Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
A |
T |
7: 119,993,587 (GRCm39) |
K1269M |
possibly damaging |
Het |
Adgrl2 |
A |
T |
3: 148,564,585 (GRCm39) |
Y332N |
probably damaging |
Het |
Adgrv1 |
C |
T |
13: 81,627,777 (GRCm39) |
V3695I |
probably benign |
Het |
Aldh1l1 |
A |
T |
6: 90,575,257 (GRCm39) |
Y848F |
probably damaging |
Het |
Ambra1 |
T |
C |
2: 91,598,103 (GRCm39) |
V88A |
possibly damaging |
Het |
Ankrd12 |
C |
T |
17: 66,292,160 (GRCm39) |
R1091Q |
probably damaging |
Het |
Apob |
T |
G |
12: 8,055,087 (GRCm39) |
V1362G |
probably damaging |
Het |
Arhgap17 |
A |
G |
7: 122,905,661 (GRCm39) |
L328P |
probably damaging |
Het |
Arhgap27 |
A |
C |
11: 103,235,367 (GRCm39) |
V9G |
probably benign |
Het |
Arhgap33 |
A |
T |
7: 30,232,434 (GRCm39) |
D34E |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,873,259 (GRCm39) |
D14G |
probably benign |
Het |
Atf6b |
T |
C |
17: 34,872,703 (GRCm39) |
Y575H |
probably damaging |
Het |
Bcl2l2 |
T |
G |
14: 55,122,058 (GRCm39) |
S74A |
probably benign |
Het |
Begain |
T |
C |
12: 109,004,794 (GRCm39) |
T73A |
possibly damaging |
Het |
Bicdl1 |
C |
T |
5: 115,808,340 (GRCm39) |
R264Q |
probably damaging |
Het |
Ccdc180 |
A |
G |
4: 45,914,588 (GRCm39) |
D701G |
probably benign |
Het |
Cd200r4 |
G |
T |
16: 44,653,529 (GRCm39) |
V146L |
probably damaging |
Het |
Cd226 |
G |
A |
18: 89,265,322 (GRCm39) |
C200Y |
probably damaging |
Het |
Cdcp3 |
T |
C |
7: 130,879,352 (GRCm39) |
|
probably null |
Het |
Cdhr18 |
T |
C |
14: 13,866,032 (GRCm38) |
T286A |
|
Het |
Cdk12 |
A |
G |
11: 98,115,451 (GRCm39) |
N864S |
unknown |
Het |
Cfhr4 |
A |
T |
1: 139,680,788 (GRCm39) |
Y243* |
probably null |
Het |
Clcnkb |
A |
T |
4: 141,135,946 (GRCm39) |
L413Q |
probably damaging |
Het |
Cldn10 |
T |
C |
14: 119,099,255 (GRCm39) |
V123A |
possibly damaging |
Het |
Cnn1 |
T |
A |
9: 22,017,078 (GRCm39) |
|
probably null |
Het |
Cpa5 |
C |
A |
6: 30,630,829 (GRCm39) |
Q364K |
probably benign |
Het |
Cstdc5 |
T |
C |
16: 36,187,809 (GRCm39) |
I19V |
probably benign |
Het |
Ddx11 |
A |
G |
17: 66,437,766 (GRCm39) |
E164G |
probably benign |
Het |
Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
Drc7 |
T |
A |
8: 95,804,549 (GRCm39) |
Y855N |
probably damaging |
Het |
Fam20b |
C |
A |
1: 156,529,968 (GRCm39) |
|
probably null |
Het |
Fip1l1 |
T |
A |
5: 74,748,736 (GRCm39) |
|
probably null |
Het |
Flt4 |
A |
G |
11: 49,525,125 (GRCm39) |
D657G |
probably null |
Het |
Fmo3 |
T |
A |
1: 162,781,857 (GRCm39) |
T499S |
possibly damaging |
Het |
Fyco1 |
C |
T |
9: 123,651,491 (GRCm39) |
G1190S |
probably benign |
Het |
Galnt17 |
C |
A |
5: 131,335,590 (GRCm39) |
|
probably benign |
Het |
Ggcx |
T |
C |
6: 72,404,987 (GRCm39) |
I465T |
probably damaging |
Het |
Gm7361 |
T |
A |
5: 26,466,116 (GRCm39) |
N159K |
probably damaging |
Het |
Golgb1 |
A |
G |
16: 36,695,663 (GRCm39) |
N54S |
unknown |
Het |
Grin2c |
G |
A |
11: 115,141,876 (GRCm39) |
P848S |
probably damaging |
Het |
Grina |
T |
C |
15: 76,133,287 (GRCm39) |
V285A |
probably damaging |
Het |
Gtpbp6 |
A |
G |
5: 110,252,478 (GRCm39) |
L381P |
probably damaging |
Het |
Herc2 |
G |
T |
7: 55,832,388 (GRCm39) |
G3028V |
probably damaging |
Het |
Ibsp |
A |
T |
5: 104,458,297 (GRCm39) |
Y278F |
probably damaging |
Het |
Ints4 |
T |
A |
7: 97,184,433 (GRCm39) |
L846* |
probably null |
Het |
Kif17 |
A |
G |
4: 138,021,077 (GRCm39) |
K849E |
probably benign |
Het |
Krt77 |
G |
A |
15: 101,777,806 (GRCm39) |
P83L |
probably benign |
Het |
Ky |
T |
G |
9: 102,419,491 (GRCm39) |
D499E |
probably damaging |
Het |
Lrp3 |
A |
T |
7: 34,902,051 (GRCm39) |
M610K |
probably damaging |
Het |
Lrrfip1 |
T |
A |
1: 91,019,338 (GRCm39) |
D156E |
probably benign |
Het |
Map6 |
C |
A |
7: 98,918,257 (GRCm39) |
H343Q |
probably benign |
Het |
Micu2 |
G |
T |
14: 58,191,606 (GRCm39) |
D148E |
probably benign |
Het |
Mks1 |
T |
A |
11: 87,747,428 (GRCm39) |
S153T |
probably benign |
Het |
Msantd5f3 |
A |
G |
4: 73,573,157 (GRCm39) |
Y132C |
probably damaging |
Het |
Muc6 |
AGGCGCAGAAACCCTGGC |
AGGC |
7: 141,214,363 (GRCm39) |
|
probably null |
Het |
Myh9 |
T |
C |
15: 77,667,672 (GRCm39) |
K587R |
probably benign |
Het |
Neb |
T |
C |
2: 52,086,368 (GRCm39) |
Y5478C |
probably damaging |
Het |
Nelfe |
G |
A |
17: 35,069,912 (GRCm39) |
|
probably null |
Het |
Nps |
T |
A |
7: 134,870,510 (GRCm39) |
L11I |
probably damaging |
Het |
Nsd1 |
A |
T |
13: 55,394,283 (GRCm39) |
D731V |
probably damaging |
Het |
Nup50 |
A |
G |
15: 84,817,859 (GRCm39) |
T93A |
probably benign |
Het |
Oprd1 |
A |
G |
4: 131,841,112 (GRCm39) |
I282T |
probably damaging |
Het |
Or4c103 |
T |
C |
2: 88,513,767 (GRCm39) |
H103R |
possibly damaging |
Het |
Or5p50 |
T |
C |
7: 107,421,782 (GRCm39) |
N298S |
probably benign |
Het |
Or6b3 |
A |
T |
1: 92,439,573 (GRCm39) |
M59K |
probably benign |
Het |
Or6d12 |
A |
G |
6: 116,492,936 (GRCm39) |
Y66C |
probably damaging |
Het |
Osbp2 |
T |
C |
11: 3,662,134 (GRCm39) |
I240V |
probably damaging |
Het |
Otub2 |
C |
A |
12: 103,359,163 (GRCm39) |
P84Q |
probably benign |
Het |
Parp9 |
A |
T |
16: 35,777,360 (GRCm39) |
I435F |
probably benign |
Het |
Pcdh18 |
C |
T |
3: 49,709,923 (GRCm39) |
R464H |
probably benign |
Het |
Pcsk6 |
G |
T |
7: 65,675,156 (GRCm39) |
|
probably null |
Het |
Ptgs2 |
G |
A |
1: 149,978,512 (GRCm39) |
R208Q |
probably benign |
Het |
Rab11b |
G |
A |
17: 33,968,841 (GRCm39) |
R51C |
probably damaging |
Het |
Rad1 |
A |
G |
15: 10,493,343 (GRCm39) |
I257V |
probably benign |
Het |
Rbms3 |
C |
T |
9: 116,415,085 (GRCm39) |
|
probably null |
Het |
Rxfp2 |
A |
T |
5: 149,983,364 (GRCm39) |
I300L |
probably benign |
Het |
Rxfp2 |
C |
A |
5: 149,983,368 (GRCm39) |
T301K |
probably benign |
Het |
Sars2 |
G |
T |
7: 28,443,733 (GRCm39) |
A112S |
probably benign |
Het |
Scn10a |
T |
C |
9: 119,442,616 (GRCm39) |
D1543G |
probably damaging |
Het |
Serpinb1b |
A |
G |
13: 33,271,406 (GRCm39) |
H59R |
probably benign |
Het |
Sgsm2 |
T |
A |
11: 74,745,319 (GRCm39) |
D661V |
possibly damaging |
Het |
Smad6 |
C |
A |
9: 63,927,688 (GRCm39) |
V207L |
probably damaging |
Het |
Son |
TCCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCAGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
TCCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,457,183 (GRCm39) |
|
probably benign |
Het |
Spata31h1 |
A |
T |
10: 82,125,161 (GRCm39) |
D2616E |
probably benign |
Het |
Tenm2 |
C |
T |
11: 35,939,956 (GRCm39) |
R1390Q |
probably damaging |
Het |
Tmem132a |
T |
A |
19: 10,844,295 (GRCm39) |
Q101L |
probably damaging |
Het |
Tmem151a |
A |
G |
19: 5,132,801 (GRCm39) |
V135A |
probably damaging |
Het |
Trappc10 |
T |
C |
10: 78,046,262 (GRCm39) |
K443E |
probably damaging |
Het |
Trrap |
A |
T |
5: 144,779,517 (GRCm39) |
N3161I |
possibly damaging |
Het |
Tspan32 |
G |
T |
7: 142,558,863 (GRCm39) |
R6L |
possibly damaging |
Het |
Tut7 |
C |
G |
13: 59,936,364 (GRCm39) |
D1246H |
probably damaging |
Het |
Ugt2a2 |
T |
C |
5: 87,608,468 (GRCm39) |
D457G |
possibly damaging |
Het |
Ulk2 |
A |
T |
11: 61,725,657 (GRCm39) |
S140T |
possibly damaging |
Het |
Upf1 |
C |
T |
8: 70,792,695 (GRCm39) |
A338T |
possibly damaging |
Het |
Usp43 |
C |
T |
11: 67,774,110 (GRCm39) |
R460Q |
probably null |
Het |
Uxs1 |
A |
G |
1: 43,856,118 (GRCm39) |
|
probably benign |
Het |
Vmn1r59 |
A |
G |
7: 5,457,725 (GRCm39) |
C12R |
probably damaging |
Het |
Wdr64 |
A |
G |
1: 175,617,499 (GRCm39) |
D693G |
probably benign |
Het |
Wnk1 |
A |
T |
6: 119,920,839 (GRCm39) |
|
probably null |
Het |
Wnt2 |
G |
T |
6: 18,028,046 (GRCm39) |
R63S |
probably benign |
Het |
Zfp418 |
A |
T |
7: 7,184,562 (GRCm39) |
Q175L |
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 |
R0538:Nup98
|
UTSW |
7 |
101,835,892 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|