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2024-03-28 23:14:06, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_003110               3132 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens Sp2 transcription factor (SP2), mRNA.
ACCESSION   NM_003110 NM_138406
VERSION     NM_003110.5  GI:125625356
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 3132)
  AUTHORS   Ito,H., Murakami,M., Furuhata,A., Gao,S., Yoshida,K., Sobue,S.,
            Hagiwara,K., Takagi,A., Kojima,T., Suzuki,M., Banno,Y., Tanaka,K.,
            Tamiya-Koizumi,K., Kyogashima,M., Nozawa,Y. and Murate,T.
  TITLE     Transcriptional regulation of neutral sphingomyelinase 2 gene
            expression of a human breast cancer cell line, MCF-7, induced by
            the anti-cancer drug, daunorubicin
  JOURNAL   Biochim. Biophys. Acta 1789 (11-12), 681-690 (2009)
   PUBMED   19698806
  REMARK    GeneRIF: Data show that three Sp1 motifs located between -148 and
            -42bp upstream of the first exon were important in basic as well as
            in DA-induced NSMase2 promoter activity.
REFERENCE   2  (bases 1 to 3132)
  AUTHORS   Wheeler,H.E., Metter,E.J., Tanaka,T., Absher,D., Higgins,J.,
            Zahn,J.M., Wilhelmy,J., Davis,R.W., Singleton,A., Myers,R.M.,
            Ferrucci,L. and Kim,S.K.
  TITLE     Sequential use of transcriptional profiling, expression
            quantitative trait mapping, and gene association implicates MMP20
            in human kidney aging
  JOURNAL   PLoS Genet. 5 (10), E1000685 (2009)
   PUBMED   19834535
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   3  (bases 1 to 3132)
  AUTHORS   Letourneur,M., Valentino,L., Travagli-Gross,J., Bertoglio,J. and
            Pierre,J.
  TITLE     Sp2 regulates interferon-gamma-mediated socs1 gene expression
  JOURNAL   Mol. Immunol. 46 (11-12), 2151-2160 (2009)
   PUBMED   19482358
  REMARK    GeneRIF: Despite the absence of Sp2 in the 5'-upstream sequence of
            the human promoter, silencing of Sp2 by RNA interference clearly
            demonstrated that Sp2 is required for IFN-gamma-induced regulation
            of socs1 mRNA both in human and mouse.
REFERENCE   4  (bases 1 to 3132)
  AUTHORS   Sun,J.M., Chen,H.Y. and Davie,J.R.
  TITLE     Differential distribution of unmodified and phosphorylated histone
            deacetylase 2 in chromatin
  JOURNAL   J. Biol. Chem. 282 (45), 33227-33236 (2007)
   PUBMED   17827154
REFERENCE   5  (bases 1 to 3132)
  AUTHORS   Das,A., Fernandez-Zapico,M.E., Cao,S., Yao,J., Fiorucci,S.,
            Hebbel,R.P., Urrutia,R. and Shah,V.H.
  TITLE     Disruption of an SP2/KLF6 repression complex by SHP is required for
            farnesoid X receptor-induced endothelial cell migration
  JOURNAL   J. Biol. Chem. 281 (51), 39105-39113 (2006)
   PUBMED   17071613
  REMARK    GeneRIF: an SP2/KLF6 repression complex by SHP is required for
            farnesoid X receptor-induced endothelial cell migration
REFERENCE   6  (bases 1 to 3132)
  AUTHORS   Moorefield,K.S., Fry,S.J. and Horowitz,J.M.
  TITLE     Sp2 DNA binding activity and trans-activation are negatively
            regulated in mammalian cells
  JOURNAL   J. Biol. Chem. 279 (14), 13911-13924 (2004)
   PUBMED   14726517
REFERENCE   7  (bases 1 to 3132)
  AUTHORS   Rotheneder,H., Geymayer,S. and Haidweger,E.
  TITLE     Transcription factors of the Sp1 family: interaction with E2F and
            regulation of the murine thymidine kinase promoter
  JOURNAL   J. Mol. Biol. 293 (5), 1005-1015 (1999)
   PUBMED   10547281
REFERENCE   8  (bases 1 to 3132)
  AUTHORS   Philipsen,S. and Suske,G.
  TITLE     A tale of three fingers: the family of mammalian Sp/XKLF
            transcription factors
  JOURNAL   Nucleic Acids Res. 27 (15), 2991-3000 (1999)
   PUBMED   10454592
  REMARK    Review article
REFERENCE   9  (bases 1 to 3132)
  AUTHORS   Scohy,S., Van Vooren,P., Szpirer,C. and Szpirer,J.
  TITLE     Assignment1 of Sp genes to rat chromosome bands 7q36 (Sp1),
            10q31-->q32.1 (Sp2), 3q24-->q31 (Sp3) and 6q33 (Sp4) and of the SP2
            gene to human chromosome bands 17q21.3-->q22 by in situ
            hybridization
  JOURNAL   Cytogenet. Cell Genet. 81 (3-4), 273-274 (1998)
   PUBMED   9730617
REFERENCE   10 (bases 1 to 3132)
  AUTHORS   Kingsley,C. and Winoto,A.
  TITLE     Cloning of GT box-binding proteins: a novel Sp1 multigene family
            regulating T-cell receptor gene expression
  JOURNAL   Mol. Cell. Biol. 12 (10), 4251-4261 (1992)
   PUBMED   1341900
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from DB451570.1, BC016680.2,
            M97190.1 and BC033814.2.
            On Feb 9, 2007 this sequence version replaced gi:41281667.
            
            Summary: This gene encodes a member of the Sp subfamily of Sp/XKLF
            transcription factors. Sp family proteins are sequence-specific
            DNA-binding proteins characterized by an amino-terminal
            trans-activation domain and three carboxy-terminal zinc finger
            motifs. This protein contains the least conserved DNA-binding
            domain within the Sp subfamily of proteins, and its DNA sequence
            specificity differs from the other Sp proteins. It localizes
            primarily within subnuclear foci associated with the nuclear
            matrix, and can activate or in some cases repress expression from
            different promoters. [provided by RefSeq, Jul 2008].
            
            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 :: BC033814.2, BC016680.2 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025083 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-107               DB451570.1         1-107
            108-743             BC016680.2         1-636
            744-1714            M97190.1           619-1589
            1715-2585           BC016680.2         1608-2478
            2586-3132           BC033814.2         2465-3011
FEATURES             Location/Qualifiers
     source          1..3132
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="17"
                     /map="17q21.32"
     gene            1..3132
                     /gene="SP2"
                     /note="Sp2 transcription factor"
                     /db_xref="GeneID:6668"
                     /db_xref="HGNC:11207"
                     /db_xref="MIM:601801"
     exon            1..144
                     /gene="SP2"
                     /inference="alignment:Splign:1.39.8"
     variation       86
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370406238"
     CDS             138..1979
                     /gene="SP2"
                     /codon_start=1
                     /product="transcription factor Sp2"
                     /protein_id="NP_003101.3"
                     /db_xref="GI:125625357"
                     /db_xref="CCDS:CCDS11521.2"
                     /db_xref="GeneID:6668"
                     /db_xref="HGNC:11207"
                     /db_xref="MIM:601801"
                     /translation="
MSDPQTSMAATAAVSPSDYLQPAASTTQDSQPSPLALLAATCSKIGPPAVEAAVTPPAPPQPTPRKLVPIKPAPLPLSPGKNSFGILSSKGNILQIQGSQLSASYPGGQLVFAIQNPTMINKGTRSNANIQYQAVPQIQASNSQTIQVQPNLTNQIQIIPGTNQAIITPSPSSHKPVPIKPAPIQKSSTTTTPVQSGANVVKLTGGGGNVTLTLPVNNLVNASDTGAPTQLLTESPPTPLSKTNKKARKKSLPASQPPVAVAEQVETVLIETTADNIIQAGNNLLIVQSPGGGQPAVVQQVQVVPPKAEQQQVVQIPQQALRVVQAASATLPTVPQKPSQNFQIQAAEPTPTQVYIRTPSGEVQTVLVQDSPPATAAATSNTTCSSPASRAPHLSGTSKKHSAAILRKERPLPKIAPAGSIISLNAAQLAAAAQAMQTININGVQVQGVPVTITNTGGQQQLTVQNVSGNNLTISGLSPTQIQLQMEQALAGETQPGEKRRRMACTCPNCKDGEKRSGEQGKKKHVCHIPDCGKTFRKTSLLRAHVRLHTGERPFVCNWFFCGKRFTRSDELQRHARTHTGDKRFECAQCQKRFMRSDHLTKHYKTHLVTKNL
"
     misc_feature    369..371
                     /gene="SP2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q02086.3); phosphorylation site"
     misc_feature    1761..1841
                     /gene="SP2"
                     /note="Zinc-finger double domain; Region: zf-H2C2_2;
                     pfam13465"
                     /db_xref="CDD:205643"
     misc_feature    1848..1919
                     /gene="SP2"
                     /note="Zinc-finger double domain; Region: zf-H2C2_2;
                     pfam13465"
                     /db_xref="CDD:205643"
     misc_feature    1893..1958
                     /gene="SP2"
                     /note="Zinc finger, C2H2 type; Region: zf-C2H2; cl15478"
                     /db_xref="CDD:210117"
     exon            145..221
                     /gene="SP2"
                     /inference="alignment:Splign:1.39.8"
     variation       167
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139803722"
     variation       195
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144611436"
     variation       207
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113705698"
     exon            222..1196
                     /gene="SP2"
                     /inference="alignment:Splign:1.39.8"
     variation       298
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112053164"
     variation       322
                     /gene="SP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201198537"
     variation       473
                     /gene="SP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376159721"
     variation       477
                     /gene="SP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370407425"
     variation       516
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369065007"
     variation       523
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373308287"
     variation       527
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377521057"
     variation       529
                     /gene="SP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:371106023"
     variation       598
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200254744"
     variation       650
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150012782"
     variation       659
                     /gene="SP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:199905768"
     variation       671
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111389976"
     variation       697
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374244316"
     variation       698
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149196682"
     variation       703
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368448436"
     variation       704
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370442344"
     variation       725
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184089381"
     variation       744
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2228253"
     variation       749
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:117736384"
     variation       759
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367582453"
     variation       769
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371850352"
     variation       783
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140739569"
     variation       791
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372866839"
     variation       794
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2228251"
     variation       803
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137884512"
     variation       815
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372732502"
     variation       816
                     /gene="SP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:150853499"
     variation       853
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150118323"
     variation       854
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2229358"
     variation       880
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371001586"
     variation       901
                     /gene="SP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373579505"
     variation       947
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149293764"
     variation       956
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147415907"
     variation       980
                     /gene="SP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200972130"
     variation       992
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370784122"
     variation       1020
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139762471"
     variation       1037
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143732446"
     variation       1044
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147446062"
     variation       1049
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148511412"
     variation       1050
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142857959"
     variation       1070
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373883531"
     variation       1089..1090
                     /gene="SP2"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:35543662"
     variation       1104
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61753877"
     variation       1115
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200257728"
     variation       1134
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202157380"
     variation       1142
                     /gene="SP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:151058054"
     variation       1172
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78896229"
     exon            1197..1509
                     /gene="SP2"
                     /inference="alignment:Splign:1.39.8"
     variation       1210
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373140962"
     variation       1211
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139815805"
     variation       1214
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141918529"
     variation       1217
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146862346"
     variation       1251
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140692820"
     variation       1275
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62067380"
     variation       1281
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114228308"
     variation       1288
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202014692"
     variation       1306
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200461216"
     variation       1313
                     /gene="SP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373795992"
     variation       1327
                     /gene="SP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373926962"
     variation       1350
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143045442"
     variation       1397
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367814481"
     variation       1400
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148217498"
     variation       1446
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184644940"
     variation       1457
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200703641"
     variation       1481
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372727470"
     exon            1510..1684
                     /gene="SP2"
                     /inference="alignment:Splign:1.39.8"
     variation       1603
                     /gene="SP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:140242891"
     variation       1619
                     /gene="SP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:3190376"
     variation       1625
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138122841"
     variation       1626
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143694248"
     variation       1631
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375180084"
     variation       1670
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147788812"
     variation       1679
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141135915"
     exon            1685..1878
                     /gene="SP2"
                     /inference="alignment:Splign:1.39.8"
     variation       1709
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78785116"
     variation       1715
                     /gene="SP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1130932"
     variation       1722
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368951804"
     variation       1747
                     /gene="SP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:202023956"
     variation       1754
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144256408"
     variation       1757
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201575491"
     variation       1790
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148743427"
     variation       1838
                     /gene="SP2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:376471731"
     variation       1847
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369515854"
     exon            1879..3112
                     /gene="SP2"
                     /inference="alignment:Splign:1.39.8"
     variation       1898
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75562971"
     variation       1937
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146350857"
     variation       1958
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139713662"
     variation       1966
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374602267"
     variation       1967
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144476806"
     variation       1973
                     /gene="SP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200755668"
     variation       1988
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375386987"
     variation       1989
                     /gene="SP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368742340"
     variation       2253
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187872777"
     variation       2361
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190836947"
     variation       2412
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183394520"
     variation       2525
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367886979"
     STS             2553..2669
                     /gene="SP2"
                     /standard_name="D17S2015"
                     /db_xref="UniSTS:69245"
     variation       2581..2584
                     /gene="SP2"
                     /replace=""
                     /replace="ct"
                     /db_xref="dbSNP:35839416"
     variation       2581
                     /gene="SP2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:199573009"
     variation       2582..2583
                     /gene="SP2"
                     /replace=""
                     /replace="ct"
                     /db_xref="dbSNP:376983576"
     variation       2586..2587
                     /gene="SP2"
                     /replace=""
                     /replace="ct"
                     /db_xref="dbSNP:72249312"
     variation       2590
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200564346"
     variation       2640
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142039420"
     STS             2651..2801
                     /gene="SP2"
                     /standard_name="RH25284"
                     /db_xref="UniSTS:92440"
     variation       2757
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115128706"
     variation       2846
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371765868"
     STS             2847..3069
                     /gene="SP2"
                     /standard_name="RH17404"
                     /db_xref="UniSTS:52979"
     variation       2860
                     /gene="SP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:113185113"
     variation       2894
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187398872"
     variation       2939
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12325753"
     polyA_signal    2946..2951
                     /gene="SP2"
     variation       2964..2968
                     /gene="SP2"
                     /replace=""
                     /replace="tttat"
                     /db_xref="dbSNP:371372163"
     polyA_site      2967
                     /gene="SP2"
     variation       2968..2973
                     /gene="SP2"
                     /replace=""
                     /replace="ttttta"
                     /db_xref="dbSNP:369393595"
     variation       3003
                     /gene="SP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192943368"
     variation       3034
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184804668"
     variation       3044
                     /gene="SP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375834257"
     polyA_signal    3080..3085
                     /gene="SP2"
     variation       3087
                     /gene="SP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:144701940"
     polyA_site      3112
                     /gene="SP2"
ORIGIN      
aatgttccaagcgcttattggtgaaggctgccgtcgctcgggcggtggcgggctccgggattggcggttgcttggcgggcggtgtcaggctctcggtggcggcggaggcggcggaggccagggaggaagatgtcgtaatgagcgatccacagaccagcatggctgccactgctgctgtgagtcccagtgactacctgcagcctgccgcctccaccacccaggactcccagccatctcccttagccctgcttgctgcaacatgtagcaaaattggccctccagcagttgaagctgctgtgacacctcctgctcccccacagcccacaccgcggaaacttgtccctatcaaacctgcccctctccctctcagccccggcaagaatagctttggaatcttgtcctccaaaggaaatatacttcagattcaggggtcacaactgagcgcctcctatcctggagggcagctggtgttcgctatccagaatcccaccatgatcaacaaagggacccgatcaaatgccaatatccagtaccaggcggtccctcagattcaggcaagcaattcccaaaccatccaagtacagcccaatctcaccaaccagatccagatcatccctggcaccaaccaagccatcatcaccccctcaccgtccagtcacaagcctgtccccatcaagccagcccccatccagaagtcgagtacgaccaccacccccgtgcagagcggggccaatgtggtgaagctgacaggtgggggcggcaatgtgacgctcactctgcccgtcaacaaccttgtgaacgccagtgacaccggggcccctactcagctcctcactgaaagccccccaaccccgctgtctaagactaacaagaaagcaaggaagaagagccttcctgcctcccagccccctgtggctgtggctgagcaggtggagacggtgctgatcgagaccaccgcggacaacatcatccaggcaggaaataacctgctcattgttcagagccctggtgggggccagccagctgtggtccagcaggtccaggtggtgccccccaaggccgagcagcagcaggtggtacagatcccccagcaggctctgcgggtggtgcaggcggcatctgccaccctccccactgtaccccagaagccctcccagaactttcagatccaggcagctgagccgacacctactcaggtctacatccgcacgccttccggtgaggtgcagacagtccttgtccaggacagccccccagcaacagctgcagccacctctaacaccacctgtagcagccctgcatcccgtgctccccatctgagtgggaccagcaaaaagcactcagctgcaattctccgaaaagagcgtcccctgccaaagattgccccagccgggagcatcatcagcctgaatgcagcccagttggcggcagctgcccaggcaatgcagaccatcaacatcaatggtgtccaggtccagggcgtgcctgtcaccatcaccaacacaggcgggcagcagcagctgacagtgcagaatgtttctgggaacaacctgaccatcagtgggctgagccccacccagatccagctgcaaatggaacaagccctggccggagagacccagcccggggagaagcggcgccgcatggcctgcacgtgtcccaactgcaaggatggggagaagaggtctggagagcagggcaagaagaagcacgtgtgccacatccccgactgtggcaagacgttccgtaagacgtccttgctgcgtgcccatgtgcgcctgcacactggcgagcggccctttgtctgcaactggttcttctgtgggaagaggttcacacggagtgacgagctccaacggcatgctcgcacccacacaggggacaaacgcttcgagtgcgcccagtgtcagaagcgcttcatgaggagtgaccacctcaccaagcattacaagacccacctggtcacgaagaacttgtaaggccaactgcggcgggaggccctgaagatgcagtcccccacctgtgtcctccctgggcccctggtggaaaggagccctgtggctgccttgggcctgccctcagccccactcctgttctgcaactgtccccacaggaaggggctctgttccctgtattgtcctccttctgaagccccttggctctgccttggcccttcccctcaccacgagctcccggcctgcccagactgtggacactggccgtgcccaatgagacgttctaaaccaggacgcgtgggaacccttatttccaaaggaaaaacatgcatttcactccgtcgaggagcaaagtgagcccctaccccccaccccgatccccgctcccaacactgccggagtcgcgtcatgccatgccccctctcctgcacctccctggccctgccggccactgtggacgccctggggcttggcacccacctctggagaaactcggggccacctccactccatgtgcccagccccgccacaacctctcctccagcacattccagctctatttaaaaagtaaagacacccaccgactcctgatccccctctttttctatggagaacgttgccttatactctacttcagatgatgaacactgtgtactgtgtgtgctttaaagaagttttatttaattgctcccttcttcctttccttgttattcacctccctgatgcctgctttcagttgagggttgggggcaatgatgagcatatgaattttttctcactctagcaattcccttttctaaatgacacagcatttaaactcaaatctggattcagataacagcacctgcacatcctgcacctcctccctctcccttcacctcacccctgcccggcccaagctctacttgtgtacagtgtatattgtataatagacaattgtgtctactacatgtttaaaaacacattgcttgttatttttgaggcttttaaattaaacaaaaatccaactttatttttagttgtaactgcttgaggtatgttttatgaattaagtgacagatttgttatcctttattaacgtactttgttggtcagcactgggctgacaaaaattttttcttgctaataaatttagttgcctgaggcaaaatcttcaaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:6668 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA
            GeneID:6668 -> Molecular function: GO:0042826 [histone deacetylase binding] evidence: IPI
            GeneID:6668 -> Molecular function: GO:0046872 [metal ion binding] evidence: IEA
            GeneID:6668 -> Biological process: GO:0001701 [in utero embryonic development] evidence: IEA
            GeneID:6668 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
            GeneID:6668 -> Biological process: GO:0006357 [regulation of transcription from RNA polymerase II promoter] evidence: TAS
            GeneID:6668 -> Biological process: GO:0006955 [immune response] evidence: TAS
            GeneID:6668 -> Biological process: GO:0035264 [multicellular organism growth] evidence: IEA
            GeneID:6668 -> Biological process: GO:0048144 [fibroblast proliferation] evidence: IEA
            GeneID:6668 -> Biological process: GO:0048568 [embryonic organ development] evidence: IEA
            GeneID:6668 -> Biological process: GO:0072358 [cardiovascular system development] evidence: IEA
            GeneID:6668 -> Cellular component: GO:0005634 [nucleus] evidence: IDA

by @meso_cacase at DBCLS
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