2024-03-29 11:09:06, GGRNA : RefSeq release 60 (20130726)
LOCUS NR_037625 4899 bp RNA linear PRI 16-JUL-2013 DEFINITION Homo sapiens bromodomain containing 2 (BRD2), transcript variant 5, non-coding RNA. ACCESSION NR_037625 VERSION NR_037625.1 GI:313747420 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 4899) 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 4899) 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 4899) 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 4899) 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 4899) 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 4899) 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 4899) 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 4899) 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 4899) 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 4899) 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, AL832722.1, DC379337.1, 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 (5) has an alternate 5' exon and an additional internal exon compared to variant 1. The transcript is a nonsense-mediated mRNA decay candidate, and may not encode a functional protein. 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. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-247 BX648109.1 3-249 248-832 AL832722.1 183-767 833-841 DC379337.1 569-577 842-2371 AL832722.1 777-2306 2372-4420 D42040.1 2367-4415 4421-4899 AL645941.11 58464-58942 FEATURES Location/Qualifiers source 1..4899 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="6" /map="6p21.3" gene 1..4899 /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" misc_RNA 1..4899 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /product="bromodomain containing 2, transcript variant 5" /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" 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" 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" misc_feature 1615..2058 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="COORDINATES: alignment:Blast2seq::RefSeq|NM_001113182.2" /note="primary ORF has stop codon >50 nucleotides from the terminal splice site; nonsense-mediated decay (NMD) candidate" 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..2039 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="alignment:Splign:1.39.8" variation 1975 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:369236359" exon 2040..2177 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="alignment:Splign:1.39.8" variation 2048 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="g" /replace="t" /db_xref="dbSNP:201582271" variation 2063 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:375792679" variation 2072 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:180909220" variation 2093 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:201754613" variation 2102 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:9378166" variation 2108 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:76146382" variation 2135 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="c" /db_xref="dbSNP:373853679" variation 2148 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:143509698" exon 2178..2316 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="alignment:Splign:1.39.8" variation 2194 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:1803864" variation 2195 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:199821934" variation 2201 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:367609858" variation 2223 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:137960007" variation 2226 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:370287964" variation 2250 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:200486677" variation 2282 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:375469443" variation 2288 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:201572264" variation 2289 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:199497657" exon 2317..2531 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="alignment:Splign:1.39.8" variation 2327 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:186277039" variation 2340 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:35952031" variation 2343 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:370807550" variation 2358 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:200381760" variation 2373 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:200917553" variation 2379..2380 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="" /replace="c" /db_xref="dbSNP:35264453" variation 2384 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:15912" variation 2418 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:176250" variation 2419 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:41270502" variation 2432 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:141377590" variation 2485 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:35294809" variation 2511 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:148978000" exon 2532..2906 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="alignment:Splign:1.39.8" variation 2540 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:374284677" variation 2570 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="t" /db_xref="dbSNP:375353506" variation 2625 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:150794546" variation 2640 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:139156709" variation 2648 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:146092849" variation 2654 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:369113238" variation 2714 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:200612980" variation 2767 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:371260391" variation 2768 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:17214085" variation 2771 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:62407971" variation 2789 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:146801767" variation 2842 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:140492558" variation 2843 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:17214092" variation 2870 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:142982923" variation 2897 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:192648574" exon 2907..3035 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="alignment:Splign:1.39.8" variation 2932 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:141044200" variation 2958 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:200770939" variation 2997 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:150234115" variation 3005 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:139231674" variation 3011 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:142112689" exon 3036..3284 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="alignment:Splign:1.39.8" variation 3047 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:55650066" variation 3056 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:200803710" variation 3084 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:201781653" variation 3090 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:199605967" variation 3101 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:145849910" variation 3110 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="c" /db_xref="dbSNP:138688346" variation 3111 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:201908033" variation 3116 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:200182536" variation 3122 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:200897288" variation 3126 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:184752888" variation 3127 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:3918143" variation 3134 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:368290193" variation 3165 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:143615833" variation 3200 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="t" /db_xref="dbSNP:200663348" variation 3201..3203 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="" /replace="gag" /db_xref="dbSNP:3918142" variation 3203 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="g" /replace="t" /db_xref="dbSNP:200978040" variation 3204 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="g" /replace="t" /db_xref="dbSNP:12822" variation 3206..3207 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="" /replace="gga" /db_xref="dbSNP:41310958" variation 3206 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:201796698" variation 3209 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:200103856" variation 3210 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:201071191" variation 3215 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:144872939" variation 3218 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:148048133" variation 3221 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:55778408" variation 3248 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="c" /db_xref="dbSNP:201425304" variation 3256 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:202033057" variation 3257 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:141740031" variation 3259 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:35773608" exon 3285..3547 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="alignment:Splign:1.39.8" variation 3305 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:191317139" variation 3337..3338 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:11555938" variation 3338 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:11037" variation 3344 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:35845948" variation 3346 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:1049369" variation 3347 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:1049372" variation 3356 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:3189517" variation 3357 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:200980274" variation 3358 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:374788375" variation 3386 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:142074834" variation 3403 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:146321913" variation 3410 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:201989394" variation 3411 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:34530779" variation 3416 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:1063379" variation 3444 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:144552033" variation 3501 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:55952113" variation 3515 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:206781" variation 3541 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:111308504" exon 3548..3852 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="alignment:Splign:1.39.8" variation 3548 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:141736131" variation 3556 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:145888786" variation 3628 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:138736016" variation 3725 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:368407034" variation 3808 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:140400525" exon 3853..3975 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="alignment:Splign:1.39.8" variation 3907 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:375635536" variation 3959 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:140096077" variation 3968 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:2066750" variation 3970 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:150287231" exon 3976..4899 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /inference="alignment:Splign:1.39.8" variation 3976 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:137898499" variation 3977 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:199954603" variation 3988 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:200578995" variation 3991 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:149549323" variation 3995 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:201375031" variation 3997 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:200164898" variation 4002 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:144861747" variation 4024 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:202018564" variation 4031 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:199887337" variation 4043 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2071876" variation 4045 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:369127190" variation 4058 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:202086051" variation 4075 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:200397640" variation 4079 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:3918140" variation 4108 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:202161102" variation 4114 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:200531629" variation 4115 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="g" /replace="t" /db_xref="dbSNP:371782351" variation 4129 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:201611634" variation 4143 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:199587809" variation 4163 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="c" /db_xref="dbSNP:200408799" variation 4165 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="c" /db_xref="dbSNP:201062187" variation 4167 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:199866893" variation 4194 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:147269908" variation 4216 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="c" /db_xref="dbSNP:201692899" variation 4221 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="c" /db_xref="dbSNP:199530843" variation 4224..4225 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:201992712" variation 4224..4225 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="" /replace="c" /replace="t" /db_xref="dbSNP:28986268" variation 4224 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="" /replace="c" /replace="cc" /replace="ct" /replace="t" /db_xref="dbSNP:368289232" variation 4224 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:1049414" variation 4225..4226 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="" /replace="t" /db_xref="dbSNP:373358187" variation 4256 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:139189753" variation 4302 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:72865897" variation 4338 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:78300601" variation 4353 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="c" /db_xref="dbSNP:10829" variation 4376 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:372641732" variation 4421 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:1049526" variation 4431 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:370640038" variation 4462 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="t" /db_xref="dbSNP:201572601" variation 4471 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:11555939" variation 4475 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="t" /db_xref="dbSNP:1803596" variation 4512 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:185910133" variation 4517 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:112975861" variation 4543 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:373317674" variation 4555..4556 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="" /replace="t" /db_xref="dbSNP:71656056" variation 4569 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="" /replace="a" /db_xref="dbSNP:3841159" variation 4569 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="t" /db_xref="dbSNP:113758837" variation 4571..4572 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="" /replace="t" /db_xref="dbSNP:71645781" variation 4586..4587 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="" /replace="tg" /db_xref="dbSNP:199828295" variation 4617 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:1803863" variation 4619 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="" /replace="c" /db_xref="dbSNP:34128205" variation 4626 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="g" /db_xref="dbSNP:191209130" variation 4648 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="g" /replace="t" /db_xref="dbSNP:115821350" variation 4731 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:182780962" variation 4755 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:187202774" variation 4769 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:1049639" variation 4788 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:16871296" variation 4812 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="a" /replace="g" /db_xref="dbSNP:60466011" variation 4846 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" /replace="c" /replace="t" /db_xref="dbSNP:73409643" polyA_signal 4870..4875 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" polyA_site 4899 /gene="BRD2" /gene_synonym="D6S113E; FSH; FSRG1; NAT; RING3; RNF3" ORIGIN
ggagggggagggctagtctgagccgcagccgccgcctcctccgctcgccctcctccctggcgctgaccgatggaccagccgctccgtggggaggactccggaccctggtgggggggcgggggggttctttcgcccccgtggcggagggcccctgagaggcggatacgggtgtgcctttgggggtgatgtggcgtgtggggggaaaggtccgagctcgcctggagggggagggtttttcccttaagtcatccctcccaggacttgctttttctgctctgagccggacgccggaatggagtttgaggaagagattcttcgctgctgctgccttaccgccgagaaccaccacccgccaggcgtcttgcggccacacccctggcgggttcaggcaggctacgcccacgcgacccctcccgtttccctgctttggccaatggaggagctacgaatggcacgacctgctcgagcttggcagtctccagttgggctgtgcatggaagcttgggaagactttgttggaaggggaggcggggagagagtgctggaggctctggggcgatggcttccgcacctcttccaaccaccctctttccctggagtcggcggaccacagctcagccaattggcttggagatgtggcgggttgccacttccctgtgggtctctgcggcactcttctgcctggtgactgacaccttggaaatgaagtttatgacgtcatcgttgcggctggccaatagaaaaagctcccgcggagaggtgttccttccccttcgactcagcttcttcacccgcgtgagcgagcgcgcgcgcgcggagggggtggggaaaagctcaagcagggtggcgcgcatgagcggcgaagctcctcctccccgcctatatataaagggctggcgcggggctcggcggcgccatttcgtgctggagtggagcagcctctagaacgagctggaggattctgcctaccgatacagagccttcgagtcgtccggggccgccattacaatccacctccatccgcttggaaatggccttcgtcccggcctatgactggtcccagcgggcagtacagaccccctagaagcccctggagctcccctttttcgggccccgcccaatcctcggagtctgtccaccccctctactccgccctcaagaggatttcaaagatggaggcggcggctccctaaaccacttttcgtgttcatccgcctccatccgagatcgaaacgggacctcgtcggccccgtaggggcccgacaagaagagggaatccctgcagaccaacagcgggctatattgacgacggtgtctgagatcggggaccgtcttttgaagagtcagtccctccttagttgcccgcctcagctgaggccgccgccattttcttgctgtccgccgtctgcagagcgcgccaagctgcccggagctctccgagaggccccaaagagactgctttcgtgccggccaggcagggggtttgtcgcctggaggcccaagaggaacggcctccccccaacttagcgggttatgctggaccgggcggtgaggggaaccgaggccacccggactttccgcggctgagggcagcgccggttccttgcggtcaagatgctgcaaaacgtgactccccacaataagctccctggggaagggaatgcagggttgctggggctgggcccagaagcagcagcaccagggaagaggattcgaaaaccctctctcttgtatgagggctttgagagccccacaatggcttcggtgcctgctttgcaacttacccctgccaacccaccacccccggaggtgtccaatcccaaaaagccaggacgagttaccaaccagctgcaatacctacacaaggtagtgatgaaggctctgtggaaacatcagttcgcatggccattccggcagcctgtggatgctgtcaaactgggtctaccgattcccacctcgggttgggagaggaccacggtggccaaaattcttagcttcttcctttccctcatgcagcccatggatagccagccccagaggattatcacaaaattataaaacagcctatggacatgggtactattaagaggagacttgaaaacaattattattgggctgcttcagagtgtatgcaagattttaataccatgttcaccaactgttacatttacaacaagcccactgatgatattgtcctaatggcacaaacgctggaaaagatattcctacagaaggttgcatcaatgccacaagaagaacaagagctggtagtgaccatccctaagaacagccacaagaagggggccaagttggcagcgctccagggcagtgttaccagtgcccatcaggtgcctgccgtctcttctgtgtcacacacagccctgtatactcctccacctgagatacctaccactgtcctcaacattccccacccatcagtcatttcctctccacttctcaagtccttgcactctgctggacccccgctccttgctgttactgcagctcctccagcccagccccttgccaagaaaaaaggcgtaaagcggaaagcagatactaccacccctacacctacagccatcttggctcctggttctccagctagccctcctgggagtcttgagcctaaggcagcacggcttccccctatgcgtagagagagtggtcgccccatcaagcccccacgcaaagacttgcctgactctcagcaacaacaccagagctctaagaaaggaaagctttcagaacagttaaaacattgcaatggcattttgaaggagttactctctaagaagcatgctgcctatgcttggcctttctataaaccagtggatgcttctgcacttggcctgcatgactaccatgacatcattaagcaccccatggacctcagcactgtcaagcggaagatggagaaccgtgattaccgggatgcacaggagtttgctgctgatgtacggcttatgttctccaactgctataagtacaatcccccagatcacgatgttgtggcaatggcacgaaagctacaggatgtatttgagttccgttatgccaagatgccagatgaaccactagaaccagggcctttaccagtctctactgccatgccccctggcttggccaaatcgtcttcagagtcctccagtgaggaaagtagcagtgagagctcctctgaggaagaggaggaggaagatgaggaggacgaggaggaagaagagagtgaaagctcagactcagaggaagaaagggctcatcgcttagcagaactacaggaacagcttcgggcagtacatgaacaactggctgctctgtcccagggtccaatatccaagcccaagaggaaaagagagaaaaaagagaaaaagaagaaacggaaggcagagaagcatcgaggccgagctggggccgatgaagatgacaaggggcctagggcaccccgcccacctcaacctaagaagtccaagaaagcaagtggcagtgggggtggcagtgctgctttaggcccttctggctttggaccttctggaggaagtggcaccaagctccccaaaaaggccacaaagacagccccacctgccctgcctacaggttatgattcagaggaggaggaagagagcaggcccatgagttacgatgagaagcggcagctgagcctggacatcaacaaattacctggggagaagctgggccgagttgtgcatataatccaagccagggagccctctttacgtgattcaaacccagaagagattgagattgattttgaaacactcaagccatccacacttagagagcttgagcgctatgtcctttcctgcctacgtaagaaaccccggaagccctacaccattaagaagcctgtgggaaagacaaaggaggaactggctttggagaaaaagcgggaattagaaaagcggttacaagatgtcagcggacagctcaattctactaaaaagccccccaagaaagcgaatgagaaaacagagtcatcctctgcacagcaagtagcagtgtcacgccttagcgcttccagctccagctcagattccagctcctcctcttcctcgtcgtcgtcttcagacaccagtgattcagactcaggctaaggggtcaggccagatggggcaggaaggctccgcaggaccggacccctagaccaccctgccccacctgccccttccccctttgctgtgacacttcttcatctcacccccccccgcccccctctaggagagctggctctgcagtgggggagggatgcagggacatttactgaaggagggacatggacaaaacaacattgaattcccagccccattggggagtgatctcttggacacagagcccccattcaaaatggggcagggcaagggtgggagtgtgcaaagccctgatctggagttacctgaggccacagctgccctattcacttctaagggccctgttttgagattgtttgttctaatttattttaagctaggtaaggctggggggagggtggggccgtggtcccctcagcctccatggggagggaagaagggggagctctttttttacgttgatttttttttttctactctgttttccctttttccttccgctccatttggggccctgggggtttcagtcatctccccatttggtcccctggactgtctttgttgattctaacttgtaaataaagaaaatattattcaagttttgagttaccttaatatttgcttttgtagtgtttcaaaaggaacatcataagaattgtcttgataattttgagggaaatattactgcagtgagaaaaggcaatagctaacctataattggattgtcttaatttttaaaccagtaggcttttgctgtgtttttaataaagtaaatatgacttttgtaaattga
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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
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