Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6820408C15Rik |
A |
G |
2: 152,284,376 (GRCm39) |
E323G |
probably damaging |
Het |
Adamts20 |
T |
C |
15: 94,243,785 (GRCm39) |
|
probably benign |
Het |
Alkbh3 |
T |
C |
2: 93,835,108 (GRCm39) |
E80G |
probably damaging |
Het |
Amfr |
T |
C |
8: 94,726,934 (GRCm39) |
Y93C |
probably damaging |
Het |
Arid2 |
T |
C |
15: 96,254,627 (GRCm39) |
Y158H |
probably damaging |
Het |
Camk1g |
T |
C |
1: 193,037,301 (GRCm39) |
Y133C |
probably damaging |
Het |
Cnnm1 |
T |
C |
19: 43,430,000 (GRCm39) |
C373R |
probably damaging |
Het |
Cnot1 |
A |
G |
8: 96,462,377 (GRCm39) |
V1691A |
probably damaging |
Het |
Cubn |
T |
C |
2: 13,367,158 (GRCm39) |
S1571G |
possibly damaging |
Het |
Dclk2 |
G |
A |
3: 86,827,342 (GRCm39) |
P46S |
probably damaging |
Het |
Dennd1b |
G |
A |
1: 138,969,654 (GRCm39) |
|
probably benign |
Het |
Dmrt2 |
C |
A |
19: 25,655,055 (GRCm39) |
T218N |
probably benign |
Het |
Drd4 |
T |
A |
7: 140,872,195 (GRCm39) |
V82E |
possibly damaging |
Het |
Fat1 |
G |
A |
8: 45,498,210 (GRCm39) |
|
probably null |
Het |
Fyn |
G |
C |
10: 39,427,451 (GRCm39) |
D445H |
probably damaging |
Het |
Igfn1 |
T |
C |
1: 135,925,586 (GRCm39) |
D56G |
probably benign |
Het |
Igkv11-125 |
T |
C |
6: 67,890,855 (GRCm39) |
F58L |
possibly damaging |
Het |
Klhdc4 |
A |
C |
8: 122,548,073 (GRCm39) |
H72Q |
probably damaging |
Het |
Kmt2c |
A |
G |
5: 25,480,733 (GRCm39) |
Y1459H |
probably damaging |
Het |
Lama2 |
C |
T |
10: 26,877,231 (GRCm39) |
E2652K |
probably benign |
Het |
Muc5b |
C |
T |
7: 141,412,496 (GRCm39) |
T1814M |
unknown |
Het |
Ntrk3 |
C |
T |
7: 78,110,263 (GRCm39) |
V324M |
probably benign |
Het |
Or52s1b |
T |
A |
7: 102,822,293 (GRCm39) |
M184L |
probably damaging |
Het |
Ptprn2 |
A |
G |
12: 116,839,800 (GRCm39) |
D441G |
probably benign |
Het |
Rbl2 |
T |
A |
8: 91,828,863 (GRCm39) |
I588N |
probably benign |
Het |
Rslcan18 |
C |
T |
13: 67,246,671 (GRCm39) |
E314K |
possibly damaging |
Het |
Ubr3 |
A |
T |
2: 69,819,184 (GRCm39) |
T1325S |
probably damaging |
Het |
Unc45a |
A |
G |
7: 79,981,294 (GRCm39) |
|
probably benign |
Het |
Vmn1r175 |
A |
G |
7: 23,508,393 (GRCm39) |
V78A |
probably benign |
Het |
|
Other mutations in Per2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01306:Per2
|
APN |
1 |
91,376,555 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01350:Per2
|
APN |
1 |
91,358,583 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01865:Per2
|
APN |
1 |
91,349,239 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01974:Per2
|
APN |
1 |
91,351,440 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02118:Per2
|
APN |
1 |
91,352,031 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02271:Per2
|
APN |
1 |
91,373,332 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02533:Per2
|
APN |
1 |
91,358,724 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02707:Per2
|
APN |
1 |
91,378,450 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02972:Per2
|
APN |
1 |
91,351,703 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL03118:Per2
|
APN |
1 |
91,372,341 (GRCm39) |
nonsense |
probably null |
|
IGL03125:Per2
|
APN |
1 |
91,378,333 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03375:Per2
|
APN |
1 |
91,351,950 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03388:Per2
|
APN |
1 |
91,372,511 (GRCm39) |
splice site |
probably benign |
|
Kortiku
|
UTSW |
1 |
91,351,551 (GRCm39) |
missense |
probably damaging |
1.00 |
obst
|
UTSW |
1 |
91,373,261 (GRCm39) |
missense |
probably benign |
0.00 |
R7092_Per2_246
|
UTSW |
1 |
91,349,153 (GRCm39) |
missense |
probably damaging |
1.00 |
rhythm
|
UTSW |
1 |
91,357,104 (GRCm39) |
critical splice donor site |
probably null |
|
ANU23:Per2
|
UTSW |
1 |
91,376,555 (GRCm39) |
missense |
probably damaging |
0.98 |
R0029:Per2
|
UTSW |
1 |
91,351,434 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0029:Per2
|
UTSW |
1 |
91,351,434 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0542:Per2
|
UTSW |
1 |
91,366,054 (GRCm39) |
critical splice donor site |
probably null |
|
R0764:Per2
|
UTSW |
1 |
91,357,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R1370:Per2
|
UTSW |
1 |
91,373,279 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1655:Per2
|
UTSW |
1 |
91,376,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R1688:Per2
|
UTSW |
1 |
91,351,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R1997:Per2
|
UTSW |
1 |
91,368,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R2891:Per2
|
UTSW |
1 |
91,373,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R2893:Per2
|
UTSW |
1 |
91,373,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R2894:Per2
|
UTSW |
1 |
91,373,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R4125:Per2
|
UTSW |
1 |
91,357,172 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4997:Per2
|
UTSW |
1 |
91,378,505 (GRCm39) |
missense |
probably benign |
0.02 |
R5110:Per2
|
UTSW |
1 |
91,357,237 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5478:Per2
|
UTSW |
1 |
91,360,590 (GRCm39) |
missense |
probably benign |
0.09 |
R5590:Per2
|
UTSW |
1 |
91,355,578 (GRCm39) |
nonsense |
probably null |
|
R5634:Per2
|
UTSW |
1 |
91,372,429 (GRCm39) |
missense |
probably benign |
0.02 |
R5654:Per2
|
UTSW |
1 |
91,373,223 (GRCm39) |
splice site |
probably null |
|
R5928:Per2
|
UTSW |
1 |
91,372,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R6241:Per2
|
UTSW |
1 |
91,349,251 (GRCm39) |
missense |
probably damaging |
0.97 |
R6295:Per2
|
UTSW |
1 |
91,377,594 (GRCm39) |
missense |
unknown |
|
R6345:Per2
|
UTSW |
1 |
91,376,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R6480:Per2
|
UTSW |
1 |
91,357,104 (GRCm39) |
critical splice donor site |
probably null |
|
R6502:Per2
|
UTSW |
1 |
91,355,485 (GRCm39) |
missense |
probably benign |
0.01 |
R6702:Per2
|
UTSW |
1 |
91,355,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R6703:Per2
|
UTSW |
1 |
91,355,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R6790:Per2
|
UTSW |
1 |
91,373,261 (GRCm39) |
missense |
probably benign |
0.00 |
R7043:Per2
|
UTSW |
1 |
91,347,130 (GRCm39) |
missense |
probably benign |
|
R7092:Per2
|
UTSW |
1 |
91,349,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R7430:Per2
|
UTSW |
1 |
91,351,705 (GRCm39) |
nonsense |
probably null |
|
R7555:Per2
|
UTSW |
1 |
91,362,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R7860:Per2
|
UTSW |
1 |
91,372,481 (GRCm39) |
missense |
probably damaging |
0.99 |
R8046:Per2
|
UTSW |
1 |
91,363,425 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8142:Per2
|
UTSW |
1 |
91,349,269 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8261:Per2
|
UTSW |
1 |
91,361,170 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8277:Per2
|
UTSW |
1 |
91,348,274 (GRCm39) |
missense |
probably benign |
0.15 |
R8534:Per2
|
UTSW |
1 |
91,351,659 (GRCm39) |
missense |
probably benign |
0.09 |
R8685:Per2
|
UTSW |
1 |
91,378,402 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8703:Per2
|
UTSW |
1 |
91,351,767 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9100:Per2
|
UTSW |
1 |
91,351,464 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9228:Per2
|
UTSW |
1 |
91,366,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R9257:Per2
|
UTSW |
1 |
91,376,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R9429:Per2
|
UTSW |
1 |
91,351,489 (GRCm39) |
missense |
probably benign |
|
X0011:Per2
|
UTSW |
1 |
91,348,311 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1176:Per2
|
UTSW |
1 |
91,349,215 (GRCm39) |
missense |
possibly damaging |
0.94 |
|