LOCUS       NM_003658               1767 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens BARX homeobox 2 (BARX2), mRNA.
ACCESSION   NM_003658
VERSION     NM_003658.4  GI:153218592
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 1767)
  AUTHORS   Long,J., Cai,Q., Sung,H., Shi,J., Zhang,B., Choi,J.Y., Wen,W.,
            Delahanty,R.J., Lu,W., Gao,Y.T., Shen,H., Park,S.K., Chen,K.,
            Shen,C.Y., Ren,Z., Haiman,C.A., Matsuo,K., Kim,M.K., Khoo,U.S.,
            Iwasaki,M., Zheng,Y., Xiang,Y.B., Gu,K., Rothman,N., Wang,W.,
            Hu,Z., Liu,Y., Yoo,K.Y., Noh,D.Y., Han,B.G., Lee,M.H., Zheng,H.,
            Zhang,L., Wu,P.E., Shieh,Y.L., Chan,S.Y., Wang,S., Xie,X.,
            Kim,S.W., Henderson,B.E., Le Marchand,L., Ito,H., Kasuga,Y.,
            Ahn,S.H., Kang,H.S., Chan,K.Y., Iwata,H., Tsugane,S., Li,C.,
            Shu,X.O., Kang,D.H. and Zheng,W.
  TITLE     Genome-wide association study in east Asians identifies novel
            susceptibility loci for breast cancer
  JOURNAL   PLoS Genet. 8 (2), E1002532 (2012)
   PUBMED   22383897
REFERENCE   2  (bases 1 to 1767)
  AUTHORS   Palmer,N.D., McDonough,C.W., Hicks,P.J., Roh,B.H., Wing,M.R.,
            An,S.S., Hester,J.M., Cooke,J.N., Bostrom,M.A., Rudock,M.E.,
            Talbert,M.E., Lewis,J.P., Ferrara,A., Lu,L., Ziegler,J.T.,
            Sale,M.M., Divers,J., Shriner,D., Adeyemo,A., Rotimi,C.N., Ng,M.C.,
            Langefeld,C.D., Freedman,B.I., Bowden,D.W., Voight,B.F.,
            Scott,L.J., Steinthorsdottir,V., Morris,A.P., Dina,C., Welch,R.P.,
            Zeggini,E., Huth,C., Aulchenko,Y.S., Thorleifsson,G.,
            McCulloch,L.J., Ferreira,T., Grallert,H., Amin,N., Wu,G.,
            Willer,C.J., Raychaudhuri,S., McCarroll,S.A., Langenberg,C.,
            Hofmann,O.M., Dupuis,J., Qi,L., Segre,A.V., van Hoek,M.,
            Navarro,P., Ardlie,K., Balkau,B., Benediktsson,R., Bennett,A.J.,
            Blagieva,R., Boerwinkle,E., Bonnycastle,L.L., Bostrom,K.B.,
            Bravenboer,B., Bumpstead,S., Burtt,N.P., Charpentier,G.,
            Chines,P.S., Cornelis,M., Couper,D.J., Crawford,G., Doney,A.S.,
            Elliott,K.S., Elliott,A.L., Erdos,M.R., Fox,C.S., Franklin,C.S.,
            Ganser,M., Gieger,C., Grarup,N., Green,T., Griffin,S., Groves,C.J.,
            Guiducci,C., Hadjadj,S., Hassanali,N., Herder,C., Isomaa,B.,
            Jackson,A.U., Johnson,P.R., Jorgensen,T., Kao,W.H., Klopp,N.,
            Kong,A., Kraft,P., Kuusisto,J., Lauritzen,T., Li,M., Lieverse,A.,
            Lindgren,C.M., Lyssenko,V., Marre,M., Meitinger,T., Midthjell,K.,
            Morken,M.A., Narisu,N., Nilsson,P., Owen,K.R., Payne,F.,
            Perry,J.R., Petersen,A.K., Platou,C., Proenca,C., Prokopenko,I.,
            Rathmann,W., Rayner,N.W., Robertson,N.R., Rocheleau,G., Roden,M.,
            Sampson,M.J., Saxena,R., Shields,B.M., Shrader,P., Sigurdsson,G.,
            Sparso,T., Strassburger,K., Stringham,H.M., Sun,Q., Swift,A.J.,
            Thorand,B., Tichet,J., Tuomi,T., van Dam,R.M., van Haeften,T.W.,
            van Herpt,T., van Vliet-Ostaptchouk,J.V., Walters,G.B.,
            Weedon,M.N., Wijmenga,C., Witteman,J., Bergman,R.N., Cauchi,S.,
            Collins,F.S., Gloyn,A.L., Gyllensten,U., Hansen,T., Hide,W.A.,
            Hitman,G.A., Hofman,A., Hunter,D.J., Hveem,K., Laakso,M.,
            Mohlke,K.L., Morris,A.D., Palmer,C.N., Pramstaller,P.P., Rudan,I.,
            Sijbrands,E., Stein,L.D., Tuomilehto,J., Uitterlinden,A.,
            Walker,M., Wareham,N.J., Watanabe,R.M., Abecasis,G.R., Boehm,B.O.,
            Campbell,H., Daly,M.J., Hattersley,A.T., Hu,F.B., Meigs,J.B.,
            Pankow,J.S., Pedersen,O., Wichmann,H.E., Barroso,I., Florez,J.C.,
            Frayling,T.M., Groop,L., Sladek,R., Thorsteinsdottir,U.,
            Wilson,J.F., Illig,T., Froguel,P., van Duijn,C.M., Stefansson,K.,
            Altshuler,D., Boehnke,M., McCarthy,M.I., Soranzo,N., Wheeler,E.,
            Glazer,N.L., Bouatia-Naji,N., Magi,R., Randall,J., Johnson,T.,
            Elliott,P., Rybin,D., Henneman,P., Dehghan,A., Hottenga,J.J.,
            Song,K., Goel,A., Egan,J.M., Lajunen,T., Doney,A., Kanoni,S.,
            Cavalcanti-Proenca,C., Kumari,M., Timpson,N.J., Zabena,C.,
            Ingelsson,E., An,P., O'Connell,J., Luan,J., Elliott,A.,
            McCarroll,S.A., Roccasecca,R.M., Pattou,F., Sethupathy,P.,
            Ariyurek,Y., Barter,P., Beilby,J.P., Ben-Shlomo,Y., Bergmann,S.,
            Bochud,M., Bonnefond,A., Borch-Johnsen,K., Bottcher,Y., Brunner,E.,
            Bumpstead,S.J., Chen,Y.D., Chines,P., Clarke,R., Coin,L.J.,
            Cooper,M.N., Crisponi,L., Day,I.N., de  Geus,E.J., Delplanque,J.,
            Fedson,A.C., Fischer-Rosinsky,A., Forouhi,N.G., Frants,R.,
            Franzosi,M.G., Galan,P., Goodarzi,M.O., Graessler,J., Grundy,S.,
            Gwilliam,R., Hallmans,G., Hammond,N., Han,X., Hartikainen,A.L.,
            Hayward,C., Heath,S.C., Hercberg,S., Hicks,A.A., Hillman,D.R.,
            Hingorani,A.D., Hui,J., Hung,J., Jula,A., Kaakinen,M., Kaprio,J.,
            Kesaniemi,Y.A., Kivimaki,M., Knight,B., Koskinen,S., Kovacs,P.,
            Kyvik,K.O., Lathrop,G.M., Lawlor,D.A., Le Bacquer,O., Lecoeur,C.,
            Li,Y., Mahley,R., Mangino,M., Manning,A.K., Martinez-Larrad,M.T.,
            McAteer,J.B., McPherson,R., Meisinger,C., Melzer,D., Meyre,D.,
            Mitchell,B.D., Mukherjee,S., Naitza,S., Neville,M.J., Oostra,B.A.,
            Orru,M., Pakyz,R., Paolisso,G., Pattaro,C., Pearson,D., Peden,J.F.,
            Pedersen,N.L., Perola,M., Pfeiffer,A.F., Pichler,I., Polasek,O.,
            Posthuma,D., Potter,S.C., Pouta,A., Province,M.A., Psaty,B.M.,
            Rayner,N.W., Rice,K., Ripatti,S., Rivadeneira,F., Rolandsson,O.,
            Sandbaek,A., Sandhu,M., Sanna,S., Sayer,A.A., Scheet,P.,
            Seedorf,U., Sharp,S.J., Shields,B., Sijbrands,E.J., Silveira,A.,
            Simpson,L., Singleton,A., Smith,N.L., Sovio,U., Swift,A.,
            Syddall,H., Syvanen,A.C., Tanaka,T., Tonjes,A., Uitterlinden,A.G.,
            van Dijk,K.W., Varma,D., Visvikis-Siest,S., Vitart,V.,
            Vogelzangs,N., Waeber,G., Wagner,P.J., Walley,A., Ward,K.L.,
            Watkins,H., Wild,S.H., Willemsen,G., Witteman,J.C., Yarnell,J.W.,
            Zelenika,D., Zethelius,B., Zhai,G., Zhao,J.H., Zillikens,M.C.,
            Borecki,I.B., Loos,R.J., Meneton,P., Magnusson,P.K., Nathan,D.M.,
            Williams,G.H., Silander,K., Salomaa,V., Smith,G.D., Bornstein,S.R.,
            Schwarz,P., Spranger,J., Karpe,F., Shuldiner,A.R., Cooper,C.,
            Dedoussis,G.V., Serrano-Rios,M., Lind,L., Palmer,L.J., Franks,P.W.,
            Ebrahim,S., Marmot,M., Kao,W.H., Pramstaller,P.P., Wright,A.F.,
            Stumvoll,M., Hamsten,A., Buchanan,T.A., Valle,T.T., Rotter,J.I.,
            Siscovick,D.S., Penninx,B.W., Boomsma,D.I., Deloukas,P.,
            Spector,T.D., Ferrucci,L., Cao,A., Scuteri,A., Schlessinger,D.,
            Uda,M., Ruokonen,A., Jarvelin,M.R., Waterworth,D.M.,
            Vollenweider,P., Peltonen,L., Mooser,V. and Sladek,R.
  CONSRTM   DIAGRAM Consortium; MAGIC Investigators
  TITLE     A genome-wide association search for type 2 diabetes genes in
            African Americans
  JOURNAL   PLoS ONE 7 (1), E29202 (2012)
   PUBMED   22238593
REFERENCE   3  (bases 1 to 1767)
  AUTHORS   Jugessur,A., Shi,M., Gjessing,H.K., Lie,R.T., Wilcox,A.J.,
            Weinberg,C.R., Christensen,K., Boyles,A.L., Daack-Hirsch,S.,
            Nguyen,T.T., Christiansen,L., Lidral,A.C. and Murray,J.C.
  TITLE     Maternal genes and facial clefts in offspring: a comprehensive
            search for genetic associations in two population-based cleft
            studies from Scandinavia
  JOURNAL   PLoS ONE 5 (7), E11493 (2010)
   PUBMED   20634891
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
            Publication Status: Online-Only
REFERENCE   4  (bases 1 to 1767)
  AUTHORS   Stevens,T.A., Iacovoni,J.S., Edelman,D.B. and Meech,R.
  TITLE     Identification of novel binding elements and gene targets for the
            homeodomain protein BARX2
  JOURNAL   J. Biol. Chem. 279 (15), 14520-14530 (2004)
   PUBMED   14744868
  REMARK    GeneRIF: BARX2 can coordinate the expression of a network of genes
            that influence the growth of tumor cells
REFERENCE   5  (bases 1 to 1767)
  AUTHORS   Herring,B.P., Kriegel,A.M. and Hoggatt,A.M.
  TITLE     Identification of Barx2b, a serum response factor-associated
            homeodomain protein
  JOURNAL   J. Biol. Chem. 276 (17), 14482-14489 (2001)
   PUBMED   11278942
REFERENCE   6  (bases 1 to 1767)
  AUTHORS   Krasner,A., Wallace,L., Thiagalingam,A., Jones,C., Lengauer,C.,
            Minahan,L., Ma,Y., Kalikin,L., Feinberg,A.P., Jabs,E.W.,
            Tunnacliffe,A., Baylin,S.B., Ball,D.W. and Nelkin,B.D.
  TITLE     Cloning and chromosomal localization of the human BARX2 homeobox
            protein gene
  JOURNAL   Gene 250 (1-2), 171-180 (2000)
   PUBMED   10854790
REFERENCE   7  (bases 1 to 1767)
  AUTHORS   Hjalt,T.A. and Murray,J.C.
  TITLE     The human BARX2 gene: genomic structure, chromosomal localization,
            and single nucleotide polymorphisms
  JOURNAL   Genomics 62 (3), 456-459 (1999)
   PUBMED   10644443
REFERENCE   8  (bases 1 to 1767)
  AUTHORS   Jones,F.S., Kioussi,C., Copertino,D.W., Kallunki,P., Holst,B.D. and
            Edelman,G.M.
  TITLE     Barx2, a new homeobox gene of the Bar class, is expressed in neural
            and craniofacial structures during development
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 94 (6), 2632-2637 (1997)
   PUBMED   9122247
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AP003775.3 and BC111432.1.
            On Jul 24, 2007 this sequence version replaced gi:21536440.
            
            Summary: This gene encodes a member of the homeobox transcription
            factor family. A highly related protein in mouse has been shown to
            influence cellular processes that control cell adhesion and
            remodeling of the actin cytoskeleton in myoblast fusion and
            chondrogenesis. The encoded protein may also play a role in cancer
            progression. [provided by RefSeq, Jul 2008].
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC069378.1, AJ243512.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025085, ERS025087 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-31                AP003775.3         75909-75939
            32-926              BC111432.1         1-895
            927-1767            AP003775.3         151362-152202
FEATURES             Location/Qualifiers
     source          1..1767
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="11"
                     /map="11q25"
     gene            1..1767
                     /gene="BARX2"
                     /note="BARX homeobox 2"
                     /db_xref="GeneID:8538"
                     /db_xref="HGNC:956"
                     /db_xref="HPRD:16074"
                     /db_xref="MIM:604823"
     STS             1..940
                     /gene="BARX2"
                     /db_xref="UniSTS:480567"
     exon            1..237
                     /gene="BARX2"
                     /inference="alignment:Splign:1.39.8"
     STS             32..926
                     /gene="BARX2"
                     /db_xref="UniSTS:483871"
     variation       39
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368286323"
     variation       44
                     /gene="BARX2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372290638"
     CDS             51..890
                     /gene="BARX2"
                     /note="BarH-like homeobox 2"
                     /codon_start=1
                     /product="homeobox protein BarH-like 2"
                     /protein_id="NP_003649.2"
                     /db_xref="GI:6633798"
                     /db_xref="CCDS:CCDS8481.1"
                     /db_xref="GeneID:8538"
                     /db_xref="HGNC:956"
                     /db_xref="HPRD:16074"
                     /db_xref="MIM:604823"
                     /translation="

MHCHAELRLSSPGQLKAARRRYKTFMIDEILSKETCDYFEKLSLYSVCPSLVVRPKPLHSCTGSPSLRAYPLLSVITRQPTVISHLVPATPGIAQALSCHQVTEAVSAEAPGGEALASSESETEQPTPRQKKPRRSRTIFTELQLMGLEKKFQKQKYLSTPDRLDLAQSLGLTQLQVKTWYQNRRMKWKKMVLKGGQEAPTKPKGRPKKNSIPTSEEIEAEEKMNSQAQGQEQLEPSQGQEELCEAQEPKARDVPLEMAEPPDPPQELPIPSSEPPPLS

"
     misc_feature    450..623
                     /gene="BARX2"
                     /note="Homeodomain;  DNA binding domains involved in the
                     transcriptional regulation of key eukaryotic developmental
                     processes; may bind to DNA as monomers or as homo- and/or
                     heterodimers, in a sequence-specific manner; Region:
                     homeodomain; cd00086"
                     /db_xref="CDD:28970"
     misc_feature    order(450..464,468..470,519..521,537..539,576..578,
                     582..587,594..599,603..611,615..620)
                     /gene="BARX2"
                     /note="DNA binding site [nucleotide binding]"
                     /db_xref="CDD:28970"
     misc_feature    order(456..458,465..467,585..587,594..599,606..608)
                     /gene="BARX2"
                     /note="specific DNA base contacts [nucleotide binding];
                     other site"
                     /db_xref="CDD:28970"
     misc_feature    630..>824
                     /gene="BARX2"
                     /note="Translocation protein Sec62; Region: Sec62;
                     cl02170"
                     /db_xref="CDD:164010"
     misc_feature    759..761
                     /gene="BARX2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     variation       55
                     /gene="BARX2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:371564225"
     variation       73
                     /gene="BARX2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376511525"
     variation       83
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139769726"
     variation       95
                     /gene="BARX2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142792520"
     variation       105
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200866072"
     variation       175
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372858784"
     variation       200
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190637588"
     exon            238..538
                     /gene="BARX2"
                     /inference="alignment:Splign:1.39.8"
     variation       240
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142822705"
     variation       272
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149699398"
     variation       299
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146663523"
     variation       311
                     /gene="BARX2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201121141"
     variation       312
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140261325"
     variation       322
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143991757"
     variation       323
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146866720"
     variation       329
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149011396"
     variation       332
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202063049"
     variation       340
                     /gene="BARX2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:377586719"
     variation       358
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377327995"
     variation       359
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369237978"
     variation       364
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143748790"
     variation       389
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372773378"
     variation       397
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201693114"
     variation       427
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377376108"
     variation       430
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370726265"
     variation       433
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200451881"
     variation       436
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148147759"
     variation       438
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375622525"
     variation       453
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376412759"
     variation       460
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200087278"
     variation       467
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140981609"
     variation       511
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150229722"
     variation       515
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61732044"
     variation       530
                     /gene="BARX2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142948782"
     exon            539..623
                     /gene="BARX2"
                     /inference="alignment:Splign:1.39.8"
     variation       548
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367573574"
     variation       566
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370794313"
     variation       592
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147038314"
     variation       601
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138172946"
     exon            624..1767
                     /gene="BARX2"
                     /inference="alignment:Splign:1.39.8"
     STS             625..1486
                     /gene="BARX2"
                     /standard_name="BARX2_2111"
                     /db_xref="UniSTS:462772"
     variation       659
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10791011"
     variation       699
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368541635"
     variation       723
                     /gene="BARX2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201994478"
     variation       755
                     /gene="BARX2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:144013495"
     variation       796
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148675839"
     variation       797
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372605659"
     variation       805
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34520023"
     variation       841
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146199848"
     variation       842
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202180662"
     variation       868
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376626609"
     variation       869
                     /gene="BARX2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:139211336"
     variation       898
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377451366"
     variation       929
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200642913"
     variation       980
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182541382"
     variation       1013
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376247287"
     variation       1017..1018
                     /gene="BARX2"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:60183112"
     variation       1017
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202123461"
     variation       1035
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113990346"
     variation       1049
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188216822"
     variation       1120
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:193170821"
     variation       1140
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112166305"
     variation       1206
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374042775"
     variation       1274
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185444315"
     variation       1281
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141031030"
     variation       1282
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12419199"
     variation       1286
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12223897"
     variation       1287
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150256721"
     variation       1295
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113446400"
     variation       1306
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116821632"
     variation       1317
                     /gene="BARX2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:114868374"
     variation       1379
                     /gene="BARX2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201046068"
     variation       1411
                     /gene="BARX2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:958476"
     variation       1439
                     /gene="BARX2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138937861"
     variation       1518..1519
                     /gene="BARX2"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:144334162"
     variation       1519..1522
                     /gene="BARX2"
                     /replace=""
                     /replace="tttt"
                     /db_xref="dbSNP:376973436"
     variation       1528
                     /gene="BARX2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370029873"
     variation       1529..1530
                     /gene="BARX2"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:71880406"
     variation       1635
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190771878"
     variation       1642
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377578616"
     variation       1672
                     /gene="BARX2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142203135"
     polyA_signal    1749..1754
                     /gene="BARX2"
     polyA_site      1767
                     /gene="BARX2"
ORIGIN      

cgggcactcgcagccgcgctcgggccggcggacgctcgcgccggctcaccatgcactgccacgccgagctgaggctgagctcgcccggccagctcaaagcagccaggcggcgctacaagactttcatgatcgacgagatcctctccaaggagacctgcgattactttgagaaactttccctctactccgtgtgcccgtcgctggtcgtgcgacccaagcccctgcattcctgtacgggctccccttccctgcgggcatatccgctcctctcggtgatcacccgccagcccactgtcatctcccacctggtccctgccaccccgggaatcgcccaggcactgtcctgccaccaggtcaccgaggcggtctctgctgaggccccagggggcgaggccctagccagcagcgagtcagagacggaacagcccacgccccgacagaagaagccccgccggagtcgcaccatcttcaccgagctgcagctcatgggcctggagaagaaattccagaagcagaagtatttgtcaaccccagacaggttggacttggctcagtctctgggactcactcagctgcaggtgaagacctggtatcagaatcgcaggatgaaatggaagaaaatggttcttaaaggtggacaggaagcacccacaaaacccaaaggtcgccccaagaagaactccatccccacatcagaagagattgaagctgaagagaagatgaacagccaggcccagggtcaggagcagctggagccctctcaggggcaggaggagctctgtgaagcacaggaaccgaaagcacgtgatgtccccttagagatggcagagccaccagacccgccccaggagttgccaataccctcttcggaacccccaccattaagctaaagtaaaacccttttgagggaagagggagactggggagaagggaaaagagagaaggcagggagagtagggagagaaaaccttccagcagcccagtaaactgcgggcgaagagatctacccgtctccctccctcccacagttaccattggccttgtcatcgcaagcatttgacaaagacttgcttgtcttgggcctgtcacctcctgaaaggctgctttagctgtggatgcccttgattaagggagagagcgcctaggagctgcctgccccagctggggtgacggctgtagggctgggtctatgttgcaagccctatatcctagcatgcagtggaaagtgcttagctctctccctcctgacctctgggcagccagtcatcaaagcagagagacgtggcggcatgtgggcagcatgcccaggttccttgctgactcagcacttatttctgtagttttaaaaaagaatttaatgtttttggttgtatttttttgggggggtgagggtgggcaaaaacatgggggtagttctgagttgttagaaatgtttctgaatcaagtttgtttgaagacacgtgtgcctttgtacccattataagatggtcataagacccaagaactgataagctttggttttttttttgttttgttttgttttttgcttcatttacccattcatgcctagggttccattattggaaccctaagcttgtgggagttatttctatcctactgctcaaggtcatcaccaagatctgatttttcataaaaaacatttgtgaccttcggcataaatgggttaaggtgccatccctgaaactgcaatgcagatatgttcagataacttttattttttaattaaaaataaatctttcaaaagga

//

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:8538 -> Molecular function: GO:0000976 [transcription regulatory region sequence-specific DNA binding] evidence: IEA
            GeneID:8538 -> Molecular function: GO:0003677 [DNA binding] evidence: IDA
            GeneID:8538 -> Molecular function: GO:0003682 [chromatin binding] evidence: IEA
            GeneID:8538 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA
            GeneID:8538 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IEA
            GeneID:8538 -> Biological process: GO:0001502 [cartilage condensation] evidence: IEA
            GeneID:8538 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
            GeneID:8538 -> Biological process: GO:0014902 [myotube differentiation] evidence: IEA
            GeneID:8538 -> Biological process: GO:0042637 [catagen] evidence: IEA
            GeneID:8538 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IEA
            GeneID:8538 -> Cellular component: GO:0005667 [transcription factor complex] evidence: IEA