Ensembl ID ENSG00000095002 Gene ID 4436 Accession 7325
Gene Symbol MSH2 Alias FCC1;COCA1;HNPCC;LCFS2;MSH-2;hMSH2;HNPCC1;LYNCH1;MMRCS2 Full Name mutS homolog 2
Position 2 : 47403067 - 47663146 Length 260080 bases Strand Plus strand
Status Confidence Main interacting RNAsN.A.RBP type Canonical_RBPs
Summary This locus is frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). When cloned, it was discovered to be a human homolog of the E. coli mismatch repair gene mutS, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]

ENSG00000095002 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000095002 MSH2 0.57 1.36e-19 BRCA
ENSG00000095002 MSH2 0.72 2.18e-16 COAD
ENSG00000095002 MSH2 1.29 1.17e-42 LUSC
ENSG00000095002 MSH2 1.27 1.83e-39 LIHC
ENSG00000095002 MSH2 1.06 8.67e-21 STAD
ENSG00000095002 MSH2 0.91 9.60e-16 UCEC
ENSG00000095002 MSH2 1.19 3.68e-15 CHOL
ENSG00000095002 MSH2 1.82 1.63e-11 CESC
ENSG00000095002 MSH2 0.93 3.46e-25 LUAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000095002 MSH2 tumor 10023718
ENSG00000095002 MSH2 tumor 10024676
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 10037723
ENSG00000095002 MSH2 colorectal cancer 10051005
ENSG00000095002 MSH2 tumors 10072435
ENSG00000095002 MSH2 hereditary nonpolyposis colon cancer 10077620
ENSG00000095002 MSH2 cancer 10077621
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 10080150
ENSG00000095002 MSH2 cancers 10086635
ENSG00000095002 MSH2 breast cancer 10098729
ENSG00000095002 MSH2 hereditary colorectal cancer 10190329
ENSG00000095002 MSH2 primary cancers 10196371
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 10200055
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 10211513
ENSG00000095002 MSH2 tumour 10323887
ENSG00000095002 MSH2 colorectal cancer 10343885
ENSG00000095002 MSH2 tumors 10348818
ENSG00000095002 MSH2 tumors 10362137
ENSG00000095002 MSH2 breast cancer 10362525
ENSG00000095002 MSH2 tumour 10369701
ENSG00000095002 MSH2 tumors 10375096
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 10378595
ENSG00000095002 MSH2 colorectal cancer 10386556
ENSG00000095002 MSH2 ovarian cancer 10388122
ENSG00000095002 MSH2 tumors 10393852
ENSG00000095002 MSH2 cancer 10397236
ENSG00000095002 MSH2 cancer 10397239
ENSG00000095002 MSH2 tumor 10397451
ENSG00000095002 MSH2 tumors 10397740
ENSG00000095002 MSH2 colorectal cancer 10404063
ENSG00000095002 MSH2 pancreatic cancer 10404064
ENSG00000095002 MSH2 cancers 10408399
ENSG00000095002 MSH2 epithelial ovarian cancer 10408416
ENSG00000095002 MSH2 colorectal cancers 10413423
ENSG00000095002 MSH2 colorectal cancer 10416884
ENSG00000095002 MSH2 tumor 10418831
ENSG00000095002 MSH2 tumours 10419591
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 10432927
ENSG00000095002 MSH2 colorectal cancer 10433009
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 10446963
ENSG00000095002 MSH2 colorectal cancer 10448273
ENSG00000095002 MSH2 AML 10450752
ENSG00000095002 MSH2 tumors 10468602
ENSG00000095002 MSH2 cancer 10469597
ENSG00000095002 MSH2 tumors 10470113
ENSG00000095002 MSH2 tumours 10470121
ENSG00000095002 MSH2 colorectal cancer 10471527
ENSG00000095002 MSH2 colorectal cancer 10480359
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 10495924
ENSG00000095002 MSH2 tumors 10496533
ENSG00000095002 MSH2 AMLs 10498615
ENSG00000095002 MSH2 colon cancer 10507723
ENSG00000095002 MSH2 tumors 10524526
ENSG00000095002 MSH2 colorectal cancer 10530344
ENSG00000095002 MSH2 colorectal cancer 10544224
ENSG00000095002 MSH2 cancer 10545954
ENSG00000095002 MSH2 colorectal cancer 10564582
ENSG00000095002 MSH2 colorectal cancer 10572231
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 10573010
ENSG00000095002 MSH2 ovarian cancer 10577927
ENSG00000095002 MSH2 cancers 10585582
ENSG00000095002 MSH2 tumour 10594000
ENSG00000095002 MSH2 colorectal tumors 10598809
ENSG00000095002 MSH2 colorectal cancer 10601588
ENSG00000095002 MSH2 colorectal cancer 10612836
ENSG00000095002 MSH2 cancer 10615127
ENSG00000095002 MSH2 tumour 10619961
ENSG00000095002 MSH2 cancers 10630171
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 10630180
ENSG00000095002 MSH2 tumor 10660333
ENSG00000095002 MSH2 pancreatic cancer 10667595
ENSG00000095002 MSH2 Hereditary nonpolyposis colon cancer 10671064
ENSG00000095002 MSH2 colorectal cancers 10673298
ENSG00000095002 MSH2 colorectal cancer 10674020
ENSG00000095002 MSH2 colorectal cancer 10680334
ENSG00000095002 MSH2 familial colorectal cancer 10682661
ENSG00000095002 MSH2 endometrial cancer 10687268
ENSG00000095002 MSH2 tumor 10688836
ENSG00000095002 MSH2 colorectal tumors 10690586
ENSG00000095002 MSH2 colorectal cancer 10706084
ENSG00000095002 MSH2 hereditary nonpolyposis colon cancer 10712226
ENSG00000095002 MSH2 rectal cancer 10713887
ENSG00000095002 MSH2 colorectal-cancer 10719736
ENSG00000095002 MSH2 tumors 10723572
ENSG00000095002 MSH2 tumors 10728595
ENSG00000095002 MSH2 Cancer 10732761
ENSG00000095002 MSH2 Colorectal cancers 10737703
ENSG00000095002 MSH2 cancer 10739686
ENSG00000095002 MSH2 colorectal cancer 10741294
ENSG00000095002 MSH2 tumors 10746679
ENSG00000095002 MSH2 colorectal cancers 10762011
ENSG00000095002 MSH2 cancer 10769643
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 10777691
ENSG00000095002 MSH2 ovarian cancer 10778972
ENSG00000095002 MSH2 tumor 10782890
ENSG00000095002 MSH2 tumor 10783165
ENSG00000095002 MSH2 hereditary nonpolyposis colon cancer 10786688
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 10793088
ENSG00000095002 MSH2 tumors 10820356
ENSG00000095002 MSH2 Hereditary nonpolyposis colorectal cancer (HNPCC) 10824932
ENSG00000095002 MSH2 tumors 10837019
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 10850409
ENSG00000095002 MSH2 colorectal cancer 10854094
ENSG00000095002 MSH2 colorectal cancer 10861262
ENSG00000095002 MSH2 colorectal cancer 10861474
ENSG00000095002 MSH2 colorectal cancer 10874005
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 10874307
ENSG00000095002 MSH2 colorectal cancer 10874318
ENSG00000095002 MSH2 colorectal cancer 10896919
ENSG00000095002 MSH2 tumours 10918209
ENSG00000095002 MSH2 tumor 10918391
ENSG00000095002 MSH2 endometrial cancer 10938395
ENSG00000095002 MSH2 tumor 10945633
ENSG00000095002 MSH2 tumors 10949383
ENSG00000095002 MSH2 tumors 10950068
ENSG00000095002 MSH2 cancer 10954253
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 10962807
ENSG00000095002 MSH2 colorectal cancer 10978352
ENSG00000095002 MSH2 tumor 10984493
ENSG00000095002 MSH2 tumors 10999752
ENSG00000095002 MSH2 colorectal tumor 11020245
ENSG00000095002 MSH2 prostate cancer 11025778
ENSG00000095002 MSH2 breast cancer 11034530
ENSG00000095002 MSH2 colorectal cancer 11048711
ENSG00000095002 MSH2 tumour 11054716
ENSG00000095002 MSH2 endometrial cancer 11059773
ENSG00000095002 MSH2 cancer 11062157
ENSG00000095002 MSH2 tumour 11066081
ENSG00000095002 MSH2 colorectal cancer 11069471
ENSG00000095002 MSH2 colorectal cancer 11074494
ENSG00000095002 MSH2 tumor 11084429
ENSG00000095002 MSH2 cancers 11093816
ENSG00000095002 MSH2 Breast cancer 11112663
ENSG00000095002 MSH2 tumor 11123866
ENSG00000095002 MSH2 tumor 11138465
ENSG00000095002 MSH2 colorectal cancer 11139242
ENSG00000095002 MSH2 tumors 11150376
ENSG00000095002 MSH2 colorectal tumors 11150379
ENSG00000095002 MSH2 tumor 11151427
ENSG00000095002 MSH2 primary cancers 11153917
ENSG00000095002 MSH2 bladder cancer 11161395
ENSG00000095002 MSH2 tumors 11166916
ENSG00000095002 MSH2 Colorectal cancer 11179758
ENSG00000095002 MSH2 tumor 11187904
ENSG00000095002 MSH2 cancers 11205208
ENSG00000095002 MSH2 hereditary breast and ovarian cancer 11205230
ENSG00000095002 MSH2 tumors 11208710
ENSG00000095002 MSH2 tumours 11213834
ENSG00000095002 MSH2 biliary tract cancers 11223838
ENSG00000095002 MSH2 sebaceous tumors 11231323
ENSG00000095002 MSH2 colon cancer 11245474
ENSG00000095002 MSH2 colorectal cancer 11268462
ENSG00000095002 MSH2 tumor 11289147
ENSG00000095002 MSH2 cancer 11291077
ENSG00000095002 MSH2 tumors 11301392
ENSG00000095002 MSH2 cancers 11302343
ENSG00000095002 MSH2 colorectal cancer 11304573
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 11306449
ENSG00000095002 MSH2 tumors 11306499
ENSG00000095002 MSH2 colorectal cancer 11309221
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 11313985
ENSG00000095002 MSH2 tumors 11332201
ENSG00000095002 MSH2 colorectal cancer 11333868
ENSG00000095002 MSH2 tumors 11334467
ENSG00000095002 MSH2 colorectal cancers 11336166
ENSG00000095002 MSH2 Tumor 11339660
ENSG00000095002 MSH2 ovarian cancer 11350971
ENSG00000095002 MSH2 tumor 11358834
ENSG00000095002 MSH2 tumours 11358903
ENSG00000095002 MSH2 breast cancer 11369138
ENSG00000095002 MSH2 colorectal cancer 11376026
ENSG00000095002 MSH2 tumors 11376800
ENSG00000095002 MSH2 colorectal cancer 11376803
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 11385712
ENSG00000095002 MSH2 colorectal cancer 11389088
ENSG00000095002 MSH2 prostate cancer 11398174
ENSG00000095002 MSH2 tumour 11407044
ENSG00000095002 MSH2 tumours 11409565
ENSG00000095002 MSH2 tumors 11416201
ENSG00000095002 MSH2 tumors 11420466
ENSG00000095002 MSH2 tumors 11422806
ENSG00000095002 MSH2 colorectal cancer 11443839
ENSG00000095002 MSH2 prostate cancer 11444857
ENSG00000095002 MSH2 ovarian cancer 11477138
ENSG00000095002 MSH2 breast cancer 11477562
ENSG00000095002 MSH2 skin tumors 11494035
ENSG00000095002 MSH2 tumors 11494037
ENSG00000095002 MSH2 tumors 11494233
ENSG00000095002 MSH2 pediatric tumors 11496300
ENSG00000095002 MSH2 Colorectal Cancer 11498787
ENSG00000095002 MSH2 tumors 11504837
ENSG00000095002 MSH2 tumours 11506498
ENSG00000095002 MSH2 tumors 11522654
ENSG00000095002 MSH2 tumors 11524701
ENSG00000095002 MSH2 colorectal cancer 11532035
ENSG00000095002 MSH2 colorectal cancer 11555625
ENSG00000095002 MSH2 tumor 11561760
ENSG00000095002 MSH2 hereditary colorectal cancer 11562928
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 11570578
ENSG00000095002 MSH2 tumor 11584201
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 11585727
ENSG00000095002 MSH2 cervical cancer 11586036
ENSG00000095002 MSH2 tumours 11592095
ENSG00000095002 MSH2 cancer 11592777
ENSG00000095002 MSH2 ovarian cancer 11592780
ENSG00000095002 MSH2 tumours 11593433
ENSG00000095002 MSH2 tumor 11598481
ENSG00000095002 MSH2 cancer 11600610
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 11601928
ENSG00000095002 MSH2 colon cancer 11604984
ENSG00000095002 MSH2 tumors 11606497
ENSG00000095002 MSH2 hereditary nonpolyposis colon cancer 11691782
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 11715474
ENSG00000095002 MSH2 germ cell tumours 11719586
ENSG00000095002 MSH2 colorectal cancer 11726306
ENSG00000095002 MSH2 tumors 11733361
ENSG00000095002 MSH2 colorectal cancer 11748856
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 11754112
ENSG00000095002 MSH2 cancers 11764381
ENSG00000095002 MSH2 colorectal cancer 11765350
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 11769399
ENSG00000095002 MSH2 malignant ovarian tumors 11775911
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 11781295
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 11782355
ENSG00000095002 MSH2 cancer 11788563
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 11801550
ENSG00000095002 MSH2 colorectal cancer 11807791
ENSG00000095002 MSH2 tumours 11829237
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 11830542
ENSG00000095002 MSH2 colorectal cancer 11839723
ENSG00000095002 MSH2 colorectal cancer 11844828
ENSG00000095002 MSH2 tumors 11851879
ENSG00000095002 MSH2 hereditary nonpolyposis colon cancer 11852345
ENSG00000095002 MSH2 cancer 11857301
ENSG00000095002 MSH2 colorectal cancer 11857362
ENSG00000095002 MSH2 skin tumors 11859205
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 11870161
ENSG00000095002 MSH2 tumours 11870540
ENSG00000095002 MSH2 cancer 11890986
ENSG00000095002 MSH2 tumors 11910346
ENSG00000095002 MSH2 colorectal cancer 11918085
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 11920650
ENSG00000095002 MSH2 tumours 11931386
ENSG00000095002 MSH2 colorectal cancers 11941977
ENSG00000095002 MSH2 tumours 11948461
ENSG00000095002 MSH2 tumour 11953861
ENSG00000095002 MSH2 endometrial cancer 11956307
ENSG00000095002 MSH2 AML 11972518
ENSG00000095002 MSH2 tumors 11975679
ENSG00000095002 MSH2 tumors 11979377
ENSG00000095002 MSH2 tumors 11979380
ENSG00000095002 MSH2 tumors 12015776
ENSG00000095002 MSH2 colorectal cancer 12019211
ENSG00000095002 MSH2 tumor 12057899
ENSG00000095002 MSH2 tumour 12060695
ENSG00000095002 MSH2 tumors 12062055
ENSG00000095002 MSH2 tumor 12063967
ENSG00000095002 MSH2 gastric cancers 12065777
ENSG00000095002 MSH2 hereditary nonpolyposis colon cancer 12067992
ENSG00000095002 MSH2 tumors 12076327
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 12095971
ENSG00000095002 MSH2 colorectal cancer 12110639
ENSG00000095002 MSH2 colorectal cancer 12112654
ENSG00000095002 MSH2 colorectal cancer 12114115
ENSG00000095002 MSH2 tumor 12115348
ENSG00000095002 MSH2 tumors 12118112
ENSG00000095002 MSH2 oral cancers 12118324
ENSG00000095002 MSH2 pancreatic cancer 12120238
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancers (HNPCC) 12124176
ENSG00000095002 MSH2 tumors 12124320
ENSG00000095002 MSH2 colorectal cancer 12124491
ENSG00000095002 MSH2 gastric cancer 12132870
ENSG00000095002 MSH2 colorectal cancer 12150741
ENSG00000095002 MSH2 tumours 12168066
ENSG00000095002 MSH2 breast cancer 12173039
ENSG00000095002 MSH2 hematological cancer 12173046
ENSG00000095002 MSH2 colorectal cancer 12174887
ENSG00000095002 MSH2 cancers 12177776
ENSG00000095002 MSH2 cancers 12200596
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 12203789
ENSG00000095002 MSH2 colon cancer 12324578
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 12352241
ENSG00000095002 MSH2 colorectal cancer 12373605
ENSG00000095002 MSH2 colorectal cancer 12377806
ENSG00000095002 MSH2 tumors 12379157
ENSG00000095002 MSH2 Colorectal Cancer 12385013
ENSG00000095002 MSH2 tumours 12386821
ENSG00000095002 MSH2 tumor 12402306
ENSG00000095002 MSH2 Hereditary Nonpolyposis Colorectal Cancer (HNPCC) 12414623
ENSG00000095002 MSH2 colorectal cancer 12419761
ENSG00000095002 MSH2 prostate cancer 12432247
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 12436451
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 12454801
ENSG00000095002 MSH2 tumors 12460887
ENSG00000095002 MSH2 colorectal cancer 12469183
ENSG00000095002 MSH2 tumour 12470655
ENSG00000095002 MSH2 hereditary breast and ovarian cancer 12475549
ENSG00000095002 MSH2 tumor 12479849
ENSG00000095002 MSH2 Hereditary nonpolyposis colorectal cancer 12494471
ENSG00000095002 MSH2 tumours 12494870
ENSG00000095002 MSH2 tumor 12496472
ENSG00000095002 MSH2 Wilms tumor 12506466
ENSG00000095002 MSH2 tumours 12509957
ENSG00000095002 MSH2 tumours 12509964
ENSG00000095002 MSH2 colon cancer 12522549
ENSG00000095002 MSH2 AML 12529664
ENSG00000095002 MSH2 colon tumors 12547705
ENSG00000095002 MSH2 tumour 12555990
ENSG00000095002 MSH2 tumours 12555992
ENSG00000095002 MSH2 cancer 12579293
ENSG00000095002 MSH2 Cancer 12591727
ENSG00000095002 MSH2 colorectal cancer 12595050
ENSG00000095002 MSH2 tumors 12627520
ENSG00000095002 MSH2 tumour 12628744
ENSG00000095002 MSH2 gastric cancer 12632492
ENSG00000095002 MSH2 lung tumors 12639995
ENSG00000095002 MSH2 endometrial cancer 12649668
ENSG00000095002 MSH2 cancer 12650804
ENSG00000095002 MSH2 tumor 12655564
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 12658575
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 12667026
ENSG00000095002 MSH2 tumors 12667388
ENSG00000095002 MSH2 colorectal cancer 12673796
ENSG00000095002 MSH2 prostate cancer 12684669
ENSG00000095002 MSH2 cancer 12684691
ENSG00000095002 MSH2 colorectal cancer 12694232
ENSG00000095002 MSH2 Hereditary nonpolyposis colorectal cancer (HNPCC) 12702580
ENSG00000095002 MSH2 bladder cancer 12712438
ENSG00000095002 MSH2 tumor 12712483
ENSG00000095002 MSH2 tumors 12769209
ENSG00000095002 MSH2 colorectal cancer 12783672
ENSG00000095002 MSH2 colorectal cancer 12792735
ENSG00000095002 MSH2 tumor 12792759
ENSG00000095002 MSH2 endometrial cancers 12792767
ENSG00000095002 MSH2 tumors 12800209
ENSG00000095002 MSH2 Cancer 12801268
ENSG00000095002 MSH2 tumors 12802583
ENSG00000095002 MSH2 tumors 12808326
ENSG00000095002 MSH2 cancer 12810667
ENSG00000095002 MSH2 pancreatic cancer 12817878
ENSG00000095002 MSH2 colorectal cancers 12823711
ENSG00000095002 MSH2 tumor 12833454
ENSG00000095002 MSH2 cancer 12842538
ENSG00000095002 MSH2 breast cancer 12851690
ENSG00000095002 MSH2 tumors 12861059
ENSG00000095002 MSH2 gastric cancer 12861399
ENSG00000095002 MSH2 tumor 12885834
ENSG00000095002 MSH2 colorectal cancer 12907901
ENSG00000095002 MSH2 tumor 12910497
ENSG00000095002 MSH2 colorectal cancers 12915883
ENSG00000095002 MSH2 colorectal cancer 12919140
ENSG00000095002 MSH2 colorectal cancer 12920072
ENSG00000095002 MSH2 colorectal cancer 12930688
ENSG00000095002 MSH2 colorectal cancer 12938096
ENSG00000095002 MSH2 non-small cell lung cancer 12948402
ENSG00000095002 MSH2 tumor 13129885
ENSG00000095002 MSH2 tumors 14499693
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 14499697
ENSG00000095002 MSH2 tumors 14500346
ENSG00000095002 MSH2 tumor 14500385
ENSG00000095002 MSH2 tumour 14504054
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 14512394
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 14514376
ENSG00000095002 MSH2 colorectal cancer 14517950
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 14518068
ENSG00000095002 MSH2 cancer 14518071
ENSG00000095002 MSH2 tumor 14518263
ENSG00000095002 MSH2 cancer 14520694
ENSG00000095002 MSH2 familial breast cancer 14520695
ENSG00000095002 MSH2 tumors 14522894
ENSG00000095002 MSH2 tumor 14562278
ENSG00000095002 MSH2 cancer 14564042
ENSG00000095002 MSH2 Hereditary nonpolyposis colorectal cancer (HNPCC) 14572584
ENSG00000095002 MSH2 cancers 14574003
ENSG00000095002 MSH2 tumor 14574004
ENSG00000095002 MSH2 ovarian cancer 14574006
ENSG00000095002 MSH2 cancer 14574010
ENSG00000095002 MSH2 tumours 14574162
ENSG00000095002 MSH2 cancer 14574163
ENSG00000095002 MSH2 colorectal cancer 14574174
ENSG00000095002 MSH2 tumors 14576472
ENSG00000095002 MSH2 cancer 14576825
ENSG00000095002 MSH2 colorectal cancer 14594944
ENSG00000095002 MSH2 tumors 14601090
ENSG00000095002 MSH2 tumors 14614055
ENSG00000095002 MSH2 ovarian endometrioid cancer 14631366
ENSG00000095002 MSH2 colorectal cancer 14635101
ENSG00000095002 MSH2 tumours 14645346
ENSG00000095002 MSH2 cancers 14645426
ENSG00000095002 MSH2 colorectal cancer 14646573
ENSG00000095002 MSH2 tumors 14652751
ENSG00000095002 MSH2 colorectal cancer 14688830
ENSG00000095002 MSH2 cancer 14696396
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 14703452
ENSG00000095002 MSH2 tumor 14708047
ENSG00000095002 MSH2 colorectal cancer 14716824
ENSG00000095002 MSH2 tumors 14726676
ENSG00000095002 MSH2 Tumors 14732226
ENSG00000095002 MSH2 tumours 14735197
ENSG00000095002 MSH2 tumor 14744764
ENSG00000095002 MSH2 sebaceous tumors 14752307
ENSG00000095002 MSH2 cancers 14760069
ENSG00000095002 MSH2 tumors 14760077
ENSG00000095002 MSH2 duodenal cancer 14762794
ENSG00000095002 MSH2 tumors 14871813
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 14871915
ENSG00000095002 MSH2 colon cancer 14960518
ENSG00000095002 MSH2 primary cancers 14961575
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 14974087
ENSG00000095002 MSH2 breast cancer 15010883
ENSG00000095002 MSH2 tumors 15015769
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 15042510
ENSG00000095002 MSH2 tumours 15048084
ENSG00000095002 MSH2 colon cancer 15059910
ENSG00000095002 MSH2 tumor 15062061
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 15063132
ENSG00000095002 MSH2 tumour 15083191
ENSG00000095002 MSH2 Tumors 15098177
ENSG00000095002 MSH2 colorectal cancer 15117997
ENSG00000095002 MSH2 endometrial cancer 15118395
ENSG00000095002 MSH2 Gastric cancer 15133479
ENSG00000095002 MSH2 tumours 15138486
ENSG00000095002 MSH2 tumors 15138928
ENSG00000095002 MSH2 stomach cancer 15142449
ENSG00000095002 MSH2 tumors 15143336
ENSG00000095002 MSH2 tumors 15161053
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 15200905
ENSG00000095002 MSH2 esophageal cancer 15201084
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 15216397
ENSG00000095002 MSH2 Tumor 15217520
ENSG00000095002 MSH2 tumors 15222003
ENSG00000095002 MSH2 tumour 15235020
ENSG00000095002 MSH2 endometrial cancer 15236168
ENSG00000095002 MSH2 colon cancer 15254659
ENSG00000095002 MSH2 pancreatic cancer 15264268
ENSG00000095002 MSH2 tumors 15279904
ENSG00000095002 MSH2 tumours 15288293
ENSG00000095002 MSH2 colorectal cancer 15289847
ENSG00000095002 MSH2 tumours 15294875
ENSG00000095002 MSH2 tumors 15297202
ENSG00000095002 MSH2 rectal cancers 15300804
ENSG00000095002 MSH2 cancer 15300854
ENSG00000095002 MSH2 colon cancer 15316055
ENSG00000095002 MSH2 cancer 15324316
ENSG00000095002 MSH2 colon cancer 15340261
ENSG00000095002 MSH2 childhood cancer 15340263
ENSG00000095002 MSH2 tumours 15342696
ENSG00000095002 MSH2 colorectal cancer 15345113
ENSG00000095002 MSH2 tumors 15350299
ENSG00000095002 MSH2 tumours 15354210
ENSG00000095002 MSH2 tumors 15362369
ENSG00000095002 MSH2 colorectal cancer 15365995
ENSG00000095002 MSH2 tumor 15365996
ENSG00000095002 MSH2 colorectal tumors 15455227
ENSG00000095002 MSH2 tumor 15467428
ENSG00000095002 MSH2 tumors 15467433
ENSG00000095002 MSH2 cancer 15475387
ENSG00000095002 MSH2 ovarian cancer 15475941
ENSG00000095002 MSH2 colorectal cancer 15480874
ENSG00000095002 MSH2 tumor 15481721
ENSG00000095002 MSH2 colorectal cancer 15483016
ENSG00000095002 MSH2 tumors 15492498
ENSG00000095002 MSH2 tumors 15492756
ENSG00000095002 MSH2 Tumors 15492759
ENSG00000095002 MSH2 colorectal cancer 15494688
ENSG00000095002 MSH2 cancer 15498213
ENSG00000095002 MSH2 colorectal cancer 15503820
ENSG00000095002 MSH2 colorectal cancers 15507669
ENSG00000095002 MSH2 colorectal cancer 15516845
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 15516847
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 15520224
ENSG00000095002 MSH2 breast cancer 15523909
ENSG00000095002 MSH2 gastric cancer 15526354
ENSG00000095002 MSH2 tumors 15540218
ENSG00000095002 MSH2 tumors 15551255
ENSG00000095002 MSH2 tumor 15563510
ENSG00000095002 MSH2 tumor 15569982
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 15571801
ENSG00000095002 MSH2 endometrial cancers 15583795
ENSG00000095002 MSH2 Cancer 15596632
ENSG00000095002 MSH2 tumors 15599934
ENSG00000095002 MSH2 lung cancers 15605365
ENSG00000095002 MSH2 colorectal cancer 15613555
ENSG00000095002 MSH2 tumors 15613860
ENSG00000095002 MSH2 tumors 15619215
ENSG00000095002 MSH2 tumors 15619218
ENSG00000095002 MSH2 breast cancer 15642167
ENSG00000095002 MSH2 tumors 15643505
ENSG00000095002 MSH2 tumor 15657659
ENSG00000095002 MSH2 colorectal cancers 15660526
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ENSG00000095002 MSH2 lymphoid tumors 9116269
ENSG00000095002 MSH2 hereditary nonpolyposis colon cancer 9137418
ENSG00000095002 MSH2 tumors 9157971
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 9218993
ENSG00000095002 MSH2 tumor 9230208
ENSG00000095002 MSH2 hereditary nonpolyposis colon cancer 9242462
ENSG00000095002 MSH2 Tumors 9244348
ENSG00000095002 MSH2 Hereditary nonpolyposis colorectal cancer (HNPCC) 9245993
ENSG00000095002 MSH2 tumor 9278518
ENSG00000095002 MSH2 colorectal cancer 9288110
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 9288790
ENSG00000095002 MSH2 colorectal tumor 9294177
ENSG00000095002 MSH2 Hereditary nonpolyposis colorectal cancer (HNPCC) 9298827
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 9307272
ENSG00000095002 MSH2 tumor 9307278
ENSG00000095002 MSH2 colorectal cancer 9311737
ENSG00000095002 MSH2 tumours 9349329
ENSG00000095002 MSH2 tumors 9354436
ENSG00000095002 MSH2 tumor 9378008
ENSG00000095002 MSH2 colon cancer 9399661
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 9419403
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 9438104
ENSG00000095002 MSH2 tumors 9445183
ENSG00000095002 MSH2 colorectal cancer 9448296
ENSG00000095002 MSH2 tumor 9469823
ENSG00000095002 MSH2 colorectal cancer 9470849
ENSG00000095002 MSH2 colorectal cancer 9490293
ENSG00000095002 MSH2 colon cancers 9491849
ENSG00000095002 MSH2 colorectal cancer 9500552
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 9506527
ENSG00000095002 MSH2 colorectal cancer 9526167
ENSG00000095002 MSH2 ovarian cancer 9538124
ENSG00000095002 MSH2 tumors 9542742
ENSG00000095002 MSH2 tumor 9546427
ENSG00000095002 MSH2 cancer 9559626
ENSG00000095002 MSH2 colorectal cancer 9559627
ENSG00000095002 MSH2 colorectal cancer 9563488
ENSG00000095002 MSH2 head and neck cancer 9568786
ENSG00000095002 MSH2 ovarian cancer 9579428
ENSG00000095002 MSH2 cancer 9587112
ENSG00000095002 MSH2 tumors 9592181
ENSG00000095002 MSH2 colorectal cancer 9592192
ENSG00000095002 MSH2 ovarian cancer 9600357
ENSG00000095002 MSH2 colorectal cancer 9611074
ENSG00000095002 MSH2 primary cancers 9621522
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 9630578
ENSG00000095002 MSH2 cancer 9633840
ENSG00000095002 MSH2 tumors 9634524
ENSG00000095002 MSH2 cancer 9648558
ENSG00000095002 MSH2 non-small cell lung cancer 9650548
ENSG00000095002 MSH2 tumor 9657101
ENSG00000095002 MSH2 cancer 9671718
ENSG00000095002 MSH2 tumors 9674699
ENSG00000095002 MSH2 tumor 9677427
ENSG00000095002 MSH2 hereditary colorectal cancer 9683794
ENSG00000095002 MSH2 tumor 9699680
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 9709044
ENSG00000095002 MSH2 colon cancer 9718327
ENSG00000095002 MSH2 colorectal cancer 9730154
ENSG00000095002 MSH2 tumors 9731891
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 9732950
ENSG00000095002 MSH2 colorectal cancer 9736731
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer (HNPCC) 9740671
ENSG00000095002 MSH2 colorectal cancer 9748699
ENSG00000095002 MSH2 colon cancer 9772075
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 9774676
ENSG00000095002 MSH2 cancers 9777938
ENSG00000095002 MSH2 tumors 9792412
ENSG00000095002 MSH2 tumor 9816148
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer 9823302
ENSG00000095002 MSH2 tumors 9824204
ENSG00000095002 MSH2 colorectal cancer 9824623
ENSG00000095002 MSH2 cancer 9833759
ENSG00000095002 MSH2 cancers 9841970
ENSG00000095002 MSH2 colorectal cancer 9845760
ENSG00000095002 MSH2 tumors 9850030
ENSG00000095002 MSH2 tumor 9850081
ENSG00000095002 MSH2 tumor 9855004
ENSG00000095002 MSH2 tumors 9892201
ENSG00000095002 MSH2 colon cancer 9916805
ENSG00000095002 MSH2 Hereditary nonpolyposis colon cancer 9927034
ENSG00000095002 MSH2 cancer PMC2736982
ENSG00000095002 MSH2 hereditary nonpolyposis colorectal cancer PMC2838404
ENSG00000095002 MSH2 cancer PMC2840013
ENSG00000095002 MSH2 cancer PMC2840014
ENSG00000095002 MSH2 colon cancers PMC3401934
ENSG00000095002 MSH2 tumor PMC5581348
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000095002 MSH2 colorectal adenocarcinoma frameshift_variant 5.366% (102/1901) 11 entries
ENSG00000095002 MSH2 colorectal adenocarcinoma sequence_alteration 5.366% (102/1901) 10 entries
ENSG00000095002 MSH2 breast ductal adenocarcinoma stop_gained 5.161% (85/1647) 3 entries
ENSG00000095002 MSH2 breast ductal adenocarcinoma missense_variant 5.161% (85/1647) 3 entries
ENSG00000095002 MSH2 Uterine Carcinosarcoma frameshift_variant 9.211% (14/152) 3 entries
ENSG00000095002 MSH2 breast ductal adenocarcinoma sequence_alteration 5.161% (85/1647) 2 entries
ENSG00000095002 MSH2 Uterine Carcinosarcoma sequence_alteration 9.211% (14/152) 2 entries
ENSG00000095002 MSH2 colorectal adenocarcinoma stop_gained 5.366% (102/1901) 10 entries
ENSG00000095002 MSH2 colorectal adenocarcinoma conservative_inframe_deletion 5.366% (102/1901) 2 entries
ENSG00000095002 MSH2 colorectal adenocarcinoma missense_variant 5.366% (102/1901) 10 entries
ENSG00000095002 MSH2 lymphoid neoplasm missense_variant 15.23% (30/197) 1 entry
ENSG00000095002 MSH2 anaplastic oligodendroglioma missense_variant 4.494% (4/89) 1 entry
ENSG00000095002 MSH2 anaplastic oligodendroglioma stop_gained 4.494% (4/89) 1 entry
ENSG00000095002 MSH2 colon adenocarcinoma sequence_alteration 3.821% (52/1361) 8 entries
ENSG00000095002 MSH2 urothelial carcinoma frameshift_variant 10.47% (9/86) 1 entry
ENSG00000095002 MSH2 T-cell acute lymphoblastic leukemia missense_variant 1.314% (11/837) 3 entries
ENSG00000095002 MSH2 chronic lymphocytic leukemia sequence_alteration 1.122% (10/891) 1 entry
ENSG00000095002 MSH2 Endometrial Endometrioid Adenocarcinoma frameshift_variant 3.655% (25/684) 3 entries
ENSG00000095002 MSH2 prostate adenocarcinoma sequence_alteration 2.596% (56/2157) 1 entry
ENSG00000095002 MSH2 Merkel cell skin cancer sequence_alteration 2.128% (2/94) 2 entries
ENSG00000095002 MSH2 oral squamous cell carcinoma sequence_alteration 2.29% (6/262) 2 entries
ENSG00000095002 MSH2 gastric adenocarcinoma sequence_alteration 2.299% (22/957) 4 entries
ENSG00000095002 MSH2 brain glioblastoma sequence_alteration 0.9562% (12/1255) 2 entries
ENSG00000095002 MSH2 Endometrial Endometrioid Adenocarcinoma stop_gained 3.655% (25/684) 3 entries
ENSG00000095002 MSH2 leiomyosarcoma missense_variant 2.0% (2/100) 1 entry
ENSG00000095002 MSH2 esophageal squamous cell carcinoma sequence_alteration 0.4386% (3/684) 2 entries
ENSG00000095002 MSH2 bladder transitional cell carcinoma missense_variant 1.961% (10/510) 2 entries
ENSG00000095002 MSH2 adrenal cortex carcinoma sequence_alteration 0.9174% (2/218) 2 entries
ENSG00000095002 MSH2 ovarian serous adenocarcinoma sequence_alteration 0.8989% (8/890) 2 entries
ENSG00000095002 MSH2 lobular breast carcinoma sequence_alteration 2.827% (8/283) 1 entry
ENSG00000095002 MSH2 female breast carcinoma sequence_alteration 0.7421% (4/539) 1 entry
ENSG00000095002 MSH2 brain glioblastoma missense_variant 0.9562% (12/1255) 2 entries
ENSG00000095002 MSH2 colon adenocarcinoma missense_variant 3.821% (52/1361) 8 entries
ENSG00000095002 MSH2 gastric adenocarcinoma missense_variant 2.299% (22/957) 3 entries
ENSG00000095002 MSH2 skin melanoma sequence_alteration 2.069% (24/1160) 3 entries
ENSG00000095002 MSH2 endometrium adenocarcinoma stop_gained 8.621% (5/58) 2 entries
ENSG00000095002 MSH2 urothelial carcinoma stop_gained 10.47% (9/86) 1 entry
ENSG00000095002 MSH2 squamous cell lung carcinoma missense_variant 1.106% (11/995) 2 entries
ENSG00000095002 MSH2 skin melanoma missense_variant 2.069% (24/1160) 4 entries
ENSG00000095002 MSH2 pancreatic ductal adenocarcinoma sequence_alteration 3.667% (63/1718) 1 entry
ENSG00000095002 MSH2 rectal adenocarcinoma missense_variant 3.292% (21/638) 3 entries
ENSG00000095002 MSH2 bladder transitional cell carcinoma sequence_alteration 1.961% (10/510) 1 entry
ENSG00000095002 MSH2 rectal adenocarcinoma frameshift_variant 3.292% (21/638) 2 entries
ENSG00000095002 MSH2 squamous cell lung carcinoma sequence_alteration 1.106% (11/995) 1 entry
ENSG00000095002 MSH2 hemangioblastoma sequence_alteration 8.571% (3/35) 1 entry
ENSG00000095002 MSH2 Cervical Small Cell Carcinoma missense_variant 37.5% (3/8) 1 entry
ENSG00000095002 MSH2 skin melanoma stop_gained 2.069% (24/1160) 2 entries
ENSG00000095002 MSH2 Endometrial Endometrioid Adenocarcinoma missense_variant 3.655% (25/684) 3 entries
ENSG00000095002 MSH2 gastric adenocarcinoma frameshift_variant 2.299% (22/957) 2 entries
ENSG00000095002 MSH2 papillary thyroid carcinoma sequence_alteration 0.818% (4/489) 1 entry
ENSG00000095002 MSH2 lung adenocarcinoma sequence_alteration 1.4% (39/2785) 3 entries
ENSG00000095002 MSH2 endometrium adenocarcinoma missense_variant 8.621% (5/58) 3 entries
ENSG00000095002 MSH2 clear cell renal carcinoma missense_variant 0.4954% (8/1615) 3 entries
ENSG00000095002 MSH2 endometrium adenocarcinoma sequence_alteration 8.621% (5/58) 2 entries
ENSG00000095002 MSH2 Mantle cell lymphoma sequence_alteration 3.774% (2/53) 1 entry
ENSG00000095002 MSH2 prostate adenocarcinoma stop_gained 2.596% (56/2157) 1 entry
ENSG00000095002 MSH2 colon adenocarcinoma frameshift_variant 3.821% (52/1361) 3 entries
ENSG00000095002 MSH2 gastric adenocarcinoma stop_gained 2.299% (22/957) 1 entry
ENSG00000095002 MSH2 pharyngeal squamous cell carcinoma missense_variant 2.098% (3/143) 1 entry
ENSG00000095002 MSH2 metaplastic breast carcinoma sequence_alteration 3.659% (3/82) 1 entry
ENSG00000095002 MSH2 breast carcinoma sequence_alteration 0.7016% (13/1853) 2 entries
ENSG00000095002 MSH2 lung adenocarcinoma stop_gained 1.4% (39/2785) 3 entries
ENSG00000095002 MSH2 breast carcinoma frameshift_variant 0.7016% (13/1853) 2 entries
ENSG00000095002 MSH2 rectal adenocarcinoma stop_gained 3.292% (21/638) 3 entries
ENSG00000095002 MSH2 squamous cell lung carcinoma stop_gained 1.106% (11/995) 1 entry
ENSG00000095002 MSH2 colon adenocarcinoma conservative_inframe_deletion 3.821% (52/1361) 2 entries
ENSG00000095002 MSH2 cecum adenocarcinoma stop_gained 3.509% (10/285) 3 entries
ENSG00000095002 MSH2 pancreatic ductal adenocarcinoma missense_variant 3.667% (63/1718) 1 entry
ENSG00000095002 MSH2 brain glioblastoma stop_gained 0.9562% (12/1255) 2 entries
ENSG00000095002 MSH2 T-cell acute lymphoblastic leukemia sequence_alteration 1.314% (11/837) 3 entries
ENSG00000095002 MSH2 diffuse large B-cell lymphoma missense_variant 1.075% (5/465) 2 entries
ENSG00000095002 MSH2 melanoma missense_variant 2.532% (4/158) 2 entries
ENSG00000095002 MSH2 bladder transitional cell carcinoma frameshift_variant 1.961% (10/510) 2 entries
ENSG00000095002 MSH2 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma missense_variant 1.838% (5/272) 2 entries
ENSG00000095002 MSH2 ovarian serous adenocarcinoma missense_variant 0.8989% (8/890) 1 entry
ENSG00000095002 MSH2 endometrial carcinoma frameshift_variant 6.897% (4/58) 3 entries
ENSG00000095002 MSH2 cecum adenocarcinoma sequence_alteration 3.509% (10/285) 2 entries
ENSG00000095002 MSH2 lung adenocarcinoma missense_variant 1.4% (39/2785) 5 entries
ENSG00000095002 MSH2 prostate carcinoma sequence_alteration 3.099% (15/484) 1 entry
ENSG00000095002 MSH2 prostate adenocarcinoma missense_variant 2.596% (56/2157) 2 entries
ENSG00000095002 MSH2 angiosarcoma sequence_alteration 6.383% (3/47) 1 entry
ENSG00000095002 MSH2 cecum adenocarcinoma missense_variant 3.509% (10/285) 2 entries
ENSG00000095002 MSH2 small cell lung carcinoma missense_variant 0.8969% (4/446) 2 entries
ENSG00000095002 MSH2 prostate carcinoma missense_variant 3.099% (15/484) 1 entry
ENSG00000095002 MSH2 clear cell renal carcinoma sequence_alteration 0.4954% (8/1615) 1 entry
ENSG00000095002 MSH2 urothelial carcinoma missense_variant 10.47% (9/86) 1 entry
ENSG00000095002 MSH2 colon adenocarcinoma stop_gained 3.821% (52/1361) 4 entries
ENSG00000095002 MSH2 Endometrial Endometrioid Adenocarcinoma sequence_alteration 3.655% (25/684) 2 entries
ENSG00000095002 MSH2 esophageal adenocarcinoma missense_variant 8.592% (47/547) 1 entry
ENSG00000095002 MSH2 rectal adenocarcinoma sequence_alteration 3.292% (21/638) 2 entries
ENSG00000095002 MSH2 T-cell acute lymphoblastic leukemia frameshift_variant 1.314% (11/837) 1 entry
ENSG00000095002 MSH2 cervical carcinoma missense_variant 12.5% (1/8) 1 entry
ENSG00000095002 MSH2 non-small cell lung carcinoma missense_variant 1.46% (2/137) 1 entry
ENSG00000095002 MSH2 Ampulla of Vater Carcinoma sequence_alteration 0.5076% (1/197) 1 entry
ENSG00000095002 MSH2 bile duct adenocarcinoma transcript_ablation 0.9479% (4/422) 1 entry
ENSG00000095002 MSH2 bile duct adenocarcinoma sequence_alteration 0.9479% (4/422) 1 entry
ENSG00000095002 MSH2 adenosquamous lung carcinoma sequence_alteration 4.545% (1/22) 1 entry
ENSG00000095002 MSH2 Lung Sarcomatoid Carcinoma missense_variant 7.143% (1/14) 1 entry
ENSG00000095002 MSH2 follicular thyroid carcinoma sequence_alteration 1.449% (1/69) 1 entry
ENSG00000095002 MSH2 undifferentiated pleomorphic sarcoma missense_variant 1.613% (1/62) 1 entry
ENSG00000095002 MSH2 hemangioblastoma missense_variant 8.571% (3/35) 1 entry
ENSG00000095002 MSH2 pancreatic neuroendocrine tumor missense_variant 5.085% (12/236) 1 entry
ENSG00000095002 MSH2 Cervical Small Cell Carcinoma sequence_alteration 37.5% (3/8) 1 entry
ENSG00000095002 MSH2 lung adenocarcinoma frameshift_variant 1.4% (39/2785) 1 entry
ENSG00000095002 MSH2 Endometrial Clear Cell Adenocarcinoma sequence_alteration 6.667% (2/30) 1 entry
ENSG00000095002 MSH2 bile duct adenocarcinoma frameshift_variant 0.9479% (4/422) 1 entry
ENSG00000095002 MSH2 papillary thyroid carcinoma stop_gained 0.818% (4/489) 1 entry
ENSG00000095002 MSH2 Duodenal Adenocarcinoma frameshift_variant 5.556% (1/18) 1 entry
ENSG00000095002 MSH2 nasopharyngeal squamous cell carcinoma stop_gained 0.6494% (2/308) 1 entry
ENSG00000095002 MSH2 marginal zone B-cell lymphoma missense_variant 3.333% (1/30) 1 entry
ENSG00000095002 MSH2 basal cell carcinoma missense_variant 2.941% (2/68) 1 entry
ENSG00000095002 MSH2 gastric intestinal type adenocarcinoma sequence_alteration 0.9709% (1/103) 1 entry
ENSG00000095002 MSH2 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma stop_gained 1.838% (5/272) 1 entry
ENSG00000095002 MSH2 sebaceous adenocarcinoma stop_gained 33.33% (1/3) 1 entry
ENSG00000095002 MSH2 neoplasm missense_variant 3.448% (1/29) 1 entry
ENSG00000095002 MSH2 Thymoma Type AB sequence_alteration 20.0% (1/5) 1 entry
ENSG00000095002 MSH2 diffuse gastric adenocarcinoma sequence_alteration 1.163% (1/86) 1 entry
ENSG00000095002 MSH2 breast phyllodes tumor missense_variant 2.174% (1/46) 1 entry
ENSG00000095002 MSH2 prostate adenocarcinoma frameshift_variant 2.596% (56/2157) 1 entry
ENSG00000095002 MSH2 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma sequence_alteration 1.838% (5/272) 1 entry
ENSG00000095002 MSH2 bile duct adenocarcinoma stop_gained 0.9479% (4/422) 1 entry
ENSG00000095002 MSH2 Pleural Mesothelioma missense_variant 0.7042% (1/142) 1 entry
ENSG00000095002 MSH2 nasopharyngeal squamous cell carcinoma missense_variant 0.6494% (2/308) 1 entry
ENSG00000095002 MSH2 endometrium adenocarcinoma frameshift_variant 8.621% (5/58) 1 entry
ENSG00000095002 MSH2 breast phyllodes tumor sequence_alteration 2.174% (1/46) 1 entry
ENSG00000095002 MSH2 Endometrial Clear Cell Adenocarcinoma missense_variant 6.667% (2/30) 1 entry
ENSG00000095002 MSH2 cecum adenocarcinoma frameshift_variant 3.509% (10/285) 1 entry
ENSG00000095002 MSH2 atypical teratoid rhabdoid tumor sequence_alteration 2.381% (1/42) 1 entry
ENSG00000095002 MSH2 bladder transitional cell carcinoma stop_gained 1.961% (10/510) 1 entry
ENSG00000095002 MSH2 pancreatic ductal adenocarcinoma stop_gained 3.667% (63/1718) 1 entry
ENSG00000095002 MSH2 Mixed Lobular and Ductal Breast Carcinoma stop_gained 1.562% (1/64) 1 entry
ENSG00000095002 MSH2 metaplastic breast carcinoma transcript_ablation 3.659% (3/82) 1 entry
ENSG00000095002 MSH2 non-small cell lung carcinoma sequence_alteration 1.46% (2/137) 1 entry
ENSG00000095002 MSH2 head and neck squamous cell carcinoma missense_variant 0.1508% (1/663) 1 entry
ENSG00000095002 MSH2 alveolar rhabdomyosarcoma missense_variant 1.562% (1/64) 1 entry
ENSG00000095002 MSH2 adenosquamous lung carcinoma missense_variant 4.545% (1/22) 1 entry
ENSG00000095002 MSH2 ovarian serous adenocarcinoma frameshift_variant 0.8989% (8/890) 1 entry
ENSG00000095002 MSH2 Parathyroid Gland Carcinoma stop_gained 2.857% (1/35) 1 entry
ENSG00000095002 MSH2 urothelial carcinoma sequence_alteration 10.47% (9/86) 1 entry
ENSG00000095002 MSH2 endometrium adenocarcinoma conservative_inframe_deletion 8.621% (5/58) 1 entry
ENSG00000095002 MSH2 ovarian serous adenocarcinoma stop_gained 0.8989% (8/890) 1 entry
ENSG00000095002 MSH2 diffuse gastric adenocarcinoma stop_gained 1.163% (1/86) 1 entry
ENSG00000095002 MSH2 Endometrial Clear Cell Adenocarcinoma frameshift_variant 6.667% (2/30) 1 entry
ENSG00000095002 MSH2 papillary thyroid carcinoma missense_variant 0.818% (4/489) 1 entry
ENSG00000095002 MSH2 lobular breast carcinoma stop_gained 2.827% (8/283) 1 entry
ENSG00000095002 MSH2 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma frameshift_variant 1.838% (5/272) 1 entry
ENSG00000095002 MSH2 laryngeal squamous cell carcinoma missense_variant 2.439% (1/41) 1 entry
ENSG00000095002 MSH2 Pancreatic Acinar Cell Carcinoma missense_variant 2.941% (1/34) 1 entry
ENSG00000095002 MSH2 Brain Stem Glioblastoma sequence_alteration 1.754% (1/57) 1 entry
ENSG00000095002 MSH2 melanoma sequence_alteration 2.532% (4/158) 1 entry
ENSG00000095002 MSH2 lobular breast carcinoma missense_variant 2.827% (8/283) 1 entry
ENSG00000095002 MSH2 essential thrombocythemia sequence_alteration 1.639% (1/61) 1 entry
ENSG00000095002 MSH2 Thyroid Gland Oncocytic Follicular Carcinoma frameshift_variant 16.67% (1/6) 1 entry
ENSG00000095002 MSH2 papillary thyroid carcinoma frameshift_variant 0.818% (4/489) 1 entry
ENSG00000095002 MSH2 prostate carcinoma frameshift_variant 3.099% (15/484) 1 entry
ENSG00000095002 MSH2 basal cell carcinoma sequence_alteration 2.941% (2/68) 1 entry
ENSG00000095002 MSH2 colorectal adenoma missense_variant 5.882% (1/17) 1 entry
ENSG00000095002 MSH2 pharyngeal squamous cell carcinoma sequence_alteration 2.098% (3/143) 1 entry
ENSG00000095002 MSH2 Prostate Small Cell Carcinoma missense_variant 5.263% (1/19) 1 entry
ENSG00000095002 MSH2 angiosarcoma stop_gained 6.383% (3/47) 1 entry
ENSG00000095002 MSH2 clear cell renal carcinoma frameshift_variant 0.4954% (8/1615) 1 entry
ENSG00000095002 MSH2 clear cell renal carcinoma stop_gained 0.4954% (8/1615) 1 entry
ENSG00000095002 MSH2 bile duct adenocarcinoma missense_variant 0.9479% (4/422) 1 entry
ENSG00000095002 MSH2 mucosal melanoma missense_variant 1.429% (1/70) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000095002 MSH2 MESO 0.037 high
ENSG00000095002 MSH2 SARC 0.00065 high
ENSG00000095002 MSH2 STAD 0.0017 low
ENSG00000095002 MSH2 PAAD 0.00034 high
ENSG00000095002 MSH2 UCEC 0.00036 high
ENSG00000095002 MSH2 LUSC 0.00063 low
ENSG00000095002 MSH2 HNSC 0.00061 low
ENSG00000095002 MSH2 READ 0.0017 low
ENSG00000095002 MSH2 KIRP 0.00063 high
ENSG00000095002 MSH2 KICH 0.0013 high
ENSG00000095002 MSH2 THYM 0.00058 low
ENSG00000095002 MSH2 ESCA 0.019 high
ENSG00000095002 MSH2 OV 0.034 high
ENSG00000095002 MSH2 PRAD 0.012 high
ENSG00000095002 MSH2 BLCA 0.044 high
ENSG00000095002 MSH2 GBM 0.049 low
ENSG00000095002 MSH2 SKCM 0.0075 low
ENSG00000095002 MSH2 CESC 0.022 low
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000095002 MSH2 LUSC Amp 3.518274 0.274131 0.572301 0.522954
ENSG00000095002 MSH2 TGCT Amp 1.008111 0.131892 0.426757 0.386667