2025-05-09 20:23:10, GGRNA : RefSeq release 60 (20130726)
LOCUS NR_002211 2872 bp RNA linear PRI 16-JUL-2013 DEFINITION Homo sapiens Meis homeobox 3 pseudogene 1 (MEIS3P1), non-coding RNA. ACCESSION NR_002211 XR_000124 VERSION NR_002211.1 GI:62632708 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 2872) AUTHORS Zody,M.C., Garber,M., Adams,D.J., Sharpe,T., Harrow,J., Lupski,J.R., Nicholson,C., Searle,S.M., Wilming,L., Young,S.K., Abouelleil,A., Allen,N.R., Bi,W., Bloom,T., Borowsky,M.L., Bugalter,B.E., Butler,J., Chang,J.L., Chen,C.K., Cook,A., Corum,B., Cuomo,C.A., de Jong,P.J., DeCaprio,D., Dewar,K., FitzGerald,M., Gilbert,J., Gibson,R., Gnerre,S., Goldstein,S., Grafham,D.V., Grocock,R., Hafez,N., Hagopian,D.S., Hart,E., Norman,C.H., Humphray,S., Jaffe,D.B., Jones,M., Kamal,M., Khodiyar,V.K., LaButti,K., Laird,G., Lehoczky,J., Liu,X., Lokyitsang,T., Loveland,J., Lui,A., Macdonald,P., Major,J.E., Matthews,L., Mauceli,E., McCarroll,S.A., Mihalev,A.H., Mudge,J., Nguyen,C., Nicol,R., O'Leary,S.B., Osoegawa,K., Schwartz,D.C., Shaw-Smith,C., Stankiewicz,P., Steward,C., Swarbreck,D., Venkataraman,V., Whittaker,C.A., Yang,X., Zimmer,A.R., Bradley,A., Hubbard,T., Birren,B.W., Rogers,J., Lander,E.S. and Nusbaum,C. TITLE DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage JOURNAL Nature 440 (7087), 1045-1049 (2006) PUBMED 16625196 REFERENCE 2 (bases 1 to 2872) AUTHORS Steelman,S., Moskow,J.J., Muzynski,K., North,C., Druck,T., Montgomery,J.C., Huebner,K., Daar,I.O. and Buchberg,A.M. TITLE Identification of a conserved family of Meis1-related homeobox genes JOURNAL Genome Res. 7 (2), 142-156 (1997) PUBMED 9049632 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC015922.17, AK054814.1, U68385.1, BQ575773.1, BM463727.1 and BU685266.1. On Apr 21, 2005 this sequence version replaced gi:41150655. Summary: This gene appears to be a retrotransposed pseudogene based on its lack of exons compared to other family members, one of which is found on chromosome 19 (MEIS3). It does appear to be transcribed and has an ORF that may encode a protein of similar size and sequence to that encoded by MEIS3. [provided by RefSeq, Jul 2008]. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-213 AC015922.17 27417-27629 214-1226 AK054814.1 213-1225 1227-1463 U68385.1 1012-1248 1464-1891 BQ575773.1 18-445 c 1892-2543 BM463727.1 99-750 2544-2872 BU685266.1 1-329 c FEATURES Location/Qualifiers source 1..2872 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="17" /map="17p12" gene 1..2872 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /note="Meis homeobox 3 pseudogene 1" /pseudo /db_xref="GeneID:4213" /db_xref="HGNC:7002" misc_RNA 1..2872 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /product="Meis homeobox 3 pseudogene 1" /pseudo /db_xref="GeneID:4213" /db_xref="HGNC:7002" exon 1..2856 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /inference="alignment:Splign:1.39.8" /pseudo variation 18 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:61731176" variation 48 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="c" /db_xref="dbSNP:376068178" variation 53..54 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="c" /db_xref="dbSNP:59447254" variation 57 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:62070981" variation 118 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:560500" variation 118 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:62070982" variation 132..134 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="ctt" /db_xref="dbSNP:200526826" variation 177 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="g" /replace="t" /db_xref="dbSNP:615514" variation 204 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:615475" variation 206 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:150739886" variation 231 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:374560624" variation 276 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:200166425" variation 299 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:558713" variation 303 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:60097079" variation 315 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:200780521" variation 332 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:202196247" variation 348 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:184509499" variation 390 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:604379" variation 398 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:188467839" variation 404 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:192775178" variation 501 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:184311786" variation 575 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:534998" variation 585 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:143985665" variation 614 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:534905" variation 630 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:534861" variation 678 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:534118" variation 689 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:371688774" variation 700 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="t" /db_xref="dbSNP:146517427" variation 723 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="c" /db_xref="dbSNP:139955530" variation 725 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:4791638" variation 765 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:533242" variation 765 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:41508544" variation 784 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="g" /replace="t" /db_xref="dbSNP:148870657" variation 821 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:61745044" variation 883 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="c" /db_xref="dbSNP:373818971" variation 956 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1054119" variation 964 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:369400567" variation 968 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="c" /db_xref="dbSNP:371710472" variation 1011 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:13877" variation 1143 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:12607" variation 1160 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:11218" variation 1190 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:376014112" variation 1219 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:10780" variation 1225 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:11766" variation 1254 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:189259395" variation 1291..1294 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="aa" /replace="aaa" /replace="aaaa" /db_xref="dbSNP:71353752" variation 1333 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:369059710" variation 1372..1374 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="ttttta" /db_xref="dbSNP:200077797" variation 1380 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="ttttta" /db_xref="dbSNP:71353753" variation 1447 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="c" /db_xref="dbSNP:589140" variation 1449 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:182209572" variation 1475 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="c" /db_xref="dbSNP:186407712" variation 1528 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:505605" variation 1571 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:189636360" variation 1735 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:112716634" variation 1801 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="a" /db_xref="dbSNP:201023088" variation 1801 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="c" /db_xref="dbSNP:202170312" variation 1869 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:502137" variation 1872 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="g" /db_xref="dbSNP:371407622" variation 1891..1893 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="aaa" /db_xref="dbSNP:201355385" variation 1910 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="aa" /db_xref="dbSNP:55918110" variation 2155 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="t" /db_xref="dbSNP:143735145" variation 2160 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:1048735" variation 2175 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:1048736" variation 2216 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:2920428" variation 2224 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="c" /db_xref="dbSNP:2955843" variation 2257 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:544509" variation 2342 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:151060655" variation 2394..2397 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="aata" /db_xref="dbSNP:200648068" variation 2448 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:181525399" variation 2475 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:186222967" variation 2487 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="g" /replace="t" /db_xref="dbSNP:112032292" variation 2502 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:1960457" variation 2517 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:146273537" variation 2654 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="c" /db_xref="dbSNP:1058178" variation 2690 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:4791639" variation 2690 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="g" /db_xref="dbSNP:201498130" variation 2700..2701 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="aaa" /db_xref="dbSNP:199975159" variation 2732 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:4792679" variation 2732 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="c" /replace="t" /db_xref="dbSNP:141822244" variation 2779 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="t" /db_xref="dbSNP:191277854" variation 2800 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="" /replace="ag" /db_xref="dbSNP:4054245" variation 2804 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="g" /replace="t" /db_xref="dbSNP:181346504" variation 2849 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="c" /db_xref="dbSNP:3169673" variation 2856 /gene="MEIS3P1" /gene_synonym="MEIS3; MEIS4; MRG2" /replace="a" /replace="c" /db_xref="dbSNP:376516394" ORIGIN
tggctacatgctctccccgtgatggggccggagctgggctggggacacccccgcggcggcgacgtctgctcctctgattccttcaacgaggacaacactgccttcgccaagcaggttcgctctgagaggcccttcttctcctccaacccagaactggacaatctgatgatccaggcaatccaagtgctgcggttccacctgctagagctggagaagggaaagatgcccatcgacctggtcatcgaggatcgggatggcggctgcagggaggacttcgaggactacccagcctcctgccccagcctcccagaccagaataatatatggattcgagaccatgaggatagcgggtctgtacatttggggaccccaggtccatccagcggggggctggcctcccagagtggggacaactccagtgaccaaggagtcgggctggacaccagcgtggcctctcccagttctggtggagaagatgaggacttggaccaggagccacggcgaaacaagaagagggggatcttccccaaggtggccaccaacatcatgcgagcctggttgttccagcacctctcacacccgtacccctcggaggagcagaagaaacagctggcgcaggacacggggcttaccatcctgcaagtcaacaactggttcattaatgcccggagacgcatcgtgcaacctatgatcgatcaatccaaccgcacagggcagggtgcagccttcagcccagagggccagcccatcgggggctataccgagacagagccacacgtggccttccgggctccagcatcagtggggatgagtttgaactcggaaggagaatggcattatctatagaggctgatgcgggagagacccagcctccggctgtgacccccagcctcacacctggctctggttcccgcctggtcctctggcttcaggatcccacctccaaaggcctctccgctcaacgcctacctccctagggccctgctgggacatgggggcctgagtgcccacccaaggggctctcaaggacaccggcaaggcctccaggctctgagccccgcttctgccttcacctctgcctgggacccgagctgggctcctgggccttggtccccagaagatggcagctagggcctcgccgcgaggacagagaagggacagggtggctgggcagtcagggaaggagggtcgcccggatccgacattttggagagattctttcaccctcctgtcccccccacctcccttctctaatttcttctttttttaatgataaagtcttaaaacacagaaaaaaaaaagacttcagagaattaggtagatgaagcactttatacagtatatatcttcagcttaaatttgttttgagtattttttttatttttaagtaggcaaagatttaaaattttttatttttagtaaatgtttgaagcaaactaaaaagacgtgggcaatatttaccaaaacaaaacagaacccaaaaaattgtacatcttgatcttagcaaatatccttattgtagagacacttaataaagagatggtattttaatatctgcagttctgaggtagggtgtaacttagttctacattgtgatttaggaatttttaaacctttcttcttcaggggagaagtgacccaggcctcgagtttagtgctaaagccactagtgtacttatgctgtcacctaaccaccacatgcgacatggaggcagaggctaaatataggggctttcttaagaaagtgagaggaaattagcaagcattattagtgtttgactactgctatcaagtgaattcaaaggaaacaggtttttatgccatatttaagttacagaaaccaggcatgcttagaatagtttctaaggtgacagagtgagactccatctcaaaaaaaaaaaaaaaaaaaagaatagtttctagaggttattggagaatagaaagctaagaaaacttggtatacatttacaattgaaatataattacactttttactctcagaatattattcagattagacttcctgtttatcttttatattcttgcattgatataatgcctgatccttcaaagttctttcacatattatatgatcttctttatgaaaaaaagtagatgctttattctgatatattcagtttcccactttaggcaaaagtggattaatagaatgatgaattcaaagtagatgaggaaaatcaggcacagagaagtaaaggtaggtacagacccaaattcacacaagataatgacatcaccagcgtttaagttgatcatcaaaggctgggctggatttgtcttgctgtatgtgtcaggaaatttatacctattacattttccattttctcaaaataagtcacatgattgtaatgtttagctgcaacttttctcctaataaatagtgtcatgaagaatgttatagtgcgaagtttgtacatttcagggtcagttatacaatgtgaactctttatctacgggaatgagaatggaggatcattgaaggccatgatataaacaaatttgcatgttgaagcctgtataaaacatggtacagtgagtgaatgcccccatccccaagaacactttatacatattaaatggatatatgattactgtgcaaaaattcattctggaaatgaacatatatttgagcactaatatgtaatgtacatcttctgccctaaggagaaaataaatcataaaacttgttttacattcaaaattactttcccgagcatgtcttagagtaatctacgtgttgatgtatgtaaattgtattttaggtaggcaaagaaacaagtctggttatttatgtaaaaactagtctaataaagtgagtggctttatcactttgaaaaaaaaaaaaaaaaaa
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:4213 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:4213 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA GeneID:4213 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
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