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2024-03-29 21:17:28, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_198700               4656 bp    mRNA    linear   PRI 24-JUN-2013
DEFINITION  Homo sapiens CUGBP, Elav-like family member 1 (CELF1), transcript
            variant 2, mRNA.
ACCESSION   NM_198700
VERSION     NM_198700.2  GI:289547569
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 4656)
  AUTHORS   Yu,T.X., Rao,J.N., Zou,T., Liu,L., Xiao,L., Ouyang,M., Cao,S.,
            Gorospe,M. and Wang,J.Y.
  TITLE     Competitive binding of CUGBP1 and HuR to occludin mRNA controls its
            translation and modulates epithelial barrier function
  JOURNAL   Mol. Biol. Cell 24 (2), 85-99 (2013)
   PUBMED   23155001
  REMARK    GeneRIF: CUGBP1 represses occludin translation by increasing
            occludin mRNA recruitment to P-bodies.
REFERENCE   2  (bases 1 to 4656)
  AUTHORS   Khaziapoul,S., Pearson,M.J., Pryme,I.F., Stern,B. and Hesketh,J.E.
  TITLE     CUG binding protein 1 binds to a specific region within the human
            albumin 3' untranslated region
  JOURNAL   Biochem. Biophys. Res. Commun. 426 (4), 539-543 (2012)
   PUBMED   22982313
  REMARK    GeneRIF: The results suggest that CUG-BP1 binds to nucleotides
            51-100 of the human albumin 3'UTR. In human cells CUG-BP1 binding
            may thus play a role in regulation of albumin expression and,
            additionally, it may have a function in post-transcriptional
            control in CHO cells.
REFERENCE   3  (bases 1 to 4656)
  AUTHORS   Chang,E.T., Donahue,J.M., Xiao,L., Cui,Y., Rao,J.N., Turner,D.J.,
            Twaddell,W.S., Wang,J.Y. and Battafarano,R.J.
  TITLE     The RNA-binding protein CUG-BP1 increases survivin expression in
            oesophageal cancer cells through enhanced mRNA stability
  JOURNAL   Biochem. J. 446 (1), 113-123 (2012)
   PUBMED   22646166
  REMARK    GeneRIF: CUG-BP1 is overexpressed in oesophageal cancer cell lines
            and human oesophageal cancer specimens. CUG-BP1 associates with the
            3'-untranslated region of survivin mRNA.
REFERENCE   4  (bases 1 to 4656)
  AUTHORS   Beisang,D., Rattenbacher,B., Vlasova-St Louis,I.A. and
            Bohjanen,P.R.
  TITLE     Regulation of CUG-binding protein 1 (CUGBP1) binding to target
            transcripts upon T cell activation
  JOURNAL   J. Biol. Chem. 287 (2), 950-960 (2012)
   PUBMED   22117072
  REMARK    GeneRIF: CUGBP1 binding to certain GRE-containing target
            transcripts decreased following T cell activation through
            activation-dependent phosphorylation of CUGBP1.
REFERENCE   5  (bases 1 to 4656)
  AUTHORS   Masuda,A., Andersen,H.S., Doktor,T.K., Okamoto,T., Ito,M.,
            Andresen,B.S. and Ohno,K.
  TITLE     CUGBP1 and MBNL1 preferentially bind to 3' UTRs and facilitate mRNA
            decay
  JOURNAL   Sci Rep 2, 209 (2012)
   PUBMED   22355723
  REMARK    GeneRIF: study suggests that regulation of CUGBP1 and MBNL1 is
            essential for accurate control of destabilization of a broad
            spectrum of mRNAs as well as of alternative splicing events
REFERENCE   6  (bases 1 to 4656)
  AUTHORS   Michalowski,S., Miller,J.W., Urbinati,C.R., Paliouras,M.,
            Swanson,M.S. and Griffith,J.
  TITLE     Visualization of double-stranded RNAs from the myotonic dystrophy
            protein kinase gene and interactions with CUG-binding protein
  JOURNAL   Nucleic Acids Res. 27 (17), 3534-3542 (1999)
   PUBMED   10446244
REFERENCE   7  (bases 1 to 4656)
  AUTHORS   Roberts,R., Timchenko,N.A., Miller,J.W., Reddy,S., Caskey,C.T.,
            Swanson,M.S. and Timchenko,L.T.
  TITLE     Altered phosphorylation and intracellular distribution of a (CUG)n
            triplet repeat RNA-binding protein in patients with myotonic
            dystrophy and in myotonin protein kinase knockout mice
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 94 (24), 13221-13226 (1997)
   PUBMED   9371827
REFERENCE   8  (bases 1 to 4656)
  AUTHORS   Timchenko,L.T., Miller,J.W., Timchenko,N.A., DeVore,D.R.,
            Datar,K.V., Lin,L., Roberts,R., Caskey,C.T. and Swanson,M.S.
  TITLE     Identification of a (CUG)n triplet repeat RNA-binding protein and
            its expression in myotonic dystrophy
  JOURNAL   Nucleic Acids Res. 24 (22), 4407-4414 (1996)
   PUBMED   8948631
REFERENCE   9  (bases 1 to 4656)
  AUTHORS   Bhagavati,S., Ghatpande,A. and Leung,B.
  TITLE     Identification of two nuclear proteins which bind to RNA CUG
            repeats: significance for myotonic dystrophy
  JOURNAL   Biochem. Biophys. Res. Commun. 228 (1), 55-62 (1996)
   PUBMED   8912635
  REMARK    Erratum:[Biochem Biophys Res Commun. 2008 Jun;370(3):530. Bhagwati,
            S [corrected to Bhagavati, S]]
REFERENCE   10 (bases 1 to 4656)
  AUTHORS   Timchenko,L.T., Timchenko,N.A., Caskey,C.T. and Roberts,R.
  TITLE     Novel proteins with binding specificity for DNA CTG repeats and RNA
            CUG repeats: implications for myotonic dystrophy
  JOURNAL   Hum. Mol. Genet. 5 (1), 115-121 (1996)
   PUBMED   8789448
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AC090559.7, BC031079.1 and
            BM737883.1.
            On Feb 24, 2010 this sequence version replaced gi:38570080.
            
            Summary: Members of the CELF/BRUNOL protein family contain two
            N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM
            domain, and a divergent segment of 160-230 aa between the second
            and third RRM domains. Members of this protein family regulate
            pre-mRNA alternative splicing and may also be involved in mRNA
            editing, and translation. This gene may play a role in myotonic
            dystrophy type 1 (DM1) via interactions with the dystrophia
            myotonica-protein kinase (DMPK) gene. Alternative splicing results
            in multiple transcript variants encoding different isoforms.
            [provided by RefSeq, Jul 2008].
            
            Transcript Variant: This variant (2) uses a different segment for
            its 5' UTR and a different internal splice site in its coding
            region, compared to variant 1. The resulting isoform (2) has an
            additional internal amino acid compared to isoform 1.
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            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 :: BC031079.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025081, ERS025082 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-177               AC090559.7         118818-118994       c
            178-1891            BC031079.1         178-1891
            1892-4582           AC090559.7         90475-93165         c
            4583-4656           BM737883.1         164-237
FEATURES             Location/Qualifiers
     source          1..4656
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="11"
                     /map="11p11"
     gene            1..4656
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="CUGBP, Elav-like family member 1"
                     /db_xref="GeneID:10658"
                     /db_xref="HGNC:2549"
                     /db_xref="HPRD:03046"
                     /db_xref="MIM:601074"
     exon            1..191
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    133..135
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="upstream in-frame stop codon"
     exon            192..379
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     CDS             202..1653
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="isoform 2 is encoded by transcript variant 2; CUG
                     RNA-binding protein; embryo deadenylation element binding
                     protein; CUG triplet repeat, RNA binding protein 1; CUG
                     triplet repeat, RNA-binding protein 1; nuclear
                     polyadenylated RNA-binding protein, 50-kD; bruno-like 2;
                     CUG-BP- and ETR-3-like factor 1; CELF-1; CUG-BP1; EDEN-BP
                     homolog; bruno-like protein 2; deadenylation factor
                     CUG-BP; RNA-binding protein BRUNOL-2; CUG triplet repeat
                     RNA-binding protein 1; 50 kDa nuclear polyadenylated
                     RNA-binding protein; embryo deadenylation element-binding
                     protein homolog"
                     /codon_start=1
                     /product="CUGBP Elav-like family member 1 isoform 2"
                     /protein_id="NP_941989.1"
                     /db_xref="GI:38570081"
                     /db_xref="CCDS:CCDS7939.1"
                     /db_xref="GeneID:10658"
                     /db_xref="HGNC:2549"
                     /db_xref="HPRD:03046"
                     /db_xref="MIM:601074"
                     /translation="
MNGTLDHPDQPDLDAIKMFVGQVPRTWSEKDLRELFEQYGAVYEINVLRDRSQNPPQSKGCCFVTFYTRKAALEAQNALHNMKVLPGMHHPIQMKPADSEKNNAVEDRKLFIGMISKKCTENDIRVMFSSFGQIEECRILRGPDGLSRGCAFVTFTTRAMAQTAIKAMHQAQTMEGCSSPMVVKFADTQKDKEQKRMAQQLQQQMQQISAASVWGNLAGLNTLGPQYLALLQQTASSGNLNTLSSLHPMGGLNAMQLQNLAALAAAASAAQNTPSGTNALTTSSSPLSVLTSSAGSSPSSSSSNSVNPIASLGALQTLAGATAGLNVGSLAGMAALNGGLGSSGLSNGTGSTMEALTQAYSGIQQYAAAALPTLYNQNLLTQQSIGAAGSQKEGPEGANLFIYHLPQEFGDQDLLQMFMPFGNVVSAKVFIDKQTNLSKCFGFVSYDNPVSAQAAIQSMNGFQIGMKRLKVQLKRSKNDSKPY
"
     misc_feature    250..489
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="RRM (RNA recognition motif), also known as RBD (RNA
                     binding domain) or RNP (ribonucleoprotein domain), is a
                     highly abundant domain in eukaryotes found in proteins
                     involved in post-transcriptional gene expression processes
                     including mRNA and rRNA...; Region: RRM; cd00590"
                     /db_xref="CDD:100104"
     misc_feature    order(256..258,382..384,388..390)
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="RNA/DNA binding site [nucleotide binding]; other
                     site"
                     /db_xref="CDD:100104"
     misc_feature    481..489
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="RRM dimerization site [polypeptide binding]; other
                     site"
                     /db_xref="CDD:100104"
     misc_feature    526..756
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="RRM (RNA recognition motif), also known as RBD (RNA
                     binding domain) or RNP (ribonucleoprotein domain), is a
                     highly abundant domain in eukaryotes found in proteins
                     involved in post-transcriptional gene expression processes
                     including mRNA and rRNA...; Region: RRM; cd00590"
                     /db_xref="CDD:100104"
     misc_feature    order(532..534,649..651,655..657)
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="RNA/DNA binding site [nucleotide binding]; other
                     site"
                     /db_xref="CDD:100104"
     misc_feature    748..756
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="RRM dimerization site [polypeptide binding]; other
                     site"
                     /db_xref="CDD:100104"
     misc_feature    1396..1620
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="RRM (RNA recognition motif), also known as RBD (RNA
                     binding domain) or RNP (ribonucleoprotein domain), is a
                     highly abundant domain in eukaryotes found in proteins
                     involved in post-transcriptional gene expression processes
                     including mRNA and rRNA...; Region: RRM; cd00590"
                     /db_xref="CDD:100104"
     misc_feature    order(1402..1404,1522..1524,1528..1530)
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="RNA/DNA binding site [nucleotide binding]; other
                     site"
                     /db_xref="CDD:100104"
     misc_feature    1612..1620
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /note="RRM dimerization site [polypeptide binding]; other
                     site"
                     /db_xref="CDD:100104"
     exon            380..462
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     exon            463..511
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     exon            512..646
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     STS             557..700
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /standard_name="MARC_11599-11600:1002739035:1"
                     /db_xref="UniSTS:267239"
     exon            647..726
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     exon            727..888
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     exon            889..952
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     exon            953..1081
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     STS             1030..1632
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /standard_name="Cugbp1"
                     /db_xref="UniSTS:479088"
     exon            1082..1195
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     exon            1196..1381
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     exon            1382..1525
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     STS             1401..1516
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /standard_name="X61451"
                     /db_xref="UniSTS:125827"
     variation       1479
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:34097581"
     exon            1526..1692
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     exon            1693..4647
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /inference="alignment:Splign:1.39.8"
     STS             1742..2380
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /standard_name="CUGBP1_2383"
                     /db_xref="UniSTS:280629"
     STS             2383..2568
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /standard_name="STS-N31747"
                     /db_xref="UniSTS:38745"
     variation       3750
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11546837"
     STS             3783..3913
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /standard_name="RH25600"
                     /db_xref="UniSTS:84245"
     variation       4010
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1062801"
     variation       4022
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1062802"
     STS             4373..4578
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /standard_name="RH36605"
                     /db_xref="UniSTS:82577"
     variation       4396
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1044269"
     polyA_signal    4628..4633
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
     polyA_site      4647
                     /gene="CELF1"
                     /gene_synonym="BRUNOL2; CUG-BP; CUGBP; CUGBP1; EDEN-BP;
                     hNab50; NAB50; NAPOR"
ORIGIN      
atactttgaaaataacagctcttttttgttccctcgtgtgtctcttcccaattgtatccctattgtattttctcatagtatgtttcagcagaaatcaaggtagacgaagtaacctcttgtcctgaattttcatagttgctcattcttaataatggcagcagaagcaacaatgagagtaactacctcctcagctcaaagaaaatgaacggcaccctggaccacccagaccaaccagatcttgatgctatcaagatgtttgtgggccaggttccaaggacctggtctgaaaaggacttgcgggaactcttcgaacagtatggtgctgtgtatgaaatcaacgtcctaagggataggagccaaaacccgcctcagagcaaagggtgctgttttgttacattttacacccgtaaagctgcattagaagctcagaatgctcttcacaacatgaaagtcctcccagggatgcatcaccctatacagatgaaacctgctgacagtgagaagaacaatgcagtggaagacaggaagctgtttattggtatgatttccaagaagtgcactgaaaatgacatccgagtcatgttctcttcgtttggacagattgaagaatgccggatattgcggggacctgatggcctgagccgaggttgtgcatttgtgacttttacaacaagagccatggcacagacggctatcaaggcaatgcaccaagcacagaccatggagggttgctcatcacccatggtggtaaaatttgctgatacacagaaggacaaagaacagaagagaatggcccagcagctccagcagcagatgcagcaaatcagcgcagcatctgtgtggggaaaccttgctggtctaaatactcttggaccccagtatttagcactccttcagcagactgcctcctctgggaacctcaacaccctgagcagcctccacccaatgggagggttgaatgcaatgcagttacagaatttggctgcactagctgctgcagctagtgcagctcagaacacaccaagtggtaccaatgctctcactacatccagcagtcccctcagcgtgctcactagttcagcagggtcctcacctagctctagcagcagtaattctgtcaaccccatagcctcacttggagccctgcagacattagctggagcaacggctggcctcaatgttggctctttggcaggaatggctgctttaaatggtggcctgggcagcagtggcctttccaatggcaccgggagcaccatggaggccctcactcaggcctactcgggtatccagcaatatgctgctgctgcgctccccactctgtacaaccagaatcttctgacacagcagagtattggtgctgctggaagccagaaggaaggtccagagggagccaacctgttcatctaccacctgccccaggagtttggtgatcaggacctgctgcagatgtttatgccctttgggaatgtcgtgtctgccaaggttttcatagacaagcagacaaacctgagcaagtgttttggttttgtaagttacgacaatcctgtttcggcccaagctgccatccagtccatgaacggctttcagattggcatgaagcggcttaaagtgcagctcaaacgttcgaagaatgacagcaagccctactgagcgtgctcccctctgagactggagtgagagggtcttctgattcctgccgtttgttcatcgttgtgcctaaagcatgtcgatgtggcgtcaagtacatcgtccaaatccctgtctcttcagcttctctgatgcttgaactctcacctttgaccttgtgttgacctttgatgctgatgtgtatttttattatgtttgtttctttcttcgtttttttttctttttttctttcctttttttttccttttgtgctgccaaattggttttgctagaacgactgctgaaggggaaatatttaaacttgcatttgaatataaaaaaaatctatttttctagaacttcataagataaccacttgattttgtgattccaattctttgtaattgtcttcagagcagccctactagcacataccgcgtggtgtttgtatttctgtgaacacacagccagtccgtttctaggctttgtttctctgtgtgcttagttttaaagacaactttgaagtaaacaatgaaataaaagatgtcactaaaacctctgaggctcctgagcacattttgctgatacagtctgtggggcttgaggagaccgcatgtattgttctttcttttgtttttcttctgagttctcaactgcggagagcacctgaaccccctttcctttttgaccgcaggctgcactttgggccccagccagccctttttctttttctttttcttttgtggttcttccctggagcgactctggggagtcctggatatcccgcctgccccttcccctcagccccatgcttgttccaacagtctccacagcaaaatgtgatgctttgatttttttgttgttgtttttgtttttgtattgtttttgtgtttttgttttgaattttttcctttcctactaagattatgcccagaaaaaagttttgcatgtttcctgctgtttcttcacaccttcgtatatatcaccttcacctctctgttttctatagtttgtgcaaaaactgatcgatttaaaagggtttcaaagaagctgttttaaattgttgtagggttgattatttttttcaagattgtattgtttaattttgaagtggcaactttctcctctattgcccttagagcgtttgcctgtgcacttagactgtcacttcgtgtggcctccaggtcttaccggggcttccgggaggctggctgctttgctcagagagggtgggaagggggcctggagagacacgagaagcagaggtagagcctagaaggtggcagcaggtgggtaagaggcttatttagcacattaggggcagtgagcacctggaggaaggagggcgctcccaatcacccgtaggaggccatctgcacaccaagcggcaattcacctgctggcgcttttcctaggtgacaagcacaatactacagtcttcacactgtttacagccctgggcaccagccacccggcactggctcttcatcacagctctgctcttgcttagctagtggggtgggggaaagggcagggatttgtttttttaattgggtggagagccaaacagctactgtccctgggtgccaagcaagccagttttttggttccctgagggaaactgaccctcctctcttgtggcaccatccagcctcagggtcttggagacttgagtaagaatgtgagtggagggggagaggtgaggagaggagcacagggtggatctgtggagggaagaggttacagggggaggagctgatgatagatcccacccagacttaagctgctggtgggtgggtgagctgggaagtaggactgtccagggaagggtggagagatgtagctaggggctggggagggggaggtggaagcgctattgagcatcctccacaccaaggttgatgaaggaagggatcccagcagggtttctgctctggggctggcaggttgcctggtattatgcccaaggccgctctgcctgggggaaagggcagccaggcagaggcccagtgtctggtaggctgctgaatttcctggaaggggtgattggatggaaagaggccagaaaccccagcctgagagactgctgtgcaccccacagtctgactgcacagagccgcctctgttggcaggaggcactgaggctccccttcctgtgtattgagaagcagtgtttgccaatatattttgctttcaattccaagaggagctctgggaaaacctgtggataaaaccaaatgccaaatgttggacgttgtttccttttccttttctctctctgattgttttaattgttctgtggtggttttaatggatttgagaccctggagcggcagctgcctttctgatttccagctgctttttgtgaataatttaaaaagaaaaaaaaaaagaaactttacattttggagacaaacctgtgtgagttttttattggtacaaacgttgtatttaacactaggggttttgtacagttttttgccttttctactagaaaacaatgtaaagtgatttcacaatgtgaagagaaaaaaaaattgccactatgaccaaacgcacagtctgttctgcagcaacaacgggattcaatcaactcagtcgtgattcagccgtagaaatgcttttcctttatcttgtttgagcttttcctttctttcctgttttgatttgcaaaagaaaatgtcttttttgtgtgaacttgtgttgtactctgtagaaaattatggattttactttaatggtttaaaaaaaggcaaggagagccctcgtcgcttttcttacctaatcacagagtttgtgtagtgaatttaaaaagaaaaaaaaattgttataagtttggagcaagggagtatgtgtttcaaaggaatctccttcctttttttgtgtgtttttccttttgtcccaatggggaacctaaatctgttttaattgcacagacacatggacaaaaagtcattttgtatctgccaagtgtggtaccttcctttgtttatttgctattaaactgtttgagaagaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:10658 -> Molecular function: GO:0000166 [nucleotide binding] evidence: IEA
            GeneID:10658 -> Molecular function: GO:0000900 [translation repressor activity, nucleic acid binding] evidence: NAS
            GeneID:10658 -> Molecular function: GO:0003723 [RNA binding] evidence: IDA
            GeneID:10658 -> Molecular function: GO:0003729 [mRNA binding] evidence: IDA
            GeneID:10658 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:10658 -> Molecular function: GO:0031369 [translation initiation factor binding] evidence: IEA
            GeneID:10658 -> Molecular function: GO:0042835 [BRE binding] evidence: IDA
            GeneID:10658 -> Biological process: GO:0006376 [mRNA splice site selection] evidence: ISS
            GeneID:10658 -> Biological process: GO:0006397 [mRNA processing] evidence: TAS
            GeneID:10658 -> Biological process: GO:0007281 [germ cell development] evidence: NAS
            GeneID:10658 -> Biological process: GO:0007286 [spermatid development] evidence: IEA
            GeneID:10658 -> Biological process: GO:0009790 [embryo development] evidence: NAS
            GeneID:10658 -> Biological process: GO:0016246 [RNA interference] evidence: NAS
            GeneID:10658 -> Biological process: GO:0040018 [positive regulation of multicellular organism growth] evidence: IEA
            GeneID:10658 -> Biological process: GO:0043484 [regulation of RNA splicing] evidence: IDA
            GeneID:10658 -> Cellular component: GO:0005634 [nucleus] evidence: NAS
            GeneID:10658 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA
            GeneID:10658 -> Cellular component: GO:0030529 [ribonucleoprotein complex] evidence: NAS

by @meso_cacase at DBCLS
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