Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp8a1 |
A |
G |
5: 67,824,777 (GRCm39) |
|
probably benign |
Het |
Bmt2 |
C |
T |
6: 13,628,609 (GRCm39) |
R358Q |
probably damaging |
Het |
C2cd6 |
A |
G |
1: 59,114,259 (GRCm39) |
I182T |
probably benign |
Het |
Calr3 |
T |
C |
8: 73,185,276 (GRCm39) |
T100A |
probably benign |
Het |
Cln3 |
T |
C |
7: 126,181,954 (GRCm39) |
K36R |
probably benign |
Het |
Ddx25 |
C |
T |
9: 35,468,974 (GRCm39) |
|
probably benign |
Het |
Dmxl2 |
A |
T |
9: 54,313,899 (GRCm39) |
V1677E |
probably damaging |
Het |
Dnah10 |
A |
G |
5: 124,850,883 (GRCm39) |
E1684G |
probably damaging |
Het |
Dnah9 |
A |
G |
11: 65,846,072 (GRCm39) |
S2989P |
probably damaging |
Het |
F5 |
A |
T |
1: 164,034,635 (GRCm39) |
T1845S |
possibly damaging |
Het |
Folh1 |
G |
T |
7: 86,383,312 (GRCm39) |
N478K |
probably benign |
Het |
Gpr22 |
T |
C |
12: 31,759,139 (GRCm39) |
I328V |
probably damaging |
Het |
Itln1 |
C |
T |
1: 171,359,097 (GRCm39) |
A128T |
probably benign |
Het |
Itprid1 |
A |
G |
6: 55,861,713 (GRCm39) |
T97A |
possibly damaging |
Het |
Kank1 |
A |
G |
19: 25,410,272 (GRCm39) |
K1322R |
probably damaging |
Het |
Klhdc2 |
A |
G |
12: 69,350,414 (GRCm39) |
Y153C |
probably damaging |
Het |
Lonp2 |
T |
A |
8: 87,350,813 (GRCm39) |
M1K |
probably null |
Het |
Mtor |
T |
A |
4: 148,630,886 (GRCm39) |
M2281K |
probably benign |
Het |
Mtor |
T |
A |
4: 148,576,104 (GRCm39) |
N1378K |
probably benign |
Het |
Myo1e |
G |
A |
9: 70,254,022 (GRCm39) |
R557H |
probably damaging |
Het |
Nedd4l |
T |
C |
18: 65,296,244 (GRCm39) |
|
probably null |
Het |
Or2r3 |
T |
C |
6: 42,449,100 (GRCm39) |
D4G |
probably benign |
Het |
Or2t46 |
A |
T |
11: 58,472,035 (GRCm39) |
M122L |
probably damaging |
Het |
Or2z9 |
T |
A |
8: 72,854,374 (GRCm39) |
F257I |
probably damaging |
Het |
Or9i16 |
A |
T |
19: 13,865,223 (GRCm39) |
M117K |
probably damaging |
Het |
Pcdh18 |
T |
C |
3: 49,699,052 (GRCm39) |
|
probably benign |
Het |
Phldb1 |
T |
C |
9: 44,626,700 (GRCm39) |
T582A |
probably damaging |
Het |
Plxna2 |
A |
T |
1: 194,428,458 (GRCm39) |
E509D |
probably benign |
Het |
Poln |
A |
T |
5: 34,286,474 (GRCm39) |
D231E |
probably damaging |
Het |
Prpf40b |
T |
C |
15: 99,204,747 (GRCm39) |
S263P |
probably damaging |
Het |
Sfmbt2 |
C |
T |
2: 10,573,194 (GRCm39) |
A574V |
probably damaging |
Het |
Slc12a3 |
T |
C |
8: 95,058,310 (GRCm39) |
I152T |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Svep1 |
T |
C |
4: 58,145,293 (GRCm39) |
I391V |
probably benign |
Het |
Tbx4 |
A |
G |
11: 85,781,720 (GRCm39) |
E80G |
probably damaging |
Het |
Vmn2r22 |
A |
G |
6: 123,614,364 (GRCm39) |
Y409H |
probably benign |
Het |
Zfp691 |
T |
G |
4: 119,027,493 (GRCm39) |
R246S |
probably damaging |
Het |
Zfp846 |
T |
C |
9: 20,499,796 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Prex2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00497:Prex2
|
APN |
1 |
11,256,876 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL00948:Prex2
|
APN |
1 |
11,240,838 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01087:Prex2
|
APN |
1 |
11,138,328 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01490:Prex2
|
APN |
1 |
11,254,769 (GRCm39) |
splice site |
probably null |
|
IGL01533:Prex2
|
APN |
1 |
11,256,965 (GRCm39) |
nonsense |
probably null |
|
IGL01661:Prex2
|
APN |
1 |
11,278,838 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01668:Prex2
|
APN |
1 |
11,223,869 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01674:Prex2
|
APN |
1 |
11,240,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01716:Prex2
|
APN |
1 |
11,336,278 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01867:Prex2
|
APN |
1 |
11,168,727 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01954:Prex2
|
APN |
1 |
11,210,235 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01990:Prex2
|
APN |
1 |
11,193,457 (GRCm39) |
splice site |
probably benign |
|
IGL02022:Prex2
|
APN |
1 |
11,367,963 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02130:Prex2
|
APN |
1 |
11,230,386 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02130:Prex2
|
APN |
1 |
11,183,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02221:Prex2
|
APN |
1 |
11,131,569 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02369:Prex2
|
APN |
1 |
11,171,393 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02477:Prex2
|
APN |
1 |
11,274,378 (GRCm39) |
missense |
probably benign |
|
IGL02492:Prex2
|
APN |
1 |
11,194,069 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03051:Prex2
|
APN |
1 |
11,212,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03154:Prex2
|
APN |
1 |
11,223,857 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL03158:Prex2
|
APN |
1 |
11,336,291 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03308:Prex2
|
APN |
1 |
11,255,399 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03338:Prex2
|
APN |
1 |
11,210,489 (GRCm39) |
missense |
probably benign |
0.01 |
R0042:Prex2
|
UTSW |
1 |
11,150,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Prex2
|
UTSW |
1 |
11,230,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Prex2
|
UTSW |
1 |
11,230,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0138:Prex2
|
UTSW |
1 |
11,355,267 (GRCm39) |
splice site |
probably benign |
|
R0206:Prex2
|
UTSW |
1 |
11,355,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0206:Prex2
|
UTSW |
1 |
11,355,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Prex2
|
UTSW |
1 |
11,355,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Prex2
|
UTSW |
1 |
11,270,281 (GRCm39) |
splice site |
probably null |
|
R0326:Prex2
|
UTSW |
1 |
11,355,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Prex2
|
UTSW |
1 |
11,159,930 (GRCm39) |
splice site |
probably null |
|
R0492:Prex2
|
UTSW |
1 |
11,256,857 (GRCm39) |
splice site |
probably benign |
|
R0512:Prex2
|
UTSW |
1 |
11,270,157 (GRCm39) |
missense |
probably benign |
|
R0515:Prex2
|
UTSW |
1 |
11,270,098 (GRCm39) |
missense |
probably damaging |
0.99 |
R0894:Prex2
|
UTSW |
1 |
11,252,122 (GRCm39) |
missense |
probably benign |
|
R1259:Prex2
|
UTSW |
1 |
11,359,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R1332:Prex2
|
UTSW |
1 |
11,274,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R1356:Prex2
|
UTSW |
1 |
11,150,316 (GRCm39) |
nonsense |
probably null |
|
R1451:Prex2
|
UTSW |
1 |
11,226,483 (GRCm39) |
missense |
probably benign |
0.01 |
R1488:Prex2
|
UTSW |
1 |
11,263,752 (GRCm39) |
missense |
probably benign |
0.05 |
R1512:Prex2
|
UTSW |
1 |
11,131,554 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1641:Prex2
|
UTSW |
1 |
11,301,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R1667:Prex2
|
UTSW |
1 |
11,256,981 (GRCm39) |
missense |
probably benign |
|
R1678:Prex2
|
UTSW |
1 |
11,355,313 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1736:Prex2
|
UTSW |
1 |
11,160,108 (GRCm39) |
splice site |
probably benign |
|
R1781:Prex2
|
UTSW |
1 |
11,270,179 (GRCm39) |
missense |
probably benign |
0.17 |
R1804:Prex2
|
UTSW |
1 |
11,202,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Prex2
|
UTSW |
1 |
11,207,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Prex2
|
UTSW |
1 |
11,232,590 (GRCm39) |
nonsense |
probably null |
|
R1900:Prex2
|
UTSW |
1 |
11,232,590 (GRCm39) |
nonsense |
probably null |
|
R2020:Prex2
|
UTSW |
1 |
11,232,536 (GRCm39) |
missense |
probably damaging |
0.98 |
R2114:Prex2
|
UTSW |
1 |
11,256,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Prex2
|
UTSW |
1 |
11,256,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R2436:Prex2
|
UTSW |
1 |
11,336,376 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2902:Prex2
|
UTSW |
1 |
11,278,838 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2915:Prex2
|
UTSW |
1 |
11,240,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2924:Prex2
|
UTSW |
1 |
11,168,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R2981:Prex2
|
UTSW |
1 |
11,252,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Prex2
|
UTSW |
1 |
11,220,078 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3832:Prex2
|
UTSW |
1 |
11,226,588 (GRCm39) |
splice site |
probably benign |
|
R3870:Prex2
|
UTSW |
1 |
11,230,416 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3963:Prex2
|
UTSW |
1 |
11,180,581 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4012:Prex2
|
UTSW |
1 |
11,254,740 (GRCm39) |
missense |
probably benign |
|
R4030:Prex2
|
UTSW |
1 |
11,278,792 (GRCm39) |
missense |
probably benign |
0.06 |
R4214:Prex2
|
UTSW |
1 |
11,355,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R4214:Prex2
|
UTSW |
1 |
11,171,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R4242:Prex2
|
UTSW |
1 |
11,226,528 (GRCm39) |
missense |
probably benign |
0.06 |
R4490:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R4491:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R4492:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R4561:Prex2
|
UTSW |
1 |
11,254,769 (GRCm39) |
splice site |
probably null |
|
R4624:Prex2
|
UTSW |
1 |
11,359,489 (GRCm39) |
nonsense |
probably null |
|
R4647:Prex2
|
UTSW |
1 |
11,232,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R4657:Prex2
|
UTSW |
1 |
11,136,049 (GRCm39) |
missense |
probably benign |
0.00 |
R4706:Prex2
|
UTSW |
1 |
11,270,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Prex2
|
UTSW |
1 |
11,138,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4900:Prex2
|
UTSW |
1 |
11,220,129 (GRCm39) |
splice site |
probably benign |
|
R4922:Prex2
|
UTSW |
1 |
11,240,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R4961:Prex2
|
UTSW |
1 |
11,168,705 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5284:Prex2
|
UTSW |
1 |
11,336,314 (GRCm39) |
nonsense |
probably null |
|
R5305:Prex2
|
UTSW |
1 |
11,177,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Prex2
|
UTSW |
1 |
11,270,256 (GRCm39) |
missense |
probably damaging |
0.99 |
R5331:Prex2
|
UTSW |
1 |
11,210,235 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5385:Prex2
|
UTSW |
1 |
11,210,204 (GRCm39) |
missense |
probably damaging |
0.99 |
R5574:Prex2
|
UTSW |
1 |
11,210,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Prex2
|
UTSW |
1 |
11,202,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R6076:Prex2
|
UTSW |
1 |
11,256,174 (GRCm39) |
missense |
probably benign |
0.09 |
R6160:Prex2
|
UTSW |
1 |
11,064,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R6177:Prex2
|
UTSW |
1 |
11,207,001 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6221:Prex2
|
UTSW |
1 |
11,336,236 (GRCm39) |
missense |
probably benign |
0.01 |
R6293:Prex2
|
UTSW |
1 |
11,232,522 (GRCm39) |
missense |
probably benign |
|
R6335:Prex2
|
UTSW |
1 |
11,180,544 (GRCm39) |
missense |
probably benign |
0.13 |
R6401:Prex2
|
UTSW |
1 |
11,256,951 (GRCm39) |
missense |
probably benign |
0.00 |
R6427:Prex2
|
UTSW |
1 |
11,252,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R6467:Prex2
|
UTSW |
1 |
11,336,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R6564:Prex2
|
UTSW |
1 |
11,171,285 (GRCm39) |
splice site |
probably null |
|
R6734:Prex2
|
UTSW |
1 |
11,150,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R6753:Prex2
|
UTSW |
1 |
11,254,680 (GRCm39) |
missense |
probably damaging |
0.98 |
R6880:Prex2
|
UTSW |
1 |
11,202,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R6973:Prex2
|
UTSW |
1 |
11,182,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R6980:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R6987:Prex2
|
UTSW |
1 |
11,240,976 (GRCm39) |
missense |
probably damaging |
0.99 |
R7085:Prex2
|
UTSW |
1 |
11,168,812 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7101:Prex2
|
UTSW |
1 |
11,223,833 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7106:Prex2
|
UTSW |
1 |
11,207,017 (GRCm39) |
missense |
probably benign |
0.33 |
R7319:Prex2
|
UTSW |
1 |
11,232,532 (GRCm39) |
missense |
probably benign |
0.10 |
R7342:Prex2
|
UTSW |
1 |
11,232,549 (GRCm39) |
missense |
probably benign |
0.00 |
R7469:Prex2
|
UTSW |
1 |
11,355,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R7528:Prex2
|
UTSW |
1 |
11,274,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R7592:Prex2
|
UTSW |
1 |
11,193,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R7650:Prex2
|
UTSW |
1 |
11,220,078 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7695:Prex2
|
UTSW |
1 |
11,232,497 (GRCm39) |
missense |
probably benign |
0.00 |
R7720:Prex2
|
UTSW |
1 |
11,252,161 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7733:Prex2
|
UTSW |
1 |
11,252,183 (GRCm39) |
missense |
probably benign |
0.31 |
R7859:Prex2
|
UTSW |
1 |
11,150,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Prex2
|
UTSW |
1 |
11,270,194 (GRCm39) |
missense |
probably benign |
|
R8300:Prex2
|
UTSW |
1 |
11,301,942 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8345:Prex2
|
UTSW |
1 |
11,270,118 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8352:Prex2
|
UTSW |
1 |
11,355,364 (GRCm39) |
missense |
probably benign |
|
R8352:Prex2
|
UTSW |
1 |
11,355,363 (GRCm39) |
missense |
probably benign |
|
R8410:Prex2
|
UTSW |
1 |
11,223,881 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8452:Prex2
|
UTSW |
1 |
11,355,364 (GRCm39) |
missense |
probably benign |
|
R8452:Prex2
|
UTSW |
1 |
11,355,363 (GRCm39) |
missense |
probably benign |
|
R8885:Prex2
|
UTSW |
1 |
11,240,799 (GRCm39) |
splice site |
probably benign |
|
R8926:Prex2
|
UTSW |
1 |
11,159,930 (GRCm39) |
splice site |
probably null |
|
R8968:Prex2
|
UTSW |
1 |
11,180,562 (GRCm39) |
nonsense |
probably null |
|
R9049:Prex2
|
UTSW |
1 |
11,256,130 (GRCm39) |
missense |
probably damaging |
0.98 |
R9398:Prex2
|
UTSW |
1 |
11,207,028 (GRCm39) |
missense |
probably benign |
0.00 |
R9452:Prex2
|
UTSW |
1 |
11,256,151 (GRCm39) |
missense |
probably benign |
0.01 |
R9549:Prex2
|
UTSW |
1 |
11,256,915 (GRCm39) |
missense |
probably damaging |
1.00 |
RF005:Prex2
|
UTSW |
1 |
11,255,390 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1177:Prex2
|
UTSW |
1 |
11,359,476 (GRCm39) |
critical splice acceptor site |
probably null |
|
|