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2020-10-26 19:16:29, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_018666               3069 bp    mRNA    linear   PRI 18-APR-2013
DEFINITION  Homo sapiens sarcoma antigen 1 (SAGE1), mRNA.
ACCESSION   NM_018666
VERSION     NM_018666.2  GI:145580596
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 3069)
  AUTHORS   Miyahara,Y., Naota,H., Wang,L., Hiasa,A., Goto,M., Watanabe,M.,
            Kitano,S., Okumura,S., Takemitsu,T., Yuta,A., Majima,Y.,
            Lemonnier,F.A., Boon,T. and Shiku,H.
  TITLE     Determination of cellularly processed HLA-A2402-restricted novel
            CTL epitopes derived from two cancer germ line genes, MAGE-A4 and
            SAGE
  JOURNAL   Clin. Cancer Res. 11 (15), 5581-5589 (2005)
   PUBMED   16061876
  REMARK    GeneRIF: MAGE-A4(143-151) and SAGE(715-723) are
            HLA-A2402-restricted CTL epitopes
REFERENCE   2  (bases 1 to 3069)
  AUTHORS   Martelange,V., De Smet,C., De Plaen,E., Lurquin,C. and Boon,T.
  TITLE     Identification on a human sarcoma of two new genes with
            tumor-specific expression
  JOURNAL   Cancer Res. 60 (14), 3848-3855 (2000)
   PUBMED   10919659
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AJ278111.1, AL953870.2,
            CD358947.1 and BF056519.1.
            This sequence is a reference standard in the RefSeqGene project.
            On Apr 20, 2007 this sequence version replaced gi:8924241.
            
            Summary: This gene belongs to a class of genes that are activated
            in tumors. These genes are expressed in tumors of different
            histologic types but not in normal tissues, except for
            spermatogenic cells and, for some, placenta. The proteins encoded
            by these genes appear to be strictly tumor specific, and hence may
            be excellent sources of antigens for cancer immunotherapy. This
            gene is expressed in sarcomas. [provided by RefSeq, Jul 2008].
            
            ##Evidence-Data-START##
            Transcript exon combination :: AJ278111.1 [ECO:0000332]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-913               AJ278111.1         1-913
            914-914             AL953870.2         11665-11665
            915-1663            AJ278111.1         915-1663
            1664-1951           CD358947.1         502-789
            1952-2580           AJ278111.1         1952-2580
            2581-3045           BF056519.1         1-465               c
            3046-3069           AJ278111.1         3046-3069
FEATURES             Location/Qualifiers
     source          1..3069
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="X"
                     /map="Xq26"
     gene            1..3069
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /note="sarcoma antigen 1"
                     /db_xref="GeneID:55511"
                     /db_xref="HGNC:30369"
                     /db_xref="MIM:300359"
     exon            1..167
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       117
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143981037"
     variation       130
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370104512"
     misc_feature    162..164
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /note="upstream in-frame stop codon"
     CDS             168..2882
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /note="cancer/testis antigen 14; putative tumor antigen"
                     /codon_start=1
                     /product="sarcoma antigen 1"
                     /protein_id="NP_061136.2"
                     /db_xref="GI:145580597"
                     /db_xref="CCDS:CCDS14652.1"
                     /db_xref="GeneID:55511"
                     /db_xref="HGNC:30369"
                     /db_xref="MIM:300359"
                     /translation="
MQASPLQTSQPTPPEELHAAAYVFTNDGQQMRSDEVNLVATGHQSKKKHSRKSKRHSSSKRRKSMSSWLDKQEDAAVTHSICEERINNGQPVADNVLSTAPPWPDATIAHNIREERMENGQSRTDKVLSTAPPQLVHMAAAGIPSMSTRDLHSTVTHNIREERMENGQPQPDNVLSTGPTGLINMAATPIPAMSARDLYATVTHNVCEQKMENVQPAPDNVLLTLRPRRINMTDTGISPMSTRDPYATITYNVPEEKMEKGQPQPDNILSTASTGLINVAGAGTPAISTNGLYSTVPHNVCEEKMENDQPQPNNVLSTVQPVIIYLTATGIPGMNTRDQYATITHNVCEERVVNNQPLPSNALSTVLPGLAYLATADMPAMSTRDQHATIIHNLREEKKDNSQPTPDNVLSAVTPELINLAGAGIPPMSTRDQYATVNHHVHEARMENGQRKQDNVLSNVLSGLINMAGASIPAMSSRDLYATITHSVREEKMESGKPQTDKVISNDAPQLGHMAAGGIPSMSTKDLYATVTQNVHEERMENNQPQPSYDLSTVLPGLTYLTVAGIPAMSTRDQYATVTHNVHEEKIKNGQAASDNVFSTVPPAFINMAATGVSSMSTRDQYAAVTHNIREEKINNSQPAPGNILSTAPPWLRHMAAAGISSTITRDLYVTATHSVHEEKMTNGQQAPDNSLSTVPPGCINLSGAGISCRSTRDLYATVIHDIQEEEMENDQTPPDGFLSNSDSPELINMTGHCMPPNALDSFSHDFTSLSKDELLYKPDSNEFAVGTKNYSVSAGDPPVTVMSLVETVPNTPQISPAMAKKINDDIKYQLMKEVRRFGQNYERIFILLEEVQGSMKVKRQFVEFTIKEAARFKKVVLIQQLEKALKEIDSHCHLRKVKHMRKR
"
     exon            168..254
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       191
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:5930805"
     variation       199
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200108643"
     variation       220
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148375834"
     exon            255..387
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       260
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141643764"
     variation       358
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150500826"
     variation       367
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143643223"
     exon            388..480
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       408
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:73226720"
     variation       423
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:141587396"
     variation       448
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146246017"
     variation       452
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12014884"
     exon            481..621
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       505
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191992256"
     variation       530
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150013472"
     variation       546
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144175318"
     variation       561
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148687005"
     variation       602
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142279610"
     variation       621
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147659975"
     exon            622..762
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       624
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:180892858"
     variation       629
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:184259780"
     variation       634
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374833451"
     variation       646
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201111165"
     variation       682
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368113626"
     variation       690
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371998107"
     variation       696
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377122684"
     variation       704
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151240146"
     variation       716
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141646494"
     variation       750
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374269888"
     variation       755
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368450526"
     variation       760
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370986426"
     exon            763..903
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       774
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145404090"
     variation       807
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:147691037"
     variation       812
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372343672"
     variation       849
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201538619"
     variation       852
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181135819"
     variation       856
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376631207"
     variation       874
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369004182"
     exon            904..1044
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       926
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374723588"
     variation       930
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369338467"
     variation       949
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150239273"
     variation       969
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:77252560"
     variation       1033
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372774863"
     variation       1038
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149941934"
     exon            1045..1185
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       1069
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149000071"
     variation       1071
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200674696"
     variation       1080
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143029955"
     variation       1095
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:138507588"
     variation       1127
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201511584"
     variation       1162
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367622228"
     exon            1186..1326
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       1186
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368384420"
     variation       1252
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141521507"
     variation       1253
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372283658"
     variation       1263
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375536886"
     variation       1272
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187385702"
     variation       1273
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146228048"
     variation       1286
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:137926286"
     variation       1299
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368948792"
     variation       1316
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372184159"
     variation       1326
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:41301507"
     exon            1327..1467
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       1337
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150553796"
     variation       1343
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139636630"
     variation       1351
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376186717"
     variation       1355
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199746856"
     variation       1358
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149311139"
     variation       1367
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144682113"
     variation       1391
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139911590"
     variation       1427
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:145348061"
     variation       1440
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145952520"
     variation       1445
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:369615050"
     variation       1458
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147700811"
     variation       1459
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:140797723"
     exon            1468..1608
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       1475
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142416061"
     variation       1486
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200716448"
     variation       1502
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201711021"
     variation       1533
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151288559"
     exon            1609..1749
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       1617
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140611917"
     variation       1618
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150494017"
     variation       1664
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:5974570"
     variation       1732
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372951066"
     exon            1750..1890
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       1783
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140250946"
     variation       1833
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145227695"
     variation       1840
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372296087"
     variation       1867
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137945651"
     exon            1891..2031
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       1899
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149476095"
     variation       1914
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143132398"
     variation       1950
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371669134"
     variation       1967
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374938226"
     variation       1977
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:6635182"
     variation       1981
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:188785844"
     variation       1987
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:148235147"
     variation       2001
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369551587"
     exon            2032..2172
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       2057
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141252399"
     variation       2064
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376122017"
     variation       2067
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:193225560"
     variation       2109
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147443347"
     variation       2112
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370856365"
     variation       2125
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139744161"
     variation       2131
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143868060"
     variation       2152
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147236070"
     variation       2156
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375231665"
     exon            2173..2313
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       2214
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373897949"
     variation       2236
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:147695949"
     variation       2248
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149788009"
     variation       2302
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191345675"
     exon            2314..2688
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       2390
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:35470903"
     variation       2410
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35098873"
     variation       2417
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142913424"
     variation       2428
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146646613"
     variation       2430
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141394144"
     variation       2460
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145270330"
     variation       2463
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146408420"
     variation       2464
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:147884544"
     variation       2465
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374548357"
     variation       2522
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150124078"
     variation       2581
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4829799"
     variation       2618
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368799672"
     variation       2630
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:4829584"
     variation       2637
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7057232"
     exon            2689..2782
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       2692
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201670376"
     variation       2698
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146979495"
     variation       2705
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200895409"
     variation       2722
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372241144"
     variation       2753
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138213839"
     variation       2766
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143701951"
     variation       2770
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200846172"
     variation       2782
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374427739"
     exon            2783..3046
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /inference="alignment:Splign:1.39.8"
     variation       2813
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369586458"
     variation       2822
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147248332"
     variation       2904
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:41302146"
     polyA_signal    3020..3025
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
     polyA_site      3046
                     /gene="SAGE1"
                     /gene_synonym="CT14; SAGE"
ORIGIN      
caggaccgctggcgccagcgggagaaccaggaagcgcagctctccccttagctgactctggtgctctctacaggtggccttcactatcaactgcacagcgggcagaggcagaggaacacagaaccttctcacacagcgggataaaagggtgaatttggagctgacagatgcaggcttctccacttcaaacgagtcaaccaactccacctgaagaacttcatgctgctgcctatgtgtttacaaatgatgggcagcaaatgaggagtgatgaagtaaatctggttgcaacagggcatcaaagcaaaaagaaacattccagaaaatccaagagacactcttcatctaagagaaggaagagtatgtcctcgtggttagacaaacaggaagatgctgcagtcactcacagcatttgtgaagagaggataaataacggccaaccagtagctgataatgtcttgtcaactgctccaccatggcctgatgctaccatcgctcacaatatccgtgaagagaggatggaaaatggccaatctcgaactgacaaagtcttgtcaactgctccaccacagcttgttcatatggctgcagctggtattccatccatgagtaccagggatctgcattctaccgtcactcacaatatccgtgaagagagaatggaaaatggccaaccccaacctgataacgtcttgtcaactggtcccacagggcttattaatatggcagcaactcctattccagccatgagtgccagagatctctatgctacagtcactcacaatgtctgtgaacagaagatggaaaatgtccaaccagcacctgataacgtgttgttgactcttcgaccacggcgtattaatatgacagacactggtatttcacccatgagtaccagggatccatatgctaccatcacttacaatgtccctgaggagaagatggaaaagggccaaccccaacctgataacatcttgtcaactgcttcaacagggcttattaatgtggcaggagctggtactccagccatcagcaccaatggcctgtattccaccgtccctcacaatgtctgtgaagagaagatggaaaatgaccaaccgcaacctaataacgtattgtcaactgttcaaccagtgattatttatttgacagcaactggtattccgggcatgaataccagggatcagtatgctaccatcactcacaatgtctgtgaagagagagtggtaaataaccaaccactacctagtaacgccttgtcaactgttctaccagggcttgcttatttggcaacagctgatatgccagccatgagtaccagggatcagcatgctaccatcattcacaatctgcgtgaagagaagaaagataacagccaaccaacccctgataacgtcttgtcagctgttacaccagagcttattaacttggcaggagctggtattccacccatgagtaccagggatcagtatgctaccgtcaatcaccatgtccatgaagcaaggatggaaaatggccaacgaaaacaggataacgtcttgtcaaatgttctatccgggcttattaatatggcaggagctagtattccagcaatgagttccagggatctgtatgctaccattactcacagtgttcgtgaagagaagatggaaagtggcaaaccccaaactgataaggtcatatcaaatgatgcaccacagcttggtcatatggctgcaggtggtattccatccatgagtaccaaggatctgtatgctaccgtcactcaaaatgtccatgaagagaggatggaaaataaccaaccacaacctagttatgacttgtcaactgttctaccaggacttacttatttgacagtagctggtattccggccatgagtaccagggatcagtatgctaccgtcactcacaatgtccatgaagagaagattaaaaatggccaagcagcatccgataatgtcttctcgactgttccaccagcatttattaatatggcagcaactggtgtttcatccatgagtaccagggatcagtatgctgcagtcactcacaacatccgtgaagagaagataaataacagccaaccagcacctggtaacatcttgtcaactgctcctccatggcttcgtcatatggcagcagctggaatttcatccacgattaccagggatctgtatgtcaccgccactcacagtgtccatgaggagaagatgacaaatggccaacaggcacctgataactccttgtcaacggttccacctggttgtattaatctgtcaggagctggtatttcatgcagaagtaccagggatctgtatgctactgtcattcacgatatccaggaggaggagatggaaaatgatcaaacccctcctgatggcttcctgtcaaattctgattcaccagagctgataaatatgacaggacattgtatgccacccaatgcattggattctttctctcacgacttcacaagtctcagcaaagatgagctgctttacaaacctgatagtaatgaatttgcggtaggcaccaaaaactacagtgtctctgcaggtgacccaccagttacagtaatgtctttggtggaaactgtgccaaatacaccacaaatatctcctgccatggcaaagaaaattaatgatgatataaaatatcaattaatgaaagaagttcgaaggtttgggcaaaattatgaaagaattttcattttgcttgaagaggtacaaggatctatgaaagtcaagagacaatttgttgaatttaccatcaaggaagcagcaaggtttaaaaaagttgtcttaattcagcaactcgagaaggcgcttaaagaaatagattcccactgccatctcagaaaagttaagcacatgagaaaaagataattgtgttagtgcaaagaccaaggagaaacaaggacatatgctgtaggatggaacaggttattgctgaagctccctataatcctgaaatgaagagaattcccttccagaagctacgaaaaagggagctgtttaaatttaataaatctctgttagtaaaagctgcaaaaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:55511 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
            GeneID:55511 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA

by @meso_cacase at DBCLS
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