Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp7 |
G |
A |
7: 28,310,553 (GRCm39) |
|
probably benign |
Het |
Adcyap1r1 |
G |
T |
6: 55,452,508 (GRCm39) |
|
probably benign |
Het |
Ankrd6 |
T |
C |
4: 32,836,424 (GRCm39) |
T44A |
probably damaging |
Het |
Ano7 |
A |
G |
1: 93,316,380 (GRCm39) |
D221G |
probably benign |
Het |
Bhlhe40 |
C |
A |
6: 108,641,711 (GRCm39) |
N218K |
probably damaging |
Het |
Bms1 |
A |
G |
6: 118,382,251 (GRCm39) |
V429A |
probably benign |
Het |
C7 |
T |
A |
15: 5,018,444 (GRCm39) |
T800S |
probably benign |
Het |
Camta2 |
G |
A |
11: 70,574,136 (GRCm39) |
T127I |
probably damaging |
Het |
Ccdc13 |
T |
A |
9: 121,627,282 (GRCm39) |
N665I |
probably damaging |
Het |
Ccdc157 |
T |
C |
11: 4,096,663 (GRCm39) |
E362G |
probably damaging |
Het |
Ccdc73 |
T |
A |
2: 104,811,352 (GRCm39) |
N310K |
probably damaging |
Het |
Cfap91 |
T |
A |
16: 38,118,659 (GRCm39) |
|
probably null |
Het |
Cmklr1 |
A |
T |
5: 113,752,578 (GRCm39) |
L141H |
probably damaging |
Het |
Cnst |
C |
A |
1: 179,407,100 (GRCm39) |
A49E |
probably benign |
Het |
Col5a3 |
C |
T |
9: 20,683,762 (GRCm39) |
R1498Q |
unknown |
Het |
Crybb3 |
T |
A |
5: 113,223,819 (GRCm39) |
I197F |
probably damaging |
Het |
Cryzl1 |
G |
A |
16: 91,504,155 (GRCm39) |
P97S |
probably benign |
Het |
Cubn |
T |
C |
2: 13,315,318 (GRCm39) |
|
probably benign |
Het |
Cyp2d37-ps |
T |
C |
15: 82,574,253 (GRCm39) |
|
noncoding transcript |
Het |
Cyp4a12b |
C |
A |
4: 115,290,117 (GRCm39) |
N223K |
probably benign |
Het |
D16Ertd472e |
A |
T |
16: 78,344,773 (GRCm39) |
C112S |
probably benign |
Het |
Dennd2a |
T |
C |
6: 39,485,233 (GRCm39) |
T349A |
probably benign |
Het |
Dock5 |
G |
A |
14: 68,060,129 (GRCm39) |
|
probably benign |
Het |
Dpp6 |
T |
C |
5: 27,857,267 (GRCm39) |
L404P |
probably damaging |
Het |
Dsc3 |
T |
A |
18: 20,104,639 (GRCm39) |
T563S |
possibly damaging |
Het |
Dync2h1 |
T |
A |
9: 7,113,182 (GRCm39) |
E214D |
possibly damaging |
Het |
Elac2 |
A |
G |
11: 64,870,136 (GRCm39) |
Y67C |
probably damaging |
Het |
Elmo1 |
A |
T |
13: 20,748,663 (GRCm39) |
K503* |
probably null |
Het |
Eng |
T |
C |
2: 32,569,149 (GRCm39) |
S559P |
probably benign |
Het |
Epc2 |
T |
A |
2: 49,427,145 (GRCm39) |
V563E |
possibly damaging |
Het |
Fancm |
A |
G |
12: 65,122,724 (GRCm39) |
Y82C |
probably damaging |
Het |
Flt4 |
A |
T |
11: 49,527,818 (GRCm39) |
M924L |
probably benign |
Het |
Gabpa |
T |
A |
16: 84,654,275 (GRCm39) |
N317K |
possibly damaging |
Het |
Gchfr |
T |
G |
2: 118,998,327 (GRCm39) |
Y3* |
probably null |
Het |
Gli3 |
G |
T |
13: 15,899,349 (GRCm39) |
G912V |
probably benign |
Het |
Gm10295 |
C |
A |
7: 71,000,361 (GRCm39) |
C73F |
unknown |
Het |
Gm10382 |
G |
T |
5: 125,466,728 (GRCm39) |
|
probably benign |
Het |
Gp1ba |
T |
C |
11: 70,531,284 (GRCm39) |
|
probably benign |
Het |
Gpr146 |
G |
A |
5: 139,364,933 (GRCm39) |
|
probably benign |
Het |
Hexd |
T |
A |
11: 121,102,969 (GRCm39) |
H62Q |
probably benign |
Het |
Hgd |
T |
A |
16: 37,431,546 (GRCm39) |
|
probably benign |
Het |
Hs6st1 |
G |
A |
1: 36,108,266 (GRCm39) |
|
probably null |
Het |
Icam4 |
A |
G |
9: 20,941,117 (GRCm39) |
Y123C |
probably damaging |
Het |
Il24 |
A |
G |
1: 130,811,674 (GRCm39) |
V134A |
probably damaging |
Het |
Iqcb1 |
G |
T |
16: 36,692,670 (GRCm39) |
A562S |
probably damaging |
Het |
Iqgap2 |
A |
C |
13: 95,867,783 (GRCm39) |
|
probably benign |
Het |
Islr2 |
T |
C |
9: 58,107,027 (GRCm39) |
T78A |
possibly damaging |
Het |
Kif1b |
A |
G |
4: 149,347,186 (GRCm39) |
I330T |
probably damaging |
Het |
Kirrel1 |
T |
C |
3: 86,997,106 (GRCm39) |
Y287C |
probably damaging |
Het |
Klf10 |
C |
T |
15: 38,297,090 (GRCm39) |
V317M |
probably benign |
Het |
Klhl9 |
T |
G |
4: 88,638,527 (GRCm39) |
K571N |
probably benign |
Het |
Lin37 |
T |
C |
7: 30,256,438 (GRCm39) |
I97V |
possibly damaging |
Het |
Lrrc37a |
C |
T |
11: 103,391,466 (GRCm39) |
V1320I |
possibly damaging |
Het |
Lrrc74a |
A |
G |
12: 86,784,569 (GRCm39) |
H99R |
probably damaging |
Het |
Me3 |
T |
A |
7: 89,435,622 (GRCm39) |
|
probably null |
Het |
Med13 |
T |
C |
11: 86,219,987 (GRCm39) |
|
probably benign |
Het |
Myh6 |
A |
T |
14: 55,185,804 (GRCm39) |
Y1490* |
probably null |
Het |
Myo10 |
T |
C |
15: 25,804,454 (GRCm39) |
L1583P |
probably damaging |
Het |
Nkx6-3 |
A |
G |
8: 23,647,722 (GRCm39) |
E227G |
possibly damaging |
Het |
Nlrp1a |
T |
A |
11: 71,004,830 (GRCm39) |
|
probably benign |
Het |
Nlrp5-ps |
A |
C |
7: 14,317,016 (GRCm39) |
|
noncoding transcript |
Het |
Obscn |
G |
A |
11: 59,019,107 (GRCm39) |
A969V |
probably benign |
Het |
Or11a4 |
T |
C |
17: 37,536,934 (GRCm39) |
L306P |
possibly damaging |
Het |
Or1j19 |
T |
A |
2: 36,677,452 (GRCm39) |
M305K |
probably benign |
Het |
Or5a1 |
G |
T |
19: 12,097,217 (GRCm39) |
D286E |
possibly damaging |
Het |
Or8k33 |
A |
T |
2: 86,384,123 (GRCm39) |
L115Q |
probably damaging |
Het |
Otogl |
T |
A |
10: 107,606,511 (GRCm39) |
|
probably benign |
Het |
Pcnx3 |
G |
A |
19: 5,715,611 (GRCm39) |
R1472W |
probably damaging |
Het |
Plekha5 |
G |
A |
6: 140,537,473 (GRCm39) |
R646K |
possibly damaging |
Het |
Plscr4 |
T |
A |
9: 92,370,814 (GRCm39) |
|
probably benign |
Het |
Pon2 |
G |
A |
6: 5,266,156 (GRCm39) |
Q288* |
probably null |
Het |
Ptpn13 |
C |
A |
5: 103,681,214 (GRCm39) |
R805S |
probably damaging |
Het |
Pyroxd2 |
A |
T |
19: 42,735,992 (GRCm39) |
V62D |
probably damaging |
Het |
Rab37 |
G |
T |
11: 115,047,790 (GRCm39) |
C44F |
probably damaging |
Het |
Rbm44 |
T |
C |
1: 91,080,069 (GRCm39) |
S52P |
probably benign |
Het |
Rgl3 |
A |
G |
9: 21,888,153 (GRCm39) |
W454R |
probably damaging |
Het |
Rita1 |
A |
G |
5: 120,747,837 (GRCm39) |
S154P |
probably benign |
Het |
Scn5a |
T |
C |
9: 119,351,665 (GRCm39) |
D772G |
probably damaging |
Het |
Sec23ip |
G |
A |
7: 128,363,129 (GRCm39) |
|
probably benign |
Het |
Skic8 |
A |
T |
9: 54,634,862 (GRCm39) |
|
probably benign |
Het |
Slc23a1 |
T |
A |
18: 35,756,032 (GRCm39) |
|
probably benign |
Het |
Slco1a8 |
A |
C |
6: 141,928,053 (GRCm39) |
|
probably benign |
Het |
Sparcl1 |
T |
A |
5: 104,237,503 (GRCm39) |
D444V |
probably damaging |
Het |
Taar6 |
C |
A |
10: 23,861,046 (GRCm39) |
V167L |
probably benign |
Het |
Tmcc3 |
T |
A |
10: 94,414,407 (GRCm39) |
N36K |
probably benign |
Het |
Tmem200c |
T |
A |
17: 69,147,543 (GRCm39) |
V42E |
probably damaging |
Het |
Trhde |
T |
C |
10: 114,338,887 (GRCm39) |
|
probably benign |
Het |
Tshz3 |
A |
G |
7: 36,469,958 (GRCm39) |
E649G |
probably benign |
Het |
Utp4 |
T |
C |
8: 107,625,169 (GRCm39) |
|
probably benign |
Het |
Vmn1r30 |
A |
G |
6: 58,412,262 (GRCm39) |
V190A |
probably benign |
Het |
Vmn1r35 |
A |
G |
6: 66,655,827 (GRCm39) |
I281T |
probably damaging |
Het |
Vmn1r58 |
G |
T |
7: 5,413,329 (GRCm39) |
H300Q |
probably benign |
Het |
Vmn1r84 |
A |
G |
7: 12,095,799 (GRCm39) |
L286P |
probably damaging |
Het |
Vmn2r54 |
A |
T |
7: 12,349,576 (GRCm39) |
C669S |
probably damaging |
Het |
Zfp623 |
T |
C |
15: 75,820,510 (GRCm39) |
S489P |
probably benign |
Het |
|
Other mutations in Nup188 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00908:Nup188
|
APN |
2 |
30,223,412 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01599:Nup188
|
APN |
2 |
30,217,537 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01938:Nup188
|
APN |
2 |
30,219,371 (GRCm39) |
missense |
probably benign |
|
IGL01973:Nup188
|
APN |
2 |
30,229,862 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02157:Nup188
|
APN |
2 |
30,219,385 (GRCm39) |
nonsense |
probably null |
|
IGL02221:Nup188
|
APN |
2 |
30,220,653 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02277:Nup188
|
APN |
2 |
30,216,523 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02335:Nup188
|
APN |
2 |
30,213,648 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02986:Nup188
|
APN |
2 |
30,197,645 (GRCm39) |
splice site |
probably null |
|
IGL03029:Nup188
|
APN |
2 |
30,212,592 (GRCm39) |
splice site |
probably benign |
|
IGL03194:Nup188
|
APN |
2 |
30,194,346 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03370:Nup188
|
APN |
2 |
30,230,653 (GRCm39) |
missense |
possibly damaging |
0.52 |
core
|
UTSW |
2 |
30,229,906 (GRCm39) |
missense |
probably damaging |
1.00 |
kern
|
UTSW |
2 |
30,227,045 (GRCm39) |
missense |
possibly damaging |
0.94 |
P0027:Nup188
|
UTSW |
2 |
30,212,693 (GRCm39) |
missense |
probably damaging |
0.99 |
R0006:Nup188
|
UTSW |
2 |
30,212,035 (GRCm39) |
missense |
probably benign |
0.27 |
R0373:Nup188
|
UTSW |
2 |
30,221,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Nup188
|
UTSW |
2 |
30,233,478 (GRCm39) |
splice site |
probably null |
|
R1411:Nup188
|
UTSW |
2 |
30,233,807 (GRCm39) |
missense |
probably benign |
0.01 |
R1670:Nup188
|
UTSW |
2 |
30,230,667 (GRCm39) |
missense |
probably benign |
0.19 |
R2034:Nup188
|
UTSW |
2 |
30,200,097 (GRCm39) |
unclassified |
probably benign |
|
R2113:Nup188
|
UTSW |
2 |
30,194,113 (GRCm39) |
nonsense |
probably null |
|
R2142:Nup188
|
UTSW |
2 |
30,226,718 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2221:Nup188
|
UTSW |
2 |
30,226,936 (GRCm39) |
splice site |
probably benign |
|
R2567:Nup188
|
UTSW |
2 |
30,231,794 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2964:Nup188
|
UTSW |
2 |
30,215,358 (GRCm39) |
missense |
probably damaging |
0.98 |
R4006:Nup188
|
UTSW |
2 |
30,199,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R4007:Nup188
|
UTSW |
2 |
30,199,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R4079:Nup188
|
UTSW |
2 |
30,199,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R4480:Nup188
|
UTSW |
2 |
30,212,141 (GRCm39) |
intron |
probably benign |
|
R4628:Nup188
|
UTSW |
2 |
30,219,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:Nup188
|
UTSW |
2 |
30,220,645 (GRCm39) |
missense |
probably benign |
0.01 |
R4814:Nup188
|
UTSW |
2 |
30,216,523 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4834:Nup188
|
UTSW |
2 |
30,229,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R5038:Nup188
|
UTSW |
2 |
30,199,232 (GRCm39) |
missense |
probably damaging |
0.98 |
R5056:Nup188
|
UTSW |
2 |
30,194,143 (GRCm39) |
missense |
probably damaging |
0.98 |
R5124:Nup188
|
UTSW |
2 |
30,220,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Nup188
|
UTSW |
2 |
30,220,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R5284:Nup188
|
UTSW |
2 |
30,220,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5548:Nup188
|
UTSW |
2 |
30,216,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R5560:Nup188
|
UTSW |
2 |
30,199,897 (GRCm39) |
missense |
probably damaging |
0.99 |
R5668:Nup188
|
UTSW |
2 |
30,226,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R5769:Nup188
|
UTSW |
2 |
30,220,747 (GRCm39) |
missense |
probably benign |
0.34 |
R5773:Nup188
|
UTSW |
2 |
30,212,208 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5774:Nup188
|
UTSW |
2 |
30,191,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R5827:Nup188
|
UTSW |
2 |
30,229,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R5919:Nup188
|
UTSW |
2 |
30,229,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R5923:Nup188
|
UTSW |
2 |
30,194,102 (GRCm39) |
missense |
probably benign |
|
R6185:Nup188
|
UTSW |
2 |
30,231,722 (GRCm39) |
missense |
probably damaging |
0.97 |
R6457:Nup188
|
UTSW |
2 |
30,212,199 (GRCm39) |
missense |
probably damaging |
0.98 |
R6529:Nup188
|
UTSW |
2 |
30,216,466 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7002:Nup188
|
UTSW |
2 |
30,213,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R7195:Nup188
|
UTSW |
2 |
30,231,842 (GRCm39) |
critical splice donor site |
probably null |
|
R7214:Nup188
|
UTSW |
2 |
30,197,566 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7345:Nup188
|
UTSW |
2 |
30,230,613 (GRCm39) |
missense |
probably benign |
0.09 |
R7853:Nup188
|
UTSW |
2 |
30,213,575 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7998:Nup188
|
UTSW |
2 |
30,220,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Nup188
|
UTSW |
2 |
30,227,277 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8080:Nup188
|
UTSW |
2 |
30,227,045 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8804:Nup188
|
UTSW |
2 |
30,220,891 (GRCm39) |
missense |
probably benign |
|
R8850:Nup188
|
UTSW |
2 |
30,217,576 (GRCm39) |
missense |
probably damaging |
0.99 |
R9110:Nup188
|
UTSW |
2 |
30,222,461 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9157:Nup188
|
UTSW |
2 |
30,188,456 (GRCm39) |
missense |
probably benign |
0.02 |
R9209:Nup188
|
UTSW |
2 |
30,232,397 (GRCm39) |
missense |
probably benign |
0.02 |
R9287:Nup188
|
UTSW |
2 |
30,226,726 (GRCm39) |
missense |
probably damaging |
0.99 |
R9325:Nup188
|
UTSW |
2 |
30,212,271 (GRCm39) |
missense |
probably damaging |
0.99 |
R9390:Nup188
|
UTSW |
2 |
30,220,777 (GRCm39) |
critical splice donor site |
probably null |
|
R9607:Nup188
|
UTSW |
2 |
30,197,724 (GRCm39) |
missense |
probably benign |
0.01 |
R9746:Nup188
|
UTSW |
2 |
30,194,300 (GRCm39) |
missense |
probably damaging |
0.99 |
R9768:Nup188
|
UTSW |
2 |
30,227,045 (GRCm39) |
missense |
probably damaging |
0.99 |
T0722:Nup188
|
UTSW |
2 |
30,212,693 (GRCm39) |
missense |
probably damaging |
0.99 |
|