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2024-03-28 17:53:52, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001134778            2825 bp    mRNA    linear   PRI 09-JUN-2013
DEFINITION  Homo sapiens pre-B-cell leukemia homeobox 3 (PBX3), transcript
            variant 2, mRNA.
ACCESSION   NM_001134778
VERSION     NM_001134778.1  GI:198041754
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 2825)
  AUTHORS   Li,Z., Zhang,Z., Li,Y., Arnovitz,S., Chen,P., Huang,H., Jiang,X.,
            Hong,G.M., Kunjamma,R.B., Ren,H., He,C., Wang,C.Z., Elkahloun,A.G.,
            Valk,P.J., Dohner,K., Neilly,M.B., Bullinger,L., Delwel,R.,
            Lowenberg,B., Liu,P.P., Morgan,R., Rowley,J.D., Yuan,C.S. and
            Chen,J.
  TITLE     PBX3 is an important cofactor of HOXA9 in leukemogenesis
  JOURNAL   Blood 121 (8), 1422-1431 (2013)
   PUBMED   23264595
  REMARK    GeneRIF: Collectively, our data suggest that PBX3 is a critical
            cofactor of HOXA9 in leukemogenesis.
REFERENCE   2  (bases 1 to 2825)
  AUTHORS   Ho,C.Y., Bar,E., Giannini,C., Marchionni,L., Karajannis,M.A.,
            Zagzag,D., Gutmann,D.H., Eberhart,C.G. and Rodriguez,F.J.
  TITLE     MicroRNA profiling in pediatric pilocytic astrocytoma reveals
            biologically relevant targets, including PBX3, NFIB, and METAP2
  JOURNAL   Neuro-oncology 15 (1), 69-82 (2013)
   PUBMED   23161775
  REMARK    GeneRIF: Increased expression of PBX3 is associated with pilocytic
            astrocytoma.
REFERENCE   3  (bases 1 to 2825)
  AUTHORS   Arrington,C.B., Dowse,B.R., Bleyl,S.B. and Bowles,N.E.
  TITLE     Non-synonymous variants in pre-B cell leukemia homeobox (PBX) genes
            are associated with congenital heart defects
  JOURNAL   Eur J Med Genet 55 (4), 235-237 (2012)
   PUBMED   22426282
  REMARK    GeneRIF: The Pbx3 Ala136Val variant is a modifier or risk allele
            for congenital heart defects.
REFERENCE   4  (bases 1 to 2825)
  AUTHORS   Li,Z., Huang,H., Li,Y., Jiang,X., Chen,P., Arnovitz,S.,
            Radmacher,M.D., Maharry,K., Elkahloun,A., Yang,X., He,C., He,M.,
            Zhang,Z., Dohner,K., Neilly,M.B., Price,C., Lussier,Y.A., Zhang,Y.,
            Larson,R.A., Le Beau,M.M., Caligiuri,M.A., Bullinger,L., Valk,P.J.,
            Delwel,R., Lowenberg,B., Liu,P.P., Marcucci,G., Bloomfield,C.D.,
            Rowley,J.D. and Chen,J.
  TITLE     Up-regulation of a HOXA-PBX3 homeobox-gene signature following
            down-regulation of miR-181 is associated with adverse prognosis in
            patients with cytogenetically abnormal AML
  JOURNAL   Blood 119 (10), 2314-2324 (2012)
   PUBMED   22251480
  REMARK    GeneRIF: Data show that up-regulation of the HOXA7, HOXA9, HOXA11,
            and PBX3 resulting from the down-regulation of miR-181 family
            members probably contribute to the poor prognosis of patients with
            nonfavorable cytogenetically abnormal AML (CA-AML).
REFERENCE   5  (bases 1 to 2825)
  AUTHORS   Ramberg,H., Alshbib,A., Berge,V., Svindland,A. and Tasken,K.A.
  TITLE     Regulation of PBX3 expression by androgen and Let-7d in prostate
            cancer
  JOURNAL   Mol. Cancer 10, 50 (2011)
   PUBMED   21548940
  REMARK    GeneRIF: PBX3 is up-regulated in prostate cancer and post-
            transcriptionally regulated by androgen through Let-7d.
            Publication Status: Online-Only
REFERENCE   6  (bases 1 to 2825)
  AUTHORS   Wistow,G., Bernstein,S.L., Wyatt,M.K., Behal,A., Touchman,J.W.,
            Bouffard,G., Smith,D. and Peterson,K.
  TITLE     Expressed sequence tag analysis of adult human lens for the NEIBank
            Project: over 2000 non-redundant transcripts, novel genes and
            splice variants
  JOURNAL   Mol. Vis. 8, 171-184 (2002)
   PUBMED   12107413
  REMARK    Publication Status: Online-Only
REFERENCE   7  (bases 1 to 2825)
  AUTHORS   Knoepfler,P.S., Sykes,D.B., Pasillas,M. and Kamps,M.P.
  TITLE     HoxB8 requires its Pbx-interaction motif to block differentiation
            of primary myeloid progenitors and of most cell line models of
            myeloid differentiation
  JOURNAL   Oncogene 20 (39), 5440-5448 (2001)
   PUBMED   11571641
REFERENCE   8  (bases 1 to 2825)
  AUTHORS   Fujino,T., Yamazaki,Y., Largaespada,D.A., Jenkins,N.A.,
            Copeland,N.G., Hirokawa,K. and Nakamura,T.
  TITLE     Inhibition of myeloid differentiation by Hoxa9, Hoxb8, and Meis
            homeobox genes
  JOURNAL   Exp. Hematol. 29 (7), 856-863 (2001)
   PUBMED   11438208
REFERENCE   9  (bases 1 to 2825)
  AUTHORS   Shen,W.F., Rozenfeld,S., Kwong,A., Kom ves,L.G., Lawrence,H.J. and
            Largman,C.
  TITLE     HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
  JOURNAL   Mol. Cell. Biol. 19 (4), 3051-3061 (1999)
   PUBMED   10082572
REFERENCE   10 (bases 1 to 2825)
  AUTHORS   Monica,K., Galili,N., Nourse,J., Saltman,D. and Cleary,M.L.
  TITLE     PBX2 and PBX3, new homeobox genes with extensive homology to the
            human proto-oncogene PBX1
  JOURNAL   Mol. Cell. Biol. 11 (12), 6149-6157 (1991)
   PUBMED   1682799
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AK309713.1, BC094883.1, CD675622.1, CN372830.1 and CN372832.1.
            
            Transcript Variant: This variant (2) utilizes an alternate first
            exon and 5'UTR; thus, the first likely translation initiation site
            corresponds to an internal methionine in variant 1. The predicted
            protein (isoform 2) is N-terminally truncated compared to isoform 1
            and is not predicted to have a signal peptide.
            
            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 :: AK309713.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025086 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-752               AK309713.1         1-752
            753-1536            BC094883.1         790-1573
            1537-1797           CD675622.1         318-578
            1798-2196           CN372830.1         355-753
            2197-2653           CN372832.1         95-551
            2654-2825           BC094883.1         2693-2864
FEATURES             Location/Qualifiers
     source          1..2825
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="9"
                     /map="9q33.3"
     gene            1..2825
                     /gene="PBX3"
                     /note="pre-B-cell leukemia homeobox 3"
                     /db_xref="GeneID:5090"
                     /db_xref="HGNC:8634"
                     /db_xref="MIM:176312"
     exon            1..230
                     /gene="PBX3"
                     /inference="alignment:Splign:1.39.8"
     variation       132..133
                     /gene="PBX3"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:373925399"
     variation       151
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12686532"
     misc_feature    199..201
                     /gene="PBX3"
                     /note="upstream in-frame stop codon"
     exon            231..304
                     /gene="PBX3"
                     /inference="alignment:Splign:1.39.8"
     CDS             256..1335
                     /gene="PBX3"
                     /note="isoform 2 is encoded by transcript variant 2;
                     pre-B-cell leukemia transcription factor 3; homeobox
                     protein PBX3"
                     /codon_start=1
                     /product="pre-B-cell leukemia transcription factor 3
                     isoform 2"
                     /protein_id="NP_001128250.1"
                     /db_xref="GI:198041755"
                     /db_xref="CCDS:CCDS48021.1"
                     /db_xref="GeneID:5090"
                     /db_xref="HGNC:8634"
                     /db_xref="MIM:176312"
                     /translation="
MKPALFSVLCEIKEKTGLSIRGAQEEDPPDPQLMRLDNMLLAEGVSGPEKGGGSAAAAAAAAASGGSSDNSIEHSDYRAKLTQIRQIYHTELEKYEQACNEFTTHVMNLLREQSRTRPISPKEIERMVGIIHRKFSSIQMQLKQSTCEAVMILRSRFLDARRKRRNFSKQATEILNEYFYSHLSNPYPSEEAKEELAKKCSITVSQVSNWFGNKRIRYKKNIGKFQEEANLYAAKTAVTAAHAVAAAVQNNQTNSPTTPNSGSSGSFNLPNSGDMFMNMQSLNGDSYQGSQVGANVQSQVDTLRHVINQTGGYSDGLGGNSLYSPHNLNANGGWQDATTPSSVTSPTEGPGSVHSDTSN
"
     misc_feature    256..732
                     /gene="PBX3"
                     /note="PBC domain; Region: PBC; pfam03792"
                     /db_xref="CDD:217730"
     misc_feature    736..918
                     /gene="PBX3"
                     /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:238039"
     misc_feature    order(736..750,754..756,814..816,832..834,871..873,
                     877..882,889..894,898..906,910..915)
                     /gene="PBX3"
                     /note="DNA binding site [nucleotide binding]"
                     /db_xref="CDD:238039"
     misc_feature    order(742..744,751..753,880..882,889..894,901..903)
                     /gene="PBX3"
                     /note="specific DNA base contacts [nucleotide binding];
                     other site"
                     /db_xref="CDD:238039"
     variation       266
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372548249"
     variation       297
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199866010"
     exon            305..546
                     /gene="PBX3"
                     /inference="alignment:Splign:1.39.8"
     variation       327
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:140051153"
     variation       419
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376106319"
     variation       437
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145687528"
     variation       complement(455)
                     /gene="PBX3"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2149989"
     variation       460
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369511204"
     variation       464
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114889309"
     variation       501
                     /gene="PBX3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:114411468"
     exon            547..737
                     /gene="PBX3"
                     /inference="alignment:Splign:1.39.8"
     variation       681
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1854706"
     exon            738..873
                     /gene="PBX3"
                     /inference="alignment:Splign:1.39.8"
     variation       801
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:117595468"
     exon            874..1039
                     /gene="PBX3"
                     /inference="alignment:Splign:1.39.8"
     variation       882
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141969948"
     variation       945
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374198859"
     variation       981
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368535684"
     variation       988
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199830900"
     variation       999
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372253003"
     variation       1019
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370710553"
     variation       1020
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114208419"
     variation       1023
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145537886"
     variation       1038
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200644689"
     exon            1040..1152
                     /gene="PBX3"
                     /inference="alignment:Splign:1.39.8"
     exon            1153..1242
                     /gene="PBX3"
                     /inference="alignment:Splign:1.39.8"
     variation       1176
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148844992"
     variation       1184
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143568685"
     variation       1195
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376665042"
     variation       1200
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138039965"
     variation       1209
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1058389"
     variation       1213
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144885113"
     variation       1219
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:76165119"
     variation       1220
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138731813"
     variation       1224
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189417832"
     variation       1228
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:114191763"
     variation       1233
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369882718"
     exon            1243..2789
                     /gene="PBX3"
                     /inference="alignment:Splign:1.39.8"
     variation       1250
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142803989"
     variation       1284
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:111373780"
     variation       1316
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115431152"
     variation       1356
                     /gene="PBX3"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:33993404"
     STS             1367..1491
                     /gene="PBX3"
                     /standard_name="WI-16961"
                     /db_xref="UniSTS:70983"
     variation       1372
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374696590"
     variation       1390
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:77899191"
     variation       1528..1529
                     /gene="PBX3"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:35298105"
     variation       1528
                     /gene="PBX3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:79152930"
     variation       1553
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186361189"
     variation       1592
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11792585"
     variation       1596
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144996442"
     variation       1599
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149098105"
     STS             1678..1820
                     /gene="PBX3"
                     /standard_name="SHGC-30429"
                     /db_xref="UniSTS:26658"
     variation       1687
                     /gene="PBX3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:192067546"
     variation       1767
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373063178"
     variation       1778
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376294286"
     STS             1821..2654
                     /gene="PBX3"
                     /standard_name="PBX3_2144"
                     /db_xref="UniSTS:280889"
     variation       1846
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:13296162"
     variation       1851
                     /gene="PBX3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113094250"
     variation       2019
                     /gene="PBX3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:151283697"
     variation       2026
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374619196"
     variation       2030
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:73667816"
     variation       2040
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:141512258"
     variation       2097
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374738745"
     STS             2166..2272
                     /gene="PBX3"
                     /standard_name="G07093"
                     /db_xref="UniSTS:274"
     variation       2180..2182
                     /gene="PBX3"
                     /replace=""
                     /replace="tta"
                     /db_xref="dbSNP:71680715"
     variation       2235
                     /gene="PBX3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:113517815"
     variation       2279
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147042624"
     variation       2371
                     /gene="PBX3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368092553"
     variation       2501
                     /gene="PBX3"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:10543594"
     variation       2510
                     /gene="PBX3"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:67765417"
     STS             2516..2724
                     /gene="PBX3"
                     /standard_name="RH45491"
                     /db_xref="UniSTS:82884"
     STS             2553..2709
                     /gene="PBX3"
                     /standard_name="A009U31"
                     /db_xref="UniSTS:56130"
     STS             2553..2709
                     /gene="PBX3"
                     /standard_name="G32849"
                     /db_xref="UniSTS:117428"
     variation       2555
                     /gene="PBX3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:183611167"
     variation       2647
                     /gene="PBX3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186955350"
ORIGIN      
ctctgcacaggagcggacgcgggagcccctccgcacccgtcccctcccccgggtcgccttcgcctgcccccggggcgaggctccccgcgcgggttcgcgtcgcgtctgcagtggccgaggctgctgcctgccgggcagatgggtccgccttgttccggctgcagctttcgccgccggggcttgctggctgtcgggaactagtcaactggagtttttgttgacttcccacggaaacatgccctgaactgtcacagaatgaaaccagcgctcttcagcgtcctgtgtgagatcaaagagaaaacaggtctcagcatcagaggagcccaggaggaggaccctcccgatccccagctaatgagactggacaatatgcttttggcagaaggggtttcaggtcctgagaaaggtgggggatcggcggcagcagctgcagccgcggcagcctctggaggttcttcagataactctattgaacactcagattacagagccaaattgacccagatcagacaaatctatcacacagaactggagaaatatgaacaggcatgtaatgaatttactacacatgtgatgaaccttctccgagaacagagtagaacacgtcccatttctccaaaagagattgaaagaatggtgggcatcatccatcgaaaatttagttccattcagatgcagctcaaacaaagcacttgtgaagcagttatgattttaagatcaaggttccttgatgccagacggaaaaggcgtaacttcagtaaacaggccacagaaatcttgaatgaatatttttactcacacctcagcaacccctaccccagtgaagaagccaaagaggagctggccaagaaatgcagcatcacagtgtcacaggtatccaattggtttggcaacaaacgaatcaggtacaagaagaacattggcaagtttcaggaagaagccaacctctatgctgcaaagacggccgtgacagctgcacacgcagtagcagcagctgtgcagaacaaccagaccaattcgcccaccacaccaaattccggttcttctggttcttttaacctcccaaattctggggacatgttcatgaacatgcagagtctgaatggggattcttaccaagggtcccaagtcggagccaatgtgcaatcacaggtggataccctccgtcatgttatcaatcagacgggaggctacagtgatggccttggaggaaattcactgtacagtccacataatttaaatgctaatggaggctggcaggacgcaacaactccatcttctgtgacttctcctacagaaggcccaggaagtgtgcactcggatacctctaactaatctctggccacacttttccctgagctacatgccttgataagtgcattcagagcaataggaggaaaaggaaagcgtttttgtagcccaccatctacagctttactgtaaaaccttgtcttattcgagaacttggtaaatctgttttttaaggaatcataatcatttgtatttatacttaaaaacacacaatgttaaaaaaaataaagcactttatccaattaggccaagatttaacattgttgacagtcctgtagctattttatcataatttattatcaatattttacattaatggtttcacagttgccaattacttggccttaagggtaaaaagtacaatatacactaaacctcaaccgttaaagcagatgcaaaaattcacctcacctaaattgaacttcttgcatatttccattactgacttggattgtctttctttcatatcactaatggagttggaataaagagctgtttgcctatccctgttaatgatggttgtgtttaagaatcttcctcgtcacgtttgtgttcagatctcttatgttataattagatcagagactggtagcatcgtttctctctctgaaagcaccagtgcccagagtctgctcggtaataaaattatggatccagattgttctgagagacgaagatacttgctgctgatagaggtgaaaacgagattgatccgtctggggttttacggtgtgcactgggtgctgcacagacttgtcaaggtttgctacgtcctctgggcatctgcaaaaggccctgctctctggagtgttgtatatagtgtagcaaaagagtatttatacatcccaccaatcaaaacacagctttattacctcatgcgaactcatacaaaccaatagaatttcaacatgttctgtagcttagagtgctcacttactacctctgaacaatactcacgctgtagtttgtctctttcttatctttttgcatcttgtaattaactctttgtttcccttcataaaatgtaatgtacattgtaatcttttaaaagaaaaatcagggttgcacttgcaacttttaaaaaaccgagtgtggaaacattgggtcttaattcaacacaggatcggtaaaactgttgtaaatactgagaaacattttgaatgttcttcatcttattactaatccatgcaaaaaaaaaaaaaaaagcagcgactaattgtgatgcattcagatttcagtattcagtactgtatatttcaccctgtgtaatggggccccctctcctttctctctttttgtattgtatgcgattctgaaactgattgagtcatgaaaataatttgtggcggtgattctaatgtattaaaaacgtttcgtgttcctttctaactggattacaccctggattgaaaaagtcttcctcgtggtagttatatgtagtttcaaacatgaataaactttttgctttcatgattaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:5090 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA
            GeneID:5090 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA
            GeneID:5090 -> Biological process: GO:0002087 [regulation of respiratory gaseous exchange by neurological system process] evidence: IEA
            GeneID:5090 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
            GeneID:5090 -> Biological process: GO:0007387 [anterior compartment pattern formation] evidence: TAS
            GeneID:5090 -> Biological process: GO:0007388 [posterior compartment specification] evidence: TAS
            GeneID:5090 -> Biological process: GO:0007585 [respiratory gaseous exchange] evidence: IEA
            GeneID:5090 -> Biological process: GO:0008344 [adult locomotory behavior] evidence: IEA
            GeneID:5090 -> Biological process: GO:0021516 [dorsal spinal cord development] evidence: IEA
            GeneID:5090 -> Biological process: GO:0048666 [neuron development] evidence: IEA
            GeneID:5090 -> Cellular component: GO:0005667 [transcription factor complex] evidence: IEA

by @meso_cacase at DBCLS
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