Other mutations in this stock |
Total: 19 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl3 |
T |
C |
5: 81,841,366 (GRCm39) |
Y816H |
probably damaging |
Het |
Clcn6 |
C |
T |
4: 148,097,073 (GRCm39) |
|
probably null |
Het |
Farp1 |
C |
T |
14: 121,494,148 (GRCm39) |
A543V |
probably damaging |
Het |
Hhat |
T |
C |
1: 192,277,394 (GRCm39) |
Y355C |
probably damaging |
Het |
Ireb2 |
A |
T |
9: 54,807,274 (GRCm39) |
H612L |
probably benign |
Het |
Kcnj3 |
A |
T |
2: 55,337,027 (GRCm39) |
I298F |
probably damaging |
Het |
Kdr |
A |
G |
5: 76,107,496 (GRCm39) |
F1016L |
probably damaging |
Het |
Klf7 |
T |
C |
1: 64,081,521 (GRCm39) |
Y269C |
probably damaging |
Het |
Klhl9 |
T |
C |
4: 88,639,207 (GRCm39) |
I345V |
probably benign |
Het |
Miga2 |
A |
T |
2: 30,268,306 (GRCm39) |
|
probably null |
Het |
Nadk |
A |
G |
4: 155,671,817 (GRCm39) |
N232S |
possibly damaging |
Het |
Ncoa6 |
T |
A |
2: 155,279,881 (GRCm39) |
D45V |
possibly damaging |
Het |
Pcnx2 |
A |
G |
8: 126,617,797 (GRCm39) |
S153P |
probably damaging |
Het |
Pik3ap1 |
G |
A |
19: 41,364,500 (GRCm39) |
A73V |
probably benign |
Het |
Plod3 |
G |
C |
5: 137,017,000 (GRCm39) |
A50P |
probably benign |
Het |
Rapsn |
A |
T |
2: 90,867,169 (GRCm39) |
D157V |
probably damaging |
Het |
Shprh |
T |
G |
10: 11,040,100 (GRCm39) |
S4R |
probably damaging |
Het |
Taar8a |
G |
A |
10: 23,953,028 (GRCm39) |
V211I |
probably benign |
Het |
Vpreb3 |
C |
T |
10: 75,779,056 (GRCm39) |
|
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 |
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 |
|