Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl3 |
T |
A |
4: 144,183,604 (GRCm39) |
|
probably benign |
Het |
Abhd16b |
A |
C |
2: 181,135,209 (GRCm39) |
D37A |
probably benign |
Het |
Acp7 |
T |
C |
7: 28,328,907 (GRCm39) |
E91G |
probably damaging |
Het |
Alms1 |
T |
A |
6: 85,599,291 (GRCm39) |
N1841K |
possibly damaging |
Het |
Arhgap25 |
T |
A |
6: 87,436,990 (GRCm39) |
D620V |
probably damaging |
Het |
Caps2 |
C |
T |
10: 112,035,632 (GRCm39) |
T371I |
possibly damaging |
Het |
Ccdc175 |
A |
G |
12: 72,186,794 (GRCm39) |
I350T |
possibly damaging |
Het |
Cdc25c |
G |
C |
18: 34,871,292 (GRCm39) |
L275V |
probably damaging |
Het |
Cdc42bpb |
A |
G |
12: 111,265,630 (GRCm39) |
L1434P |
probably damaging |
Het |
Cdkl3 |
A |
T |
11: 51,917,666 (GRCm39) |
E321V |
probably damaging |
Het |
Clec2d |
G |
T |
6: 129,160,153 (GRCm39) |
V56L |
possibly damaging |
Het |
Cops3 |
A |
T |
11: 59,715,136 (GRCm39) |
S301T |
possibly damaging |
Het |
Crygd |
T |
C |
1: 65,102,405 (GRCm39) |
D19G |
probably damaging |
Het |
Dnah2 |
T |
C |
11: 69,387,432 (GRCm39) |
I931M |
possibly damaging |
Het |
Dst |
A |
T |
1: 34,250,251 (GRCm39) |
R4068S |
probably damaging |
Het |
Fas |
C |
T |
19: 34,297,953 (GRCm39) |
|
probably benign |
Het |
G6pd2 |
T |
A |
5: 61,967,594 (GRCm39) |
D456E |
probably damaging |
Het |
Galnt18 |
G |
A |
7: 111,153,809 (GRCm39) |
R272W |
probably damaging |
Het |
Grb2 |
C |
A |
11: 115,536,651 (GRCm39) |
G200W |
probably damaging |
Het |
Herc4 |
A |
G |
10: 63,099,832 (GRCm39) |
N85S |
probably benign |
Het |
Ighv7-2 |
T |
C |
12: 113,875,727 (GRCm39) |
D92G |
probably damaging |
Het |
Itih3 |
A |
G |
14: 30,631,792 (GRCm39) |
V765A |
possibly damaging |
Het |
Itm2b |
T |
C |
14: 73,600,560 (GRCm39) |
N247D |
probably benign |
Het |
Kcnd3 |
T |
C |
3: 105,574,315 (GRCm39) |
V500A |
probably benign |
Het |
Lrp2 |
C |
T |
2: 69,338,187 (GRCm39) |
G1198R |
probably damaging |
Het |
Ltb4r2 |
A |
G |
14: 55,999,444 (GRCm39) |
T22A |
probably damaging |
Het |
Mdga2 |
A |
G |
12: 66,702,136 (GRCm39) |
V355A |
probably damaging |
Het |
Megf8 |
T |
A |
7: 25,053,163 (GRCm39) |
V1778E |
probably benign |
Het |
Mroh2b |
G |
A |
15: 4,974,448 (GRCm39) |
E1143K |
probably damaging |
Het |
Nbn |
A |
T |
4: 15,979,389 (GRCm39) |
Y458F |
probably damaging |
Het |
Nlrc3 |
A |
G |
16: 3,781,856 (GRCm39) |
C534R |
probably benign |
Het |
Or5w11 |
A |
G |
2: 87,459,173 (GRCm39) |
Y122C |
probably damaging |
Het |
Plcl2 |
A |
G |
17: 50,913,857 (GRCm39) |
T289A |
probably benign |
Het |
Ptprs |
C |
T |
17: 56,741,990 (GRCm39) |
R7Q |
probably null |
Het |
Rab3ip |
A |
T |
10: 116,754,865 (GRCm39) |
D198E |
possibly damaging |
Het |
Scaf4 |
A |
T |
16: 90,049,323 (GRCm39) |
F255I |
unknown |
Het |
Senp6 |
T |
C |
9: 80,033,437 (GRCm39) |
S475P |
probably benign |
Het |
Shpk |
T |
C |
11: 73,094,785 (GRCm39) |
L67P |
probably damaging |
Het |
Sik3 |
T |
A |
9: 46,130,801 (GRCm39) |
Y1246N |
probably damaging |
Het |
Slc44a2 |
A |
G |
9: 21,265,020 (GRCm39) |
Y686C |
probably damaging |
Het |
Slc6a19 |
A |
G |
13: 73,848,685 (GRCm39) |
V23A |
probably benign |
Het |
Slit3 |
A |
T |
11: 35,435,575 (GRCm39) |
I169F |
possibly damaging |
Het |
Stxbp5l |
A |
G |
16: 37,056,637 (GRCm39) |
V379A |
possibly damaging |
Het |
Tex2 |
T |
C |
11: 106,397,690 (GRCm39) |
|
probably null |
Het |
Tnpo3 |
A |
G |
6: 29,586,143 (GRCm39) |
V149A |
possibly damaging |
Het |
Vmn1r158 |
T |
A |
7: 22,489,815 (GRCm39) |
R131S |
probably benign |
Het |
Vmn2r24 |
T |
A |
6: 123,792,358 (GRCm39) |
C562S |
probably damaging |
Het |
Wipi1 |
T |
C |
11: 109,468,490 (GRCm39) |
N368S |
probably benign |
Het |
Zbtb41 |
T |
C |
1: 139,351,831 (GRCm39) |
S315P |
probably damaging |
Het |
|
Other mutations in Nup155 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00228:Nup155
|
APN |
15 |
8,150,939 (GRCm39) |
splice site |
probably benign |
|
IGL00426:Nup155
|
APN |
15 |
8,186,278 (GRCm39) |
makesense |
probably null |
|
IGL00765:Nup155
|
APN |
15 |
8,182,712 (GRCm39) |
missense |
probably benign |
0.16 |
IGL00936:Nup155
|
APN |
15 |
8,157,889 (GRCm39) |
splice site |
probably benign |
|
IGL01124:Nup155
|
APN |
15 |
8,183,163 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01739:Nup155
|
APN |
15 |
8,165,272 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02013:Nup155
|
APN |
15 |
8,143,132 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02066:Nup155
|
APN |
15 |
8,187,250 (GRCm39) |
unclassified |
probably benign |
|
IGL02231:Nup155
|
APN |
15 |
8,173,548 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02246:Nup155
|
APN |
15 |
8,172,486 (GRCm39) |
missense |
probably benign |
|
IGL02289:Nup155
|
APN |
15 |
8,160,977 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02608:Nup155
|
APN |
15 |
8,138,955 (GRCm39) |
missense |
probably benign |
|
IGL02749:Nup155
|
APN |
15 |
8,163,560 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02813:Nup155
|
APN |
15 |
8,159,605 (GRCm39) |
splice site |
probably benign |
|
IGL03102:Nup155
|
APN |
15 |
8,176,768 (GRCm39) |
missense |
probably benign |
0.00 |
H8930:Nup155
|
UTSW |
15 |
8,187,142 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02835:Nup155
|
UTSW |
15 |
8,172,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R0314:Nup155
|
UTSW |
15 |
8,176,736 (GRCm39) |
missense |
probably benign |
0.00 |
R0365:Nup155
|
UTSW |
15 |
8,161,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R0586:Nup155
|
UTSW |
15 |
8,159,716 (GRCm39) |
missense |
probably benign |
0.39 |
R0764:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R0839:Nup155
|
UTSW |
15 |
8,175,071 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0844:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1066:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1067:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1085:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1137:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1162:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1166:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1202:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1203:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1219:Nup155
|
UTSW |
15 |
8,146,822 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1385:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1421:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Nup155
|
UTSW |
15 |
8,141,890 (GRCm39) |
missense |
probably benign |
0.44 |
R1611:Nup155
|
UTSW |
15 |
8,159,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Nup155
|
UTSW |
15 |
8,184,464 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1863:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Nup155
|
UTSW |
15 |
8,145,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R1894:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1976:Nup155
|
UTSW |
15 |
8,165,311 (GRCm39) |
missense |
probably benign |
0.01 |
R2024:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R2026:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R2027:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Nup155
|
UTSW |
15 |
8,150,951 (GRCm39) |
missense |
probably benign |
0.45 |
R2921:Nup155
|
UTSW |
15 |
8,183,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R2936:Nup155
|
UTSW |
15 |
8,172,533 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3108:Nup155
|
UTSW |
15 |
8,146,790 (GRCm39) |
missense |
probably null |
1.00 |
R3161:Nup155
|
UTSW |
15 |
8,177,867 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3162:Nup155
|
UTSW |
15 |
8,177,867 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3162:Nup155
|
UTSW |
15 |
8,177,867 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3522:Nup155
|
UTSW |
15 |
8,186,162 (GRCm39) |
splice site |
probably benign |
|
R4423:Nup155
|
UTSW |
15 |
8,150,948 (GRCm39) |
missense |
probably damaging |
0.99 |
R4451:Nup155
|
UTSW |
15 |
8,180,366 (GRCm39) |
missense |
probably benign |
0.02 |
R4498:Nup155
|
UTSW |
15 |
8,183,157 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4780:Nup155
|
UTSW |
15 |
8,187,187 (GRCm39) |
missense |
probably benign |
0.00 |
R4822:Nup155
|
UTSW |
15 |
8,158,010 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5013:Nup155
|
UTSW |
15 |
8,153,722 (GRCm39) |
missense |
probably benign |
0.00 |
R5064:Nup155
|
UTSW |
15 |
8,165,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5172:Nup155
|
UTSW |
15 |
8,139,026 (GRCm39) |
missense |
probably benign |
0.06 |
R5406:Nup155
|
UTSW |
15 |
8,183,122 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5551:Nup155
|
UTSW |
15 |
8,177,817 (GRCm39) |
missense |
probably benign |
0.09 |
R5588:Nup155
|
UTSW |
15 |
8,148,737 (GRCm39) |
critical splice donor site |
probably null |
|
R5977:Nup155
|
UTSW |
15 |
8,159,721 (GRCm39) |
critical splice donor site |
probably null |
|
R6035:Nup155
|
UTSW |
15 |
8,173,577 (GRCm39) |
missense |
probably benign |
|
R6035:Nup155
|
UTSW |
15 |
8,173,577 (GRCm39) |
missense |
probably benign |
|
R6036:Nup155
|
UTSW |
15 |
8,157,895 (GRCm39) |
missense |
probably benign |
0.16 |
R6036:Nup155
|
UTSW |
15 |
8,157,895 (GRCm39) |
missense |
probably benign |
0.16 |
R6085:Nup155
|
UTSW |
15 |
8,177,842 (GRCm39) |
missense |
probably damaging |
0.98 |
R6188:Nup155
|
UTSW |
15 |
8,139,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R6232:Nup155
|
UTSW |
15 |
8,138,963 (GRCm39) |
missense |
probably benign |
0.02 |
R6257:Nup155
|
UTSW |
15 |
8,180,282 (GRCm39) |
nonsense |
probably null |
|
R6262:Nup155
|
UTSW |
15 |
8,186,225 (GRCm39) |
missense |
probably benign |
0.03 |
R6267:Nup155
|
UTSW |
15 |
8,182,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R6296:Nup155
|
UTSW |
15 |
8,182,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Nup155
|
UTSW |
15 |
8,157,922 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6303:Nup155
|
UTSW |
15 |
8,147,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R6304:Nup155
|
UTSW |
15 |
8,147,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R6763:Nup155
|
UTSW |
15 |
8,165,379 (GRCm39) |
nonsense |
probably null |
|
R6958:Nup155
|
UTSW |
15 |
8,176,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R7088:Nup155
|
UTSW |
15 |
8,186,177 (GRCm39) |
missense |
probably benign |
0.11 |
R7313:Nup155
|
UTSW |
15 |
8,184,406 (GRCm39) |
missense |
probably damaging |
0.96 |
R7451:Nup155
|
UTSW |
15 |
8,175,091 (GRCm39) |
nonsense |
probably null |
|
R7560:Nup155
|
UTSW |
15 |
8,184,531 (GRCm39) |
missense |
probably benign |
0.39 |
R7633:Nup155
|
UTSW |
15 |
8,138,937 (GRCm39) |
missense |
probably damaging |
0.99 |
R7670:Nup155
|
UTSW |
15 |
8,183,180 (GRCm39) |
missense |
probably damaging |
0.99 |
R7726:Nup155
|
UTSW |
15 |
8,151,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R7752:Nup155
|
UTSW |
15 |
8,145,926 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7889:Nup155
|
UTSW |
15 |
8,150,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R7899:Nup155
|
UTSW |
15 |
8,148,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R7901:Nup155
|
UTSW |
15 |
8,145,926 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8429:Nup155
|
UTSW |
15 |
8,141,904 (GRCm39) |
missense |
probably damaging |
0.96 |
R8467:Nup155
|
UTSW |
15 |
8,151,015 (GRCm39) |
missense |
probably benign |
0.00 |
R8507:Nup155
|
UTSW |
15 |
8,177,044 (GRCm39) |
nonsense |
probably null |
|
R8860:Nup155
|
UTSW |
15 |
8,159,640 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8994:Nup155
|
UTSW |
15 |
8,172,645 (GRCm39) |
critical splice donor site |
probably null |
|
R9046:Nup155
|
UTSW |
15 |
8,157,919 (GRCm39) |
frame shift |
probably null |
|
R9086:Nup155
|
UTSW |
15 |
8,177,830 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9500:Nup155
|
UTSW |
15 |
8,141,800 (GRCm39) |
missense |
probably damaging |
1.00 |
RF003:Nup155
|
UTSW |
15 |
8,148,660 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF048:Nup155
|
UTSW |
15 |
8,148,660 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z1177:Nup155
|
UTSW |
15 |
8,149,973 (GRCm39) |
missense |
probably benign |
0.23 |
|