2025-05-09 20:00:02, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_005924 2383 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens mesenchyme homeobox 2 (MEOX2), mRNA. ACCESSION NM_005924 VERSION NM_005924.4 GI:84105334 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 2383) AUTHORS Douville,J.M., Cheung,D.Y., Herbert,K.L., Moffatt,T. and Wigle,J.T. TITLE Mechanisms of MEOX1 and MEOX2 regulation of the cyclin dependent kinase inhibitors p21 and p16 in vascular endothelial cells JOURNAL PLoS ONE 6 (12), E29099 (2011) PUBMED 22206000 REMARK GeneRIF: MEOX1 and MEOX2 activate p16(INK4a) in a DNA binding dependent manner, whereas they induce p21(CIP1/WAF1) in a DNA binding independent manner. REFERENCE 2 (bases 1 to 2383) AUTHORS Chen,Y., Rabson,A.B. and Gorski,D.H. TITLE MEOX2 regulates nuclear factor-kappaB activity in vascular endothelial cells through interactions with p65 and IkappaBbeta JOURNAL Cardiovasc. Res. 87 (4), 723-731 (2010) PUBMED 20421348 REMARK GeneRIF: Report of an interaction between a homeobox protein and IkappaBbeta in endothelial cells and suggest that MEOX2 modulates the activity of the RelA complex through direct interaction with its components. REFERENCE 3 (bases 1 to 2383) AUTHORS Ohshima,J., Haruta,M., Arai,Y., Kasai,F., Fujiwara,Y., Ariga,T., Okita,H., Fukuzawa,M., Hata,J., Horie,H. and Kaneko,Y. TITLE Two candidate tumor suppressor genes, MEOX2 and SOSTDC1, identified in a 7p21 homozygous deletion region in a Wilms tumor JOURNAL Genes Chromosomes Cancer 48 (12), 1037-1050 (2009) PUBMED 19760604 REMARK GeneRIF: Loss of MEOX2 gene is associated with Wilms tumor. REFERENCE 4 (bases 1 to 2383) AUTHORS Irelan,J.T., Gutierrez Del Arroyo,A., Gutierrez,A., Peters,G., Quon,K.C., Miraglia,L. and Chanda,S.K. TITLE A functional screen for regulators of CKDN2A reveals MEOX2 as a transcriptional activator of INK4a JOURNAL PLoS ONE 4 (4), E5067 (2009) PUBMED 19340300 REMARK GeneRIF: MEOX2-induced senescence is dependent upon INK4a activity, and chromatin immunoprecipitation studies indicate that MEOX2 directly binds the INK4a promoter REFERENCE 5 (bases 1 to 2383) AUTHORS Valcourt,U., Thuault,S., Pardali,K., Heldin,C.H. and Moustakas,A. TITLE Functional role of Meox2 during the epithelial cytostatic response to TGF-beta JOURNAL Mol Oncol 1 (1), 55-71 (2007) PUBMED 19383287 REMARK GeneRIF: ectopic Meox2 suppressed epithelial cell proliferation in cooperation with TGF-beta1, and mediated induction of the cell cycle inhibitor gene p21. REFERENCE 6 (bases 1 to 2383) AUTHORS Quinn,L.M., Latham,S.E. and Kalionis,B. TITLE The homeobox genes MSX2 and MOX2 are candidates for regulating epithelial-mesenchymal cell interactions in the human placenta JOURNAL Placenta 21 (SUPPL A), S50-S54 (2000) PUBMED 10831122 REFERENCE 7 (bases 1 to 2383) AUTHORS Quinn,L.M., Johnson,B.V., Nicholl,J., Sutherland,G.R. and Kalionis,B. TITLE Isolation and identification of homeobox genes from the human placenta including a novel member of the Distal-less family, DLX4 JOURNAL Gene 187 (1), 55-61 (1997) PUBMED 9073066 REFERENCE 8 (bases 1 to 2383) AUTHORS Grigoriou,M., Kastrinaki,M.C., Modi,W.S., Theodorakis,K., Mankoo,B., Pachnis,V. and Karagogeos,D. TITLE Isolation of the human MOX2 homeobox gene and localization to chromosome 7p22.1-p21.3 JOURNAL Genomics 26 (3), 550-555 (1995) PUBMED 7607679 REFERENCE 9 (bases 1 to 2383) AUTHORS LePage,D.F., Altomare,D.A., Testa,J.R. and Walsh,K. TITLE Molecular cloning and localization of the human GAX gene to 7p21 JOURNAL Genomics 24 (3), 535-540 (1994) PUBMED 7713505 REFERENCE 10 (bases 1 to 2383) AUTHORS Reardon,W., McManus,S.P., Summers,D. and Winter,R.M. TITLE Cytogenetic evidence that the Saethre-Chotzen gene maps to 7p21.2 JOURNAL Am. J. Med. Genet. 47 (5), 633-636 (1993) PUBMED 8266988 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DA586635.1, BC017021.1 and BQ025060.1. This sequence is a reference standard in the RefSeqGene project. On Dec 30, 2005 this sequence version replaced gi:55956906. Summary: This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease. [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 :: BC017021.1, X82629.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025084 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-512 DA586635.1 1-512 513-2049 BC017021.1 410-1946 2050-2383 BQ025060.1 1-334 c FEATURES Location/Qualifiers source 1..2383 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="7" /map="7p22.1-p21.3" gene 1..2383 /gene="MEOX2" /gene_synonym="GAX; MOX2" /note="mesenchyme homeobox 2" /db_xref="GeneID:4223" /db_xref="HGNC:7014" /db_xref="MIM:600535" exon 1..798 /gene="MEOX2" /gene_synonym="GAX; MOX2" /inference="alignment:Splign:1.39.8" variation 243 /gene="MEOX2" /gene_synonym="GAX; MOX2" /replace="c" /replace="t" /db_xref="dbSNP:1050290" misc_feature 246..248 /gene="MEOX2" /gene_synonym="GAX; MOX2" /note="upstream in-frame stop codon" CDS 282..1196 /gene="MEOX2" /gene_synonym="GAX; MOX2" /note="growth arrest-specific homeobox" /codon_start=1 /product="homeobox protein MOX-2" /protein_id="NP_005915.2" /db_xref="GI:84105335" /db_xref="CCDS:CCDS34605.1" /db_xref="GeneID:4223" /db_xref="HGNC:7014" /db_xref="MIM:600535" /translation="
MEHPLFGCLRSPHATAQGLHPFSQSSLALHGRSDHMSYPELSTSSSSCIIAGYPNEEGMFASQHHRGHHHHHHHHHHHHHQQQQHQALQTNWHLPQMSSPPSAARHSLCLQPDSGGPPELGSSPPVLCSNSSSLGSSTPTGAACAPGDYGRQALSPAEAEKRSGGKRKSDSSDSQEGNYKSEVNSKPRKERTAFTKEQIRELEAEFAHHNYLTRLRRYEIAVNLDLTERQVKVWFQNRRMKWKRVKGGQQGAAAREKELVNVKKGTLLPSELSGIGAATLQQTGDSIANEDSHDSDHSSEHAHL
" misc_feature 843..1019 /gene="MEOX2" /gene_synonym="GAX; MOX2" /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(843..857,861..863,912..914,930..932,969..971, 975..980,987..992,996..1004,1008..1013) /gene="MEOX2" /gene_synonym="GAX; MOX2" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:28970" misc_feature order(849..851,858..860,978..980,987..992,999..1001) /gene="MEOX2" /gene_synonym="GAX; MOX2" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:28970" STS 537..687 /gene="MEOX2" /gene_synonym="GAX; MOX2" /standard_name="MEOX2" /db_xref="UniSTS:503608" exon 799..971 /gene="MEOX2" /gene_synonym="GAX; MOX2" /inference="alignment:Splign:1.39.8" STS 818..878 /gene="MEOX2" /gene_synonym="GAX; MOX2" /standard_name="MEOX2" /db_xref="UniSTS:23282" exon 972..2371 /gene="MEOX2" /gene_synonym="GAX; MOX2" /inference="alignment:Splign:1.39.8" STS 1374..1695 /gene="MEOX2" /gene_synonym="GAX; MOX2" /standard_name="G60276" /db_xref="UniSTS:137381" STS 1376..1709 /gene="MEOX2" /gene_synonym="GAX; MOX2" /standard_name="SHGC-12960" /db_xref="UniSTS:44537" variation 1438 /gene="MEOX2" /gene_synonym="GAX; MOX2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:17199" variation 1468 /gene="MEOX2" /gene_synonym="GAX; MOX2" /replace="g" /replace="t" /db_xref="dbSNP:1131061" variation 1604 /gene="MEOX2" /gene_synonym="GAX; MOX2" /replace="a" /replace="g" /db_xref="dbSNP:1050291" STS 2071..2204 /gene="MEOX2" /gene_synonym="GAX; MOX2" /standard_name="D7S2109E" /db_xref="UniSTS:24755" polyA_signal 2349..2354 /gene="MEOX2" /gene_synonym="GAX; MOX2" polyA_site 2371 /gene="MEOX2" /gene_synonym="GAX; MOX2" ORIGIN
gaaagcagttctctgggaccaccttcttttggcttcaacctctcccactcttgacatctgagtagctcagggaagctcttccaggtccgactgttcatatgtaaaggagactggccgctggggctcaggaccgggattatccgagctctgcagaagtgcaccgctattgctttgggaggttaaaaaaaaaatcacacggtttccagtgaaaaagtgacagagggtggtggcctttggaaccgccgtgaagtcttctgcctggaacccgaaacttgcatgctatggaacacccgctctttggctgcctgcgcagccctcacgccacggcgcaaggcttgcacccgttctcccaatcctctctcgccctccatggaagatctgaccatatgtcttaccccgagctctctacttcttcctcatcttgcataatcgcgggataccccaacgaagagggcatgtttgccagccagcatcacagggggcaccaccaccaccaccaccaccaccaccatcaccaccatcagcagcagcagcaccaggctctgcaaaccaactggcacctcccgcagatgtcttccccaccgagtgcggctcggcacagcctctgcctccagcccgactctggagggcccccagagttggggagcagcccgcccgtcctgtgctccaactcttccagcttgggctccagcaccccgactggggccgcgtgcgcgccgggggactacggccgccaggcactgtcacctgcggaggcggagaagcgaagcggcggcaagaggaaaagcgacagctcagactcccaggaaggaaattacaagtcagaagtcaacagcaaacccaggaaagaaaggacagcatttaccaaagagcaaatcagagaacttgaagcagaatttgcccatcataattatctcaccagactgaggcgatacgagatagcagtgaatctggatctcactgaaagacaggtgaaagtctggttccaaaacaggcggatgaagtggaagagggtaaagggtggacagcaaggagctgcggctcgggaaaaggaactggtgaatgtgaaaaagggaacacttctcccatcagagctgtcgggaattggtgcagccaccctccagcaaacaggggactctatagcaaatgaagacagtcacgacagtgaccacagctcagagcatgcgcacttatgatataaacagaggaccagctccattctcaggaaagaaatgttgtgatggcaagccttacccaaatatcgtttacacagagagatgactatggcagtgatgtttaatattattaaatccaggcatttcgaatctgtttttcatgatttatagagggtttacacaaagtgccacttattaaagagcttccacagtgaagatggagaaggtgaacttgctttgaatattccagatgtgtttggtcgtgcgtatggcagtgagcaggtatgtgtttgcttttgcttgcactgaaaattaaattgctatcaagagcaaactatgaacggttttttattcaagatgtctccagagtgaagatgccgaggatgaacttgcattgaacattccagatgtgtgagatcatgtgtattacagtgggcaggtatttgcttttgcttgcactgaaaattaaattgctatcaagaataaaccatgaaacattttatcctgaacagccacagtgcctgaattcactcaagtggataaaaagtgtattttaactctgtatatattacccttaagtcattttcctgtcttcactaatttagcaatgcattcatattagctgatgaaaataggcactcacaatgacaaccagagccagtttcttgtcttttttatacattttgtcatcccagagacaatcagtatgtgcttacctgtgttcaagtagagaaaaatacagtagagtctgataggacatattcttgtaccacagacaaaacaaatcttatgttgcatttactatcaactgctgctaatacgttattataaaacttacctagctcctgaattcttcctatcttatagcttaaaacaattaggatcataggcaaatcagttaccttgcagaaagagctttgtatgacagacattgtcttattttatttctgtaaaatattagctgtatgaatatgatttaattaacaagaaaacatttcttcctgattgacaacagtgttagacaaggtgcaaagcgaaactggttgctcaagttgatagaaaacaaaattctgaatatcttcaaattaaattcggtaaaaacacattattttttcatatgtgatgtattcatgcagaacaactatctttgtattttgtttttaaaatgtgtttaataaatgatcctttgtaaataaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:4223 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:4223 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:4223 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IDA GeneID:4223 -> Biological process: GO:0001525 [angiogenesis] evidence: IEA GeneID:4223 -> Biological process: GO:0001757 [somite specification] evidence: IEA GeneID:4223 -> Biological process: GO:0007275 [multicellular organismal development] evidence: TAS GeneID:4223 -> Biological process: GO:0007519 [skeletal muscle tissue development] evidence: IEA GeneID:4223 -> Biological process: GO:0008015 [blood circulation] evidence: TAS GeneID:4223 -> Biological process: GO:0060021 [palate development] evidence: IEA GeneID:4223 -> Biological process: GO:0060173 [limb development] evidence: IEA GeneID:4223 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA GeneID:4223 -> Cellular component: GO:0016607 [nuclear speck] evidence: IEA
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