Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
T |
C |
10: 28,849,863 (GRCm39) |
D191G |
probably benign |
Het |
Ankrd39 |
C |
T |
1: 36,581,062 (GRCm39) |
G96R |
probably damaging |
Het |
Cdh12 |
C |
T |
15: 21,492,740 (GRCm39) |
T253I |
probably damaging |
Het |
Cox4i2 |
C |
T |
2: 152,599,011 (GRCm39) |
T56I |
possibly damaging |
Het |
Cpsf1 |
A |
C |
15: 76,481,527 (GRCm39) |
D1141E |
possibly damaging |
Het |
Dennd5b |
T |
C |
6: 148,920,847 (GRCm39) |
|
probably null |
Het |
Dnah6 |
A |
T |
6: 73,128,672 (GRCm39) |
D1194E |
probably damaging |
Het |
Dst |
C |
A |
1: 34,228,409 (GRCm39) |
H1676N |
probably benign |
Het |
Eif4a3l1 |
T |
C |
6: 136,306,568 (GRCm39) |
V343A |
probably damaging |
Het |
Fitm1 |
A |
G |
14: 55,813,154 (GRCm39) |
T6A |
probably benign |
Het |
Galnt5 |
T |
A |
2: 57,904,922 (GRCm39) |
V495E |
probably damaging |
Het |
Gtf2h2 |
C |
A |
13: 100,617,544 (GRCm39) |
R206L |
possibly damaging |
Het |
Heatr5a |
A |
T |
12: 52,005,734 (GRCm39) |
Y80* |
probably null |
Het |
Il17ra |
A |
G |
6: 120,455,434 (GRCm39) |
R348G |
probably benign |
Het |
Mmp28 |
A |
T |
11: 83,334,733 (GRCm39) |
Y340* |
probably null |
Het |
Mrgprb8 |
A |
T |
7: 48,038,778 (GRCm39) |
T150S |
probably benign |
Het |
Ms4a10 |
A |
T |
19: 10,945,484 (GRCm39) |
|
probably null |
Het |
Muc5b |
A |
T |
7: 141,417,679 (GRCm39) |
I3542F |
probably benign |
Het |
Mybbp1a |
T |
C |
11: 72,336,998 (GRCm39) |
L578P |
probably damaging |
Het |
N4bp2l1 |
G |
A |
5: 150,496,420 (GRCm39) |
R65* |
probably null |
Het |
Nhsl3 |
GGTG |
GGTGTG |
4: 129,117,773 (GRCm39) |
|
probably null |
Het |
Or8b3b |
T |
C |
9: 38,584,600 (GRCm39) |
I60V |
probably benign |
Het |
Or8s5 |
T |
A |
15: 98,238,253 (GRCm39) |
T206S |
probably benign |
Het |
Pbrm1 |
T |
A |
14: 30,827,381 (GRCm39) |
C1257S |
probably damaging |
Het |
Pcdh8 |
T |
C |
14: 80,004,942 (GRCm39) |
T1028A |
probably damaging |
Het |
Pramel16 |
C |
T |
4: 143,676,550 (GRCm39) |
E185K |
probably benign |
Het |
Qars1 |
C |
T |
9: 108,390,117 (GRCm39) |
P348S |
possibly damaging |
Het |
Qrfpr |
T |
A |
3: 36,276,075 (GRCm39) |
Q105L |
possibly damaging |
Het |
Slc10a5 |
A |
T |
3: 10,399,377 (GRCm39) |
Y428N |
probably benign |
Het |
Slc16a5 |
A |
T |
11: 115,360,630 (GRCm39) |
Y271F |
probably benign |
Het |
Slc1a4 |
T |
A |
11: 20,254,429 (GRCm39) |
Q479L |
possibly damaging |
Het |
Slc38a1 |
C |
T |
15: 96,488,355 (GRCm39) |
G143S |
probably damaging |
Het |
Susd1 |
G |
A |
4: 59,369,577 (GRCm39) |
T364M |
probably benign |
Het |
Tmem132c |
T |
A |
5: 127,628,587 (GRCm39) |
Y496* |
probably null |
Het |
Tmem63b |
A |
G |
17: 45,975,884 (GRCm39) |
I523T |
probably damaging |
Het |
Tnrc6c |
T |
C |
11: 117,651,669 (GRCm39) |
S1731P |
possibly damaging |
Het |
Ttll3 |
T |
A |
6: 113,370,078 (GRCm39) |
W139R |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,187,401 (GRCm39) |
T3823M |
probably damaging |
Het |
Vangl1 |
T |
A |
3: 102,091,762 (GRCm39) |
D108V |
possibly damaging |
Het |
Vmn1r120 |
T |
C |
7: 20,787,482 (GRCm39) |
I76M |
probably benign |
Het |
Wdr17 |
A |
G |
8: 55,156,886 (GRCm39) |
Y17H |
probably damaging |
Het |
Xkr4 |
C |
T |
1: 3,287,153 (GRCm39) |
A346T |
probably damaging |
Het |
Zfp267 |
C |
G |
3: 36,219,640 (GRCm39) |
H554Q |
possibly damaging |
Het |
Zfp600 |
T |
A |
4: 146,133,019 (GRCm39) |
S562R |
possibly damaging |
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 |
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 |
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 |
|