Other mutations in this stock |
Total: 129 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578I07Rik |
A |
T |
14: 67,175,823 (GRCm39) |
H6L |
unknown |
Het |
Abca13 |
G |
A |
11: 9,217,622 (GRCm39) |
|
probably null |
Het |
Acad12 |
C |
T |
5: 121,745,511 (GRCm39) |
R260Q |
possibly damaging |
Het |
Actn1 |
G |
A |
12: 80,306,874 (GRCm39) |
|
probably benign |
Het |
Acvrl1 |
A |
G |
15: 101,034,030 (GRCm39) |
T182A |
probably damaging |
Het |
Adam23 |
T |
C |
1: 63,607,003 (GRCm39) |
|
probably benign |
Het |
Adamtsl1 |
A |
T |
4: 86,261,358 (GRCm39) |
T1190S |
probably benign |
Het |
Adh6b |
A |
T |
3: 138,063,411 (GRCm39) |
Y330F |
probably benign |
Het |
Ak7 |
A |
G |
12: 105,732,876 (GRCm39) |
E540G |
probably damaging |
Het |
Akr1c19 |
T |
A |
13: 4,287,099 (GRCm39) |
L106Q |
probably damaging |
Het |
Ankrd12 |
A |
T |
17: 66,356,847 (GRCm39) |
S57T |
probably damaging |
Het |
Aoc3 |
G |
A |
11: 101,222,964 (GRCm39) |
R400Q |
possibly damaging |
Het |
Arel1 |
A |
T |
12: 84,988,611 (GRCm39) |
I46N |
probably damaging |
Het |
Armc5 |
A |
G |
7: 127,843,463 (GRCm39) |
D752G |
probably damaging |
Het |
Atp11b |
T |
C |
3: 35,891,163 (GRCm39) |
V812A |
probably damaging |
Het |
Axin1 |
A |
G |
17: 26,403,215 (GRCm39) |
H131R |
possibly damaging |
Het |
Bpifb3 |
A |
G |
2: 153,765,789 (GRCm39) |
E184G |
probably benign |
Het |
Cacna2d2 |
T |
C |
9: 107,401,582 (GRCm39) |
|
probably benign |
Het |
Catsperd |
T |
C |
17: 56,969,828 (GRCm39) |
F641L |
probably benign |
Het |
Ccdc83 |
A |
C |
7: 89,877,591 (GRCm39) |
L284V |
probably damaging |
Het |
Ccn2 |
T |
A |
10: 24,472,364 (GRCm39) |
C136S |
probably damaging |
Het |
Ccnt2 |
T |
A |
1: 127,730,902 (GRCm39) |
V593E |
probably damaging |
Het |
Cd53 |
T |
A |
3: 106,669,444 (GRCm39) |
I185F |
probably benign |
Het |
Cep350 |
A |
T |
1: 155,724,366 (GRCm39) |
D3077E |
possibly damaging |
Het |
Ces1h |
C |
A |
8: 94,083,628 (GRCm39) |
|
probably null |
Het |
Chrna3 |
T |
A |
9: 54,923,290 (GRCm39) |
T173S |
probably benign |
Het |
Clca4b |
T |
C |
3: 144,627,717 (GRCm39) |
D418G |
probably benign |
Het |
Col11a2 |
T |
C |
17: 34,270,302 (GRCm39) |
|
probably benign |
Het |
Coq2 |
T |
A |
5: 100,815,889 (GRCm39) |
I97F |
possibly damaging |
Het |
Cr2 |
A |
G |
1: 194,842,667 (GRCm39) |
|
probably benign |
Het |
D2hgdh |
A |
G |
1: 93,754,099 (GRCm39) |
Y24C |
probably damaging |
Het |
D630045J12Rik |
G |
A |
6: 38,168,628 (GRCm39) |
R974C |
probably damaging |
Het |
Dach1 |
A |
G |
14: 98,140,715 (GRCm39) |
V429A |
possibly damaging |
Het |
Ddr1 |
G |
A |
17: 35,995,899 (GRCm39) |
T660I |
probably damaging |
Het |
Dlg1 |
A |
C |
16: 31,615,682 (GRCm39) |
|
probably null |
Het |
Dmbt1 |
T |
C |
7: 130,651,631 (GRCm39) |
|
probably benign |
Het |
Dmxl2 |
A |
T |
9: 54,301,120 (GRCm39) |
D2330E |
probably benign |
Het |
Dnai4 |
T |
C |
4: 102,953,815 (GRCm39) |
N128S |
possibly damaging |
Het |
Doc2a |
A |
G |
7: 126,447,983 (GRCm39) |
T5A |
probably benign |
Het |
Dock2 |
G |
A |
11: 34,595,545 (GRCm39) |
|
probably benign |
Het |
Dok4 |
T |
A |
8: 95,591,866 (GRCm39) |
Y290F |
probably damaging |
Het |
Dop1a |
A |
G |
9: 86,367,550 (GRCm39) |
D11G |
probably damaging |
Het |
E230025N22Rik |
T |
C |
18: 36,821,987 (GRCm39) |
H235R |
probably benign |
Het |
Ear6 |
A |
G |
14: 52,091,909 (GRCm39) |
D152G |
probably damaging |
Het |
Ecscr |
T |
A |
18: 35,846,689 (GRCm39) |
|
probably benign |
Het |
Eml6 |
A |
T |
11: 29,710,010 (GRCm39) |
|
probably benign |
Het |
Epha4 |
T |
A |
1: 77,365,178 (GRCm39) |
Q607L |
probably damaging |
Het |
Exoc4 |
A |
G |
6: 33,948,998 (GRCm39) |
N947S |
probably benign |
Het |
Flg |
A |
G |
3: 93,186,767 (GRCm39) |
E73G |
probably damaging |
Het |
Fndc1 |
C |
T |
17: 8,003,173 (GRCm39) |
|
probably benign |
Het |
Gad1-ps |
T |
C |
10: 99,280,854 (GRCm39) |
|
noncoding transcript |
Het |
Gata6 |
A |
G |
18: 11,064,771 (GRCm39) |
T528A |
probably benign |
Het |
Gjd4 |
T |
C |
18: 9,280,244 (GRCm39) |
E278G |
probably benign |
Het |
Gm20091 |
T |
A |
10: 96,244,864 (GRCm39) |
|
noncoding transcript |
Het |
Gnb3 |
G |
A |
6: 124,812,659 (GRCm39) |
Q266* |
probably null |
Het |
Grm3 |
A |
G |
5: 9,562,446 (GRCm39) |
V468A |
possibly damaging |
Het |
Igf1r |
C |
T |
7: 67,857,574 (GRCm39) |
R1085C |
probably damaging |
Het |
Igsf10 |
T |
C |
3: 59,227,527 (GRCm39) |
T2049A |
probably damaging |
Het |
Jak3 |
A |
T |
8: 72,138,126 (GRCm39) |
D859V |
probably benign |
Het |
Kcnb2 |
G |
T |
1: 15,783,108 (GRCm39) |
|
probably benign |
Het |
Kcnh3 |
G |
A |
15: 99,138,839 (GRCm39) |
G858D |
probably benign |
Het |
Kif1a |
C |
A |
1: 92,971,360 (GRCm39) |
R1006L |
probably damaging |
Het |
Klhl23 |
C |
T |
2: 69,654,757 (GRCm39) |
A209V |
probably benign |
Het |
Mapk13 |
T |
C |
17: 28,994,229 (GRCm39) |
Y104H |
probably damaging |
Het |
Mbd4 |
A |
G |
6: 115,826,443 (GRCm39) |
S183P |
probably damaging |
Het |
Mga |
T |
C |
2: 119,750,187 (GRCm39) |
|
probably null |
Het |
Mipol1 |
G |
A |
12: 57,461,197 (GRCm39) |
|
probably null |
Het |
Mmp14 |
A |
G |
14: 54,676,166 (GRCm39) |
T299A |
possibly damaging |
Het |
Mmrn1 |
A |
G |
6: 60,953,453 (GRCm39) |
E578G |
probably benign |
Het |
Mov10l1 |
G |
A |
15: 88,879,063 (GRCm39) |
C193Y |
possibly damaging |
Het |
Mppe1 |
A |
G |
18: 67,370,548 (GRCm39) |
C50R |
probably damaging |
Het |
Msantd1 |
C |
A |
5: 35,075,069 (GRCm39) |
R44S |
probably damaging |
Het |
Myt1l |
T |
C |
12: 29,892,570 (GRCm39) |
V69A |
possibly damaging |
Het |
Nav1 |
A |
T |
1: 135,392,430 (GRCm39) |
|
probably benign |
Het |
Ncan |
A |
G |
8: 70,561,252 (GRCm39) |
S572P |
possibly damaging |
Het |
Nck2 |
T |
C |
1: 43,608,304 (GRCm39) |
|
probably benign |
Het |
Nemf |
A |
T |
12: 69,403,088 (GRCm39) |
D31E |
probably damaging |
Het |
Nlrp12 |
T |
C |
7: 3,297,892 (GRCm39) |
D93G |
possibly damaging |
Het |
Nsmaf |
A |
T |
4: 6,419,930 (GRCm39) |
|
probably null |
Het |
Oog2 |
C |
A |
4: 143,922,654 (GRCm39) |
Y306* |
probably null |
Het |
Or13a18 |
A |
T |
7: 140,190,297 (GRCm39) |
N73Y |
probably damaging |
Het |
Or6ae1 |
A |
T |
7: 139,742,144 (GRCm39) |
S240T |
probably damaging |
Het |
Or6b2b |
A |
T |
1: 92,419,055 (GRCm39) |
C141S |
possibly damaging |
Het |
Osmr |
A |
G |
15: 6,871,419 (GRCm39) |
|
probably benign |
Het |
P2rx6 |
A |
G |
16: 17,386,162 (GRCm39) |
N275S |
probably benign |
Het |
Pbxip1 |
G |
T |
3: 89,354,926 (GRCm39) |
G482W |
possibly damaging |
Het |
Pcsk4 |
T |
G |
10: 80,161,168 (GRCm39) |
I249L |
probably damaging |
Het |
Pou4f2 |
C |
T |
8: 79,162,291 (GRCm39) |
G104E |
probably damaging |
Het |
Pramel28 |
T |
A |
4: 143,691,653 (GRCm39) |
T357S |
possibly damaging |
Het |
Prkdc |
G |
T |
16: 15,651,652 (GRCm39) |
R3763L |
probably damaging |
Het |
Ptpre |
A |
T |
7: 135,265,044 (GRCm39) |
I207F |
probably damaging |
Het |
Rapgef3 |
A |
T |
15: 97,655,698 (GRCm39) |
|
probably benign |
Het |
Rasgrp1 |
T |
G |
2: 117,115,428 (GRCm39) |
K685T |
probably benign |
Het |
Rnf148 |
C |
T |
6: 23,654,237 (GRCm39) |
R253Q |
probably damaging |
Het |
Rock1 |
T |
C |
18: 10,132,227 (GRCm39) |
I241V |
possibly damaging |
Het |
Rp1l1 |
T |
G |
14: 64,259,541 (GRCm39) |
V61G |
probably damaging |
Het |
Scin |
A |
C |
12: 40,131,770 (GRCm39) |
S255A |
probably damaging |
Het |
Scn8a |
A |
T |
15: 100,933,505 (GRCm39) |
K1570* |
probably null |
Het |
Sec14l4 |
A |
C |
11: 3,990,018 (GRCm39) |
M106L |
probably benign |
Het |
Sec63 |
G |
A |
10: 42,674,795 (GRCm39) |
R226H |
probably benign |
Het |
Septin2 |
T |
A |
1: 93,429,345 (GRCm39) |
N271K |
probably damaging |
Het |
Serac1 |
G |
T |
17: 6,099,101 (GRCm39) |
|
probably benign |
Het |
Shc2 |
T |
A |
10: 79,465,974 (GRCm39) |
|
probably benign |
Het |
Sipa1l1 |
T |
A |
12: 82,471,873 (GRCm39) |
D1284E |
probably benign |
Het |
Slc11a2 |
A |
G |
15: 100,306,097 (GRCm39) |
L105P |
probably damaging |
Het |
Slc1a3 |
T |
A |
15: 8,680,406 (GRCm39) |
T151S |
probably benign |
Het |
Smarca2 |
G |
T |
19: 26,668,762 (GRCm39) |
K920N |
probably damaging |
Het |
Sugp2 |
G |
A |
8: 70,711,598 (GRCm39) |
E964K |
probably damaging |
Het |
Tas2r122 |
A |
C |
6: 132,688,778 (GRCm39) |
N38K |
probably benign |
Het |
Tecpr1 |
G |
A |
5: 144,143,092 (GRCm39) |
R730C |
probably damaging |
Het |
Tent2 |
A |
T |
13: 93,312,123 (GRCm39) |
|
probably benign |
Het |
Themis3 |
G |
T |
17: 66,900,265 (GRCm39) |
N34K |
possibly damaging |
Het |
Traf3ip1 |
A |
G |
1: 91,427,341 (GRCm39) |
T104A |
unknown |
Het |
Trappc11 |
A |
G |
8: 47,956,447 (GRCm39) |
V843A |
probably benign |
Het |
Trmt61a |
T |
A |
12: 111,645,361 (GRCm39) |
L99Q |
probably damaging |
Het |
Trp53tg5 |
T |
A |
2: 164,313,401 (GRCm39) |
K91N |
probably damaging |
Het |
Ufsp2 |
T |
C |
8: 46,445,187 (GRCm39) |
S339P |
probably damaging |
Het |
Usp20 |
T |
A |
2: 30,894,462 (GRCm39) |
V126E |
probably damaging |
Het |
Vmn1r75 |
T |
A |
7: 11,614,797 (GRCm39) |
N176K |
probably damaging |
Het |
Vmn2r24 |
A |
G |
6: 123,793,012 (GRCm39) |
S780G |
probably benign |
Het |
Vmn2r89 |
A |
G |
14: 51,695,048 (GRCm39) |
|
probably null |
Het |
Vps13d |
A |
T |
4: 144,771,665 (GRCm39) |
S4038T |
probably damaging |
Het |
Vwa7 |
A |
G |
17: 35,241,627 (GRCm39) |
T421A |
probably damaging |
Het |
Wdr95 |
C |
A |
5: 149,504,271 (GRCm39) |
L332I |
probably damaging |
Het |
Wrn |
T |
A |
8: 33,826,119 (GRCm39) |
K181I |
probably damaging |
Het |
Zc3h6 |
T |
A |
2: 128,859,143 (GRCm39) |
I1058N |
possibly damaging |
Het |
Zfp423 |
T |
A |
8: 88,508,713 (GRCm39) |
I544F |
probably damaging |
Het |
Zfp446 |
T |
A |
7: 12,713,516 (GRCm39) |
S161T |
possibly damaging |
Het |
Zmym6 |
T |
A |
4: 127,017,162 (GRCm39) |
M889K |
probably benign |
Het |
|
Other mutations in Nup98 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00662:Nup98
|
APN |
7 |
101,844,194 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00789:Nup98
|
APN |
7 |
101,803,178 (GRCm39) |
missense |
probably benign |
|
IGL00798:Nup98
|
APN |
7 |
101,796,411 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01562:Nup98
|
APN |
7 |
101,835,125 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01942:Nup98
|
APN |
7 |
101,843,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02109:Nup98
|
APN |
7 |
101,832,693 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02490:Nup98
|
APN |
7 |
101,801,573 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03184:Nup98
|
APN |
7 |
101,832,752 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4519001:Nup98
|
UTSW |
7 |
101,784,171 (GRCm39) |
missense |
probably benign |
0.00 |
R0040:Nup98
|
UTSW |
7 |
101,841,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R0133:Nup98
|
UTSW |
7 |
101,788,859 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0309:Nup98
|
UTSW |
7 |
101,801,635 (GRCm39) |
missense |
probably null |
|
R0471:Nup98
|
UTSW |
7 |
101,788,004 (GRCm39) |
missense |
probably benign |
0.13 |
R0650:Nup98
|
UTSW |
7 |
101,801,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R0881:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R0900:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1120:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1159:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Nup98
|
UTSW |
7 |
101,788,008 (GRCm39) |
missense |
probably benign |
0.00 |
R1469:Nup98
|
UTSW |
7 |
101,788,008 (GRCm39) |
missense |
probably benign |
0.00 |
R1470:Nup98
|
UTSW |
7 |
101,796,513 (GRCm39) |
missense |
probably damaging |
0.98 |
R1470:Nup98
|
UTSW |
7 |
101,796,513 (GRCm39) |
missense |
probably damaging |
0.98 |
R1545:Nup98
|
UTSW |
7 |
101,784,087 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1775:Nup98
|
UTSW |
7 |
101,784,144 (GRCm39) |
missense |
probably benign |
0.03 |
R1889:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Nup98
|
UTSW |
7 |
101,829,631 (GRCm39) |
missense |
probably damaging |
0.96 |
R3423:Nup98
|
UTSW |
7 |
101,834,084 (GRCm39) |
missense |
probably benign |
0.03 |
R4361:Nup98
|
UTSW |
7 |
101,794,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Nup98
|
UTSW |
7 |
101,834,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Nup98
|
UTSW |
7 |
101,802,403 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4910:Nup98
|
UTSW |
7 |
101,845,007 (GRCm39) |
missense |
unknown |
|
R4924:Nup98
|
UTSW |
7 |
101,784,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Nup98
|
UTSW |
7 |
101,794,862 (GRCm39) |
missense |
probably benign |
0.00 |
R5069:Nup98
|
UTSW |
7 |
101,794,862 (GRCm39) |
missense |
probably benign |
0.00 |
R5233:Nup98
|
UTSW |
7 |
101,845,029 (GRCm39) |
missense |
unknown |
|
R5779:Nup98
|
UTSW |
7 |
101,801,568 (GRCm39) |
missense |
probably benign |
|
R5922:Nup98
|
UTSW |
7 |
101,803,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R6010:Nup98
|
UTSW |
7 |
101,829,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Nup98
|
UTSW |
7 |
101,784,002 (GRCm39) |
missense |
probably benign |
|
R6039:Nup98
|
UTSW |
7 |
101,784,002 (GRCm39) |
missense |
probably benign |
|
R6343:Nup98
|
UTSW |
7 |
101,843,957 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6364:Nup98
|
UTSW |
7 |
101,825,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R6462:Nup98
|
UTSW |
7 |
101,844,223 (GRCm39) |
missense |
probably benign |
0.03 |
R6577:Nup98
|
UTSW |
7 |
101,778,053 (GRCm39) |
splice site |
probably null |
|
R6900:Nup98
|
UTSW |
7 |
101,835,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R7205:Nup98
|
UTSW |
7 |
101,844,248 (GRCm39) |
missense |
unknown |
|
R7218:Nup98
|
UTSW |
7 |
101,841,107 (GRCm39) |
splice site |
probably null |
|
R7235:Nup98
|
UTSW |
7 |
101,774,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7307:Nup98
|
UTSW |
7 |
101,784,002 (GRCm39) |
missense |
probably benign |
|
R7402:Nup98
|
UTSW |
7 |
101,784,144 (GRCm39) |
missense |
probably benign |
0.00 |
R7427:Nup98
|
UTSW |
7 |
101,784,208 (GRCm39) |
splice site |
probably null |
|
R7428:Nup98
|
UTSW |
7 |
101,784,208 (GRCm39) |
splice site |
probably null |
|
R7584:Nup98
|
UTSW |
7 |
101,825,596 (GRCm39) |
missense |
probably benign |
0.02 |
R7646:Nup98
|
UTSW |
7 |
101,803,242 (GRCm39) |
missense |
probably benign |
0.01 |
R7648:Nup98
|
UTSW |
7 |
101,773,404 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7742:Nup98
|
UTSW |
7 |
101,802,464 (GRCm39) |
splice site |
probably null |
|
R7827:Nup98
|
UTSW |
7 |
101,773,569 (GRCm39) |
missense |
probably benign |
0.10 |
R7884:Nup98
|
UTSW |
7 |
101,825,556 (GRCm39) |
missense |
probably benign |
0.12 |
R7943:Nup98
|
UTSW |
7 |
101,844,029 (GRCm39) |
missense |
probably benign |
0.10 |
R8034:Nup98
|
UTSW |
7 |
101,794,930 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8952:Nup98
|
UTSW |
7 |
101,835,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R9060:Nup98
|
UTSW |
7 |
101,783,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R9099:Nup98
|
UTSW |
7 |
101,844,173 (GRCm39) |
missense |
probably damaging |
0.98 |
R9146:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9148:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9223:Nup98
|
UTSW |
7 |
101,834,167 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9246:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9249:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9272:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9274:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9283:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9326:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9466:Nup98
|
UTSW |
7 |
101,818,611 (GRCm39) |
missense |
probably benign |
0.05 |
R9492:Nup98
|
UTSW |
7 |
101,778,252 (GRCm39) |
missense |
probably benign |
0.11 |
R9661:Nup98
|
UTSW |
7 |
101,782,019 (GRCm39) |
nonsense |
probably null |
|
T0970:Nup98
|
UTSW |
7 |
101,835,959 (GRCm39) |
unclassified |
probably benign |
|
X0054:Nup98
|
UTSW |
7 |
101,796,415 (GRCm39) |
missense |
probably damaging |
1.00 |
|