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2024-03-29 21:49:27, 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:

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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