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Previous release (v1)
2024-04-19 06:32:00, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_005193 1642 bp mRNA linear PRI 20-MAR-2023 DEFINITION Homo sapiens caudal type homeobox 4 (CDX4), mRNA. ACCESSION NM_005193 VERSION NM_005193.2 KEYWORDS RefSeq; MANE Select. 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 1642) AUTHORS Luck K, Kim DK, Lambourne L, Spirohn K, Begg BE, Bian W, Brignall R, Cafarelli T, Campos-Laborie FJ, Charloteaux B, Choi D, Cote AG, Daley M, Deimling S, Desbuleux A, Dricot A, Gebbia M, Hardy MF, Kishore N, Knapp JJ, Kovacs IA, Lemmens I, Mee MW, Mellor JC, Pollis C, Pons C, Richardson AD, Schlabach S, Teeking B, Yadav A, Babor M, Balcha D, Basha O, Bowman-Colin C, Chin SF, Choi SG, Colabella C, Coppin G, D'Amata C, De Ridder D, De Rouck S, Duran-Frigola M, Ennajdaoui H, Goebels F, Goehring L, Gopal A, Haddad G, Hatchi E, Helmy M, Jacob Y, Kassa Y, Landini S, Li R, van Lieshout N, MacWilliams A, Markey D, Paulson JN, Rangarajan S, Rasla J, Rayhan A, Rolland T, San-Miguel A, Shen Y, Sheykhkarimli D, Sheynkman GM, Simonovsky E, Tasan M, Tejeda A, Tropepe V, Twizere JC, Wang Y, Weatheritt RJ, Weile J, Xia Y, Yang X, Yeger-Lotem E, Zhong Q, Aloy P, Bader GD, De Las Rivas J, Gaudet S, Hao T, Rak J, Tavernier J, Hill DE, Vidal M, Roth FP and Calderwood MA. TITLE A reference map of the human binary protein interactome JOURNAL Nature 580 (7803), 402-408 (2020) PUBMED 32296183 REFERENCE 2 (bases 1 to 1642) AUTHORS Fragoza R, Das J, Wierbowski SD, Liang J, Tran TN, Liang S, Beltran JF, Rivera-Erick CA, Ye K, Wang TY, Yao L, Mort M, Stenson PD, Cooper DN, Wei X, Keinan A, Schimenti JC, Clark AG and Yu H. TITLE Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations JOURNAL Nat Commun 10 (1), 4141 (2019) PUBMED 31515488 REMARK Publication Status: Online-Only REFERENCE 3 (bases 1 to 1642) AUTHORS Creamer JP, Dege C, Ren Q, Ho JTK, Valentine MC, Druley TE and Sturgeon CM. TITLE Human definitive hematopoietic specification from pluripotent stem cells is regulated by mesodermal expression of CDX4 JOURNAL Blood 129 (22), 2988-2992 (2017) PUBMED 28408465 REMARK GeneRIF: Gene expression analyses on WNT-dependent KDR(+)CD235a(-) definitive hematopoietic mesoderm and WNT-independent KDR(+)CD235a(+) primitive hematopoietic mesoderm revealed strong CDX gene expression within definitive hematopoietic mesoderm. Temporal expression analyses revealed that CDX4 was expressed exclusively within definitive hematopoietic KDR(+)CD235a(-) mesoderm in a WNT- and fibroblast growth factor-dependent manner REFERENCE 4 (bases 1 to 1642) AUTHORS Yin Y, Morgunova E, Jolma A, Kaasinen E, Sahu B, Khund-Sayeed S, Das PK, Kivioja T, Dave K, Zhong F, Nitta KR, Taipale M, Popov A, Ginno PA, Domcke S, Yan J, Schubeler D, Vinson C and Taipale J. TITLE Impact of cytosine methylation on DNA binding specificities of human transcription factors JOURNAL Science 356 (6337) (2017) PUBMED 28473536 REFERENCE 5 (bases 1 to 1642) AUTHORS Yang X, Coulombe-Huntington J, Kang S, Sheynkman GM, Hao T, Richardson A, Sun S, Yang F, Shen YA, Murray RR, Spirohn K, Begg BE, Duran-Frigola M, MacWilliams A, Pevzner SJ, Zhong Q, Wanamaker SA, Tam S, Ghamsari L, Sahni N, Yi S, Rodriguez MD, Balcha D, Tan G, Costanzo M, Andrews B, Boone C, Zhou XJ, Salehi-Ashtiani K, Charloteaux B, Chen AA, Calderwood MA, Aloy P, Roth FP, Hill DE, Iakoucheva LM, Xia Y and Vidal M. TITLE Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing JOURNAL Cell 164 (4), 805-817 (2016) PUBMED 26871637 REFERENCE 6 (bases 1 to 1642) AUTHORS Frohling S, Scholl C, Bansal D and Huntly BJ. TITLE HOX gene regulation in acute myeloid leukemia: CDX marks the spot? JOURNAL Cell Cycle 6 (18), 2241-2245 (2007) PUBMED 17881901 REMARK Review article REFERENCE 7 (bases 1 to 1642) AUTHORS Bansal D, Scholl C, Frohling S, McDowell E, Lee BH, Dohner K, Ernst P, Davidson AJ, Daley GQ, Zon LI, Gilliland DG and Huntly BJ. TITLE Cdx4 dysregulates Hox gene expression and generates acute myeloid leukemia alone and in cooperation with Meis1a in a murine model JOURNAL Proc Natl Acad Sci U S A 103 (45), 16924-16929 (2006) PUBMED 17068127 REFERENCE 8 (bases 1 to 1642) AUTHORS Zambidis ET, Peault B, Park TS, Bunz F and Civin CI. TITLE Hematopoietic differentiation of human embryonic stem cells progresses through sequential hematoendothelial, primitive, and definitive stages resembling human yolk sac development JOURNAL Blood 106 (3), 860-870 (2005) PUBMED 15831705 REFERENCE 9 (bases 1 to 1642) AUTHORS Lohnes D. TITLE The Cdx1 homeodomain protein: an integrator of posterior signaling in the mouse JOURNAL Bioessays 25 (10), 971-980 (2003) PUBMED 14505364 REMARK Review article REFERENCE 10 (bases 1 to 1642) AUTHORS Horn JM and Ashworth A. TITLE A member of the caudal family of homeobox genes maps to the X-inactivation centre region of the mouse and human X chromosomes JOURNAL Hum Mol Genet 4 (6), 1041-1047 (1995) PUBMED 7655457 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AL450108.12. On Sep 14, 2020 this sequence version replaced NM_005193.1. Summary: This gene encodes a member of a small subfamily of homeobox containing transcription factors. The encoded protein may regulate homeobox gene expression during anteroposterior patterning and hematopoiesis. [provided by RefSeq, Aug 2012]. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: SRR14038194.88973.1, BC128233.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2147596, SAMEA2161674 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000373514.3/ ENSP00000362613.1 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-703 AL450108.12 78161-78863 704-849 AL450108.12 84625-84770 850-1642 AL450108.12 85487-86279 FEATURES Location/Qualifiers source 1..1642 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="X" /map="Xq13.2" gene 1..1642 /gene="CDX4" /note="caudal type homeobox 4" /db_xref="GeneID:1046" /db_xref="HGNC:HGNC:1808" /db_xref="MIM:300025" exon 1..703 /gene="CDX4" /inference="alignment:Splign:2.1.0" variation 1 /gene="CDX4" /replace="a" /replace="t" /db_xref="dbSNP:979068345" variation 9 /gene="CDX4" /replace="c" /replace="g" /db_xref="dbSNP:2057072126" variation 14 /gene="CDX4" /replace="c" /replace="g" /db_xref="dbSNP:2057072136" variation 17 /gene="CDX4" /replace="c" /replace="t" /db_xref="dbSNP:2057072152" variation 21 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:2057072162" variation 35 /gene="CDX4" /replace="a" /replace="c" /db_xref="dbSNP:2057072181" variation 38 /gene="CDX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:938918964" variation 40 /gene="CDX4" /replace="c" /replace="t" /db_xref="dbSNP:2057072199" variation 41 /gene="CDX4" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1055772598" variation 42 /gene="CDX4" /replace="c" /replace="t" /db_xref="dbSNP:2057072227" variation 43 /gene="CDX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:937020993" variation 46 /gene="CDX4" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:915907082" variation 56 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:2057072267" variation 60 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:746328235" variation 63 /gene="CDX4" /replace="g" /replace="t" /db_xref="dbSNP:867922326" variation 66 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:2057072296" variation 69 /gene="CDX4" /replace="g" /replace="t" /db_xref="dbSNP:151110728" variation 70 /gene="CDX4" /replace="a" /replace="c" /db_xref="dbSNP:2057072321" variation 73 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:755211512" variation 75 /gene="CDX4" /replace="g" /replace="t" /db_xref="dbSNP:1430537311" variation 76 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:2057072356" variation 77 /gene="CDX4" /replace="c" /replace="g" /db_xref="dbSNP:2057072371" variation 78 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:1263577150" variation 79 /gene="CDX4" /replace="c" /replace="t" /db_xref="dbSNP:2057072396" variation 82 /gene="CDX4" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:767541558" variation 90..91 /gene="CDX4" /replace="t" /replace="tt" /db_xref="dbSNP:1487909229" variation 92 /gene="CDX4" /replace="c" /replace="g" /db_xref="dbSNP:2057072440" variation 93 /gene="CDX4" /replace="a" /replace="c" /db_xref="dbSNP:1283736810" variation 97 /gene="CDX4" /replace="a" /replace="c" /db_xref="dbSNP:41303721" variation 98 /gene="CDX4" /replace="c" /replace="t" /db_xref="dbSNP:1603327709" variation 99 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:776203203" variation 100 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:1439747927" variation 102 /gene="CDX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:993320301" variation 105 /gene="CDX4" /replace="g" /replace="t" /db_xref="dbSNP:2057072500" variation 106 /gene="CDX4" /replace="" /replace="t" /db_xref="dbSNP:1374946494" variation 107 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:763374803" variation 111 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:1390162408" variation 131 /gene="CDX4" /replace="c" /replace="t" /db_xref="dbSNP:2057072553" variation 136 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:2057072564" variation 140 /gene="CDX4" /replace="a" /replace="t" /db_xref="dbSNP:1052035777" variation 141 /gene="CDX4" /replace="c" /replace="t" /db_xref="dbSNP:2147487745" variation 142 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:2057072588" variation 144 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:2057072600" variation 151 /gene="CDX4" /replace="a" /replace="c" /db_xref="dbSNP:2057072612" variation 156 /gene="CDX4" /replace="a" /replace="c" /db_xref="dbSNP:754540125" variation 158 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:1569494043" variation 159 /gene="CDX4" /replace="g" /replace="t" /db_xref="dbSNP:2057072653" variation 162 /gene="CDX4" /replace="a" /replace="c" /db_xref="dbSNP:1468517050" variation 163 /gene="CDX4" /replace="c" /replace="t" /db_xref="dbSNP:1176592483" variation 167 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:1279204768" variation 170 /gene="CDX4" /replace="c" /replace="t" /db_xref="dbSNP:778407288" variation 172 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:1399839093" misc_feature 175..177 /gene="CDX4" /note="upstream in-frame stop codon" variation 176 /gene="CDX4" /replace="a" /replace="aa" /db_xref="dbSNP:745830531" variation 181 /gene="CDX4" /replace="a" /replace="g" /db_xref="dbSNP:752132664" variation 182 /gene="CDX4" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1171950084" variation 189 /gene="CDX4" /replace="c" /replace="t" /db_xref="dbSNP:1375078890" variation 200 /gene="CDX4" /replace="a" /replace="c" /db_xref="dbSNP:1381546555" CDS 202..1056 /gene="CDX4" /note="caudal type homeobox transcription factor 4; caudal-type homeobox protein 4" /codon_start=1 /product="homeobox protein CDX-4" /protein_id="NP_005184.1" /db_xref="CCDS:CCDS14424.1" /db_xref="GeneID:1046" /db_xref="HGNC:HGNC:1808" /db_xref="MIM:300025" /translation="
MYGSCLLEKEAGMYPGTLMSPGGDGTAGTGGTGGGGSPMPASNFAAAPAFSHYMGYPHMPSMDPHWPSLGVWGSPYSPPREDWSVYPGPSSTMGTVPVNDVTSSPAAFCSTDYSNLGPVGGGTSGSSLPGQAGGSLVPTDAGAAKASSPSRSRHSPYAWMRKTVQVTGKTRTKEKYRVVYTDHQRLELEKEFHCNRYITIQRKSELAVNLGLSERQVKIWFQNRRAKERKMIKKKISQFENSGGSVQSDSDSISPGELPNTFFTTPSAVRGFQPIEIQQVIVSE"
misc_feature 238..687
/gene="CDX4"
/note="Caudal like protein activation region; Region:
Caudal_act; pfam04731"
/db_xref="CDD:398418"
misc_feature 244..321
/gene="CDX4"
/note="propagated from UniProtKB/Swiss-Prot (O14627.1);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 559..666
/gene="CDX4"
/note="propagated from UniProtKB/Swiss-Prot (O14627.1);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature order(724..735,739..741,790..792,808..810,847..849,
853..858,865..870,874..882,886..891)
/gene="CDX4"
/note="DNA binding site [nucleotide binding]"
/db_xref="CDD:238039"
misc_feature order(727..729,736..738,856..858,865..870,877..879)
/gene="CDX4"
/note="specific DNA base contacts [nucleotide binding];
other site"
/db_xref="CDD:238039"
misc_feature 730..891
/gene="CDX4"
/note="Homeobox domain; Region: Homeobox; pfam00046"
/db_xref="CDD:395001"
misc_feature 913..978
/gene="CDX4"
/note="propagated from UniProtKB/Swiss-Prot (O14627.1);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
variation 202
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057072766"
variation 204
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:758096608"
variation 205
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:777240076"
variation 207
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352874940"
variation 208
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442057914"
variation 218
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057072855"
variation 221
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:746867826"
variation 222
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:1315307303"
variation 229
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057072909"
variation 232
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:770630184"
variation 234
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:1232558185"
variation 239
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:375681941"
variation 244
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303217198"
variation 246
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:367670478"
variation 247
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219499209"
variation 248
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057073013"
variation 255
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007422840"
variation 256
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057073055"
variation 259
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:756210535"
variation 261
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:778908953"
variation 262
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057073092"
variation 265..269
/gene="CDX4"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:768685151"
variation 265
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1243376766"
variation 266
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057073140"
variation 267
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:199592731"
variation 269
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057073170"
variation 270
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458874418"
variation 271..289
/gene="CDX4"
/replace="gacggcacagctgggacag"
/replace="gacggcacagctgggacagacggcacagctgggacag"
/db_xref="dbSNP:2057073205"
variation 273
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:775744896"
variation 274
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:370175012"
variation 277
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:2147487828"
variation 278
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:1478459209"
variation 279
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:2057073269"
variation 280
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:768973829"
variation 281
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057073304"
variation 283
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057073320"
variation 284
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:150836467"
variation 285
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:886601996"
variation 287
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1171650431"
variation 289
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057073360"
variation 290
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057073371"
variation 291
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1403078383"
variation 297..298
/gene="CDX4"
/replace=""
/replace="ag"
/db_xref="dbSNP:1439412257"
variation 297
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1325627457"
variation 298
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:940984524"
variation 299
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1436701181"
variation 304
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:767759680"
variation 305
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057073496"
variation 309
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217670762"
variation 310
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:773507655"
variation 312
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1852984960"
variation 314
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:1336819105"
variation 315
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761170974"
variation 318
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439287647"
variation 319
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:774580628"
variation 322
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057073589"
variation 329
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:532670975"
variation 333
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2147487873"
variation 334
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761975244"
variation 338
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1246151225"
variation 339
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:757822096"
variation 344
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057073650"
variation 346
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:868273091"
variation 353
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252102110"
variation 354
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451985214"
variation 355
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1020672167"
variation 357
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:1201197981"
variation 359
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:763877364"
variation 362
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1475247187"
variation 365
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171457058"
variation 366
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057073799"
variation 367
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:966881465"
variation 368
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1401163615"
variation 369
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:758155962"
variation 370
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:996183726"
variation 371
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057073874"
variation 373
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:373883804"
variation 377
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:1464271318"
variation 383
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057073922"
variation 388
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1391847961"
variation 389
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1242345960"
variation 392
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057073982"
variation 394
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057073997"
variation 398
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057074013"
variation 400
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781141901"
variation 401
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:145092385"
variation 402
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1603327772"
variation 404
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:368078652"
variation 406
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:372222815"
variation 408..410
/gene="CDX4"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1278241652"
variation 410
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:749426657"
variation 412
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:201550677"
variation 420
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:774690724"
variation 422
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:149578736"
variation 426
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211408987"
variation 428
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281957446"
variation 430
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:772215407"
variation 432
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:773593959"
variation 433
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1197556333"
variation 434
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760976173"
variation 436
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:777088488"
variation 439
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057074298"
variation 440
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:200133821"
variation 441
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:111725575"
variation 442
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:751019321"
variation 444
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1020140442"
variation 448..449
/gene="CDX4"
/replace=""
/replace="tg"
/db_xref="dbSNP:1157181555"
variation 453
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:146093321"
variation 456
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:767231207"
variation 467
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:750293125"
variation 469
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361827942"
variation 472
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:755944689"
variation 473
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:780209125"
variation 476
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:749168322"
variation 479
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:754885067"
variation 480..482
/gene="CDX4"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2147488004"
variation 482
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:778861857"
variation 484
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:748215000"
variation 485
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:2147488011"
variation 487
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2147488013"
variation 488
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282901466"
variation 490
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:772299390"
variation 491
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:777946946"
variation 492
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:747411736"
variation 495
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:919308508"
variation 498
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1444831609"
variation 499
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:929389049"
variation 501
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484694612"
variation 502
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057074657"
variation 509
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:777000029"
variation 512
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:770299385"
variation 514
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140116090"
variation 515
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057074734"
variation 516
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257024462"
variation 517
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750486027"
variation 519
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:760805148"
variation 526
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314440437"
variation 527
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057074819"
variation 529
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057074833"
variation 530
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:750098739"
variation 531
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:760603470"
variation 533
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:766289002"
variation 534
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:753601065"
variation 536
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754902561"
variation 537
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:778856271"
variation 539
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:1301726875"
variation 543
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:752765305"
variation 547
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1397674801"
variation 554
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057075007"
variation 555
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326799801"
variation 557
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:1375799815"
variation 558
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1221890522"
variation 561
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:143815058"
variation 562
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057075090"
variation 565
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:778033453"
variation 574
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1268309313"
variation 575
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:747248108"
variation 579
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:146389652"
variation 600
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057075173"
variation 604
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1603327826"
variation 606
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1603327828"
variation 614
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:781445620"
variation 615
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:148593166"
variation 617
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1194523878"
variation 621
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057075246"
variation 622
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2147488126"
variation 623
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:746199378"
variation 627..633
/gene="CDX4"
/replace="cgcc"
/replace="cgccgcc"
/db_xref="dbSNP:778831035"
variation 629
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:770253641"
variation 630
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251575409"
variation 631
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057075304"
variation 632
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:776034454"
variation 633
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057075336"
variation 635
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:761482989"
variation 639
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201939178"
variation 642
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:771697726"
variation 643
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:2057075376"
variation 644..648
/gene="CDX4"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:2057075414"
variation 644
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772788049"
variation 645
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1166018687"
variation 647
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057075447"
variation 653
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1399454936"
variation 657
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057075471"
variation 658
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:760407288"
variation 660
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:766014861"
variation 661
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:753593735"
variation 668
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:1386375753"
variation 669
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:1302260279"
variation 672
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:759350426"
variation 673
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1421439491"
variation 675
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:765124044"
variation 678
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057075613"
variation 679
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2147488174"
variation 682
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:752673817"
variation 684
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057075625"
variation 687
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057075635"
variation 690
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1319184347"
variation 692
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201114866"
variation 695
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251478324"
variation 697
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258553201"
variation 699
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157994337"
variation 701
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057075704"
variation 703
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010547256"
exon 704..849
/gene="CDX4"
/inference="alignment:Splign:2.1.0"
variation 704
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1195667489"
variation 706
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208013756"
variation 708
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:751046644"
variation 714
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423229477"
variation 718
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2147490555"
variation 719
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:1165186271"
variation 721
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1463443044"
variation 724
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1172097625"
variation 726
/gene="CDX4"
/replace=""
/replace="g"
/db_xref="dbSNP:2057096143"
variation 726
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057096117"
variation 730
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1351444146"
variation 731
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:753589935"
variation 743
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:1451846225"
variation 746
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:762912423"
variation 749
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:763974997"
variation 751
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057096234"
variation 752
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057096252"
variation 758
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:377257604"
variation 759
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057096302"
variation 762
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1291589953"
variation 766
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057096355"
variation 770
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057096387"
variation 771
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:757329545"
variation 772
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:767700268"
variation 778
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057096434"
variation 781
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:750645875"
variation 785..793
/gene="CDX4"
/replace="ata"
/replace="atagatata"
/db_xref="dbSNP:748313062"
variation 785
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057096463"
variation 789
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:759013295"
variation 790
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1603328727"
variation 791
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057096523"
variation 792
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:780470070"
variation 793
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057096545"
variation 795..799
/gene="CDX4"
/replace="ca"
/replace="cacca"
/db_xref="dbSNP:1297254519"
variation 795
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:749628903"
variation 809
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:755563266"
variation 814
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057096615"
variation 820
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235290726"
variation 827
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:2057096660"
variation 829
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:779540280"
variation 840..841
/gene="CDX4"
/replace=""
/replace="ctgtta"
/db_xref="dbSNP:2057096759"
variation 840
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:746554552"
variation 841
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1029678890"
variation 845
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770467036"
variation 848
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:1978848757"
exon 850..1642
/gene="CDX4"
/inference="alignment:Splign:2.1.0"
variation 850
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057099595"
variation 852
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1569494381"
variation 855
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1312899852"
variation 856
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1235178976"
variation 859
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057099643"
variation 860
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057099656"
variation 871
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:868321760"
variation 872
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1456440419"
variation 876
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:371721540"
variation 878
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:750400645"
variation 882
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1441746956"
variation 886
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:760987259"
variation 890
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435553254"
variation 891
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:867743464"
variation 894
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:766658172"
variation 895
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:754303817"
variation 896
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:941508566"
variation 899
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057099857"
variation 901
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353251015"
variation 903
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057099890"
variation 906
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:755359564"
variation 908
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332422111"
variation 909
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:779626316"
variation 914
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037163713"
variation 916
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:2057099953"
variation 918
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:753231858"
variation 919
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:758770897"
variation 921
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:762696148"
variation 924
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1280200354"
variation 929
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259736429"
variation 931..932
/gene="CDX4"
/replace=""
/replace="a"
/db_xref="dbSNP:2057100059"
variation 932
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:151132225"
variation 935
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:897378141"
variation 936
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315965332"
variation 940..943
/gene="CDX4"
/replace=""
/replace="caaa"
/db_xref="dbSNP:2057100182"
variation 940
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:202058995"
variation 945
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258428092"
variation 946..953
/gene="CDX4"
/replace=""
/replace="gactctga"
/db_xref="dbSNP:2057100254"
variation 946
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:749148546"
variation 948..951
/gene="CDX4"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1194961088"
variation 948
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:993186468"
variation 949
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1196960024"
variation 950
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1246355304"
variation 955..960
/gene="CDX4"
/replace="tc"
/replace="tccatc"
/db_xref="dbSNP:2057100357"
variation 955
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:768427209"
variation 957..958
/gene="CDX4"
/replace=""
/replace="gt"
/db_xref="dbSNP:2057100377"
variation 957
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208840351"
variation 960
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057100395"
variation 961
/gene="CDX4"
/replace="a"
/replace="attaaaaaaa"
/db_xref="dbSNP:2057100415"
variation 970
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:770591459"
variation 971
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057100447"
variation 977
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1421624096"
variation 980
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465525582"
variation 983
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:761817164"
variation 984
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:1569494408"
variation 993
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771862536"
variation 995
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1228804605"
variation 997
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:199967021"
variation 1000
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1740306367"
variation 1001
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1323391133"
variation 1002
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330135368"
variation 1009
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760648974"
variation 1010
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:140658145"
variation 1021
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:754107817"
variation 1023
/gene="CDX4"
/replace=""
/replace="t"
/db_xref="dbSNP:1178655664"
variation 1024
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301691506"
variation 1029
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057100740"
variation 1032
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:760035317"
variation 1035
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:752965907"
variation 1039
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057100818"
variation 1043
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1319656688"
variation 1044
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207825498"
variation 1046
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1047421263"
variation 1050
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:889777082"
variation 1051
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:758968054"
variation 1055..1063
/gene="CDX4"
/replace="gaaag"
/replace="gaaagaaag"
/db_xref="dbSNP:2057100903"
variation 1059
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:767137357"
variation 1070
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371770160"
variation 1074..1076
/gene="CDX4"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1261058070"
variation 1075
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:2057100971"
variation 1077
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:749990964"
variation 1080
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:1194942919"
variation 1082
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1033071233"
variation 1085
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:755621721"
variation 1086..1092
/gene="CDX4"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:772171166"
variation 1090
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:779744412"
variation 1092
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1472129343"
variation 1094
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057101097"
variation 1097
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1569494421"
variation 1101
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1163018655"
variation 1102
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:2057101153"
variation 1107
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343528341"
variation 1108
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057101175"
variation 1111
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:753208549"
variation 1114
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017141789"
variation 1115
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1185851517"
variation 1117
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:964257070"
variation 1126
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057101267"
variation 1129
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:1252780727"
variation 1134
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010037055"
variation 1138
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:190288861"
variation 1139
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338497579"
variation 1141
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:758951329"
variation 1148
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057101363"
variation 1150
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057101371"
variation 1151
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246737218"
variation 1157
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:2057101393"
variation 1159
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:971257374"
variation 1164
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057101412"
variation 1168
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057101421"
variation 1171
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:2147491134"
variation 1176
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057101431"
variation 1176
/gene="CDX4"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2057101447"
variation 1178
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230298180"
variation 1188
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1292629709"
variation 1190
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057101493"
variation 1193
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:778309010"
variation 1204
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057101537"
variation 1206
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:764742678"
variation 1216
/gene="CDX4"
/replace=""
/replace="c"
/db_xref="dbSNP:2057101574"
variation 1216
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2147491145"
variation 1217
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:2057101588"
variation 1218
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:2057101598"
variation 1223..1225
/gene="CDX4"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1412360499"
variation 1226
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057101615"
variation 1230
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:868173453"
variation 1233
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1310653228"
variation 1240
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057101658"
variation 1249
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1321126783"
variation 1250
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:751915592"
variation 1257
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:988191839"
variation 1260
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057101739"
variation 1264
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057101755"
variation 1287
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057101767"
variation 1288
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:958368608"
variation 1292
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:144067429"
variation 1293
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:968134810"
variation 1298
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:376889376"
variation 1300
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057101891"
variation 1308
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057101905"
variation 1310
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:908922720"
variation 1311
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057101949"
variation 1314
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1181708627"
variation 1316
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436233422"
variation 1320
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057101985"
variation 1322
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269742209"
variation 1329
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:2057102014"
variation 1330
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:2057102030"
variation 1351
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211368514"
variation 1355
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:961777579"
variation 1356
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057102100"
variation 1358
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057102120"
variation 1362
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250867155"
variation 1363
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:750616747"
variation 1365
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1231451239"
variation 1371
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330587361"
variation 1375
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057102199"
variation 1376
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:375275847"
variation 1379
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057102243"
variation 1383
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:918754200"
variation 1385
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1333586658"
variation 1386
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:758414257"
variation 1393
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2147491196"
variation 1395
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1325147080"
variation 1399
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1183170975"
variation 1404
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330208174"
variation 1407
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:2057102342"
variation 1410
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:757657716"
variation 1413
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1324462720"
variation 1419
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:937864486"
variation 1421
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:1390036625"
variation 1426
/gene="CDX4"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1158433804"
variation 1431
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1468693591"
variation 1435
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781369624"
variation 1438
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:917875753"
variation 1445
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252207895"
variation 1447
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1211604255"
variation 1454
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1466149228"
variation 1463
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:181531849"
variation 1464
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057102508"
variation 1466..1473
/gene="CDX4"
/replace="agaag"
/replace="agaagaag"
/db_xref="dbSNP:2057102519"
variation 1470
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1203989204"
variation 1471
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057102542"
variation 1475
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057102550"
variation 1478
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:2057102564"
variation 1480
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347989679"
variation 1481
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:942695942"
variation 1487
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370695454"
variation 1490
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1301626160"
variation 1492
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047454292"
variation 1493
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:748037565"
variation 1504
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057102645"
variation 1511
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:2147491250"
variation 1513
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318271541"
variation 1515
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399000266"
variation 1520
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392608383"
variation 1527
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057102674"
variation 1533
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1173365887"
variation 1534
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057102698"
variation 1542..1548
/gene="CDX4"
/replace="ataa"
/replace="ataataa"
/db_xref="dbSNP:1428332248"
variation 1542
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:893174883"
variation 1545
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057102733"
variation 1551
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:1038821039"
variation 1554
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451128549"
variation 1566
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:2057102768"
variation 1569
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248548764"
variation 1576
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057102788"
variation 1578
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:900210831"
variation 1579
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2147491265"
variation 1580
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:1019063230"
variation 1582
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:769687831"
variation 1584
/gene="CDX4"
/replace="c"
/replace="g"
/db_xref="dbSNP:2057102849"
variation 1585
/gene="CDX4"
/replace="a"
/replace="c"
/db_xref="dbSNP:1444772675"
variation 1589
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:997029771"
variation 1602
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1280197087"
variation 1604
/gene="CDX4"
/replace="a"
/replace="t"
/db_xref="dbSNP:746119865"
variation 1605
/gene="CDX4"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:796177523"
variation 1611
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277785947"
variation 1614
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231006363"
regulatory 1616..1621
/regulatory_class="polyA_signal_sequence"
/gene="CDX4"
/note="hexamer: AATAAA"
variation 1617
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450631547"
variation 1618
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1041846905"
variation 1619..1624
/gene="CDX4"
/replace="aaaaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:1270126160"
variation 1619
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057102949"
variation 1621
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1429315176"
variation 1624
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057102988"
variation 1626
/gene="CDX4"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1378694589"
variation 1629
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334840617"
variation 1630
/gene="CDX4"
/replace="g"
/replace="t"
/db_xref="dbSNP:2057103031"
variation 1633
/gene="CDX4"
/replace="c"
/replace="t"
/db_xref="dbSNP:2057103038"
variation 1634
/gene="CDX4"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1382888172"
variation 1639
/gene="CDX4"
/replace=""
/replace="t"
/db_xref="dbSNP:2057103048"
polyA_site 1642
/gene="CDX4"
/note="major polyA site"
variation 1642
/gene="CDX4"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057103061"
ORIGIN
attggtggcctatctatacagggctgctagtcacctggataccctcgtaagaaacgtgggatggagtagcctgaggggtgcaaaagagcttgcggcacaactacgtactgataagtttattctctgctgcttctcaaagtcgagttggggccttacagggacttcaggatggcttagggagcgccttctacccaagacacgatgtacggaagctgtcttttggagaaagaagcaggcatgtacccgggcactctcatgagccctgggggcgacggcacagctgggacaggcggcacagggggcggtgggagtccgatgccagcctccaatttcgctgcggcaccggctttctcgcactatatggggtatcctcatatgcccagcatggatcctcactggccgtctctgggagtctggggctcaccctacagtcccccgcgagaagactggagcgtgtatcctgggccgtctagtacaatgggcacagtgccggtgaacgacgtgacctctagccccgccgctttctgctcgaccgactacagcaacttgggccctgtgggcggtggaactagcggcagcagcctaccaggccaggctggcgggtcgcttgtcccgacggacgcaggcgccgccaaggccagttcccccagcaggagccgccacagcccctatgcatggatgcgcaagacggtgcaggtgacggggaaaaccaggacaaaagaaaagtatcgtgtagtttacactgatcatcaaagattggagctggaaaaggaattccattgcaatagatatatcaccatccagagaaaatcagagctggcagttaacctgggcctttccgagagacaggtgaaaatctggtttcagaatcgcagagccaaggagagaaagatgatcaaaaagaaaatctcccagtttgagaatagtggaggctcggtgcaaagtgactctgactccatcagccctggggaactacctaacacttttttcaccacaccatctgctgttcgtggatttcaacctattgagatacagcaggttatagtctccgaatgaaagaaagcaaagagaaatttaaagtgccctttttttagtgatgtcttttgggtctctaagctatctacaggggagttggagcagggtgtaattccctgtaaggcagtatttggaacagatggatgcacaatgggttgaagataatttaggggactcttacttttagaaactatccccagaaaactcctgtcacgtgctgtgctatatgtcagtcactcaggaatcttagtggtaaggtatataattaaaagctagaatcacaggcccttccaactctgttcacaatttcagaaacttgcttatgaatagactgtaaaatacaattttgccagaaagcacatttgtgtatgtgtacttctgtttgttatttgatgctaggtgttttcttttatgctatctttaaggagtgagaagaaggtaaaccgaagtttatctatctttagctacctttccaagtgtttaattcaaaagctaacagaatttttataataagataaatgttttaaaaatcatcagaaggtgattctgattccattgtcactgcttaacaagaataaccaataaaaaagacaattttggccctcaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]