2025-05-09 20:29:59, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001172509 5730 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens SATB homeobox 2 (SATB2), transcript variant 1, mRNA. ACCESSION NM_001172509 VERSION NM_001172509.1 GI:289547595 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 5730) AUTHORS Zhou,L.Q., Wu,J., Wang,W.T., Yu,W., Zhao,G.N., Zhang,P., Xiong,J., Li,M., Xue,Z., Wang,X., Xie,X.M., Guo,Z.C., Lv,X. and Liu,D.P. TITLE The AT-rich DNA-binding protein SATB2 promotes expression and physical association of human (G)gamma- and (A)gamma-globin genes JOURNAL J. Biol. Chem. 287 (36), 30641-30652 (2012) PUBMED 22825848 REMARK GeneRIF: results establish SATB2 as a novel gamma-globin gene regulator and provide a glimpse of the differential and cooperative roles of SATB family proteins in modulating clustered genes transcription REFERENCE 2 (bases 1 to 5730) AUTHORS Wei,J.D., Lin,Y.L., Tsai,C.H., Shieh,H.S., Lin,P.I., Ho,W.P. and Chen,R.M. TITLE SATB2 participates in regulation of menadione-induced apoptotic insults to osteoblasts JOURNAL J. Orthop. Res. 30 (7), 1058-1066 (2012) PUBMED 22570222 REMARK GeneRIF: SATB2 may play a crucial role in protecting against oxidative stress-induced osteoblast apoptosis. REFERENCE 3 (bases 1 to 5730) AUTHORS Liu,T.R., Xu,L.H., Yang,A.K., Zhong,Q., Song,M., Li,M.Z., Hu,L.J., Chen,F.J., Hu,Z.D., Han,P. and Zeng,M.S. TITLE Decreased expression of SATB2: a novel independent prognostic marker of worse outcome in laryngeal carcinoma patients JOURNAL PLoS ONE 7 (7), E40704 (2012) PUBMED 22815795 REMARK GeneRIF: SATB2 might involve in the development and progression of laryngeal squamous cell carcinoma. REFERENCE 4 (bases 1 to 5730) AUTHORS Chung,J., Grant,R.I., Kaplan,D.R. and Irwin,M.S. TITLE Special AT-rich binding protein-2 (SATB2) differentially affects disease-causing p63 mutant proteins JOURNAL J. Biol. Chem. 286 (47), 40671-40680 (2011) PUBMED 21965674 REMARK GeneRIF: SATB2 as the first p63 binding partner that differentially influences AEC and EEC p63 mutant proteins REFERENCE 5 (bases 1 to 5730) AUTHORS Magnusson,K., de Wit,M., Brennan,D.J., Johnson,L.B., McGee,S.F., Lundberg,E., Naicker,K., Klinger,R., Kampf,C., Asplund,A., Wester,K., Gry,M., Bjartell,A., Gallagher,W.M., Rexhepaj,E., Kilpinen,S., Kallioniemi,O.P., Belt,E., Goos,J., Meijer,G., Birgisson,H., Glimelius,B., Borrebaeck,C.A., Navani,S., Uhlen,M., O'Connor,D.P., Jirstrom,K. and Ponten,F. TITLE SATB2 in combination with cytokeratin 20 identifies over 95% of all colorectal carcinomas JOURNAL Am. J. Surg. Pathol. 35 (7), 937-948 (2011) PUBMED 21677534 REMARK GeneRIF: SATB2 in combination with cytokeratin 20 identifies over 95% of all colorectal carcinomas. REFERENCE 6 (bases 1 to 5730) AUTHORS Rosenfeld,J.A., Ballif,B.C., Lucas,A., Spence,E.J., Powell,C., Aylsworth,A.S., Torchia,B.A. and Shaffer,L.G. TITLE Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome JOURNAL PLoS ONE 4 (8), E6568 (2009) PUBMED 19668335 REMARK GeneRIF: results suggest that deletion of SATB2 is responsible for several of the clinical features associated with 2q32q33 microdeletion syndrome Publication Status: Online-Only REFERENCE 7 (bases 1 to 5730) AUTHORS Beaty,T.H., Hetmanski,J.B., Fallin,M.D., Park,J.W., Sull,J.W., McIntosh,I., Liang,K.Y., Vanderkolk,C.A., Redett,R.J., Boyadjiev,S.A., Jabs,E.W., Chong,S.S., Cheah,F.S., Wu-Chou,Y.H., Chen,P.K., Chiu,Y.F., Yeow,V., Ng,I.S., Cheng,J., Huang,S., Ye,X., Wang,H., Ingersoll,R. and Scott,A.F. TITLE Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations JOURNAL Hum. Genet. 120 (4), 501-518 (2006) PUBMED 16953426 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 8 (bases 1 to 5730) AUTHORS Vieira,A.R., Avila,J.R., Daack-Hirsch,S., Dragan,E., Felix,T.M., Rahimov,F., Harrington,J., Schultz,R.R., Watanabe,Y., Johnson,M., Fang,J., O'Brien,S.E., Orioli,I.M., Castilla,E.E., Fitzpatrick,D.R., Jiang,R., Marazita,M.L. and Murray,J.C. TITLE Medical sequencing of candidate genes for nonsyndromic cleft lip and palate JOURNAL PLoS Genet. 1 (6), E64 (2005) PUBMED 16327884 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 9 (bases 1 to 5730) AUTHORS Dobreva,G., Dambacher,J. and Grosschedl,R. TITLE SUMO modification of a novel MAR-binding protein, SATB2, modulates immunoglobulin mu gene expression JOURNAL Genes Dev. 17 (24), 3048-3061 (2003) PUBMED 14701874 REFERENCE 10 (bases 1 to 5730) AUTHORS FitzPatrick,D.R., Carr,I.M., McLaren,L., Leek,J.P., Wightman,P., Williamson,K., Gautier,P., McGill,N., Hayward,C., Firth,H., Markham,A.F., Fantes,J.A. and Bonthron,D.T. TITLE Identification of SATB2 as the cleft palate gene on 2q32-q33 JOURNAL Hum. Mol. Genet. 12 (19), 2491-2501 (2003) PUBMED 12915443 REMARK GeneRIF: SATB2 is identified as the cleft palate gene on chromosome pair 2 which undergoes translocation. COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK056638.1 and AC016746.8. Summary: This gene encodes a DNA binding protein that specifically binds nuclear matrix attachment regions. The encoded protein is involved in transcription regulation and chromatin remodeling. Defects in this gene are associated with isolated cleft palate and mental retardation. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Feb 2010]. Transcript Variant: This variant (1) represents the longest transcript. Variants 1, 2 and 3 encode the same protein. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AK056638.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025084, ERS025088 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-1471 AK056638.1 2-1472 1472-1472 AC016746.8 136075-136075 c 1473-3369 AK056638.1 1474-3370 3370-5730 AC016746.8 36925-39285 c FEATURES Location/Qualifiers source 1..5730 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="2" /map="2q33" gene 1..5730 /gene="SATB2" /note="SATB homeobox 2" /db_xref="GeneID:23314" /db_xref="HGNC:21637" /db_xref="MIM:608148" exon 1..758 /gene="SATB2" /inference="alignment:Splign:1.39.8" misc_feature 638..640 /gene="SATB2" /note="upstream in-frame stop codon" exon 759..986 /gene="SATB2" /inference="alignment:Splign:1.39.8" CDS 818..3019 /gene="SATB2" /note="SATB family member 2; special AT-rich sequence-binding protein 2" /codon_start=1 /product="DNA-binding protein SATB2" /protein_id="NP_001165980.1" /db_xref="GI:289547596" /db_xref="CCDS:CCDS2327.1" /db_xref="GeneID:23314" /db_xref="HGNC:21637" /db_xref="MIM:608148" /translation="
MERRSESPCLRDSPDRRSGSPDVKGPPPVKVARLEQNGSPMGARGRPNGAVAKAVGGLMIPVFCVVEQLDGSLEYDNREEHAEFVLVRKDVLFSQLVETALLALGYSHSSAAQAQGIIKLGRWNPLPLSYVTDAPDATVADMLQDVYHVVTLKIQLQSCSKLEDLPAEQWNHATVRNALKELLKEMNQSTLAKECPLSQSMISSIVNSTYYANVSATKCQEFGRWYKKYKKIKVERVERENLSDYCVLGQRPMHLPNMNQLASLGKTNEQSPHSQIHHSTPIRNQVPALQPIMSPGLLSPQLSPQLVRQQIAMAHLINQQIAVSRLLAHQHPQAINQQFLNHPPIPRAVKPEPTNSSVEVSPDIYQQVRDELKRASVSQAVFARVAFNRTQGLLSEILRKEEDPRTASQSLLVNLRAMQNFLNLPEVERDRIYQDERERSMNPNVSMVSSASSSPSSSRTPQAKTSTPTTDLPIKVDGANINITAAIYDEIQQEMKRAKVSQALFAKVAANKSQGWLCELLRWKENPSPENRTLWENLCTIRRFLNLPQHERDVIYEEESRHHHSERMQHVVQLPPEPVQVLHRQQSQPAKESSPPREEAPPPPPPTEDSCAKKPRSRTKISLEALGILQSFIHDVGLYPDQEAIHTLSAQLDLPKHTIIKFFQNQRYHVKHHGKLKEHLGSAVDVAEYKDEELLTESEENDSEEGSEEMYKVEAEEENADKSKAAPAEIDQR
" misc_feature 995..1282 /gene="SATB2" /note="N-terminal domain of SATB1 and similar proteins; Region: SATB1_N; cd11585" /db_xref="CDD:211426" misc_feature order(998..1000,1004..1006,1055..1069,1073..1075, 1169..1171,1175..1177,1184..1189,1205..1216,1238..1243, 1250..1258,1262..1267) /gene="SATB2" /note="tetramer interface [polypeptide binding]; other site" /db_xref="CDD:211426" misc_feature 1871..2128 /gene="SATB2" /note="CUT domain; Region: CUT; pfam02376" /db_xref="CDD:202226" misc_feature 2240..2485 /gene="SATB2" /note="CUT domain; Region: CUT; pfam02376" /db_xref="CDD:202226" misc_feature 2660..2839 /gene="SATB2" /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(2660..2674,2678..2680,2732..2734,2750..2752, 2789..2791,2795..2800,2807..2812,2816..2824,2828..2833) /gene="SATB2" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:28970" misc_feature order(2666..2668,2675..2677,2798..2800,2807..2812, 2819..2821) /gene="SATB2" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:28970" exon 987..1163 /gene="SATB2" /inference="alignment:Splign:1.39.8" exon 1164..1290 /gene="SATB2" /inference="alignment:Splign:1.39.8" exon 1291..1414 /gene="SATB2" /inference="alignment:Splign:1.39.8" exon 1415..1517 /gene="SATB2" /inference="alignment:Splign:1.39.8" exon 1518..1990 /gene="SATB2" /inference="alignment:Splign:1.39.8" exon 1991..2203 /gene="SATB2" /inference="alignment:Splign:1.39.8" exon 2204..2359 /gene="SATB2" /inference="alignment:Splign:1.39.8" exon 2360..2557 /gene="SATB2" /inference="alignment:Splign:1.39.8" exon 2558..5730 /gene="SATB2" /inference="alignment:Splign:1.39.8" STS 3470..3703 /gene="SATB2" /standard_name="RH80503" /db_xref="UniSTS:87202" variation 4252 /gene="SATB2" /replace="c" /replace="t" /db_xref="dbSNP:11543297" STS 5334..5414 /gene="SATB2" /standard_name="Satb2" /db_xref="UniSTS:498445" STS 5561..5722 /gene="SATB2" /standard_name="D2S2708" /db_xref="UniSTS:21036" STS 5561..5690 /gene="SATB2" /standard_name="RH91707" /db_xref="UniSTS:91093" polyA_signal 5707..5712 /gene="SATB2" polyA_site 5730 /gene="SATB2" ORIGIN
aaattattattttgaaggcgctagatctggggaccgaaagggggagggggagaaatcggaaaccgaggacaacccaaaaggactcactttgcctgatgactcaacgcaactaataatcatctccctctcagtgtgtctctctctgcggcttgtcagtgagtccggctctggctgctggcagaggcggccgagaggggagaggctggaggtgacagcttgggcggccgccgcgtttcctcccgcgcgcggtcccgggtccctgcgtcttctcggctcttggtgttaccggtcccaccgctctggccgcgcctcctcgcgagctagccgccctgcgaaccagcagccccggctcgccgccgccgccgccgcctccgggttctcagccctttctctccagaacgggtctccttcccgaaggtgtgaaaaggctctttcagcctccttctcttcccccctcctccgccgtcccctcccccgctcgctcgggtgtccctttggaggagtcctttccctctcctcctcctccccctcctccctccccccatcatcatcataacaaccatctccgcaccagaagaagacaccctgacccaggaccttaaacattaggacctggggaagagggaaggggaaggagtaaagaggaagactaggagaacactgcaaagccaagcaccagaaactttccaccctggattctctacttttgctccatggacagagccccagtcagccaagtttcagacagaccgtgagcagtccctgtgcgttttattgcgacctgccggtgggaactttgtctccgagtcggagcagcatggagcggcggagcgagagcccgtgtctgcgggacagccccgaccggcggagcggcagcccggacgtcaaggggcctcccccagtgaaggtggcccggctggagcagaacggcagccccatgggagcccgcgggaggcccaacggcgccgtggccaaggccgtgggaggtttgatgattcctgtcttttgtgtcgtggagcagttggacggctctcttgaatatgacaacagagaagaacacgccgagtttgtcctggtgcggaaagatgtgctttttagccagctggtggagactgcgctcctggccctggggtattctcacagctctgcggcccaggcccaaggaataatcaagctgggaaggtggaaccctctccccctcagttatgtgacagatgcacccgacgcgacagtggccgacatgctacaagatgtctatcatgttgtgacgttgaaaatccaattacaaagttgttcaaagttggaagacttgcctgcggagcagtggaaccatgccacagtccgcaatgccttaaaggaactgctcaaagagatgaaccagagcacattagccaaagaatgccctctctcccagagtatgatttcatccattgtaaatagcacatattatgccaatgtgtcagcaaccaagtgccaggagtttgggagatggtataaaaagtacaagaagattaaagtggaaagagtggaacgagaaaacctttcagactattgtgttctgggccagcgtccaatgcatttaccaaatatgaaccagctggcatccctggggaaaaccaacgaacagtctcctcacagccaaattcaccacagtactccaatccgaaaccaagtgcccgcattacagcccatcatgagccctggtcttctttctccccagcttagtccacaacttgtaaggcaacaaatagccatggcccatctgataaaccaacagattgccgttagccggctcctggctcaccagcatcctcaagccatcaaccagcagttcctgaaccatccacccatccccagagcagttaagccagagccaaccaactcttccgtggaagtctctccagatatctaccagcaagtcagagatgagctgaagagggccagtgtgtcccaagctgtctttgcaagagtggcattcaaccgcacacagggattgttgtctgagattctgcgtaaggaagaagaccctcggacagcctctcagtctcttctagtaaacctgagggccatgcagaatttcctcaatctgccagaagtggagcgagatcgcatctaccaggatgagagggagcggagcatgaatcccaatgtgagcatggtctcctcggcctccagcagtcccagctcctcccgaacccctcaggccaaaacctcgacaccgacaacagacctccctattaaggtggacggcgccaacatcaacatcacagctgccatttatgacgagatccaacaggagatgaaaagggccaaggtgtctcaagccctgtttgccaaagtggctgcaaataaaagtcagggctggctgtgtgaactgctccgctggaaggagaacccaagcccagaaaaccgcaccctctgggaaaacctctgtaccatccgtcgcttcctgaaccttccccagcatgagagggatgtcatctatgaggaggagtcaaggcatcaccacagcgaacgcatgcaacacgtggtccagcttccccctgagccggtgcaggtacttcatagacagcagtctcagccagccaaggagagttcccctcccagagaagaagcgcctcccccacctcctccgactgaagacagttgtgccaaaaagccccggtctcgcacaaagatctccttagaagccctggggatcctccaaagctttattcatgatgtaggcctgtacccagaccaggaagccatccacactctttcggctcagctggatctccccaaacacaccatcatcaagttcttccagaaccagcggtaccacgtgaagcaccacgggaagctgaaagagcacctgggctccgcggtggacgtggctgaatataaggacgaggagctgctgaccgagtcagaggagaacgacagcgaggaaggctccgaggagatgtacaaagtggaggctgaggaggaaaatgctgacaaaagcaaggcagcacctgccgaaattgaccagagataatgtgaacttctactaggcaaagcaatacatcggtccaaggattttctgctttcatttctttaaaagttttttgttagtttgttttttgtttttgtttttgggtttttttggctttatttttgtctttttatgtctgttttgtttttcttacccttttggacatttctttgttgcacaggatacacctatagactgaataagttcagtatttccgaatcagacatcgccttggcaaagacactaaagcgttacactttatcccgtctctatgactggatcatagtcattataatcacaggagactctgccttcattatccttgcacttaacggaagttacatcaggcaagtaccaggatgaaaagaactatgaaataaatgaaggaagctacaagtgtgtgtgtatatgtatatgtatatatctctatatttacatatatatattaaaattgcatgggacagagactttgcaatccgaaagaatagactgtgaaatgagttcttaaagaaaagacttgtttatgtattaaaaaaaccacttcacagtgagtcgctttggctttttgataaactgcggcctgctctcagggtggggtgactatttttgaattcctatttattttttgtgtttgtccctgattttttttttttaattctatggcttcctatctggcagcttaatgggtaatttttgaggtatgtatttaacaaaataaacgacactgccgaaaaaaaaaaaagtgaagtgaaaacaatcagggcacattaaaatgatacaagtcaaataaatcttaaagacacaatgcacacttaaaatgactcaataaaatgacttgctacgttccgttattcaatttgtcattactgtagtgaacagatgcatttctgtggaattccaaataagtaaaactgaaattcagtgcagagaaaactttgtccactagtgcaagtcttgatcaaatgacattttgacattggacatatggaattcatagtatgagccacattttgttgtgaaatttatttacctgcttgtggcttcaaatctgaaaattaataagcctgctcgtttaaaagttgtttgttgttgctgtttttttgtctttttgttttttactagaaaatagttcagtgtaatattaagttagaaaagaagttgctgcccagttaaaggggctccctctcaaataaatctccatccttccctctcccaaaagacatttctgatttctgcttcactttgggcttcctcttcttcgtacacattccatctacctaatcaaacattttcagtccctgatctctcctgtcccttttcctgggatgacagccctaacaagaactgtttttgaatcgttgtgcagctccaggcaatagagtatgtgaagcgatttcagtagaatcacttactcatcctaaaagaaaacattatcccagttacctacatcgcaattaccttatgtaaagcagaactaatgctgactggatgtttaatgggatgagcattaaagctgcaatctactatagtactccagatctctttcggcttcctatgagaaacaccagaagcattactttccacttctacttacagtaattgcaagaggagacctcacattcaggactggcctagtgaacgtaatccatgctttaaactggccattaaacagtcccacatggttggattttttttttttttttgagttgtgctttcacaaaaccttgtcaaagacctcatgcaatatcactttgaaagttattttctgtttactacacaaacattgtaatataactgttaatactatttatatatttgaaaggtataaaaggtaggagttaaaaaaaaaacctctatgtgtagatattaactcagaacttacaatatacagggagaagacatgttgcaatacaagctaattctagctgctcagtaacctctggagtttttaaagggacattttcctgtactttttcaaataatgatgtttaaaaattatcttgacataagcgtcatatacctttgcaaaaggatggttgtttgcagttagccctggccccatccttcctatttctgtagtatgctgcagctttaatcagaaagtccatggttgctgcttcctgatctccgagttactctttccaaattgtcttcttacactgttgctgaaggtcactctgtacacgtaatggaaactgattttgccaagctcttacaaggtggttcatctatcgatggcatccgcatttggtatcttttacacttcaaccaaaaatttattaggtatttttcaatgctaagtcttgccttttattttttaatttcactgccaagtttgcagtggttctaagtgaatctgtgggcattttagcctgtggtcttgccagatctttgcgaattacaatgcatatatgtctatttattcaatatctgtcatataatatctatttggaagaagaaactttctcttgtagtgcctcttgacaaagcacaatttcccgcctttttttttttttgtgaaatgaaaaaaacaaattgtgttttattgcggtatcaacaatgtgaataaggattaacatattgtaaatgttcttttttccatgtaaatcaactatctttgttatcactaagtgataattaatttttaacttatgtgcattgttaggctgttagaattttttggttgttaaaataaacgcattcaataaatatga
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:23314 -> Molecular function: GO:0003682 [chromatin binding] evidence: IEA GeneID:23314 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:23314 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA GeneID:23314 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IEA GeneID:23314 -> Biological process: GO:0001764 [neuron migration] evidence: IEA GeneID:23314 -> Biological process: GO:0002076 [osteoblast development] evidence: IEA GeneID:23314 -> Biological process: GO:0006338 [chromatin remodeling] evidence: IEA GeneID:23314 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA GeneID:23314 -> Biological process: GO:0009880 [embryonic pattern specification] evidence: IEA GeneID:23314 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IEA GeneID:23314 -> Biological process: GO:0048704 [embryonic skeletal system morphogenesis] evidence: IEA GeneID:23314 -> Biological process: GO:0051216 [cartilage development] evidence: IEA GeneID:23314 -> Biological process: GO:0060021 [palate development] evidence: IEA GeneID:23314 -> Biological process: GO:0071310 [cellular response to organic substance] evidence: IEA GeneID:23314 -> Cellular component: GO:0000118 [histone deacetylase complex] evidence: IEA GeneID:23314 -> Cellular component: GO:0005634 [nucleus] evidence: IDA GeneID:23314 -> Cellular component: GO:0005667 [transcription factor complex] evidence: IEA GeneID:23314 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA GeneID:23314 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA GeneID:23314 -> Cellular component: GO:0016363 [nuclear matrix] evidence: IEA
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