Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl7b |
A |
G |
4: 56,741,173 (GRCm39) |
Y62H |
probably damaging |
Het |
Cfap52 |
A |
G |
11: 67,829,881 (GRCm39) |
I296T |
probably damaging |
Het |
Col14a1 |
A |
G |
15: 55,351,937 (GRCm39) |
|
probably null |
Het |
Daam2 |
G |
T |
17: 49,793,529 (GRCm39) |
D329E |
probably benign |
Het |
Defb26 |
A |
G |
2: 152,349,902 (GRCm39) |
V126A |
probably benign |
Het |
Fasn |
A |
T |
11: 120,703,621 (GRCm39) |
I1535N |
possibly damaging |
Het |
Fbxw15 |
A |
T |
9: 109,384,219 (GRCm39) |
Y431N |
probably benign |
Het |
Fbxw26 |
T |
G |
9: 109,575,087 (GRCm39) |
I13L |
probably damaging |
Het |
Fggy |
A |
T |
4: 95,710,301 (GRCm39) |
H300L |
probably damaging |
Het |
Fndc3c1 |
G |
A |
X: 105,464,307 (GRCm39) |
T1277I |
probably benign |
Het |
Gigyf1 |
G |
T |
5: 137,523,952 (GRCm39) |
V1041L |
possibly damaging |
Het |
Kif26b |
G |
A |
1: 178,742,946 (GRCm39) |
R567H |
probably benign |
Het |
Kpna6 |
G |
A |
4: 129,549,314 (GRCm39) |
T156M |
probably damaging |
Het |
Lrrc37a |
C |
T |
11: 103,388,499 (GRCm39) |
E2309K |
unknown |
Het |
Lyn |
T |
C |
4: 3,780,931 (GRCm39) |
Y357H |
possibly damaging |
Het |
Mki67 |
A |
G |
7: 135,297,219 (GRCm39) |
V2605A |
probably benign |
Het |
Mtmr3 |
T |
C |
11: 4,437,385 (GRCm39) |
D1023G |
probably damaging |
Het |
Muc5b |
G |
T |
7: 141,418,514 (GRCm39) |
R3820L |
probably benign |
Het |
Mus81 |
A |
G |
19: 5,534,991 (GRCm39) |
|
probably benign |
Het |
Pgd |
A |
T |
4: 149,249,685 (GRCm39) |
V29D |
probably damaging |
Het |
Plch2 |
T |
C |
4: 155,071,371 (GRCm39) |
S244G |
probably benign |
Het |
Rapgef5 |
C |
A |
12: 117,694,294 (GRCm39) |
T372K |
probably damaging |
Het |
Rb1 |
A |
G |
14: 73,520,306 (GRCm39) |
|
probably null |
Het |
Ryr3 |
A |
T |
2: 112,586,944 (GRCm39) |
V2680E |
possibly damaging |
Het |
Sgsm3 |
A |
C |
15: 80,895,855 (GRCm39) |
|
probably null |
Het |
Slc38a1 |
C |
T |
15: 96,477,228 (GRCm39) |
V362I |
possibly damaging |
Het |
Sun1 |
T |
A |
5: 139,216,886 (GRCm39) |
D308E |
probably damaging |
Het |
Tns1 |
C |
T |
1: 74,025,053 (GRCm39) |
V387M |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,582,083 (GRCm39) |
G22937C |
probably damaging |
Het |
Ubr1 |
C |
A |
2: 120,725,641 (GRCm39) |
A1258S |
probably benign |
Het |
Vmn2r74 |
A |
G |
7: 85,607,265 (GRCm39) |
F153L |
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 |
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 |
R0360:Nup188
|
UTSW |
2 |
30,216,491 (GRCm39) |
missense |
probably null |
0.93 |
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 |
|