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2024-03-29 15:02:45, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001005333            2928 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens melanoma antigen family D, 1 (MAGED1), transcript
            variant 1, mRNA.
ACCESSION   NM_001005333
VERSION     NM_001005333.1  GI:52632380
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 2928)
  AUTHORS   Zeng,Z.L., Wu,W.J., Yang,J., Tang,Z.J., Chen,D.L., Qiu,M.Z.,
            Luo,H.Y., Wang,Z.Q., Jin,Y., Wang,D.S. and Xu,R.H.
  TITLE     Prognostic relevance of melanoma antigen D1 expression in
            colorectal carcinoma
  JOURNAL   J Transl Med 10, 181 (2012)
   PUBMED   22935435
  REMARK    GeneRIF: Univariate and multivariate analyses indicated that MAGED1
            expression was an independent prognostic factor in colorectal
            carcinoma
            Publication Status: Online-Only
REFERENCE   2  (bases 1 to 2928)
  AUTHORS   Reddy,E.M., Chettiar,S.T., Kaur,N., Ganeshkumar,R., Shepal,V.,
            Shanbhag,N.C. and Shiras,A.
  TITLE     Dlxin-1, a member of MAGE family, inhibits cell proliferation,
            invasion and tumorigenicity of glioma stem cells
  JOURNAL   Cancer Gene Ther. 18 (3), 206-218 (2011)
   PUBMED   21109781
  REMARK    GeneRIF: we establish the roles for Dlxin-1, one as an
            anti-tumorigenic and anti-invasive protein in high-grade gliomas
            and the other as an inducer of differentiation of glioma stem
            cells.
REFERENCE   3  (bases 1 to 2928)
  AUTHORS   Xue,X.Y., Liu,Z.H., Jing,F.M., Li,Y.G., Liu,H.Z. and Gao,X.S.
  TITLE     Relationship between NRAGE and the radioresistance of esophageal
            carcinoma cell line TE13R120
  JOURNAL   Chin J Cancer 29 (10), 900-906 (2010)
   PUBMED   20868560
  REMARK    GeneRIF: NRAGE may participate in the formation of radioresistance
            of TE13R120 cells by changing its subcellular localization, but its
            relationship with cell apoptosis has not been confirmed.
REFERENCE   4  (bases 1 to 2928)
  AUTHORS   Davila,S., Froeling,F.E., Tan,A., Bonnard,C., Boland,G.J.,
            Snippe,H., Hibberd,M.L. and Seielstad,M.
  TITLE     New genetic associations detected in a host response study to
            hepatitis B vaccine
  JOURNAL   Genes Immun. 11 (3), 232-238 (2010)
   PUBMED   20237496
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   5  (bases 1 to 2928)
  AUTHORS   Matluk,N., Rochira,J.A., Karaczyn,A., Adams,T. and Verdi,J.M.
  TITLE     A role for NRAGE in NF-kappaB activation through the non-canonical
            BMP pathway
  JOURNAL   BMC Biol. 8, 7 (2010)
   PUBMED   20100315
  REMARK    GeneRIF: Data report that NRAGE, via the same XIAP-Tak1-Tab1
            complex, is required for the phosphorylation of IKK -alpha/beta and
            subsequent transcriptional activation of the p65 subunit of
            NF-kappaB.
            Publication Status: Online-Only
REFERENCE   6  (bases 1 to 2928)
  AUTHORS   Masuda,Y., Sasaki,A., Shibuya,H., Ueno,N., Ikeda,K. and Watanabe,K.
  TITLE     Dlxin-1, a novel protein that binds Dlx5 and regulates its
            transcriptional function
  JOURNAL   J. Biol. Chem. 276 (7), 5331-5338 (2001)
   PUBMED   11084035
REFERENCE   7  (bases 1 to 2928)
  AUTHORS   Zhang,C.G., Xing,G.C., Wei,H.D., Yu,Y.T. and He,F.C.
  TITLE     [A new melanoma antigen-encoding gene subfamily in human chromosome
            X]
  JOURNAL   Yi Chuan Xue Bao 28 (3), 197-203 (2001)
   PUBMED   11280991
REFERENCE   8  (bases 1 to 2928)
  AUTHORS   Kubu,C.J., Goldhawk,D.G., Barker,P.A. and Verdi,J.M.
  TITLE     Identification of the translational initiation codon in human
            MAGED1
  JOURNAL   Genomics 70 (1), 150-152 (2000)
   PUBMED   11087672
REFERENCE   9  (bases 1 to 2928)
  AUTHORS   Salehi,A.H., Roux,P.P., Kubu,C.J., Zeindler,C., Bhakar,A.,
            Tannis,L.L., Verdi,J.M. and Barker,P.A.
  TITLE     NRAGE, a novel MAGE protein, interacts with the p75 neurotrophin
            receptor and facilitates nerve growth factor-dependent apoptosis
  JOURNAL   Neuron 27 (2), 279-288 (2000)
   PUBMED   10985348
REFERENCE   10 (bases 1 to 2928)
  AUTHORS   Pold,M., Zhou,J., Chen,G.L., Hall,J.M., Vescio,R.A. and
            Berenson,J.R.
  TITLE     Identification of a new, unorthodox member of the MAGE gene family
  JOURNAL   Genomics 59 (2), 161-167 (1999)
   PUBMED   10409427
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BX422007.2, BC014070.2 and
            AF132205.1.
            
            Summary: This gene is a member of the melanoma antigen gene (MAGE)
            family. Most of the genes of this family encode tumor specific
            antigens that are not expressed in normal adult tissues except
            testis. Although the protein encoded by this gene shares strong
            homology with members of the MAGE family, it is expressed in almost
            all normal adult tissues. This gene has been demonstrated to be
            involved in the p75 neurotrophin receptor mediated programmed cell
            death pathway. Three transcript variants encoding two different
            isoforms have been found for this gene. [provided by RefSeq, Jul
            2008].
            
            Transcript Variant: This variant (1) represents the longest
            transcript and encodes the longer isoform (a).
            
            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 :: BC014070.2 [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
            1-37                BX422007.2         1-37
            38-2912             BC014070.2         1-2875
            2913-2928           AF132205.1         1372-1387
FEATURES             Location/Qualifiers
     source          1..2928
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="X"
                     /map="Xp11.23"
     gene            1..2928
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /note="melanoma antigen family D, 1"
                     /db_xref="GeneID:9500"
                     /db_xref="HGNC:6813"
                     /db_xref="HPRD:02202"
                     /db_xref="MIM:300224"
     exon            1..154
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       66..67
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:11541163"
     misc_feature    146..148
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /note="upstream in-frame stop codon"
     exon            155..235
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     CDS             191..2695
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /note="isoform a is encoded by transcript variant 1;
                     neurotrophin receptor-interacting MAGE homolog;
                     melanoma-associated antigen D1; MAGE-D1 antigen; MAGE
                     tumor antigen CCF"
                     /codon_start=1
                     /product="melanoma-associated antigen D1 isoform a"
                     /protein_id="NP_001005333.1"
                     /db_xref="GI:52632381"
                     /db_xref="CCDS:CCDS35279.1"
                     /db_xref="GeneID:9500"
                     /db_xref="HGNC:6813"
                     /db_xref="HPRD:02202"
                     /db_xref="MIM:300224"
                     /translation="
MAQKMDCGAGLLGFQNPDACRAVCHPLPQPPASTLPLSAFPTLCDPPYSQLRDPPAVLSCYCTPLGASPAPAEASVEDSALLMQTLMEAIQISEAPPTNQATAAASPQSSQPPTANEMADIQVSAAAARPKSAFKVQNATTKGPNGVYDFSQAHNAKDVPNTQPKAAFKSQNATPKGPNAAYDFSQAATTGELAANKSEMAFKAQNATTKVGPNATYNFSQSLNANDLANSRPKTPFKAWNDTTKAPTADTQTQNVNQAKMATSQADIETDPGISEPDGATAQTSADGSQAQNLESRTIIRGKRTRKINNLNVEENSSGDQRRAPLAAGTWRSAPVPVTTQNPPGAPPNVLWQTPLAWQNPSGWQNQTARQTPPARQSPPARQTPPAWQNPVAWQNPVIWPNPVIWQNPVIWPNPIVWPGPVVWPNPLAWQNPPGWQTPPGWQTPPGWQGPPDWQGPPDWPLPPDWPLPPDWPLPTDWPLPPDWIPADWPIPPDWQNLRPSPNLRPSPNSRASQNPGAAQPRDVALLQERANKLVKYLMLKDYTKVPIKRSEMLRDIIREYTDVYPEIIERACFVLEKKFGIQLKEIDKEEHLYILISTPESLAGILGTTKDTPKLGLLLVILGVIFMNGNRASEAVLWEALRKMGLRPGVRHPLLGDLRKLLTYEFVKQKYLDYRRVPNSNPPEYEFLWGLRSYHETSKMKVLRFIAEVQKRDPRDWTAQFMEAADEALDALDAAAAEAEARAEARTRMGIGDEAVSGPWSWDDIEFELLTWDEEGDFGDPWSRIPFTFWARYHQNARSRFPQTFAGPIIGPGGTASANFAANFGAIGFFWVE
"
     misc_feature    632..634
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    632..634
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    1790..2299
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /note="MAGE family; Region: MAGE; pfam01454"
                     /db_xref="CDD:201804"
     exon            236..403
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       279
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372507787"
     variation       315
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141749849"
     variation       351
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369340329"
     variation       354
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377536231"
     variation       359
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145588024"
     variation       396
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371038613"
     exon            404..1111
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       416
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200403502"
     variation       530
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370800331"
     variation       533
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375273111"
     variation       572
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201938318"
     variation       588
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202085108"
     variation       633
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151112988"
     variation       665
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141080853"
     variation       702
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:113823505"
     variation       703
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200269066"
     variation       704
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:137856838"
     variation       802
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144264968"
     variation       824
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200672367"
     variation       833
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373610127"
     variation       862
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183944548"
     variation       1020
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:187608453"
     variation       1044
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372248500"
     variation       1070
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:12689461"
     exon            1112..1780
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       1172
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:41307638"
     variation       1179
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200760701"
     variation       1225
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140810987"
     variation       1251
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374985036"
     variation       1271
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144665907"
     variation       1307
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369211587"
     variation       1317
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373153783"
     variation       1420
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138624949"
     variation       1437
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202231305"
     variation       1528
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141719497"
     variation       1571
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:199911189"
     variation       1603
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376126768"
     variation       1609
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370215151"
     variation       1648
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184387756"
     variation       1649
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200856189"
     variation       1685
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377687584"
     variation       1740
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144566171"
     variation       1751
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148038224"
     exon            1781..1844
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     exon            1845..1924
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       1900
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367685368"
     exon            1925..2016
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       1963
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141770812"
     variation       1990
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150589159"
     exon            2017..2096
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       2047
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371683752"
     variation       2084
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375975220"
     exon            2097..2139
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     exon            2140..2202
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       2153
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199703705"
     exon            2203..2317
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     exon            2318..2703
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       2350
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201229700"
     variation       2356
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140668837"
     variation       2383
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144656819"
     variation       2410
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368745871"
     variation       2411
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147478214"
     variation       2417
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:3199687"
     variation       2584
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200548781"
     variation       2601
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150014410"
     variation       2621
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145319637"
     variation       2653
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149192593"
     variation       2665
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142436276"
     variation       2694
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145598419"
     exon            2704..2912
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       2718
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:58080956"
     variation       2731
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:193192478"
     variation       2745
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376570677"
     variation       2763
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1136500"
     variation       2777
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1136504"
     variation       2792
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11541165"
     variation       2858..2859
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35938097"
     polyA_signal    2887..2892
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
     polyA_site      2912
                     /gene="MAGED1"
                     /gene_synonym="DLXIN-1; NRAGE"
ORIGIN      
ggcgaagaggcggggtcgcccaagctgccgcgctggcattttctcctggacaaggagagagtgcggctgctgagagccgagcccagcaatcccgatcctctgagtcgtgaagaagggaggcagcgagggggttggggttggggcctgaggcaagcccccaggctccgctcttgccagagggacaggagccatggctcagaaaatggactgtggtgcgggcctcctcggcttccagaatcctgacgcttgtagagcagtctgtcaccccctcccccagcctcctgcctccaccctccctctttctgcattccccactctgtgcgaccccccttattctcaactccgcgatccgcctgccgtcctgagctgctactgcacgcctcttggagcgtccccggctcctgctgaggcctccgtagaagacagcgccttgcttatgcagaccttgatggaggccatccagatctcagaggctccacctactaaccaggccaccgcagctgctagtccccagagttcacagcccccaactgccaatgagatggctgacattcaggtttcagcagctgccgctaggcctaagtcagcctttaaagtccagaatgccaccacaaaaggcccaaatggtgtctatgatttctctcaggctcataatgccaaggatgtgcccaacacgcagcccaaggcagcctttaagtcccaaaatgctaccccaaagggtccaaatgctgcctatgatttttcccaggcagcaaccactggtgagttagctgctaacaagtctgagatggccttcaaggcccagaatgccactactaaagtgggcccaaatgccacctacaatttctctcagtctctcaatgccaatgacctggccaacagcaggcctaagacccctttcaaggcttggaatgataccactaaggccccaacagctgatacccagacccagaatgtaaatcaggccaaaatggccacttcccaggctgacatagagaccgacccaggtatctctgaacctgacggtgcaactgcacagacatcagcagatggttcccaggctcagaatctggagtcccggacaataattcggggcaagaggacccgcaagattaataacttgaatgttgaagagaacagcagtggggatcagaggcgggccccactggctgcagggacctggaggtctgcaccagttccagtgaccactcagaacccacctggcgcaccccccaatgtgctctggcagacgccattggcttggcagaacccctcaggctggcaaaaccagacagccaggcagaccccaccagcacgtcagagccctccagctaggcagaccccaccagcctggcagaacccagtcgcttggcagaacccagtgatttggccaaacccagtaatctggcagaacccagtgatctggccaaaccccattgtctggcccggccctgttgtctggccgaatccactggcctggcagaatccacctggatggcagactccacctggatggcagaccccaccgggctggcagggtcctccagactggcaaggtcctcctgactggccgctaccacccgactggccactgccacctgattggccacttcccactgactggccactaccacctgactggatccccgctgattggccaattccacctgactggcagaacctgcgcccctcgcctaacctgcgcccttctcccaactcgcgtgcctcacagaacccaggtgctgcacagccccgagatgtggcccttcttcaggaaagagcaaataagttggtcaagtacttgatgcttaaggactacacaaaggtgcccatcaagcgctcagaaatgctgagagatatcatccgtgaatacactgatgtttatccagaaatcattgaacgtgcatgctttgtcctagagaagaaatttgggattcaactgaaagaaattgacaaagaagaacacctgtatattctcatcagtacccccgagtccctggctggcatactgggaacgaccaaagacacacccaagctcggtctcctcttggtgattctgggtgtcatcttcatgaatggcaaccgtgccagtgaggctgtcctctgggaggcactacgcaagatgggactgcgtcctggggtgagacatcccctccttggagatctaaggaaacttctcacctatgagtttgtaaagcagaaatacctggactacagacgagtgcccaacagcaaccccccggagtatgagttcctctggggcctccgttcctaccatgagactagcaagatgaaagtgctgagattcattgcagaggttcagaaaagagaccctcgtgactggactgcacagttcatggaggctgcagatgaggccttggatgctctggatgctgctgcagctgaggccgaagcccgggctgaagcaagaacccgcatgggaattggagatgaggctgtgtctgggccctggagctgggatgacattgagtttgagctgctgacctgggatgaggaaggagattttggagatccctggtccagaattccatttaccttctgggccagataccaccagaatgcccgctccagattccctcagacctttgccggtcccattattggtcctggtggtacagccagtgccaacttcgctgccaactttggtgccattggtttcttctgggttgagtgagatgttggatattgctatcaatcgcagtagtctttcccctgtgtgaggctgaagcctcagattccttctaaacacagctatctagagagccacatcctgttgactgaaagtggcatgcaagataaatttatttgctgttccttgtctactgctttttttccccttgtgtgctgtcaagttttggtatcagaaataaacattgaaattgcaaagtgaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:9500 -> Molecular function: GO:0003713 [transcription coactivator activity] evidence: IEA
            GeneID:9500 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:9500 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: TAS
            GeneID:9500 -> Biological process: GO:0006357 [regulation of transcription from RNA polymerase II promoter] evidence: IEA
            GeneID:9500 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
            GeneID:9500 -> Biological process: GO:0042981 [regulation of apoptotic process] evidence: TAS
            GeneID:9500 -> Biological process: GO:0043065 [positive regulation of apoptotic process] evidence: TAS
            GeneID:9500 -> Biological process: GO:0043406 [positive regulation of MAP kinase activity] evidence: IEA
            GeneID:9500 -> Biological process: GO:0045892 [negative regulation of transcription, DNA-dependent] evidence: IEA
            GeneID:9500 -> Biological process: GO:0045893 [positive regulation of transcription, DNA-dependent] evidence: IEA
            GeneID:9500 -> Biological process: GO:0048011 [neurotrophin TRK receptor signaling pathway] evidence: TAS
            GeneID:9500 -> Biological process: GO:0050680 [negative regulation of epithelial cell proliferation] evidence: IDA
            GeneID:9500 -> Biological process: GO:0090190 [positive regulation of branching involved in ureteric bud morphogenesis] evidence: IEA
            GeneID:9500 -> Biological process: GO:0097190 [apoptotic signaling pathway] evidence: TAS
            GeneID:9500 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA
            GeneID:9500 -> Cellular component: GO:0005886 [plasma membrane] evidence: IEA
            GeneID:9500 -> Cellular component: GO:0043234 [protein complex] evidence: IDA

by @meso_cacase at DBCLS
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