2024-04-20 05:14:02, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001184961 6628 bp mRNA linear PRI 08-JUL-2013 DEFINITION Homo sapiens paternally expressed 10 (PEG10), transcript variant 1, mRNA. ACCESSION NM_001184961 VERSION NM_001184961.1 GI:296785057 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 6628) 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 6628) 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 6628) 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 6628) 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 6628) 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 6628) 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 6628) 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 6628) 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 6628) 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 6628) 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 BP250746.1, AB049150.1, AF216076.1, DA683494.1 and AC069292.12. 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 (1) represents the predominant transcript and contains two overlapping reading frames, RF1 and RF1/RF2. It initiates translation from an in-frame, upstream non-AUG (CUG) codon compared to variant 1. This isoform (5), encoded by RF1/RF2, has a longer N-terminus compared to isoform 1, and is the product of -1 translational frame-shifting. 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 :: DA501267.1, AB049150.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025082, ERS025084 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## imprinted gene :: PMID: 11318613 non-AUG initiation codon :: PMID: 20084274 ribosomal slippage :: PMID: 15611116, 15767280 ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-221 BP250746.1 1-221 222-2872 AB049150.1 1-2651 2873-4379 AF216076.1 2404-3910 4380-4381 DA683494.1 26-27 4382-4910 AF216076.1 3913-4441 4911-4912 AC069292.12 94200-94201 4913-6628 AF216076.1 4443-6158 FEATURES Location/Qualifiers source 1..6628 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="7" /map="7q21" gene 1..6628 /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..256 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /inference="alignment:Splign:1.39.8" variation 40 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:191439025" misc_feature 255..257 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="upstream in-frame stop codon" exon 257..6618 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /inference="alignment:Splign:1.39.8" variation 267 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:112688289" variation 371 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:369601878" CDS join(378..1436,1436..2605) /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /ribosomal_slippage /note="; isoform 5 is encoded by transcript variant 1; non-AUG (CUG) translation initiation codon; 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 5" /protein_id="NP_001171890.1" /db_xref="GI:296785058" /db_xref="GeneID:23089" /db_xref="HGNC:14005" /db_xref="MIM:609810" /translation="
MGPDCPPPPPPPPPNNNNNNNSKHTGHKSACVPNMTERRRDELSEEINNLREKVMKQSEENNNLQSQVQKLTEENTTLREQVEPTPEDEDDDIELRGAAAAAAPPPPIEEECPEDLPEKFDGNPDMLAPFMAQCQIFMEKSTRDFSVDRVRVCFVTSMMTGRAARWASAKLERSHYLMHNYPAFMMEMKHVFEDPQRREVAKRKIRRLRQGMGSVIDYSNAFQMIAQDLDWNEPALIDQYHEGLSDHIQEELSHLEVAKSLSALIGQCIHIERRLARAAAARKPRSPPRALVLPHIASHHQVDPTEPVGGARMRLTQEEKERRRKLNLCLYCGTGGHYADNCPAKASKSSPAGKLPGPAVEGPSATGPEIIRSPQDDASSPHLQVMLQIHLPGRHTLFVRAMIDSGASGNFIDHEYVAQNGIPLRIKDWPILVEAIDGRPIASGPVVHETHDLIVDLGDHREVLSFDVTQSPFFPVVLGVRWLSTHDPNITWSTRSIVFDSEYCRYHCRMYSPIPPSLPPPAPQPPLYYPVDGYRVYQPVRYYYVQNVYTPVDEHVYPDHRLVDPHIEMIPGAHSIPSGHVYSLSEPEMAALRDFVARNVKDGLITPTIAPNGAQVLQVKRGWKLQVSYDCRAPNNFTIQNQYPRLSIPNLEDQAHLATYTEFVPQIPGYQTYPTYAAYPTYPVGFAWYPVGRDGQGRSLYVPVMITWNPHWYRQPPVPQYPPPQPPPPPPPPPPPPSYSTL
" misc_feature <486..623 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="basic region leucin zipper; Region: BRLZ; smart00338" /db_xref="CDD:197664" misc_feature 834..1115 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="Retrotransposon gag protein; Region: Retrotrans_gag; pfam03732" /db_xref="CDD:146393" misc_feature 1571..1825 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="Retropepsins; pepsin-like aspartate proteases; Region: retropepsin_like; cd00303" /db_xref="CDD:133136" misc_feature order(1586..1588,1592..1594,1598..1600,1673..1681, 1805..1807) /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="inhibitor binding site; inhibition site" /db_xref="CDD:133136" misc_feature 1586..1594 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="catalytic motif [active]" /db_xref="CDD:133136" misc_feature 1586..1588 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="Catalytic residue [active]" /db_xref="CDD:133136" misc_feature order(1673..1684,1694..1702,1712..1714) /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="Active site flap [active]" /db_xref="CDD:133136" variation 392 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:71562863" variation 399 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:71562864" variation 408 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:71562865" variation 437..442 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="caactc" /db_xref="dbSNP:374577874" variation 446 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:373794887" STS 457..1491 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /db_xref="UniSTS:481964" variation 473 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:376814465" variation 485 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:367923171" variation 550 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:372443374" variation 636 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:375463611" variation 641 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:200610645" variation 663 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:147863226" variation 740 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:201501752" variation 762 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:374803366" variation 802 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:368939059" variation 823 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:372959401" variation 895 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:375994845" variation 919 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:148903291" variation 934 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:199644223" variation 936 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:181931446" variation 949 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:373696772" variation 1036 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:200638421" variation 1080 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:371583344" variation 1082 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:202101917" variation 1085 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:367821311" variation 1115 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:370323324" variation 1136 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:3209061" variation 1221 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:374669576" variation 1241 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:371597071" variation 1311 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:376581536" variation 1358 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:368311963" variation 1378 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:372378066" misc_feature 1433..1439 /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 1436 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /note="-1 ribosomal frame-shift site" variation 1563 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:375398177" variation 1581 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:187567019" variation 1609 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:189856221" variation 1705 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:373004121" variation 1745 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:181708979" variation 1789 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:376322331" variation 1818 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:148037544" variation 1842 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:140813381" variation 1891 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:200375561" variation 1968 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:201023812" variation 1982 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:201604172" variation 2042 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:185617764" variation 2090 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:369503620" variation 2165 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:190428861" variation 2286 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:369421203" variation 2293 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:3750105" variation 2345 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:200290306" variation 2408 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:369566255" variation 2409 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:182259108" variation 2410 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:185785639" variation 2448 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:112535663" variation 2538 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:199593658" variation 2581 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:150121454" variation 2593 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:35039803" variation 2696 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:78966738" variation 2757 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:35237090" variation 2794 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:72615135" variation 2797 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:113951929" variation 2818 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:191035277" variation 2929 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:75890579" variation 2930 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:78249742" variation 2953 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:138576679" variation 3029 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:141573011" variation 3042 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:183720152" variation 3065 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:146181651" variation 3106 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:189106507" variation 3198 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:3750106" variation 3243 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:112079331" variation 3574 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:371237508" variation 3658 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:374308979" variation 3696 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:137861769" variation 3771 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:372624616" variation 3834 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:367756779" variation 3921 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:11549144" variation 3951 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:190424869" variation 4031 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:368587365" variation 4064 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:183061000" variation 4099 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:149435445" variation 4101 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:375735183" variation 4159 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:74802312" variation 4167 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:117152307" variation 4321 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:371957260" variation 4380 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:13073" variation 4404 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:13226637" variation 4413 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:377389610" variation 4421 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:1136429" variation 4732 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:186982647" variation 4744 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="t" /db_xref="dbSNP:375638047" variation 4782 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:116616252" variation 4790 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:73223849" STS 4843..5643 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /standard_name="PEG10_8006" /db_xref="UniSTS:467823" variation 4886 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="t" /db_xref="dbSNP:191522451" variation 4903 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:200749134" variation 4904 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:201879623" variation 4905 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:200078595" variation 4905 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="t" /db_xref="dbSNP:10707840" variation 4911 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:78537188" variation 4912 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:77252058" variation 4996 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:184904316" variation 5081 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:12671285" STS 5238..5337 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /standard_name="WI-12157" /db_xref="UniSTS:83417" variation 5258 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:148567462" variation 5261..5264 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="aatt" /db_xref="dbSNP:199565534" variation 5310 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:1059224" variation 5312..5313 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="tt" /db_xref="dbSNP:71660247" variation 5319 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:187513909" variation 5419 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:192748781" variation 5422 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:62466562" variation 5425 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:7810469" variation 5431 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="t" /db_xref="dbSNP:14444" variation 5468 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:147284109" variation 5492..5493 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="tt" /db_xref="dbSNP:61078050" variation 5595 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:114854087" STS 5610..5769 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /standard_name="STS-H51766" /db_xref="UniSTS:1756" variation 5656 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /db_xref="dbSNP:368821741" variation 5673 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="a" /db_xref="dbSNP:139770503" variation 5726 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:185496776" variation 5849..5852 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="" /replace="ctgt" /db_xref="dbSNP:67946661" variation 6048 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:1059044" variation 6201 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:76468647" STS 6237..6497 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /standard_name="WI-20034" /db_xref="UniSTS:23610" variation 6463 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:144674472" variation 6524 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="g" /replace="t" /db_xref="dbSNP:371406587" variation 6538 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="c" /db_xref="dbSNP:11981011" variation 6541 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="c" /replace="g" /db_xref="dbSNP:190747409" polyA_signal 6581..6586 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" polyA_signal 6592..6597 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" variation 6616 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:113002760" polyA_site 6618 /gene="PEG10" /gene_synonym="EDR; HB-1; Mar2; Mart2; MEF3L; RGAG3" ORIGIN
ctcctcggtgcaacctatataaggctcacagtctgcgctcctggtacacgcgcttcaacttcggttggtgtgtgtcgaagaaacctgactgcgccctgaggagaacagcggagaaggtccaccgagcctggcgaaaggtccgctgagcgggctgtcgtccggagccactccgggctgcggagcacccagtggagaccgcgcctggctcaggtgtgggaccccatccttcctgtcttcgcagaggagtcctcgcgtgaaataagcgggttttgaaaacaaaaaaaagaaggagtggaagagggggccaggatccaggcctccatccccacagaagtgaagctacagctgggaggtctcctcccaccccaaccgtcaccctgggtcccgactgcccacctcctcctcctccccctccccccaacaacaacaacaacaacaactccaagcacaccggccataagagtgcgtgtgtccccaacatgaccgaacgaagaagggacgagctctctgaagagatcaacaacttaagagagaaggtcatgaagcagtcggaggagaacaacaacctgcagagccaggtgcagaagctcacagaggagaacaccacccttcgagagcaagtggaacccacccctgaggatgaggatgatgacatcgagctccgcggtgctgcagcagctgctgccccaccccctccaatagaggaagagtgcccagaagacctcccagagaagttcgatggcaacccagacatgctggctcctttcatggcccagtgccagatcttcatggaaaagagcaccagggatttctcagttgatcgtgtccgtgtctgcttcgtgacaagcatgatgaccggccgtgctgcccgttgggcctcagcaaagctggagcgctcccactacctgatgcacaactacccagctttcatgatggaaatgaagcatgtctttgaagaccctcagaggcgagaggttgccaaacgcaagatcagacgcctgcgccaaggcatggggtctgtcatcgactactccaatgctttccagatgattgcccaggacctggattggaacgagcctgcgctgattgaccagtaccacgagggcctcagcgaccacattcaggaggagctctcccacctcgaggtcgccaagtcgctgtctgctctgattgggcagtgcattcacattgagagaaggctggccagggctgctgcagctcgcaagccacgctcgccaccccgggcgctggtgttgcctcacattgcaagccaccaccaggtagatccaaccgagccggtgggaggtgcccgcatgcgcctgacgcaggaagaaaaagaaagacgcagaaagctgaacctgtgcctctactgtggaacaggaggtcactacgctgacaattgtcctgccaaggcctcaaagtcttcgccggcgggaaactccccggccccgctgtagagggaccttcagcgaccgggccagaaataataaggtccccacaagatgatgcctcatctccacacttgcaagtgatgctccagattcatcttccgggcagacacaccctgttcgtccgagccatgatcgattctggtgcttctggcaacttcattgatcacgaatatgttgctcaaaatggaattcctctaagaatcaaggactggccaatacttgtggaagcaattgatgggcgccccatagcatcgggcccagttgtccacgaaactcacgacctgatagttgacctgggagatcaccgagaggtgctgtcatttgatgtgactcagtctccattcttccctgtcgtcctaggggttcgctggctgagcacacatgatcccaatatcacatggagcactcgatctatcgtctttgattctgaatactgccgctaccactgccggatgtattctccaataccaccatcgctcccaccaccagcaccacaaccgccactctattatccagtagatggatacagagtttaccaaccagtgaggtattactatgtccagaatgtgtacactccagtagatgagcacgtctacccagatcaccgcctggttgaccctcacatagaaatgatacctggagcacacagtattcccagtggacatgtgtattcactgtccgaacctgaaatggcagctcttcgagattttgtggcaagaaatgtaaaagatgggctaattactccaacgattgcacctaatggagcccaagttctccaggtgaagagggggtggaaactgcaagtttcttatgattgccgagctccaaacaattttactatccagaatcagtatcctcgcctatctattccaaatttagaagaccaagcacacctggcaacgtacactgaattcgtacctcaaatacctggataccaaacataccccacatatgccgcgtacccgacctacccagtaggattcgcctggtacccagtgggacgagacggacaaggaagatcactatatgtacctgtgatgatcacttggaatccacactggtaccgccagcctccggtaccacagtacccgccgccacagccgccgcctccaccaccaccaccgccgccgcctccatcttacagtaccctgtaaatacctgtcatgtccttcaggatctctgccctcaaaatttattcctgttcagcttctcaatcagtgactgtgtgctaaattttaggctactgtatcttcaggccacctgaggcacatcctctctgaaacggctatggaaggttagggccactctggactggcacacatcctaaagcaccaaaagaccttcaacattttctgagagcaacagagtatttgccaataaatgatctctcatttttccaccttgactgccaatctaactaaaataattaataagtttactttccagccagtcctggaagtctgggttttacctgccaaaacctccatcaccatctaaattataggctgccaaatttgctgtttaacatttacagagaagctgatacaaacgcaggaaatgctgatttctttatggagggggagacgaggaggaggaggacatgacttttcttgcggtttcggtaccctctttttaaatcactggaggactgaggccttattaaggaagccaaaattatcggtgcagtgtggaaaggcttccgtgatcctctcgctgcacccttagaaacttcaccgtcttcaaactccatttccatggttctgttaattctcaaggagcagcaactcgactggttctcccaggagcaggaaaaacccttgtgacatgaaacatctcaggcctgaaaagaaagtgctctctcagatggactcttgcatgttaagactatgtcttcacatcatggtgcaaatcacatgtacccaatgactccggctttgacacaacaccttaccatcatcatgccatgatggcttccacaaagcattaaacctggtaaccagagattactggtggctccagcgttgttagatgttcatgaaatgtgaccacctctcaatcacctttgagggctaaagagtagcacatcaaaaggactccaaaatcccatacccaactcttaagagatttgtcctggtacttcagaaagaattttcatgagtgttcttaattggctggaaaagcaccagctgacgttttggaagaatctatccatgtgtctgcctccatatgcatctgggcatttcatcttcagtcccctcattagactgtagcattaggatgtgtggagagaggagaaatgatttagcacccagattcacactcctatgcctggaagggggacatctttgaagaagaggaattagggctgtggacactgtcttgaggatgtggacttccttagtgagctccacattacttgatggtaaccacttcaaaaggatcagaatccacgtaatgaaaaaggtccctctagaggatggagctgatgtgaagctgccaatggatgaaaagcctcagaaagcaactcaaaggactcaaagcaacggacaacacaagagttgtcttcagcccagtgacacctctgatgtcccctggaagctttgtgctaacctgggactgcctgacttcctttagcctggtcccttgctactaccttgaactgttttatctaacctctctttttctgtttaattctttgctactgccattgaccctgctgcaggatttgtgtcattttcctgcctggttgctgagactccattttgctgccacacacagagatgtaagaggcaggctttaattgccaaagcacagtttgagcagtagaaaacaacatggtgtatatctcaaattgcctgacatgaagaggagtctaacggtgaagtttcacttttcatcagcatcatctttcacatgttcattatcatctgctcttattcttgcatgtttaaacacttaaaatttttagtataatttttagtgtgttttgaagtggtgactaggctttcaaaaacttccattgaattacaaagcactatccagttcttattgttaaactaagtaaaaatgataagtaacatagtgtaaaatattcctttactgtgaacttcttacaatgctgtgaatgagaggctcctcagaactggagcatttgtataataattcatcctgttcatcttcaattttaacatcatatataatttcaattctatcaattgggcctttaaaaatcatataaaaggatataaaatttgaaaagagaaacctaattggctatttaatccaaaacaactttttttttccttcaatggaatcagaaagcttgtcaatcactcatgtgttttagagtaattacttttaaaatggtgcatttgtgcttctgaactattttgaagagtcacttctgtttacctcaagtatcaattcatcctccatacatttgaattcaagttgtttttttgtcaaatttacagttgtcaattgatcttcaagctgcagggtgcctagaaatgggccgttgtctgtagccctggcatgtgcacacggacatttgccaccactgcaagcaaaagtctggagaagttcaccaacgacaagaacgattagggaaaatatgctgctgtgggttaacaactcagaaagtccctgatccacatttggctgtttactaaagcttgtgattaactttttggcagtgtgtactatgctctattgctatatatgctatctataaatgtagatgttaaggataagtaattctaaatttattattctatagttttgaagtttggttaagtttcctttcactcaattgatttattttgttgttaatcaaatttatgttaattggatcctttaaattttttttggcattttccaacaaaaatggctttattcataagaaaggaaaaaaatcaatggaatttgatatctaaagaagttagaaagggagcaaaataaaaaacataaaggagatagatgaattagtaagcaaatcagtagtcgagtttttcaaactggcaaaattaattaattgacttttagcccaaatttacattgttaattaaatcaagaaggaagaagatctaagagctcccattgataggcaagcctagagagaactagctaaatttatcatgctaggatattgaaacacagaaagtttacatacatttatgaagggtcaatttagtttggacagtgaggtatttgtcttagtggaaaaaaggagaattagtctgatcaaatcgtgaagtaatacagtgaacttgcaggtgcacaaaataagagggccacatctatatggtgcagtctggaattctgtttaagtttgtaggtacctcttggacttctgaattgatccagttgtcatccaccacagacatctcacatcagatacagacagttccaagattgacaacagagaacaacctgctggaaagacctgggcagaaatggagagccctgcgggaaccatgctacattttcatctaaagagagaatgcacatctgatgagactgaaagttctttgttgttttagattgtagaatggtattgaattggtctgtggaaaattgcattgcttttatttctttgtgtaatcaagtttaagtaataggggatatataatcataagcattttagggtgggagggactattaagtaattttaagtgggtggggttatttagaatgttagaataatattatgtattagatatcgctataagtggacatgcgtacttacttgtaaccctttaccctataattgctatccttaaagatttcaaataaactcggagggaactgcagggagaccaacttatttagagcgaattggacatggataaaaaccccagtgggagaaagttcaaaggtgattagattaataatttaatagaggatgagtgacctctgataaattactgctagaatgaacttgtcaatgatggatggtaaattttcatggaagttataaaagtgataaataaaaacccttgcttttacccctgtcagtagccctcctcctaccactgaaccccattgcccctacccctccttctaactttattgctgtattctcttcactctatatttctctctatttgctaatattgcattgctgttacaataaaaattcaataaagatttagtggttaagtgcaaaaaaaaaaaaa
//
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
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.