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2025-05-09 19:39:21, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_014868 3864 bp mRNA linear PRI 15-JUN-2013
DEFINITION Homo sapiens ring finger protein 10 (RNF10), mRNA.
ACCESSION NM_014868
VERSION NM_014868.4 GI:156630998
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 3864)
AUTHORS Sandholm,N., Salem,R.M., McKnight,A.J., Brennan,E.P., Forsblom,C.,
Isakova,T., McKay,G.J., Williams,W.W., Sadlier,D.M., Makinen,V.P.,
Swan,E.J., Palmer,C., Boright,A.P., Ahlqvist,E., Deshmukh,H.A.,
Keller,B.J., Huang,H., Ahola,A.J., Fagerholm,E., Gordin,D.,
Harjutsalo,V., He,B., Heikkila,O., Hietala,K., Kyto,J., Lahermo,P.,
Lehto,M., Lithovius,R., Osterholm,A.M., Parkkonen,M.,
Pitkaniemi,J., Rosengard-Barlund,M., Saraheimo,M., Sarti,C.,
Soderlund,J., Soro-Paavonen,A., Syreeni,A., Thorn,L.M.,
Tikkanen,H., Tolonen,N., Tryggvason,K., Tuomilehto,J., Waden,J.,
Gill,G.V., Prior,S., Guiducci,C., Mirel,D.B., Taylor,A.,
Hosseini,S.M., Parving,H.H., Rossing,P., Tarnow,L., Ladenvall,C.,
Alhenc-Gelas,F., Lefebvre,P., Rigalleau,V., Roussel,R.,
Tregouet,D.A., Maestroni,A., Maestroni,S., Falhammar,H., Gu,T.,
Mollsten,A., Cimponeriu,D., Ioana,M., Mota,M., Mota,E.,
Serafinceanu,C., Stavarachi,M., Hanson,R.L., Nelson,R.G.,
Kretzler,M., Colhoun,H.M., Panduru,N.M., Gu,H.F., Brismar,K.,
Zerbini,G., Hadjadj,S., Marre,M., Groop,L., Lajer,M., Bull,S.B.,
Waggott,D., Paterson,A.D., Savage,D.A., Bain,S.C., Martin,F.,
Hirschhorn,J.N., Godson,C., Florez,J.C., Groop,P.H. and
Maxwell,A.P.
CONSRTM DCCT/EDIC Research Group
TITLE New susceptibility loci associated with kidney disease in type 1
diabetes
JOURNAL PLoS Genet. 8 (9), E1002921 (2012)
PUBMED 23028342
REFERENCE 2 (bases 1 to 3864)
AUTHORS Hoshikawa,S., Ogata,T., Fujiwara,S., Nakamura,K. and Tanaka,S.
TITLE A novel function of RING finger protein 10 in transcriptional
regulation of the myelin-associated glycoprotein gene and myelin
formation in Schwann cells
JOURNAL PLoS ONE 3 (10), E3464 (2008)
PUBMED 18941509
REMARK GeneRIF: RNF10 is a trans-acting protein regulating MAG expression
and is required for myelin formation.
REFERENCE 3 (bases 1 to 3864)
AUTHORS Oh,J.H., Yang,J.O., Hahn,Y., Kim,M.R., Byun,S.S., Jeon,Y.J.,
Kim,J.M., Song,K.S., Noh,S.M., Kim,S., Yoo,H.S., Kim,Y.S. and
Kim,N.S.
TITLE Transcriptome analysis of human gastric cancer
JOURNAL Mamm. Genome 16 (12), 942-954 (2005)
PUBMED 16341674
REFERENCE 4 (bases 1 to 3864)
AUTHORS Stelzl,U., Worm,U., Lalowski,M., Haenig,C., Brembeck,F.H.,
Goehler,H., Stroedicke,M., Zenkner,M., Schoenherr,A., Koeppen,S.,
Timm,J., Mintzlaff,S., Abraham,C., Bock,N., Kietzmann,S.,
Goedde,A., Toksoz,E., Droege,A., Krobitsch,S., Korn,B.,
Birchmeier,W., Lehrach,H. and Wanker,E.E.
TITLE A human protein-protein interaction network: a resource for
annotating the proteome
JOURNAL Cell 122 (6), 957-968 (2005)
PUBMED 16169070
REFERENCE 5 (bases 1 to 3864)
AUTHORS Lin,J., Friesen,M.T., Bocangel,P., Cheung,D., Rawszer,K. and
Wigle,J.T.
TITLE Characterization of Mesenchyme Homeobox 2 (MEOX2) transcription
factor binding to RING finger protein 10
JOURNAL Mol. Cell. Biochem. 275 (1-2), 75-84 (2005)
PUBMED 16335786
REMARK GeneRIF: MEOX2 and Meox2 binding to RNF10 protein was
characterized.
REFERENCE 6 (bases 1 to 3864)
AUTHORS Seki,N., Hattori,A., Sugano,S., Muramatsu,M. and Saito,T.
TITLE cDNA cloning, expression profile, and genomic structure of human
and mouse RNF10/Rnf 10 genes, encoding a novel RING finger protein
JOURNAL J. Hum. Genet. 45 (1), 38-42 (2000)
PUBMED 10697961
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DA103961.1, BC016622.1,
DB526099.1 and BQ015862.1.
On Aug 31, 2007 this sequence version replaced gi:34452680.
Summary: The protein encoded by this gene contains a ring finger
motif, which is known to be involved in protein-protein
interactions. The specific function of this protein has not yet
been determined. EST data suggests the existence of multiple
alternatively spliced transcript variants, however, their full
length nature is not known. [provided by RefSeq, Jul 2008].
##Evidence-Data-START##
Transcript exon combination :: BC016622.1, AB027196.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025082 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-36 DA103961.1 8-43
37-3141 BC016622.1 1-3105
3142-3419 DB526099.1 152-429
3420-3864 BQ015862.1 1-445 c
FEATURES Location/Qualifiers
source 1..3864
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12q24.31"
gene 1..3864
/gene="RNF10"
/gene_synonym="RIE2"
/note="ring finger protein 10"
/db_xref="GeneID:9921"
/db_xref="HGNC:10055"
/db_xref="HPRD:11496"
exon 1..640
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 202
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="g"
/db_xref="dbSNP:11542860"
variation 265..267
/gene="RNF10"
/gene_synonym="RIE2"
/replace=""
/replace="cct"
/db_xref="dbSNP:140042315"
variation 265
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:541126"
misc_feature 421..423
/gene="RNF10"
/gene_synonym="RIE2"
/note="upstream in-frame stop codon"
variation 453
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043097"
variation 455
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="g"
/db_xref="dbSNP:113139244"
CDS 484..2919
/gene="RNF10"
/gene_synonym="RIE2"
/codon_start=1
/product="RING finger protein 10"
/protein_id="NP_055683.3"
/db_xref="GI:34452681"
/db_xref="CCDS:CCDS9201.1"
/db_xref="GeneID:9921"
/db_xref="HGNC:10055"
/db_xref="HPRD:11496"
/translation="
MPLSSPNAAATASDMDKNSGSNSSSASSGSSKGQQPPRSASAGPAGESKPKSDGKNSSGSKRYNRKRELSYPKNESFNNQSRRSSSQKSKTFNKMPPQRGGGSSKLFSSSFNGGRRDEVAEAQRAEFSPAQFSGPKKINLNHLLNFTFEPRGQTGHFEGSGHGSWGKRNKWGHKPFNKELFLQANCQFVVSEDQDYTAHFADPDTLVNWDFVEQVRICSHEVPSCPICLYPPTAAKITRCGHIFCWACILHYLSLSEKTWSKCPICYSSVHKKDLKSVVATESHQYVVGDTITMQLMKREKGVLVALPKSKWMNVDHPIHLGDEQHSQYSKLLLASKEQVLHRVVLEEKVALEQQLAEEKHTPESCFIEAAIQELKTREEALSGLAGSRREVTGVVAALEQLVLMAPLAKESVFQPRKGVLEYLSAFDEETTEVCSLDTPSRPLALPLVEEEEAVSEPEPEGLPEACDDLELADDNLKEGTICTESSQQEPITKSGFTRLSSSPCYYFYQAEDGQHMFLHPVNVRCLVREYGSLERSPEKISATVVEIAGYSMSEDVRQRHRYLSHLPLTCEFSICELALQPPVVSKETLEMFSDDIEKRKRQRQKKAREERRRERRIEIEENKKQGKYPEVHIPLENLQQFPAFNSYTCSSDSALGPTSTEGHGALSISPLSRSPGSHADFLLTPLSPTASQGSPSFCVGSLEEDSPFPSFAQMLRVGKAKADVWPKTAPKKDENSLVPPAPVDSDGESDNSDRVPVPSFQNSFSQAIEAAFMKLDTPATSDPLSEEKGGKKRKKQKQKLLFSTSVVHTK
"
misc_feature 784..1038
/gene="RNF10"
/gene_synonym="RIE2"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q8N5U6.2);
Region: Interaction with MEOX2"
misc_feature 1153..1293
/gene="RNF10"
/gene_synonym="RIE2"
/note="RING-finger (Really Interesting New Gene) domain, a
specialized type of Zn-finger of 40 to 60 residues that
binds two atoms of zinc; defined by the 'cross-brace'
motif C-X2-C-X(9-39)-C-X(1-3)-
H-X(2-3)-(N/C/H)-X2-C-X(4-48)C-X2-C; probably involved
in...; Region: RING; cd00162"
/db_xref="CDD:29102"
misc_feature 1153..1281
/gene="RNF10"
/gene_synonym="RIE2"
/note="Zinc finger, C3HC4 type (RING finger); Region:
zf-C3HC4_2; pfam13923"
/db_xref="CDD:206094"
misc_feature order(1156..1158,1165..1167,1201..1203,1207..1209,
1216..1218,1225..1227,1270..1272,1279..1281)
/gene="RNF10"
/gene_synonym="RIE2"
/note="cross-brace motif; other site"
/db_xref="CDD:29102"
variation 576
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:184077395"
variation 624
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374593114"
variation 625
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:377054423"
exon 641..837
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 654
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146802529"
variation 668
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376427405"
variation 672
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:61741840"
variation 677
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:111483466"
variation 683
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:140614674"
variation 699
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:144374907"
variation 714
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="c"
/db_xref="dbSNP:186748904"
variation 770
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201217014"
variation 773
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:114775205"
variation 780
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150282383"
variation 784
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:137902657"
variation 787
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141915839"
variation 822
/gene="RNF10"
/gene_synonym="RIE2"
/replace="g"
/replace="t"
/db_xref="dbSNP:201659121"
exon 838..1037
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 876
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368183309"
variation 896
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="t"
/db_xref="dbSNP:370551365"
variation 928
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="t"
/db_xref="dbSNP:189978208"
variation 993
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145779566"
exon 1038..1128
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 1043
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200200679"
variation 1053
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201585715"
variation 1116
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372583460"
exon 1129..1313
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 1162
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142763100"
variation 1183
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372493264"
variation 1256
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:202018576"
variation 1260
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144536329"
variation 1276
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201588245"
exon 1314..1450
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 1319
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376818128"
variation 1361
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200683852"
variation 1430
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:148043070"
exon 1451..1611
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 1453
/gene="RNF10"
/gene_synonym="RIE2"
/replace="g"
/replace="t"
/db_xref="dbSNP:182592988"
variation 1455
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150600491"
variation 1460
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:77933939"
variation 1479
/gene="RNF10"
/gene_synonym="RIE2"
/replace="g"
/replace="t"
/db_xref="dbSNP:17852961"
variation 1510
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201672608"
variation 1515
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367963197"
variation 1544
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200354349"
variation 1554
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370511084"
variation 1563
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139972463"
variation 1567
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:377026080"
variation 1568
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="g"
/db_xref="dbSNP:143542654"
variation 1592
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374875330"
exon 1612..1737
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 1627
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371485318"
variation 1631
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:146309808"
variation 1632
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374784902"
variation 1641
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:139601055"
variation 1642
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:116727495"
variation 1666
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368896123"
variation 1682
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:187060835"
variation 1709
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145343225"
variation 1710
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:61760870"
STS 1733..2001
/gene="RNF10"
/gene_synonym="RIE2"
/standard_name="AA675014"
/db_xref="UniSTS:159429"
exon 1738..2014
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 1779
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:151315852"
variation 1782
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="t"
/db_xref="dbSNP:16950277"
variation 1783
/gene="RNF10"
/gene_synonym="RIE2"
/replace="g"
/replace="t"
/db_xref="dbSNP:145736802"
variation 1867
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369715030"
variation 1890
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="g"
/db_xref="dbSNP:138683853"
variation 1896
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373656404"
variation 1978
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:150334309"
variation 1991..1992
/gene="RNF10"
/gene_synonym="RIE2"
/replace=""
/replace="t"
/db_xref="dbSNP:35590307"
variation 1991
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="g"
/db_xref="dbSNP:138031591"
exon 2015..2148
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 2069
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:192832337"
variation 2076
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:149497258"
variation 2098
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375098491"
variation 2114
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:377456759"
variation 2135
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:184918703"
exon 2149..2266
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 2171
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="c"
/db_xref="dbSNP:191921489"
variation 2223
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="g"
/db_xref="dbSNP:144046411"
variation 2251
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:147370516"
exon 2267..2368
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 2288
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374298144"
variation 2304
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138738342"
variation 2324
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141882801"
variation 2336
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376525062"
exon 2369..2524
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 2376
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:146297351"
variation 2381
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369126447"
variation 2391
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201728776"
variation 2423
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="g"
/db_xref="dbSNP:113560686"
variation 2430
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:139558500"
variation 2435
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:183419563"
variation 2441
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="c"
/db_xref="dbSNP:201228341"
variation 2457
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200377129"
variation 2466
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374793380"
variation 2480
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:61760871"
variation 2497
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370094183"
variation 2513
/gene="RNF10"
/gene_synonym="RIE2"
/replace="g"
/replace="t"
/db_xref="dbSNP:201421747"
exon 2525..2625
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 2526
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="c"
/db_xref="dbSNP:150629669"
variation 2532
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139788197"
variation 2570
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:149816443"
variation 2581
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200686697"
exon 2626..2683
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 2654
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:147936384"
variation 2658
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370334473"
exon 2684..2842
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 2718
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:140165853"
variation 2745
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="g"
/db_xref="dbSNP:375902863"
variation 2769
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145695976"
variation 2788
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="c"
/db_xref="dbSNP:147768290"
exon 2843..3847
/gene="RNF10"
/gene_synonym="RIE2"
/inference="alignment:Splign:1.39.8"
variation 2853..2854
/gene="RNF10"
/gene_synonym="RIE2"
/replace="g"
/replace="t"
/db_xref="dbSNP:10056"
variation 2904
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:188863621"
variation 2905
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:148836482"
variation 2928
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200696006"
STS 2931..3072
/gene="RNF10"
/gene_synonym="RIE2"
/standard_name="D12S1173E"
/db_xref="UniSTS:151454"
variation 2952
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199883755"
variation 2963..2964
/gene="RNF10"
/gene_synonym="RIE2"
/replace=""
/replace="t"
/db_xref="dbSNP:368403066"
variation 2972
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:3203671"
STS 3018..3117
/gene="RNF10"
/gene_synonym="RIE2"
/standard_name="D12S1147E"
/db_xref="UniSTS:55522"
STS 3019..3118
/gene="RNF10"
/gene_synonym="RIE2"
/standard_name="D12S1196E"
/db_xref="UniSTS:151460"
variation 3035
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368045439"
polyA_signal 3120..3125
/gene="RNF10"
/gene_synonym="RIE2"
polyA_site 3141
/gene="RNF10"
/gene_synonym="RIE2"
variation 3157
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145527012"
variation 3167
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="c"
/db_xref="dbSNP:148849373"
STS 3171..3291
/gene="RNF10"
/gene_synonym="RIE2"
/standard_name="RH45155"
/db_xref="UniSTS:48512"
variation 3251
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="c"
/db_xref="dbSNP:10505"
variation 3254
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145288520"
variation 3291
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="g"
/db_xref="dbSNP:3088345"
polyA_signal 3401..3406
/gene="RNF10"
/gene_synonym="RIE2"
polyA_site 3424
/gene="RNF10"
/gene_synonym="RIE2"
variation 3449..3450
/gene="RNF10"
/gene_synonym="RIE2"
/replace=""
/replace="t"
/db_xref="dbSNP:71690132"
STS 3546..3729
/gene="RNF10"
/gene_synonym="RIE2"
/standard_name="A007E11"
/db_xref="UniSTS:60614"
STS 3566..3702
/gene="RNF10"
/gene_synonym="RIE2"
/standard_name="RH17496"
/db_xref="UniSTS:46125"
variation 3581
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145867367"
variation 3618
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:10515974"
STS 3676..3822
/gene="RNF10"
/gene_synonym="RIE2"
/standard_name="SHGC-33949"
/db_xref="UniSTS:79733"
variation 3754
/gene="RNF10"
/gene_synonym="RIE2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148143877"
polyA_signal 3821..3826
/gene="RNF10"
/gene_synonym="RIE2"
variation 3826
/gene="RNF10"
/gene_synonym="RIE2"
/replace="a"
/replace="g"
/db_xref="dbSNP:192333533"
polyA_site 3841
/gene="RNF10"
/gene_synonym="RIE2"
polyA_site 3847
/gene="RNF10"
/gene_synonym="RIE2"
ORIGIN
atacagtccatccgggttctttgagatgctgtttggcgactcgtcgccattcccggagcaggtcggcctcggcccaggggcgagtatccgttgctgtgtcggagacactagtccccgacaccgagacagccagccctctcccctgcctcgcggcgggagagcgtgtccggccggccggccggcggggctcgcgcaacctccctcgcctccccttcccccgcagcctccgccccgccaggcccggcccggactcccgagccccggcctcctcgtcctcggtcgccgctgccgccgggcttaacagccccgtccgccgcttctcttcctagtttgagaagccaaggaaggaaacagggaaaaatgtcgccatgaaggccgagaaccgctgccgccgccgacccccgccggccctgaacgccatgagcctgggtccccgccgcgcccgctccgctccgactgccgtcgccgccgaggcccccgttgatgccgctgagctcccccaacgccgccgccaccgcctccgacatggacaagaacagcggctccaacagctcctccgcctcttcgggcagcagcaaagggcaacagccgccccgctccgcctcggcggggccagccggcgagtctaaacccaagagcgatggaaagaactccagtggatccaagcgttataatcgcaaacgtgaactttcctaccccaaaaatgaaagttttaacaaccagtcccgtcgctccagttcacagaaaagcaagacttttaacaagatgcctcctcaaaggggcggcggcagcagcaaactctttagctcttcttttaatggtggaagacgagatgaggtagcagaggctcaacgggcagagtttagccctgcccagttctctggtcctaagaagatcaacctgaaccacttgttgaatttcacttttgaaccccgtggccagacgggtcactttgaaggcagtggacatggtagctggggaaagaggaacaagtggggacataagccttttaacaaggaactctttttacaggccaactgccaatttgtggtgtctgaagaccaagactacacagctcattttgctgatcctgatacattagttaactgggactttgtggaacaagtgcgcatttgtagccatgaagtgccatcttgcccaatatgcctctatccacctactgcagccaagataacccgttgtggacacatcttctgctgggcatgcatcctgcactatctttcactgagtgagaagacgtggagtaaatgtcccatctgttacagttctgtgcataagaaggatctcaagagtgttgttgccacagagtcacatcagtatgttgttggtgataccattacgatgcagctgatgaagagggagaaaggggtgttggtggctttgcccaaatccaaatggatgaatgtagaccatcccattcatctaggagatgaacagcacagccagtactccaagttgctgctggcctctaaggagcaggtgctgcaccgggtagttctggaggagaaagtagcactagagcagcagctggcagaggagaagcacactcccgagtcctgctttattgaggcagctatccaggagctcaagactcgggaagaggctctgtcgggattggccggaagcagaagggaggtcactggtgttgtggctgctctggaacaactggtgctgatggctcccttggcgaaggagtctgtttttcaacccaggaagggtgtgctggagtatctgtctgccttcgatgaagaaaccacggaagtttgttctctggacactccttctagacctcttgctctccctctggtagaagaggaggaagcagtgtctgaaccagagcctgaggggttgccagaggcctgtgatgacttggagttagcagatgacaatcttaaagaggggaccatttgcactgagtccagccagcaggaacccatcaccaagtcaggcttcacacgcctcagcagctctccttgttactacttttaccaagcggaagatggacagcatatgttcctgcaccctgtgaatgtgcgctgcctcgtgcgggagtacggcagcctggagaggagccccgagaagatctcagcaactgtggtggagattgctggctactccatgtctgaggatgttcgacagcgtcacagatatctctctcacttgccactcacctgtgagttcagcatctgtgaactggctttgcaacctcctgtggtctctaaggaaaccctagagatgttctcagatgacattgagaagaggaaacgtcagcgccaaaagaaggctcgggaggaacgccgccgagagcgcaggattgagatagaggagaacaagaaacagggcaagtacccagaagtccacattcccctcgagaatctacagcagtttcctgccttcaattcttatacctgctcctctgattctgctttgggtcccaccagcaccgagggccatggggccctctccatttctcctctcagcagaagtccaggttcccatgcagactttctgctgacccctctgtcacccactgccagtcagggcagtccctcattctgcgttgggagtctggaagaagactctcccttcccttcctttgcccagatgctgagggttggaaaagcaaaagcagatgtgtggcccaaaactgctccaaagaaagatgagaacagcttagttcctcctgcccctgtggacagcgacggggagagtgataattcagaccgtgttcctgtgcccagttttcaaaattccttcagccaagctattgaagcagccttcatgaaactggacacaccagctacttcagatcccctctctgaagagaaaggaggaaagaaaagaaaaaaacagaaacagaagctcctgttcagcacctcagtcgtccacaccaagtgacactactggcccaggctaccttctccatctggtttttgtttttgtttttttttcccccatgcttttgtttggctgctgtaatttttaagtatttgagtttgaacagattagctctggggggagggggtttccacaatgtgagggggaaccaagaaaattttaaatacagtgtattttccagcttcctgtctttacaccaaaataaagtattgacacaagagatctcttcctgccaaggtttttagttcattgccagtttagtctttttgacccatgtgtaattaatttttctcaacccaaagtaagattgagtcccctttgagatgcattagagcagtccaacccagaatggcacacactgctctgctgtagcatcatgtcagggcttcctggactcagtacacctctcagtttgtcttttaaaaaacagctgaatctttactacctatttagttctccttgttaaagaaacaggggtgggaataaaatggatttaggacacccagtttgaattgcagtttttttttttctgacacatggccaggctgtggtgccagcttaatggagtaggctgtccttggcacttgcatgtgtgaaaggagggttttgcctcttcttgagcatggcttgagttggtaaggaaagctgtaactcacgaagccctgagacctgctacccctaagatcgagcttgttttcagtgactggcttgagtcataggaggaggagtctggtacagctgcaggagagcagggccatctgaagcggtagcattgccaccatctccctctcatctagagcagttttcttatgccttggtttgagctgaatttgatgtgaattcttttgctgcttaataaagtgacctctaggtgcattagaatgcgaaggcaaatagttgcaataaatcacctgcacaagcattgtgaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:9921 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:9921 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA
GeneID:9921 -> Molecular function: GO:0044212 [transcription regulatory region DNA binding] evidence: ISS
GeneID:9921 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
GeneID:9921 -> Biological process: GO:0010626 [negative regulation of Schwann cell proliferation] evidence: ISS
GeneID:9921 -> Biological process: GO:0031643 [positive regulation of myelination] evidence: ISS
GeneID:9921 -> Biological process: GO:0045893 [positive regulation of transcription, DNA-dependent] evidence: IDA
GeneID:9921 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: ISS
GeneID:9921 -> Cellular component: GO:0005634 [nucleus] evidence: ISS
GeneID:9921 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
by
@meso_cacase at
DBCLS
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