Other mutations in this stock |
Total: 17 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
A |
C |
5: 114,342,866 (GRCm39) |
S911R |
possibly damaging |
Het |
Acap1 |
G |
A |
11: 69,777,864 (GRCm39) |
R125C |
probably damaging |
Het |
Car7 |
A |
T |
8: 105,274,851 (GRCm39) |
S131C |
probably benign |
Het |
Erich6 |
G |
T |
3: 58,531,727 (GRCm39) |
T423N |
probably benign |
Het |
Insr |
T |
C |
8: 3,234,972 (GRCm39) |
H174R |
possibly damaging |
Het |
Lrch3 |
A |
G |
16: 32,734,647 (GRCm39) |
S46G |
possibly damaging |
Het |
Meis3 |
G |
T |
7: 15,912,695 (GRCm39) |
R144L |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,952,474 (GRCm39) |
E4162G |
probably damaging |
Het |
Or10ak9 |
A |
T |
4: 118,726,118 (GRCm39) |
I47F |
possibly damaging |
Het |
Or4m1 |
T |
C |
14: 50,558,149 (GRCm39) |
T48A |
probably benign |
Het |
Prdm11 |
C |
T |
2: 92,810,967 (GRCm39) |
A211T |
probably benign |
Het |
Pygl |
A |
G |
12: 70,244,256 (GRCm39) |
S471P |
probably damaging |
Het |
Reln |
A |
T |
5: 22,115,842 (GRCm39) |
N3055K |
probably damaging |
Het |
Spata31 |
A |
C |
13: 65,068,703 (GRCm39) |
N284H |
probably benign |
Het |
Stk36 |
A |
T |
1: 74,662,472 (GRCm39) |
D530V |
probably damaging |
Het |
Stxbp5l |
G |
T |
16: 37,007,083 (GRCm39) |
D703E |
probably benign |
Het |
Usp24 |
A |
G |
4: 106,249,599 (GRCm39) |
I1439V |
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 |
|
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 |
R3109:Per2
|
UTSW |
1 |
91,373,297 (GRCm39) |
missense |
probably benign |
0.02 |
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 |
|