Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts3 |
T |
A |
5: 90,009,282 (GRCm39) |
H127L |
probably benign |
Het |
Adamtsl3 |
T |
C |
7: 82,244,579 (GRCm39) |
V419A |
possibly damaging |
Het |
Arhgap31 |
T |
A |
16: 38,423,287 (GRCm39) |
L926F |
probably damaging |
Het |
Asgr2 |
A |
T |
11: 69,988,877 (GRCm39) |
|
probably null |
Het |
C3ar1 |
T |
A |
6: 122,828,194 (GRCm39) |
T8S |
probably benign |
Het |
Caskin2 |
T |
C |
11: 115,695,543 (GRCm39) |
I273V |
probably damaging |
Het |
Ccnl2 |
T |
A |
4: 155,904,856 (GRCm39) |
C242S |
probably damaging |
Het |
Cdkn2a |
A |
T |
4: 89,212,569 (GRCm39) |
|
probably null |
Het |
Cfap45 |
T |
G |
1: 172,361,616 (GRCm39) |
M231R |
probably damaging |
Het |
Clcn7 |
A |
C |
17: 25,374,350 (GRCm39) |
N464H |
probably benign |
Het |
Col20a1 |
T |
A |
2: 180,651,161 (GRCm39) |
|
probably benign |
Het |
Col7a1 |
T |
A |
9: 108,797,067 (GRCm39) |
|
probably benign |
Het |
Cops7a |
T |
C |
6: 124,939,379 (GRCm39) |
D90G |
probably benign |
Het |
Ctcf |
T |
C |
8: 106,396,864 (GRCm39) |
V363A |
probably benign |
Het |
Cyp2j12 |
A |
G |
4: 96,021,306 (GRCm39) |
V100A |
probably benign |
Het |
Dcaf1 |
T |
A |
9: 106,736,800 (GRCm39) |
F1085Y |
possibly damaging |
Het |
Drc7 |
T |
A |
8: 95,800,760 (GRCm39) |
F594Y |
possibly damaging |
Het |
Ehbp1l1 |
C |
A |
19: 5,768,277 (GRCm39) |
E1009* |
probably null |
Het |
Epg5 |
C |
A |
18: 78,028,316 (GRCm39) |
R1286S |
probably damaging |
Het |
Etv1 |
T |
C |
12: 38,885,060 (GRCm39) |
|
probably benign |
Het |
Exosc7 |
T |
C |
9: 122,964,956 (GRCm39) |
|
probably benign |
Het |
Fam227a |
T |
C |
15: 79,496,747 (GRCm39) |
D610G |
possibly damaging |
Het |
Fat4 |
T |
A |
3: 39,033,923 (GRCm39) |
M2525K |
probably benign |
Het |
Gimap5 |
G |
T |
6: 48,729,999 (GRCm39) |
A190S |
probably damaging |
Het |
Glcci1 |
T |
A |
6: 8,579,596 (GRCm39) |
S79T |
probably damaging |
Het |
Gpnmb |
C |
T |
6: 49,024,384 (GRCm39) |
T233I |
probably null |
Het |
Hdac1-ps |
T |
C |
17: 78,799,558 (GRCm39) |
V183A |
probably damaging |
Het |
Hyls1 |
T |
C |
9: 35,473,363 (GRCm39) |
I18V |
probably benign |
Het |
Ighv1-63 |
C |
T |
12: 115,459,274 (GRCm39) |
E108K |
probably damaging |
Het |
Ighv5-12 |
C |
A |
12: 113,665,927 (GRCm39) |
R57L |
probably damaging |
Het |
Igkv5-37 |
T |
C |
6: 69,940,323 (GRCm39) |
Y107C |
probably damaging |
Het |
Il20ra |
T |
A |
10: 19,631,591 (GRCm39) |
V264D |
probably damaging |
Het |
Jph1 |
A |
T |
1: 17,167,608 (GRCm39) |
V74E |
probably damaging |
Het |
Kcnab1 |
C |
T |
3: 65,265,695 (GRCm39) |
L280F |
probably damaging |
Het |
Kcnk1 |
T |
C |
8: 126,751,826 (GRCm39) |
F144S |
probably damaging |
Het |
Kcnq1 |
G |
A |
7: 142,738,241 (GRCm39) |
E294K |
possibly damaging |
Het |
Kdm4b |
T |
A |
17: 56,704,355 (GRCm39) |
V813E |
probably damaging |
Het |
Ldb2 |
G |
A |
5: 44,637,586 (GRCm39) |
R241W |
probably damaging |
Het |
Lgr5 |
T |
C |
10: 115,288,319 (GRCm39) |
N703S |
probably damaging |
Het |
Map4k1 |
A |
T |
7: 28,688,032 (GRCm39) |
M227L |
possibly damaging |
Het |
Mbnl1 |
T |
A |
3: 60,520,940 (GRCm39) |
M268K |
possibly damaging |
Het |
Mcm2 |
C |
A |
6: 88,868,708 (GRCm39) |
G350C |
probably damaging |
Het |
Myh2 |
A |
T |
11: 67,082,599 (GRCm39) |
T1390S |
possibly damaging |
Het |
Npat |
T |
A |
9: 53,469,526 (GRCm39) |
|
probably benign |
Het |
Nr2e1 |
T |
A |
10: 42,443,969 (GRCm39) |
D251V |
possibly damaging |
Het |
Or1x2 |
A |
G |
11: 50,918,162 (GRCm39) |
N111S |
probably benign |
Het |
Or4d10 |
C |
T |
19: 12,051,421 (GRCm39) |
V192I |
probably benign |
Het |
Or5b107 |
C |
A |
19: 13,142,767 (GRCm39) |
P130T |
probably damaging |
Het |
Plekha5 |
T |
A |
6: 140,470,621 (GRCm39) |
H87Q |
probably damaging |
Het |
Polr3a |
A |
G |
14: 24,529,256 (GRCm39) |
V368A |
probably damaging |
Het |
Psmb8 |
T |
A |
17: 34,419,168 (GRCm39) |
L154Q |
probably damaging |
Het |
Rab40c |
A |
C |
17: 26,103,644 (GRCm39) |
C140G |
probably damaging |
Het |
Ranbp17 |
G |
A |
11: 33,437,689 (GRCm39) |
T183I |
probably benign |
Het |
Ruvbl2 |
T |
C |
7: 45,078,122 (GRCm39) |
E117G |
probably damaging |
Het |
Serpinb3b |
T |
A |
1: 107,082,368 (GRCm39) |
M299L |
probably benign |
Het |
Smpdl3a |
A |
G |
10: 57,678,530 (GRCm39) |
H111R |
probably damaging |
Het |
Sspo |
C |
A |
6: 48,452,821 (GRCm39) |
P2843H |
probably damaging |
Het |
Stk39 |
T |
C |
2: 68,144,908 (GRCm39) |
T389A |
probably benign |
Het |
Synrg |
T |
A |
11: 83,910,531 (GRCm39) |
F1000Y |
probably benign |
Het |
Thbs2 |
C |
T |
17: 14,908,076 (GRCm39) |
S229N |
probably benign |
Het |
Thsd1 |
G |
A |
8: 22,742,247 (GRCm39) |
C305Y |
probably damaging |
Het |
Ticrr |
C |
A |
7: 79,344,297 (GRCm39) |
D1387E |
probably benign |
Het |
Tmem145 |
G |
T |
7: 25,010,816 (GRCm39) |
A383S |
probably damaging |
Het |
Tmprss4 |
A |
G |
9: 45,090,718 (GRCm39) |
V187A |
probably damaging |
Het |
Unc13c |
T |
A |
9: 73,600,524 (GRCm39) |
M1407L |
probably benign |
Het |
Vps39 |
C |
T |
2: 120,153,609 (GRCm39) |
G655D |
probably benign |
Het |
Wwtr1 |
T |
C |
3: 57,482,241 (GRCm39) |
|
probably benign |
Het |
Xrn1 |
T |
C |
9: 95,930,397 (GRCm39) |
S1535P |
probably damaging |
Het |
|
Other mutations in Kntc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Kntc1
|
APN |
5 |
123,928,222 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00514:Kntc1
|
APN |
5 |
123,929,590 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01103:Kntc1
|
APN |
5 |
123,902,283 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01106:Kntc1
|
APN |
5 |
123,900,666 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01357:Kntc1
|
APN |
5 |
123,895,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01367:Kntc1
|
APN |
5 |
123,896,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01538:Kntc1
|
APN |
5 |
123,919,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01546:Kntc1
|
APN |
5 |
123,903,068 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01595:Kntc1
|
APN |
5 |
123,941,758 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01725:Kntc1
|
APN |
5 |
123,902,253 (GRCm39) |
missense |
probably benign |
|
IGL01916:Kntc1
|
APN |
5 |
123,939,976 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01942:Kntc1
|
APN |
5 |
123,916,330 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01973:Kntc1
|
APN |
5 |
123,904,021 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01982:Kntc1
|
APN |
5 |
123,947,159 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02145:Kntc1
|
APN |
5 |
123,900,661 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02510:Kntc1
|
APN |
5 |
123,957,125 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02611:Kntc1
|
APN |
5 |
123,950,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02669:Kntc1
|
APN |
5 |
123,893,727 (GRCm39) |
splice site |
probably benign |
|
IGL02737:Kntc1
|
APN |
5 |
123,957,183 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02793:Kntc1
|
APN |
5 |
123,916,340 (GRCm39) |
splice site |
probably null |
|
IGL02809:Kntc1
|
APN |
5 |
123,914,645 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02860:Kntc1
|
APN |
5 |
123,907,936 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02875:Kntc1
|
APN |
5 |
123,916,340 (GRCm39) |
splice site |
probably null |
|
IGL02931:Kntc1
|
APN |
5 |
123,937,874 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03169:Kntc1
|
APN |
5 |
123,913,884 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03267:Kntc1
|
APN |
5 |
123,896,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Kntc1
|
UTSW |
5 |
123,927,201 (GRCm39) |
missense |
probably benign |
0.19 |
R0006:Kntc1
|
UTSW |
5 |
123,927,201 (GRCm39) |
missense |
probably benign |
0.19 |
R0017:Kntc1
|
UTSW |
5 |
123,919,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Kntc1
|
UTSW |
5 |
123,903,120 (GRCm39) |
splice site |
probably benign |
|
R0324:Kntc1
|
UTSW |
5 |
123,916,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R0580:Kntc1
|
UTSW |
5 |
123,941,732 (GRCm39) |
missense |
probably benign |
0.00 |
R0608:Kntc1
|
UTSW |
5 |
123,924,137 (GRCm39) |
missense |
probably damaging |
0.98 |
R0725:Kntc1
|
UTSW |
5 |
123,907,767 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0733:Kntc1
|
UTSW |
5 |
123,928,979 (GRCm39) |
missense |
probably null |
|
R0781:Kntc1
|
UTSW |
5 |
123,937,965 (GRCm39) |
splice site |
probably benign |
|
R0787:Kntc1
|
UTSW |
5 |
123,934,167 (GRCm39) |
missense |
probably benign |
|
R1250:Kntc1
|
UTSW |
5 |
123,922,262 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1253:Kntc1
|
UTSW |
5 |
123,948,925 (GRCm39) |
frame shift |
probably null |
|
R1467:Kntc1
|
UTSW |
5 |
123,925,047 (GRCm39) |
missense |
probably benign |
0.04 |
R1467:Kntc1
|
UTSW |
5 |
123,925,047 (GRCm39) |
missense |
probably benign |
0.04 |
R1481:Kntc1
|
UTSW |
5 |
123,916,338 (GRCm39) |
missense |
probably benign |
0.00 |
R1572:Kntc1
|
UTSW |
5 |
123,910,176 (GRCm39) |
missense |
probably damaging |
0.99 |
R1624:Kntc1
|
UTSW |
5 |
123,896,540 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1749:Kntc1
|
UTSW |
5 |
123,927,162 (GRCm39) |
missense |
probably benign |
0.00 |
R1993:Kntc1
|
UTSW |
5 |
123,948,874 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1993:Kntc1
|
UTSW |
5 |
123,897,162 (GRCm39) |
critical splice donor site |
probably null |
|
R2071:Kntc1
|
UTSW |
5 |
123,932,340 (GRCm39) |
splice site |
probably null |
|
R2237:Kntc1
|
UTSW |
5 |
123,941,733 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2239:Kntc1
|
UTSW |
5 |
123,941,733 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2366:Kntc1
|
UTSW |
5 |
123,919,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R2367:Kntc1
|
UTSW |
5 |
123,919,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R2382:Kntc1
|
UTSW |
5 |
123,898,411 (GRCm39) |
missense |
probably damaging |
0.99 |
R2389:Kntc1
|
UTSW |
5 |
123,919,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R2413:Kntc1
|
UTSW |
5 |
123,902,212 (GRCm39) |
missense |
probably benign |
0.01 |
R2442:Kntc1
|
UTSW |
5 |
123,948,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Kntc1
|
UTSW |
5 |
123,916,410 (GRCm39) |
nonsense |
probably null |
|
R2943:Kntc1
|
UTSW |
5 |
123,935,847 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3116:Kntc1
|
UTSW |
5 |
123,940,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R4107:Kntc1
|
UTSW |
5 |
123,900,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R4176:Kntc1
|
UTSW |
5 |
123,914,680 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4275:Kntc1
|
UTSW |
5 |
123,905,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R4440:Kntc1
|
UTSW |
5 |
123,932,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R4575:Kntc1
|
UTSW |
5 |
123,904,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Kntc1
|
UTSW |
5 |
123,904,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4578:Kntc1
|
UTSW |
5 |
123,904,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Kntc1
|
UTSW |
5 |
123,950,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R4704:Kntc1
|
UTSW |
5 |
123,949,496 (GRCm39) |
missense |
probably damaging |
0.96 |
R4720:Kntc1
|
UTSW |
5 |
123,903,086 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4784:Kntc1
|
UTSW |
5 |
123,954,825 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4785:Kntc1
|
UTSW |
5 |
123,954,825 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4824:Kntc1
|
UTSW |
5 |
123,928,196 (GRCm39) |
nonsense |
probably null |
|
R4847:Kntc1
|
UTSW |
5 |
123,940,337 (GRCm39) |
missense |
probably benign |
0.18 |
R4849:Kntc1
|
UTSW |
5 |
123,897,128 (GRCm39) |
missense |
probably benign |
0.02 |
R4904:Kntc1
|
UTSW |
5 |
123,916,396 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4922:Kntc1
|
UTSW |
5 |
123,940,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R5080:Kntc1
|
UTSW |
5 |
123,900,649 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5114:Kntc1
|
UTSW |
5 |
123,919,118 (GRCm39) |
critical splice donor site |
probably null |
|
R5171:Kntc1
|
UTSW |
5 |
123,937,907 (GRCm39) |
missense |
probably benign |
0.01 |
R5220:Kntc1
|
UTSW |
5 |
123,950,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R5226:Kntc1
|
UTSW |
5 |
123,932,235 (GRCm39) |
missense |
probably benign |
0.09 |
R5278:Kntc1
|
UTSW |
5 |
123,919,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R5329:Kntc1
|
UTSW |
5 |
123,902,254 (GRCm39) |
missense |
probably benign |
0.02 |
R5496:Kntc1
|
UTSW |
5 |
123,922,245 (GRCm39) |
missense |
probably benign |
0.00 |
R5503:Kntc1
|
UTSW |
5 |
123,957,939 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5633:Kntc1
|
UTSW |
5 |
123,957,120 (GRCm39) |
missense |
probably damaging |
0.99 |
R5638:Kntc1
|
UTSW |
5 |
123,956,538 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5697:Kntc1
|
UTSW |
5 |
123,903,070 (GRCm39) |
missense |
probably benign |
0.00 |
R5757:Kntc1
|
UTSW |
5 |
123,945,372 (GRCm39) |
critical splice donor site |
probably null |
|
R5773:Kntc1
|
UTSW |
5 |
123,932,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R5940:Kntc1
|
UTSW |
5 |
123,924,258 (GRCm39) |
missense |
probably benign |
0.05 |
R6019:Kntc1
|
UTSW |
5 |
123,900,579 (GRCm39) |
missense |
probably benign |
0.03 |
R6230:Kntc1
|
UTSW |
5 |
123,927,072 (GRCm39) |
splice site |
probably null |
|
R6437:Kntc1
|
UTSW |
5 |
123,907,754 (GRCm39) |
missense |
probably damaging |
0.98 |
R6888:Kntc1
|
UTSW |
5 |
123,949,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R6907:Kntc1
|
UTSW |
5 |
123,939,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R7123:Kntc1
|
UTSW |
5 |
123,919,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R7262:Kntc1
|
UTSW |
5 |
123,925,036 (GRCm39) |
missense |
probably benign |
0.18 |
R7381:Kntc1
|
UTSW |
5 |
123,948,971 (GRCm39) |
missense |
probably benign |
0.12 |
R7485:Kntc1
|
UTSW |
5 |
123,925,019 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7512:Kntc1
|
UTSW |
5 |
123,929,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R7581:Kntc1
|
UTSW |
5 |
123,954,818 (GRCm39) |
missense |
probably benign |
0.05 |
R7687:Kntc1
|
UTSW |
5 |
123,897,152 (GRCm39) |
missense |
probably benign |
0.01 |
R7798:Kntc1
|
UTSW |
5 |
123,957,180 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7798:Kntc1
|
UTSW |
5 |
123,924,357 (GRCm39) |
missense |
probably benign |
|
R7871:Kntc1
|
UTSW |
5 |
123,922,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R7876:Kntc1
|
UTSW |
5 |
123,913,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R7947:Kntc1
|
UTSW |
5 |
123,919,951 (GRCm39) |
missense |
unknown |
|
R7997:Kntc1
|
UTSW |
5 |
123,916,117 (GRCm39) |
missense |
probably damaging |
0.96 |
R8231:Kntc1
|
UTSW |
5 |
123,920,959 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8257:Kntc1
|
UTSW |
5 |
123,896,586 (GRCm39) |
critical splice donor site |
probably null |
|
R8345:Kntc1
|
UTSW |
5 |
123,924,993 (GRCm39) |
missense |
probably benign |
0.37 |
R8354:Kntc1
|
UTSW |
5 |
123,916,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R8732:Kntc1
|
UTSW |
5 |
123,928,180 (GRCm39) |
missense |
probably benign |
0.00 |
R8754:Kntc1
|
UTSW |
5 |
123,897,115 (GRCm39) |
missense |
probably benign |
0.01 |
R8947:Kntc1
|
UTSW |
5 |
123,925,041 (GRCm39) |
missense |
probably benign |
0.01 |
R9041:Kntc1
|
UTSW |
5 |
123,927,093 (GRCm39) |
missense |
probably benign |
0.00 |
R9182:Kntc1
|
UTSW |
5 |
123,940,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R9432:Kntc1
|
UTSW |
5 |
123,925,112 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9460:Kntc1
|
UTSW |
5 |
123,941,378 (GRCm39) |
nonsense |
probably null |
|
R9468:Kntc1
|
UTSW |
5 |
123,954,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R9643:Kntc1
|
UTSW |
5 |
123,949,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R9646:Kntc1
|
UTSW |
5 |
123,897,119 (GRCm39) |
missense |
probably benign |
0.01 |
R9721:Kntc1
|
UTSW |
5 |
123,939,948 (GRCm39) |
missense |
probably benign |
0.01 |
R9789:Kntc1
|
UTSW |
5 |
123,898,706 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0027:Kntc1
|
UTSW |
5 |
123,948,992 (GRCm39) |
missense |
probably benign |
0.00 |
X0065:Kntc1
|
UTSW |
5 |
123,916,100 (GRCm39) |
nonsense |
probably null |
|
X0067:Kntc1
|
UTSW |
5 |
123,916,137 (GRCm39) |
unclassified |
probably benign |
|
|