2024-03-29 17:36:55, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001172438 6602 bp mRNA linear PRI 07-JUL-2013 DEFINITION Homo sapiens paternally expressed 10 (PEG10), transcript variant 2, mRNA. ACCESSION NM_001172438 VERSION NM_001172438.1 GI:289176997 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 6602) AUTHORS Chen,H., Sun,M., Zhao,G., Liu,J., Gao,W., Si,S. and Meng,T. TITLE Elevated expression of PEG10 in human placentas from preeclamptic pregnancies JOURNAL Acta Histochem. 114 (6), 589-593 (2012) PUBMED 22137777 REMARK GeneRIF: elevated expression of PEG10 is likely to be involved in the pathophysiology of preeclampsia REFERENCE 2 (bases 1 to 6602) AUTHORS Xiong,J., Qin,J., Zheng,Y., Peng,X., Luo,Y. and Meng,X. TITLE PEG10 promotes the migration of human Burkitt's lymphoma cells by up-regulating the expression of matrix metalloproteinase-2 and -9 JOURNAL Clin Invest Med 35 (3), E117-E125 (2012) PUBMED 22673314 REMARK GeneRIF: promotes migration of Burkitt's lymphoma cells via upregulation of matrix metalloproteinase-2 and -9 Publication Status: Online-Only REFERENCE 3 (bases 1 to 6602) AUTHORS Liu,D.C., Yang,Z.L. and Jiang,S. TITLE Identification of PEG10 and TSG101 as carcinogenesis, progression, and poor-prognosis related biomarkers for gallbladder adenocarcinoma JOURNAL Pathol. Oncol. Res. 17 (4), 859-866 (2011) PUBMED 21455631 REMARK GeneRIF: Overexpression of PEG10 and TSG101 was detected in gallbladder adenocarcinoma. REFERENCE 4 (bases 1 to 6602) AUTHORS Dong,H., Zhang,H., Liang,J., Yan,H., Chen,Y., Shen,Y., Kong,Y., Wang,S., Zhao,G. and Jin,W. TITLE Digital karyotyping reveals probable target genes at 7q21.3 locus in hepatocellular carcinoma JOURNAL BMC Med Genomics 4, 60 (2011) PUBMED 21767414 REMARK GeneRIF: the mRNA expression level of PEG10 were significantly up-regulated in tumorous liver tissues compared with corresponding nontumorous counterparts. Publication Status: Online-Only REFERENCE 5 (bases 1 to 6602) AUTHORS Lux,A., Beil,C., Majety,M., Barron,S., Gallione,C.J., Kuhn,H.M., Berg,J.N., Kioschis,P., Marchuk,D.A. and Hafner,M. TITLE Human retroviral gag- and gag-pol-like proteins interact with the transforming growth factor-beta receptor activin receptor-like kinase 1 JOURNAL J. Biol. Chem. 280 (9), 8482-8493 (2005) PUBMED 15611116 REMARK GeneRIF: PEG10 contains two overlapping reading frames from which two proteins are translated by a -1 ribosomal frameshift mechanism. REFERENCE 6 (bases 1 to 6602) AUTHORS Smallwood,A., Papageorghiou,A., Nicolaides,K., Alley,M.K., Jim,A., Nargund,G., Ojha,K., Campbell,S. and Banerjee,S. TITLE Temporal regulation of the expression of syncytin (HERV-W), maternally imprinted PEG10, and SGCE in human placenta JOURNAL Biol. Reprod. 69 (1), 286-293 (2003) PUBMED 12620933 REMARK GeneRIF: placental PEG10 is downregulated at early hypoxic phase, and highly activated at 11-12 wk of gestation REFERENCE 7 (bases 1 to 6602) AUTHORS Okabe,H., Satoh,S., Furukawa,Y., Kato,T., Hasegawa,S., Nakajima,Y., Yamaoka,Y. and Nakamura,Y. TITLE Involvement of PEG10 in human hepatocellular carcinogenesis through interaction with SIAH1 JOURNAL Cancer Res. 63 (12), 3043-3048 (2003) PUBMED 12810624 REMARK GeneRIF: Exogenous expression of PEG10 conferred oncogenic activity. PEG10 protein associated with SIAH1, a mediator of apoptosis, and overexpression of PEG10 decreased the cell death mediated by SIAH1. REFERENCE 8 (bases 1 to 6602) AUTHORS Shigemoto,K., Brennan,J., Walls,E., Watson,C.J., Stott,D., Rigby,P.W. and Reith,A.D. TITLE Identification and characterisation of a developmentally regulated mammalian gene that utilises -1 programmed ribosomal frameshifting JOURNAL Nucleic Acids Res. 29 (19), 4079-4088 (2001) PUBMED 11574691 REFERENCE 9 (bases 1 to 6602) AUTHORS Ono,R., Kobayashi,S., Wagatsuma,H., Aisaka,K., Kohda,T., Kaneko-Ishino,T. and Ishino,F. TITLE A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21 JOURNAL Genomics 73 (2), 232-237 (2001) PUBMED 11318613 REMARK GeneRIF: PEG10 gene is imprinted, with preferential expression from the paternal allele. REFERENCE 10 (bases 1 to 6602) AUTHORS Volff,J., Korting,C. and Schartl,M. TITLE Ty3/Gypsy retrotransposon fossils in mammalian genomes: did they evolve into new cellular functions? JOURNAL Mol. Biol. Evol. 18 (2), 266-270 (2001) PUBMED 11158386 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK299837.1, AF216076.1, DA683494.1 and DA297295.1. Summary: This is a paternally expressed imprinted gene that encodes transcripts containing two overlapping open reading frames (ORFs), RF1 and RF1/RF2, as well as retroviral-like slippage and pseudoknot elements, which can induce a -1 nucleotide frame-shift. ORF1 encodes a shorter isoform with a CCHC-type zinc finger motif containing a sequence characteristic of gag proteins of most retroviruses and some retrotransposons. The longer isoform is the result of -1 translational frame-shifting leading to translation of a gag/pol-like protein combining RF1 and RF2. It contains the active-site consensus sequence of the protease domain of pol proteins. Additional isoforms resulting from alternatively spliced transcript variants, as well as from use of upstream non-AUG (CUG) start codon, have been reported for this gene. Increased expression of this gene is associated with hepatocellular carcinomas. [provided by RefSeq, May 2010]. Transcript Variant: This variant (2) uses an alternate donor splice site at the 5' terminal exon compared to variant 1, resulting in translation initiation from an in-frame, upstream AUG. It contains two overlapping reading frames, RF1 and RF1/RF2. This isoform (4), encoded by RF1, is shorter with a distinct N-terminus compared to isoform 1. Isoform 4 is synthesized when -1 translational frame-shifting does not occur. 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 :: AK299837.1, AL560233.3 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025082, ERS025084 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## imprinted gene :: PMID: 11318613 ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-2586 AK299837.1 1-2586 2587-4345 AF216076.1 2152-3910 4346-4756 DA683494.1 26-436 4757-4980 DA297295.1 357-580 4981-6602 AF216076.1 4545-6166 FEATURES Location/Qualifiers source 1..6602 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="7" /map="7q21" gene 1..6602 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="paternally expressed 10" /db_xref="GeneID:23089" /db_xref="HGNC:14005" /db_xref="MIM:609810" exon 1..222 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /inference="alignment:Splign:1.39.8" misc_feature 41..43 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="upstream in-frame stop codon" CDS 218..1423 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="isoform 4 is encoded by transcript variant 2; retrotransposon gag domain containing 3; retrotransposon-derived protein PEG10; embryonal carcinoma differentiation regulated; MEF3 like 1; MEF3-like protein 1; ty3/Gypsy-like protein; paternally expressed gene 10 protein; myelin expression factor 3-like protein 1; mammalian retrotransposon-derived protein 2; retrotransposon-derived gag-like polyprotein; retrotransposon gag domain-containing protein 3; embryonal carcinoma differentiation-regulated protein" /codon_start=1 /product="retrotransposon-derived protein PEG10 isoform 4" /protein_id="NP_001165909.1" /db_xref="GI:289176998" /db_xref="GeneID:23089" /db_xref="HGNC:14005" /db_xref="MIM:609810" /translation="
MRNKRVLKTKKRRSGRGGQDPGLHPHRSEATAGRSPPTPTVTLGPDCPPPPPPPPPNNNNNNNSKHTGHKSACVPNMTERRRDELSEEINNLREKVMKQSEENNNLQSQVQKLTEENTTLREQVEPTPEDEDDDIELRGAAAAAAPPPPIEEECPEDLPEKFDGNPDMLAPFMAQCQIFMEKSTRDFSVDRVRVCFVTSMMTGRAARWASAKLERSHYLMHNYPAFMMEMKHVFEDPQRREVAKRKIRRLRQGMGSVIDYSNAFQMIAQDLDWNEPALIDQYHEGLSDHIQEELSHLEVAKSLSALIGQCIHIERRLARAAAARKPRSPPRALVLPHIASHHQVDPTEPVGGARMRLTQEEKERRRKLNLCLYCGTGGHYADNCPAKASKSSPAGNSPAPL
" misc_feature 800..1081 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="Retrotransposon gag protein; Region: Retrotrans_gag; pfam03732" /db_xref="CDD:146393" exon 223..6584 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /inference="alignment:Splign:1.39.8" variation 233 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:112688289" variation 337 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:369601878" variation 358 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:71562863" variation 365 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:71562864" variation 374 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:71562865" variation 403..408 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="caactc" /db_xref="dbSNP:374577874" variation 412 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:373794887" STS 423..1457 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /db_xref="UniSTS:481964" variation 439 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:376814465" variation 451 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:367923171" variation 516 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:372443374" variation 602 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:375463611" variation 607 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:200610645" variation 629 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:147863226" variation 706 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:201501752" variation 728 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:374803366" variation 768 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:368939059" variation 789 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:372959401" variation 861 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:375994845" variation 885 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:148903291" variation 900 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:199644223" variation 902 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:181931446" variation 915 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:373696772" variation 1002 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:200638421" variation 1046 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:371583344" variation 1048 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:202101917" variation 1051 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:367821311" variation 1081 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:370323324" variation 1102 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:3209061" variation 1187 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:374669576" variation 1207 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:371597071" variation 1277 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:376581536" variation 1324 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:368311963" variation 1344 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:372378066" misc_feature 1399..1405 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="the nucleotide sequence surrounding the frame-shift site is highly conserved; Region: conserved frame-shift core sequence" misc_feature 1402 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="-1 ribosomal frame-shift at this site generates the longer isoform" variation 1529 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:375398177" variation 1547 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:187567019" variation 1575 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:189856221" variation 1671 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:373004121" variation 1711 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:181708979" variation 1755 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:376322331" variation 1784 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:148037544" variation 1808 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:140813381" variation 1857 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:200375561" variation 1934 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:201023812" variation 1948 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:201604172" variation 2008 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:185617764" variation 2056 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:369503620" variation 2131 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:190428861" variation 2252 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:369421203" variation 2259 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:3750105" variation 2311 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:200290306" variation 2374 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:369566255" variation 2375 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:182259108" variation 2376 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:185785639" variation 2414 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:112535663" variation 2504 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:199593658" variation 2547 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:150121454" variation 2559 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:35039803" variation 2662 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:78966738" variation 2723 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:35237090" variation 2760 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:72615135" variation 2763 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:113951929" variation 2784 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:191035277" variation 2895 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:75890579" variation 2896 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:78249742" variation 2919 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:138576679" variation 2995 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:141573011" variation 3008 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:183720152" variation 3031 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:146181651" variation 3072 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:189106507" variation 3164 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:3750106" variation 3209 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:112079331" variation 3540 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:371237508" variation 3624 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:374308979" variation 3662 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:137861769" variation 3737 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:372624616" variation 3800 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:367756779" variation 3887 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:11549144" variation 3917 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:190424869" variation 3997 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:368587365" variation 4030 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:183061000" variation 4065 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:149435445" variation 4067 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:375735183" variation 4125 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:74802312" variation 4133 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:117152307" variation 4287 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:371957260" variation 4346 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:13073" variation 4370 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:13226637" variation 4379 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:377389610" variation 4387 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:1136429" variation 4698 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:186982647" variation 4710 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="t" /db_xref="dbSNP:375638047" variation 4748 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:116616252" variation 4756 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:73223849" STS 4809..5609 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /standard_name="PEG10_8006" /db_xref="UniSTS:467823" variation 4852 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:191522451" variation 4869 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:200749134" variation 4870 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:201879623" variation 4871 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:200078595" variation 4871 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="t" /db_xref="dbSNP:10707840" variation 4877 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:78537188" variation 4878 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:77252058" variation 4962 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:184904316" variation 5047 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:12671285" STS 5204..5303 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /standard_name="WI-12157" /db_xref="UniSTS:83417" variation 5224 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:148567462" variation 5227..5230 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="aatt" /db_xref="dbSNP:199565534" variation 5276 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:1059224" variation 5278..5279 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="tt" /db_xref="dbSNP:71660247" variation 5285 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:187513909" variation 5385 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:192748781" variation 5388 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:62466562" variation 5391 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:7810469" variation 5397 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:14444" variation 5434 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:147284109" variation 5458..5459 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="tt" /db_xref="dbSNP:61078050" variation 5561 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:114854087" STS 5576..5735 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /standard_name="STS-H51766" /db_xref="UniSTS:1756" variation 5622 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:368821741" variation 5639 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="a" /db_xref="dbSNP:139770503" variation 5692 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:185496776" variation 5815..5818 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="ctgt" /db_xref="dbSNP:67946661" variation 6014 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:1059044" variation 6167 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:76468647" STS 6203..6463 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /standard_name="WI-20034" /db_xref="UniSTS:23610" variation 6429 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:144674472" variation 6490 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:371406587" variation 6504 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:11981011" variation 6507 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:190747409" polyA_signal 6547..6552 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" polyA_signal 6558..6563 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" variation 6582 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:113002760" polyA_site 6584 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" ORIGIN
acacgcgcttcaacttcggttggtgtgtgtcgaagaaacctgactgcgccctgaggagaacagcggagaaggtccaccgagcctggcgaaaggtccgctgagcgggctgtcgtccggagccactccgggctgcggagcacccagtggagaccgcgcctggctcaggtgtgggaccccatccttcctgtcttcgcagaggagtcctcgcgtggtgagtatgcgaaataagcgggttttgaaaacaaaaaaaagaaggagtggaagagggggccaggatccaggcctccatccccacagaagtgaagctacagctgggaggtctcctcccaccccaaccgtcaccctgggtcccgactgcccacctcctcctcctccccctccccccaacaacaacaacaacaacaactccaagcacaccggccataagagtgcgtgtgtccccaacatgaccgaacgaagaagggacgagctctctgaagagatcaacaacttaagagagaaggtcatgaagcagtcggaggagaacaacaacctgcagagccaggtgcagaagctcacagaggagaacaccacccttcgagagcaagtggaacccacccctgaggatgaggatgatgacatcgagctccgcggtgctgcagcagctgctgccccaccccctccaatagaggaagagtgcccagaagacctcccagagaagttcgatggcaacccagacatgctggctcctttcatggcccagtgccagatcttcatggaaaagagcaccagggatttctcagttgatcgtgtccgtgtctgcttcgtgacaagcatgatgaccggccgtgctgcccgttgggcctcagcaaagctggagcgctcccactacctgatgcacaactacccagctttcatgatggaaatgaagcatgtctttgaagaccctcagaggcgagaggttgccaaacgcaagatcagacgcctgcgccaaggcatggggtctgtcatcgactactccaatgctttccagatgattgcccaggacctggattggaacgagcctgcgctgattgaccagtaccacgagggcctcagcgaccacattcaggaggagctctcccacctcgaggtcgccaagtcgctgtctgctctgattgggcagtgcattcacattgagagaaggctggccagggctgctgcagctcgcaagccacgctcgccaccccgggcgctggtgttgcctcacattgcaagccaccaccaggtagatccaaccgagccggtgggaggtgcccgcatgcgcctgacgcaggaagaaaaagaaagacgcagaaagctgaacctgtgcctctactgtggaacaggaggtcactacgctgacaattgtcctgccaaggcctcaaagtcttcgccggcgggaaactccccggccccgctgtagagggaccttcagcgaccgggccagaaataataaggtccccacaagatgatgcctcatctccacacttgcaagtgatgctccagattcatcttccgggcagacacaccctgttcgtccgagccatgatcgattctggtgcttctggcaacttcattgatcacgaatatgttgctcaaaatggaattcctctaagaatcaaggactggccaatacttgtggaagcaattgatgggcgccccatagcatcgggcccagttgtccacgaaactcacgacctgatagttgacctgggagatcaccgagaggtgctgtcatttgatgtgactcagtctccattcttccctgtcgtcctaggggttcgctggctgagcacacatgatcccaatatcacatggagcactcgatctatcgtctttgattctgaatactgccgctaccactgccggatgtattctccaataccaccatcgctcccaccaccagcaccacaaccgccactctattatccagtagatggatacagagtttaccaaccagtgaggtattactatgtccagaatgtgtacactccagtagatgagcacgtctacccagatcaccgcctggttgaccctcacatagaaatgatacctggagcacacagtattcccagtggacatgtgtattcactgtccgaacctgaaatggcagctcttcgagattttgtggcaagaaatgtaaaagatgggctaattactccaacgattgcacctaatggagcccaagttctccaggtgaagagggggtggaaactgcaagtttcttatgattgccgagctccaaacaattttactatccagaatcagtatcctcgcctatctattccaaatttagaagaccaagcacacctggcaacgtacactgaattcgtacctcaaatacctggataccaaacataccccacatatgccgcgtacccgacctacccagtaggattcgcctggtacccagtgggacgagacggacaaggaagatcactatatgtacctgtgatgatcacttggaatccacactggtaccgccagcctccggtaccacagtacccgccgccacagccgccgcctccaccaccaccaccgccgccgcctccatcttacagtaccctgtaaatacctgtcatgtccttcaggatctctgccctcaaaatttattcctgttcagcttctcaatcagtgactgtgtgctaaattttaggctactgtatcttcaggccacctgaggcacatcctctctgaaacggctatggaaggttagggccactctggactggcacacatcctaaagcaccaaaagaccttcaacattttctgagagcaacagagtatttgccaataaatgatctctcatttttccaccttgactgccaatctaactaaaataattaataagtttactttccagccagtcctggaagtctgggttttacctgccaaaacctccatcaccatctaaattataggctgccaaatttgctgtttaacatttacagagaagctgatacaaacgcaggaaatgctgatttctttatggagggggagacgaggaggaggaggacatgacttttcttgcggtttcggtaccctctttttaaatcactggaggactgaggccttattaaggaagccaaaattatcggtgcagtgtggaaaggcttccgtgatcctctcgctgcacccttagaaacttcaccgtcttcaaactccatttccatggttctgttaattctcaaggagcagcaactcgactggttctcccaggagcaggaaaaacccttgtgacatgaaacatctcaggcctgaaaagaaagtgctctctcagatggactcttgcatgttaagactatgtcttcacatcatggtgcaaatcacatgtacccaatgactccggctttgacacaacaccttaccatcatcatgccatgatggcttccacaaagcattaaacctggtaaccagagattactggtggctccagcgttgttagatgttcatgaaatgtgaccacctctcaatcacctttgagggctaaagagtagcacatcaaaaggactccaaaatcccatacccaactcttaagagatttgtcctggtacttcagaaagaattttcatgagtgttcttaattggctggaaaagcaccagctgacgttttggaagaatctatccatgtgtctgcctccatatgcatctgggcatttcatcttcagtcccctcattagactgtagcattaggatgtgtggagagaggagaaatgatttagcacccagattcacactcctatgcctggaagggggacatctttgaagaagaggaattagggctgtggacactgtcttgaggatgtggacttccttagtgagctccacattacttgatggtaaccacttcaaaaggatcagaatccacgtaatgaaaaaggtccctctagaggatggagctgatgtgaagctgccaatggatgaaaagcctcagaaagcaactcaaaggactcaaagcaacggacaacacaagagttgtcttcagcccagtgacacctctgatgtcccctggaagctttgtgctaacctgggactgcctgacttcctttagcctggtcccttgctactaccttgaactgttttatctaacctctctttttctgtttaattctttgctactgccattgaccctgctgcaggatttgtgtcattttcctgcctggttgctgagactccattttgctgccacacacagagatgtaagaggcaggctttaattgccaaagcacagtttgagcagtagaaaacaacatggtgtatatctcaaattgcctgacatgaagaggagtctaacggtgaagtttcacttttcatcagcatcatctttcacatgttcattatcatctgctcttattcttgcatgtttaaacacttaaaatttttagtataatttttagtgtgttttgaagtggtgactaggctttcaaaaacttccattgaattacaaagcactatccagttcttattgttaaactaagtaaaaatgataagtaacatagtgtaaaatattcctttactgtgaacttcttacaatgctgtgaatgagaggctcctcagaactggagcatttgtataataattcatcctgttcatcttcaattttaacatcatatataatttcaattctatcaattgggcctttaaaaatcatataaaaggatataaaatttgaaaagagaaacctaattggctatttaatccaaaacaactttttttttccttcaatggaatcagaaagcttgtcaatcactcatgtgttttagagtaattacttttaaaatggtgcatttgtgcttctgaactattttgaagagtcacttctgtttacctcaagtatcaattcatcctccatacatttgaattcaagttgtttttttgtcaaatttacagttgtcaattgatcttcaagctgcagggtgcctagaaatgggccgttgtctgtagccctggcatgtgcacacggacatttgccaccactgcaagcaaaagtctggagaagttcaccaacgacaagaacgattagggaaaatatgctgctgtgggttaacaactcagaaagtccctgatccacatttggctgtttactaaagcttgtgattaactttttggcagtgtgtactatgctctattgctatatatgctatctataaatgtagatgttaaggataagtaattctaaatttattattctatagttttgaagtttggttaagtttcctttcactcaattgatttattttgttgttaatcaaatttatgttaattggatcctttaaattttttttggcattttccaacaaaaatggctttattcataagaaaggaaaaaaatcaatggaatttgatatctaaagaagttagaaagggagcaaaataaaaaacataaaggagatagatgaattagtaagcaaatcagtagtcgagtttttcaaactggcaaaattaattaattgacttttagcccaaatttacattgttaattaaatcaagaaggaagaagatctaagagctcccattgataggcaagcctagagagaactagctaaatttatcatgctaggatattgaaacacagaaagtttacatacatttatgaagggtcaatttagtttggacagtgaggtatttgtcttagtggaaaaaaggagaattagtctgatcaaatcgtgaagtaatacagtgaacttgcaggtgcacaaaataagagggccacatctatatggtgcagtctggaattctgtttaagtttgtaggtacctcttggacttctgaattgatccagttgtcatccaccacagacatctcacatcagatacagacagttccaagattgacaacagagaacaacctgctggaaagacctgggcagaaatggagagccctgcgggaaccatgctacattttcatctaaagagagaatgcacatctgatgagactgaaagttctttgttgttttagattgtagaatggtattgaattggtctgtggaaaattgcattgcttttatttctttgtgtaatcaagtttaagtaataggggatatataatcataagcattttagggtgggagggactattaagtaattttaagtgggtggggttatttagaatgttagaataatattatgtattagatatcgctataagtggacatgcgtacttacttgtaaccctttaccctataattgctatccttaaagatttcaaataaactcggagggaactgcagggagaccaacttatttagagcgaattggacatggataaaaaccccagtgggagaaagttcaaaggtgattagattaataatttaatagaggatgagtgacctctgataaattactgctagaatgaacttgtcaatgatggatggtaaattttcatggaagttataaaagtgataaataaaaacccttgcttttacccctgtcagtagccctcctcctaccactgaaccccattgcccctacccctccttctaactttattgctgtattctcttcactctatatttctctctatttgctaatattgcattgctgttacaataaaaattcaataaagatttagtggttaagtgcaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:23089 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA GeneID:23089 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:23089 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA GeneID:23089 -> Biological process: GO:0001890 [placenta development] evidence: IEA GeneID:23089 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA GeneID:23089 -> Biological process: GO:0030154 [cell differentiation] evidence: IEA GeneID:23089 -> Biological process: GO:0030512 [negative regulation of transforming growth factor beta receptor signaling pathway] evidence: IDA GeneID:23089 -> Cellular component: GO:0005634 [nucleus] evidence: IEA GeneID:23089 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
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