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2024-04-17 06:41:34, 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 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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