been described for
this gene. [provided by RefSeq, Dec 2010].
Transcript Variant: This variant (4) has an alternate 5' exon,
resulting in a downstream AUG start codon compared to variant 1.
The resulting isoform (3) is shorter at the N-terminus, as compared
to 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 :: BX647233.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025085 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-1485 BX647233.1 1-1485
1486-2731 D42040.1 3170-4415
2732-3210 AL645941.11 58464-58942
FEATURES Location/Qualifiers
source 1..3210
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="6"
/map="6p21.3"
gene 1..3210
/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..46
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
exon 47..350
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 50
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:35974351"
variation 72
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3752528"
variation 85
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55650502"
variation 88
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:368437378"
variation 90
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:371937442"
variation 110
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:516535"
variation 132
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:143451360"
variation 133
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:376209743"
variation 136
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200307380"
variation 137
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:148450256"
variation 140
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:11555090"
CDS 159..2423
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="isoform 3 is encoded by transcript variant 4;
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 3"
/protein_id="NP_001186385.1"
/db_xref="GI:313747419"
/db_xref="CCDS:CCDS56421.1"
/db_xref="GeneID:6046"
/db_xref="HGNC:1103"
/db_xref="MIM:601540"
/translation="
MASVPALQLTPANPPPPEVSNPKKPGRVTNQLQYLHKVVMKALWKHQFAWPFRQPVDAVKLGLPDYHKIIKQPMDMGTIKRRLENNYYWAASECMQDFNTMFTNCYIYNKPTDDIVLMAQTLEKIFLQKVASMPQEEQELVVTIPKNSHKKGAKLAALQGSVTSAHQVPAVSSVSHTALYTPPPEIPTTVLNIPHPSVISSPLLKSLHSAGPPLLAVTAAPPAQPLAKKKGVKRKADTTTPTPTAILAPGSPASPPGSLEPKAARLPPMRRESGRPIKPPRKDLPDSQQQHQSSKKGKLSEQLKHCNGILKELLSKKHAAYAWPFYKPVDASALGLHDYHDIIKHPMDLSTVKRKMENRDYRDAQEFAADVRLMFSNCYKYNPPDHDVVAMARKLQDVFEFRYAKMPDEPLEPGPLPVSTAMPPGLAKSSSESSSEESSSESSSEEEEEEDEEDEEEEESESSDSEEERAHRLAELQEQLRAVHEQLAALSQGPISKPKRKREKKEKKKKRKAEKHRGRAGADEDDKGPRAPRPPQPKKSKKASGSGGGSAALGPSGFGPSGGSGTKLPKKATKTAPPALPTGYDSEEEEESRPMSYDEKRQLSLDINKLPGEKLGRVVHIIQAREPSLRDSNPEEIEIDFETLKPSTLRELERYVLSCLRKKPRKPYTIKKPVGKTKEELALEKKRELEKRLQDVSGQLNSTKKPPKKANEKTESSSAQQVAVSRLSASSSSSDSSSSSSSSSSSDTSDSDSG
"
misc_feature 237..557
/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(324..326,345..347,354..356,471..473,483..485,
501..503)
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="acetyllysine binding site; other site"
/db_xref="CDD:99929"
misc_feature 1062..1367
/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(1143..1145,1164..1166,1173..1175,1290..1292,
1302..1304,1320..1322)
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/note="acetyllysine binding site; other site"
/db_xref="CDD:99930"
variation 159
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:369193752"
variation 162
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:55669504"
variation 163
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:3918144"
variation 163
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="gc"
/replace="tg"
/db_xref="dbSNP:375083792"
variation 194
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:138097363"
variation 197
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:56109539"
variation 208
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:146881536"
variation 209
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199590043"
variation 218
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:115120098"
variation 224
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:376374651"
variation 225
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="a"
/db_xref="dbSNP:35261809"
variation 232
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201647382"
variation 247
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368792346"
variation 251
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374628062"
variation 266
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150476702"
variation 302
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:375791386"
variation 305
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374599253"
variation 331
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:138290874"
exon 351..488
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 359
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:201582271"
variation 374
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:375792679"
variation 383
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:180909220"
variation 404
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201754613"
variation 413
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:9378166"
variation 419
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:76146382"
STS 421..596
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="RH79050"
/db_xref="UniSTS:39777"
variation 446
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:373853679"
variation 459
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143509698"
exon 489..627
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 505
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1803864"
variation 506
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199821934"
STS 507..740
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="STS-T87864"
/db_xref="UniSTS:53679"
variation 512
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:367609858"
variation 534
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:137960007"
variation 537
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370287964"
STS 547..683
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="G67884"
/db_xref="UniSTS:225610"
variation 561
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:200486677"
STS 582..657
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb741"
/db_xref="UniSTS:240935"
variation 593
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:375469443"
variation 599
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201572264"
variation 600
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199497657"
exon 628..842
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 638
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:186277039"
STS 640..780
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb250"
/db_xref="UniSTS:240929"
variation 651
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:35952031"
variation 654
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370807550"
variation 669
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200381760"
variation 684
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200917553"
variation 690..691
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:35264453"
variation 695
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:15912"
variation 729
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:176250"
variation 730
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:41270502"
variation 743
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141377590"
variation 796
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:35294809"
variation 822
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:148978000"
exon 843..1217
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 851
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:374284677"
variation 881
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:375353506"
variation 936
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:150794546"
variation 951
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139156709"
variation 959
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146092849"
variation 965
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:369113238"
variation 1025
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200612980"
variation 1078
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:371260391"
variation 1079
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:17214085"
variation 1082
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:62407971"
variation 1100
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146801767"
variation 1153
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:140492558"
variation 1154
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:17214092"
variation 1181
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142982923"
variation 1208
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:192648574"
exon 1218..1346
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 1243
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:141044200"
variation 1269
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200770939"
variation 1308
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150234115"
variation 1316
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139231674"
variation 1322
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142112689"
exon 1347..1595
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 1358
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55650066"
variation 1367
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200803710"
variation 1395
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201781653"
variation 1401
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:199605967"
variation 1412
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:145849910"
variation 1421
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:138688346"
variation 1422
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201908033"
variation 1427
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200182536"
variation 1433
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200897288"
variation 1437
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:184752888"
variation 1438
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:3918143"
variation 1445
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368290193"
variation 1476
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143615833"
variation 1511
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:200663348"
variation 1512..1514
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="gag"
/db_xref="dbSNP:3918142"
variation 1514
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:200978040"
variation 1515
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:12822"
variation 1517..1518
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="gga"
/db_xref="dbSNP:41310958"
variation 1517
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201796698"
STS 1518..1643
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="SGC31960"
/db_xref="UniSTS:63641"
variation 1520
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200103856"
variation 1521
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201071191"
variation 1526
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:144872939"
variation 1529
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:148048133"
variation 1532
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:55778408"
variation 1559
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201425304"
variation 1567
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:202033057"
variation 1568
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141740031"
variation 1570
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:35773608"
exon 1596..1858
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
STS 1605..1710
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="CGCb369"
/db_xref="UniSTS:240931"
variation 1616
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:191317139"
variation 1648..1649
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555938"
variation 1649
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:11037"
variation 1655
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:35845948"
variation 1657
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049369"
variation 1658
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049372"
variation 1667
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3189517"
variation 1668
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200980274"
variation 1669
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374788375"
variation 1697
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:142074834"
variation 1714
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:146321913"
variation 1721
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201989394"
variation 1722
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:34530779"
variation 1727
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1063379"
variation 1755
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:144552033"
variation 1812
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:55952113"
variation 1826
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:206781"
variation 1852
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:111308504"
exon 1859..2163
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 1859
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:141736131"
variation 1867
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:145888786"
variation 1939
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:138736016"
variation 2036
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:368407034"
variation 2119
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:140400525"
exon 2164..2286
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2218
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:375635536"
variation 2270
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:140096077"
variation 2279
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2066750"
variation 2281
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:150287231"
exon 2287..3210
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/inference="alignment:Splign:1.39.8"
variation 2287
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:137898499"
variation 2288
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199954603"
STS 2292..3143
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="BRD2_3857"
/db_xref="UniSTS:462062"
variation 2299
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200578995"
variation 2302
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:149549323"
variation 2306
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201375031"
variation 2308
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200164898"
variation 2313
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:144861747"
variation 2335
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:202018564"
variation 2342
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199887337"
variation 2354
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2071876"
variation 2356
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:369127190"
variation 2369
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:202086051"
variation 2386
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200397640"
variation 2390
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:3918140"
variation 2419
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:202161102"
variation 2425
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200531629"
variation 2426
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:371782351"
variation 2440
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201611634"
variation 2454
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199587809"
variation 2474
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:200408799"
variation 2476
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201062187"
variation 2478
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199866893"
variation 2505
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:147269908"
variation 2527
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201692899"
variation 2532
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:199530843"
variation 2535..2536
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201992712"
variation 2535..2536
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/replace="t"
/db_xref="dbSNP:28986268"
variation 2535
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/replace="cc"
/replace="ct"
/replace="t"
/db_xref="dbSNP:368289232"
variation 2535
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049414"
variation 2536..2537
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:373358187"
STS 2543..2655
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="D6S1894"
/db_xref="UniSTS:67698"
variation 2567
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:139189753"
STS 2578..2775
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="RH18121"
/db_xref="UniSTS:26631"
variation 2613
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:72865897"
variation 2649
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:78300601"
variation 2664
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="c"
/db_xref="dbSNP:10829"
variation 2687
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:372641732"
variation 2732
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049526"
variation 2742
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:370640038"
variation 2773
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:201572601"
variation 2782
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11555939"
variation 2786
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1803596"
variation 2823
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:185910133"
variation 2828
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:112975861"
variation 2854
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:373317674"
variation 2866..2867
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:71656056"
variation 2880
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="a"
/db_xref="dbSNP:3841159"
variation 2880
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="t"
/db_xref="dbSNP:113758837"
variation 2882..2883
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="t"
/db_xref="dbSNP:71645781"
STS 2885..2985
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="NIB1722"
/db_xref="UniSTS:42553"
variation 2897..2898
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="tg"
/db_xref="dbSNP:199828295"
variation 2928
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1803863"
variation 2930
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace=""
/replace="c"
/db_xref="dbSNP:34128205"
variation 2937
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="g"
/db_xref="dbSNP:191209130"
variation 2959
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="g"
/replace="t"
/db_xref="dbSNP:115821350"
variation 3042
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:182780962"
STS 3056..3170
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/standard_name="A008D22"
/db_xref="UniSTS:22045"
variation 3066
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:187202774"
variation 3080
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049639"
variation 3099
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:16871296"
variation 3123
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="a"
/replace="g"
/db_xref="dbSNP:60466011"
variation 3157
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
/replace="c"
/replace="t"
/db_xref="dbSNP:73409643"
polyA_signal 3181..3186
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
polyA_site 3210
/gene="BRD2"
/gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3"
ORIGIN
ggaacggtggtggcggctcggctactgctcgtggaggggaatacaggctccctggggaagggaatgcagggttgctggggctgggcccagaagcagcagcaccagggaagaggattcgaaaaccctctctcttgtatgagggctttgagagccccacaatggcttcggtgcctgctttgcaacttacccctgccaacccaccacccccggaggtgtccaatcccaaaaagccaggacgagttaccaaccagctgcaatacctacacaaggtagtgatgaaggctctgtggaaacatcagttcgcatggccattccggcagcctgtggatgctgtcaaactgggtctaccggattatcacaaaattataaaacagcctatggacatgggtactattaagaggagacttgaaaacaattattattgggctgcttcagagtgtatgcaagattttaataccatgttcaccaactgttacatttacaacaagcccactgatgatattgtcctaatggcacaaacgctggaaaagatattcctacagaaggttgcatcaatgccacaagaagaacaagagctggtagtgaccatccctaagaacagccacaagaagggggccaagttggcagcgctccagggcagtgttaccagtgcccatcaggtgcctgccgtctcttctgtgtcacacacagccctgtatactcctccacctgagatacctaccactgtcctcaacattccccacccatcagtcatttcctctccacttctcaagtccttgcactctgctggacccccgctccttgctgttactgcagctcctccagcccagccccttgccaagaaaaaaggcgtaaagcggaaagcagatactaccacccctacacctacagccatcttggctcctggttctccagctagccctcctgggagtcttgagcctaaggcagcacggcttccccctatgcgtagagagagtggtcgccccatcaagcccccacgcaaagacttgcctgactctcagcaacaacaccagagctctaagaaaggaaagctttcagaacagttaaaacattgcaatggcattttgaaggagttactctctaagaagcatgctgcctatgcttggcctttctataaaccagtggatgcttctgcacttggcctgcatgactaccatgacatcattaagcaccccatggacctcagcactgtcaagcggaagatggagaaccgtgattaccgggatgcacaggagtttgctgctgatgtacggcttatgttctccaactgctataagtacaatcccccagatcacgatgttgtggcaatggcacgaaagctacaggatgtatttgagttccgttatgccaagatgccagatgaaccactagaaccagggcctttaccagtctctactgccatgccccctggcttggccaaatcgtcttcagagtcctccagtgaggaaagtagcagtgagagctcctctgaggaagaggaggaggaagatgaggaggacgaggaggaagaagagagtgaaagctcagactcagaggaagaaagggctcatcgcttagcagaactacaggaacagcttcgggcagtacatgaacaactggctgctctgtcccagggtccaatatccaagcccaagaggaaaagagagaaaaaagagaaaaagaagaaacggaaggcagagaagcatcgaggccgagctggggccgatgaagatgacaaggggcctagggcaccccgcccacctcaacctaagaagtccaagaaagcaagtggcagtgggggtggcagtgctgctttaggcccttctggctttggaccttctggaggaagtggcaccaagctccccaaaaaggccacaaagacagccccacctgccctgcctacaggttatgattcagaggaggaggaagagagcaggcccatgagttacgatgagaagcggcagctgagcctggacatcaacaaattacctggggagaagctgggccgagttgtgcatataatccaagccagggagccctctttacgtgattcaaacccagaagagattgagattgattttgaaacactcaagccatccacacttagagagcttgagcgctatgtcctttcctgcctacgtaagaaaccccggaagccctacaccattaagaagcctgtgggaaagacaaaggaggaactggctttggagaaaaagcgggaattagaaaagcggttacaagatgtcagcggacagctcaattctactaaaaagccccccaagaaagcgaatgagaaaacagagtcatcctctgcacagcaagtagcagtgtcacgccttagcgcttccagctccagctcagattccagctcctcctcttcctcgtcgtcgtcttcagacaccagtgattcagactcaggctaaggggtcaggccagatggggcaggaaggctccgcaggaccggacccctagaccaccctgccccacctgccccttccccctttgctgtgacacttcttcatctcacccccccccgcccccctctaggagagctggctctgcagtgggggagggatgcagggacatttactgaaggagggacatggacaaaacaacattgaattcccagccccattggggagtgatctcttggacacagagcccccattcaaaatggggcagggcaagggtgggagtgtgcaaagccctgatctggagttacctgaggccacagctgccctattcacttctaagggccctgttttgagattgtttgttctaatttattttaagctaggtaaggctggggggagggtggggccgtggtcccctcagcctccatggggagggaagaagggggagctctttttttacgttgatttttttttttctactctgttttccctttttccttccgctccatttggggccctgggggtttcagtcatctccccatttggtcccctggactgtctttgttgattctaacttgtaaataaagaaaatattattcaagttttgagttaccttaatatttgcttttgtagtgtttcaaaaggaacatcataagaattgtcttgataattttgagggaaatattactgcagtgagaaaaggcaatagctaacctataattggattgtcttaatttttaaaccagtaggcttttgctgtgtttttaataaagtaaatatgacttttgtaaattga
//
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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