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Previous release (v1)
2024-04-20 08:39:43, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001101389 690 bp mRNA linear PRI 17-DEC-2022 DEFINITION Homo sapiens claudin 25 (CLDN25), mRNA. ACCESSION NM_001101389 XM_927777 XM_938396 VERSION NM_001101389.1 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 690) AUTHORS Berndt P, Winkler L, Cording J, Breitkreuz-Korff O, Rex A, Dithmer S, Rausch V, Blasig R, Richter M, Sporbert A, Wolburg H, Blasig IE and Haseloff RF. TITLE Tight junction proteins at the blood-brain barrier: far more than claudin-5 JOURNAL Cell Mol Life Sci 76 (10), 1987-2002 (2019) PUBMED 30734065 REFERENCE 2 (bases 1 to 690) AUTHORS Lal-Nag M and Morin PJ. TITLE The claudins JOURNAL Genome Biol 10 (8), 235 (2009) PUBMED 19706201 REMARK Review article REFERENCE 3 (bases 1 to 690) AUTHORS Krause G, Winkler L, Mueller SL, Haseloff RF, Piontek J and Blasig IE. TITLE Structure and function of claudins JOURNAL Biochim Biophys Acta 1778 (3), 631-645 (2008) PUBMED 18036336 REMARK Review article REFERENCE 4 (bases 1 to 690) AUTHORS Katoh M and Katoh M. TITLE CLDN23 gene, frequently down-regulated in intestinal-type gastric cancer, is a novel member of CLAUDIN gene family JOURNAL Int J Mol Med 11 (6), 683-689 (2003) PUBMED 12736707 COMMENT INFERRED REFSEQ: This record is predicted by genome sequence analysis and is not yet supported by experimental evidence. The reference sequence was derived from CH471065.1. On or before Oct 4, 2007 this sequence version replaced XM_927777.1, XM_938396.1. Summary: This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. [provided by RefSeq, Jun 2010]. Sequence Note: This RefSeq record was created from genomic sequence data because no transcript was available for the gene. The extent of this transcript is supported by orthologous data. ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000453129.3/ ENSP00000396304.2 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## FEATURES Location/Qualifiers source 1..690 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="11" /map="11q23.2" gene 1..690 /gene="CLDN25" /note="claudin 25" /db_xref="GeneID:644672" /db_xref="HGNC:HGNC:37218" CDS 1..690 /gene="CLDN25" /codon_start=1 /product="putative claudin-25" /protein_id="NP_001094859.1" /db_xref="CCDS:CCDS44736.1" /db_xref="GeneID:644672" /db_xref="HGNC:HGNC:37218" /translation="
MAWSFRAKVQLGGLLLSLLGWVCSCVTTILPQWKTLNLELNEMETWIMGIWEVCVDREEVATVCKAFESFLSLPQELQVARILMVASHGLGLLGLLLCSFGSECFQFHRIRWVFKRRLGLLGRTLEASASATTLLPVSWVAHATIQDFWDDSIPDIIPRWEFGGALYLGWAAGIFLALGGLLLIFSACLGKEDVPFPLMAGPTVPLSCAPVEESDGSFHLMLRPRNLVI"
misc_feature 31..93
/gene="CLDN25"
/note="propagated from UniProtKB/Swiss-Prot (C9JDP6.1);
transmembrane region"
misc_feature 76..549
/gene="CLDN25"
/note="PMP-22/EMP/MP20/Claudin family; Region:
PMP22_Claudin; cl21598"
/db_xref="CDD:451326"
misc_feature 244..306
/gene="CLDN25"
/note="propagated from UniProtKB/Swiss-Prot (C9JDP6.1);
transmembrane region"
misc_feature 373..435
/gene="CLDN25"
/note="propagated from UniProtKB/Swiss-Prot (C9JDP6.1);
transmembrane region"
misc_feature 493..555
/gene="CLDN25"
/note="propagated from UniProtKB/Swiss-Prot (C9JDP6.1);
transmembrane region"
exon 1..690
/gene="CLDN25"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224286935"
variation 2
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1200330516"
variation 7
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:2134912628"
variation 8
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:1937796141"
variation 10
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937796164"
variation 11
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:768889315"
variation 14
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776813904"
variation 16
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:918393061"
variation 17
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:764892613"
variation 18
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1199620128"
variation 20
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:765295086"
variation 21
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:371018780"
variation 22
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:375569415"
variation 24
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766841470"
variation 25
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339497601"
variation 27
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286726231"
variation 33
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:751896747"
variation 34..39
/gene="CLDN25"
/replace="gggggg"
/replace="ggggggg"
/db_xref="dbSNP:772015749"
variation 34
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:367566026"
variation 35
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:753506514"
variation 36
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:2134912695"
variation 37
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:368739845"
variation 38
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778582555"
variation 39
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:745321540"
variation 41
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:758302636"
variation 46
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:866477480"
variation 48
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:779993191"
variation 50
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746830020"
variation 51
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:370403067"
variation 54
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226628907"
variation 56
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:768410561"
variation 59
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:373997049"
variation 62
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748354515"
variation 63
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:769944171"
variation 65
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:1591429666"
variation 67
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1166069623"
variation 68
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023165732"
variation 71
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1211591766"
variation 80..81
/gene="CLDN25"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1937797440"
variation 80
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:969055014"
variation 81
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220050151"
variation 82
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:773169116"
variation 83
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:541402454"
variation 86
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1937797610"
variation 87..88
/gene="CLDN25"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1183649519"
variation 91
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1259241763"
variation 92
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015858364"
variation 94
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1432169181"
variation 96
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1937797791"
variation 101
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1054481490"
variation 103
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:766813269"
variation 106
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:893220944"
variation 113
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:774895409"
variation 114..115
/gene="CLDN25"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1937797978"
variation 119
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:971804554"
variation 123
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:17115958"
variation 124
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:371879188"
variation 128
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:756977984"
variation 129
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:367712273"
variation 132
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:556650979"
variation 133
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:868828897"
variation 134
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374339626"
variation 135
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465217329"
variation 139..162
/gene="CLDN25"
/replace="atcatggggatttgggaggtctgc"
/replace="atcatggggatttgggaggtctgcatcatggggatttgggaggtctgc
"
/db_xref="dbSNP:375691427"
variation 142
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937798357"
variation 144
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:1937798390"
variation 145
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749924583"
variation 146
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:538478199"
variation 151
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:757904523"
variation 156
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1937798733"
variation 158
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:907346246"
variation 159
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1273854766"
variation 162
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:779897572"
variation 163
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:746964341"
variation 164
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1239390615"
variation 166
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1380706855"
variation 169
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754824119"
variation 170
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:371445026"
variation 172
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:747871346"
variation 174
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937799121"
variation 180
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:773431568"
variation 181
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:749373712"
variation 182
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277435518"
variation 183
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220164217"
variation 184
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937799331"
variation 186
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:374737042"
variation 187
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390111036"
variation 188
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:774785286"
variation 191
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:760135741"
variation 195..196
/gene="CLDN25"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1937799590"
variation 195
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:375224880"
variation 196
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:866329317"
variation 198
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1937799728"
variation 202
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:190938380"
variation 205
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:761076385"
variation 207
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441404234"
variation 210
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:764847351"
variation 211
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750060970"
variation 213
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:368118465"
variation 214
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:1421969305"
variation 220
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273593983"
variation 221
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457198405"
variation 223
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320645208"
variation 224
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:896006391"
variation 225
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1937800514"
variation 228
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:962361402"
variation 230
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274698285"
variation 234
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1468594263"
variation 235
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:765901652"
variation 236
/gene="CLDN25"
/replace="a"
/replace="t"
/db_xref="dbSNP:1937800711"
variation 240
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:182753809"
variation 241
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200887183"
variation 242
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:781067415"
variation 245
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256434367"
variation 247
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044652121"
variation 251
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1404860856"
variation 252..253
/gene="CLDN25"
/replace=""
/replace="c"
/db_xref="dbSNP:1937801027"
variation 252
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:888715901"
variation 254..264
/gene="CLDN25"
/replace=""
/replace="tagcctcccat"
/db_xref="dbSNP:1937801052"
variation 255
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315111495"
variation 258
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1162720947"
variation 259
/gene="CLDN25"
/replace="a"
/replace="t"
/db_xref="dbSNP:147182065"
variation 262
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:2134912987"
variation 266
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462110337"
variation 267
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:757357516"
variation 271
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378516320"
variation 272
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777892536"
variation 276
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1016348772"
variation 277
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:372181019"
variation 278..279
/gene="CLDN25"
/replace=""
/replace="tg"
/db_xref="dbSNP:1361594460"
variation 280
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:770971339"
variation 281
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:779056527"
variation 288
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1298020343"
variation 289
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:201126561"
variation 291
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1937801583"
variation 293
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1937801638"
variation 294
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:772732542"
variation 297
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:776123054"
variation 303
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:761162254"
variation 304
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:769061794"
variation 307
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:140547989"
variation 315
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:765879630"
variation 320
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1937801899"
variation 324
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243228469"
variation 328
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1565292758"
variation 329
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1937801990"
variation 331
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:751099592"
variation 334
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:758997931"
variation 337
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:767488166"
variation 341
/gene="CLDN25"
/replace="a"
/replace="t"
/db_xref="dbSNP:1937802122"
variation 345
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:955204579"
variation 347
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1489039590"
variation 349
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:368993117"
variation 350
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:202065177"
variation 351
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937802301"
variation 355
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199984262"
variation 356
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:1318651294"
variation 357
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:1591429816"
variation 358
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1937802434"
variation 359
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:1358522794"
variation 361..372
/gene="CLDN25"
/replace="ct"
/replace="ctgggaaggact"
/db_xref="dbSNP:1445812109"
variation 362
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:911120544"
variation 363..365
/gene="CLDN25"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:747219472"
variation 363
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314646642"
variation 364..365
/gene="CLDN25"
/replace=""
/replace="t"
/db_xref="dbSNP:1565292781"
variation 364
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334266009"
variation 365
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1355582986"
variation 366
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937802723"
variation 367
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:2134913103"
variation 368
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:753511689"
variation 369
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:2134913112"
variation 370
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:757534339"
variation 371
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:954727747"
variation 372..379
/gene="CLDN25"
/replace="tttggagg"
/replace="tttggagggtttggagg"
/db_xref="dbSNP:1937802887"
variation 374
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779232461"
variation 378
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937802987"
variation 379
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:201922794"
variation 382
/gene="CLDN25"
/replace="a"
/replace="t"
/db_xref="dbSNP:1277797538"
variation 384
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:772247740"
variation 385
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201592139"
variation 389
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:538673377"
variation 392
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209407226"
variation 397..398
/gene="CLDN25"
/replace=""
/replace="ac"
/db_xref="dbSNP:1260203126"
variation 397
/gene="CLDN25"
/replace="a"
/replace="t"
/db_xref="dbSNP:1937803518"
variation 398
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486053629"
variation 399
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1457807681"
variation 400
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:946050881"
variation 401
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777057182"
variation 405
/gene="CLDN25"
/replace="a"
/replace="t"
/db_xref="dbSNP:748420331"
variation 407
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1937803919"
variation 410
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:770638676"
variation 413
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1937804040"
variation 415
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:1937804094"
variation 416
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:773970022"
variation 420
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:2134913178"
variation 421
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:187854554"
variation 423
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432593131"
variation 425
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1041778162"
variation 426
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:907311151"
variation 427
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:759083664"
variation 428
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423979060"
variation 430
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1192014075"
variation 431
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408720192"
variation 433
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305568679"
variation 434
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:767006139"
variation 437
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1426536637"
variation 439
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:779540850"
variation 441
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1937804944"
variation 444
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:760672655"
variation 447
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:753693627"
variation 451
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1937805168"
variation 453
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:765601504"
variation 455
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:750669515"
variation 459
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:376808395"
variation 460
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758610171"
variation 462
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:780295757"
variation 463
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204544964"
variation 464..466
/gene="CLDN25"
/replace="aca"
/replace="acaca"
/db_xref="dbSNP:869204019"
variation 466
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1248585903"
variation 467
/gene="CLDN25"
/replace=""
/replace="t"
/db_xref="dbSNP:1555037413"
variation 469
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1250981734"
variation 472
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:746991778"
variation 474
/gene="CLDN25"
/replace="a"
/replace="t"
/db_xref="dbSNP:755539012"
variation 475
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:781501145"
variation 476
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:192382861"
variation 479
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:200964173"
variation 481
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937806205"
variation 482
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774053184"
variation 485
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428963594"
variation 487
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937806732"
variation 490
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166075007"
variation 491
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:745503566"
variation 494..496
/gene="CLDN25"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1410019498"
variation 495
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1937806920"
variation 500
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:373881888"
variation 505
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937807040"
variation 508
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1565292847"
variation 510
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937807134"
variation 511
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:775015220"
variation 513..524
/gene="CLDN25"
/replace="t"
/replace="tgctggtatttt"
/db_xref="dbSNP:1937807237"
variation 515
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400325731"
variation 517
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:760058243"
variation 518
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166969448"
variation 520
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:764144573"
variation 522
/gene="CLDN25"
/replace="a"
/replace="t"
/db_xref="dbSNP:776406132"
variation 525
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:761739420"
variation 527
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037281726"
variation 530
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765114746"
variation 532
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1937807687"
variation 536
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1341616780"
variation 538
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:750188759"
variation 539..542
/gene="CLDN25"
/replace="ggct"
/replace="ggctggct"
/db_xref="dbSNP:768799652"
variation 539
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196409317"
variation 543
/gene="CLDN25"
/replace="a"
/replace="t"
/db_xref="dbSNP:551863211"
variation 548
/gene="CLDN25"
/replace="a"
/replace="t"
/db_xref="dbSNP:1467259995"
variation 549
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453565997"
variation 557
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:766666126"
variation 558
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:751679089"
variation 575
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1591429933"
variation 577
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:754987182"
variation 578
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1190985685"
variation 580
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:781740262"
variation 582..584
/gene="CLDN25"
/replace="gcc"
/replace="gccggccgggcgcggtggctcacgcc"
/db_xref="dbSNP:776869580"
variation 582
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:898141320"
variation 583..584
/gene="CLDN25"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1272325308"
variation 584
/gene="CLDN25"
/replace="c"
/replace="cggccgggcgcggtggctcacgcctgtaatcccagcac"
/db_xref="dbSNP:762115636"
variation 584
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1937808524"
variation 586
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:748598202"
variation 587..588
/gene="CLDN25"
/replace=""
/replace="aa"
/db_xref="dbSNP:765637066"
variation 590
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1937808640"
variation 592
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1162055181"
variation 596
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1391851181"
variation 598
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:756527897"
variation 599
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:201639185"
variation 603
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:1591429955"
variation 605
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256779605"
variation 608
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025377027"
variation 610
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1395719129"
variation 612..616
/gene="CLDN25"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1381984576"
variation 612
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007283022"
variation 614
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:749585439"
variation 615
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371223196"
variation 616
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1312121358"
variation 618
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1228254429"
variation 620
/gene="CLDN25"
/replace="c"
/replace="g"
/db_xref="dbSNP:1448087100"
variation 622
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:199947437"
variation 625
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:768046540"
variation 630
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1215863889"
variation 632
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274009305"
variation 634
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:1937809391"
variation 635
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:761672821"
variation 637
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:2134913415"
variation 639
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1203116157"
variation 640
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:1591429982"
variation 647
/gene="CLDN25"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1263766310"
variation 653
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:963877315"
variation 654
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:373289613"
variation 655
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:35111413"
variation 657
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:1937809719"
variation 661
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:762784616"
variation 663
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:751696048"
variation 665..666
/gene="CLDN25"
/replace="ta"
/replace="tata"
/db_xref="dbSNP:773559827"
variation 665
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:539640434"
variation 666
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:767481514"
variation 670
/gene="CLDN25"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1387796680"
variation 671
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:201126695"
variation 676
/gene="CLDN25"
/replace="a"
/replace="c"
/db_xref="dbSNP:200276274"
variation 678
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031573443"
variation 679
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:778206832"
variation 681
/gene="CLDN25"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1294169104"
variation 682
/gene="CLDN25"
/replace="g"
/replace="t"
/db_xref="dbSNP:754251495"
variation 688
/gene="CLDN25"
/replace="c"
/replace="t"
/db_xref="dbSNP:1937810266"
variation 689
/gene="CLDN25"
/replace="a"
/replace="g"
/db_xref="dbSNP:1937810301"
ORIGIN
atggcctggagtttccgtgcaaaagtccagctcggggggctacttctctccctccttggctgggtctgctcctgtgttaccaccatcctgccccagtggaagactcttaatctggaactgaacgagatggagacctggatcatggggatttgggaggtctgcgtggatcgagaggaagtcgccactgtgtgcaaggcctttgaatccttcttgtctctgccccaggagctccaggtagcccgcatcctcatggtagcctcccatgggctgggcctattggggcttttgctctgcagctttgggtctgaatgcttccagtttcacaggatcagatgggtattcaagaggcggcttggtctcctgggaaggactttggaggcatccgcttcagccactaccctccttccagtctcctgggtggcccatgccacaatccaagacttctgggatgacagcatccctgacatcatacctcggtgggagtttggaggtgccctctacttgggctgggctgctggtattttcctggctcttggtgggctactcctcatcttctcggcctgcctgggaaaagaagatgtgccttttcctttgatggctggtcccacagtccccctatcctgtgctccagtggaggagtcagatggctccttccacctcatgctaagacctaggaacctggtcatctag
//
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]