Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahcyl2 |
A |
G |
6: 29,903,266 (GRCm39) |
R516G |
probably damaging |
Het |
Aldh3b3 |
A |
G |
19: 4,014,549 (GRCm39) |
M95V |
probably benign |
Het |
Ankrd34a |
T |
C |
3: 96,505,816 (GRCm39) |
L340P |
possibly damaging |
Het |
Arid1a |
T |
A |
4: 133,412,482 (GRCm39) |
R1186W |
unknown |
Het |
Arpc4 |
T |
A |
6: 113,361,092 (GRCm39) |
M95K |
possibly damaging |
Het |
Atrnl1 |
A |
G |
19: 57,684,744 (GRCm39) |
E790G |
possibly damaging |
Het |
C130074G19Rik |
T |
C |
1: 184,606,624 (GRCm39) |
N103D |
probably damaging |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Camsap2 |
T |
C |
1: 136,198,678 (GRCm39) |
T782A |
|
Het |
Catsperd |
A |
G |
17: 56,971,055 (GRCm39) |
I706M |
probably benign |
Het |
Cbx2 |
T |
C |
11: 118,919,941 (GRCm39) |
V502A |
probably damaging |
Het |
Cd72 |
T |
G |
4: 43,454,515 (GRCm39) |
I5L |
possibly damaging |
Het |
Celsr3 |
A |
G |
9: 108,720,777 (GRCm39) |
Y2609C |
probably benign |
Het |
Col19a1 |
C |
T |
1: 24,356,788 (GRCm39) |
G632R |
probably damaging |
Het |
Efcc1 |
T |
C |
6: 87,707,972 (GRCm39) |
V33A |
probably damaging |
Het |
Eif4enif1 |
T |
A |
11: 3,177,709 (GRCm39) |
L367* |
probably null |
Het |
Eml2 |
T |
A |
7: 18,940,066 (GRCm39) |
L627* |
probably null |
Het |
F13b |
A |
G |
1: 139,435,433 (GRCm39) |
T193A |
probably benign |
Het |
Hif3a |
G |
A |
7: 16,776,560 (GRCm39) |
T462I |
possibly damaging |
Het |
Ifna7 |
T |
A |
4: 88,734,913 (GRCm39) |
I150N |
probably damaging |
Het |
Man2b2 |
G |
A |
5: 36,967,657 (GRCm39) |
H904Y |
probably damaging |
Het |
Midn |
A |
G |
10: 79,991,156 (GRCm39) |
T389A |
possibly damaging |
Het |
Myo19 |
A |
T |
11: 84,776,626 (GRCm39) |
H94L |
probably benign |
Het |
Naglu |
T |
C |
11: 100,962,725 (GRCm39) |
Y177H |
probably damaging |
Het |
Nek1 |
T |
A |
8: 61,583,179 (GRCm39) |
D1272E |
probably benign |
Het |
Nxn |
A |
T |
11: 76,152,378 (GRCm39) |
V372E |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,984,242 (GRCm39) |
R1738C |
probably damaging |
Het |
Pcm1 |
A |
G |
8: 41,714,410 (GRCm39) |
E266G |
probably benign |
Het |
Pkd1l1 |
T |
C |
11: 8,879,441 (GRCm39) |
N920S |
|
Het |
Pkd1l3 |
C |
A |
8: 110,359,947 (GRCm39) |
T944K |
probably damaging |
Het |
Prl7d1 |
C |
A |
13: 27,894,168 (GRCm39) |
E133* |
probably null |
Het |
Qser1 |
G |
A |
2: 104,619,859 (GRCm39) |
L228F |
probably damaging |
Het |
Rasa3 |
A |
G |
8: 13,664,605 (GRCm39) |
I69T |
possibly damaging |
Het |
Rb1 |
A |
T |
14: 73,506,577 (GRCm39) |
S391T |
probably damaging |
Het |
Rnf220 |
T |
C |
4: 117,153,333 (GRCm39) |
Y301C |
possibly damaging |
Het |
Sertm1 |
A |
G |
3: 54,806,749 (GRCm39) |
V92A |
possibly damaging |
Het |
Slfn5 |
A |
G |
11: 82,851,442 (GRCm39) |
K580E |
probably damaging |
Het |
Stard4 |
T |
C |
18: 33,338,377 (GRCm39) |
Y111C |
unknown |
Het |
Tagap |
C |
A |
17: 8,152,422 (GRCm39) |
Q536K |
possibly damaging |
Het |
Tank |
T |
C |
2: 61,480,513 (GRCm39) |
C351R |
probably damaging |
Het |
Tarbp2 |
A |
T |
15: 102,430,169 (GRCm39) |
M144L |
probably benign |
Het |
Tdrd9 |
T |
C |
12: 111,951,476 (GRCm39) |
Y89H |
probably damaging |
Het |
Tecpr2 |
C |
A |
12: 110,934,873 (GRCm39) |
T1373K |
probably benign |
Het |
Tle1 |
G |
A |
4: 72,055,349 (GRCm39) |
P434L |
probably damaging |
Het |
Tmed5 |
A |
G |
5: 108,272,495 (GRCm39) |
V201A |
probably benign |
Het |
Ust |
A |
G |
10: 8,266,650 (GRCm39) |
|
probably null |
Het |
Vmn2r94 |
T |
C |
17: 18,477,767 (GRCm39) |
T215A |
probably benign |
Het |
Zfp273 |
A |
T |
13: 67,973,251 (GRCm39) |
Q126H |
probably benign |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
|
Other mutations in Ak9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
Mean
|
UTSW |
10 |
41,233,559 (GRCm39) |
missense |
possibly damaging |
0.59 |
BB006:Ak9
|
UTSW |
10 |
41,259,944 (GRCm39) |
missense |
|
|
BB016:Ak9
|
UTSW |
10 |
41,259,944 (GRCm39) |
missense |
|
|
R0057:Ak9
|
UTSW |
10 |
41,268,724 (GRCm39) |
missense |
probably benign |
0.04 |
R0605:Ak9
|
UTSW |
10 |
41,221,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Ak9
|
UTSW |
10 |
41,223,218 (GRCm39) |
missense |
probably damaging |
0.98 |
R1696:Ak9
|
UTSW |
10 |
41,203,585 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1738:Ak9
|
UTSW |
10 |
41,211,917 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1815:Ak9
|
UTSW |
10 |
41,213,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R2900:Ak9
|
UTSW |
10 |
41,300,751 (GRCm39) |
missense |
unknown |
|
R3123:Ak9
|
UTSW |
10 |
41,234,576 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3715:Ak9
|
UTSW |
10 |
41,233,508 (GRCm39) |
missense |
probably damaging |
0.96 |
R4092:Ak9
|
UTSW |
10 |
41,265,140 (GRCm39) |
missense |
probably benign |
0.29 |
R4193:Ak9
|
UTSW |
10 |
41,211,941 (GRCm39) |
missense |
probably benign |
0.14 |
R4598:Ak9
|
UTSW |
10 |
41,259,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R4621:Ak9
|
UTSW |
10 |
41,282,887 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4681:Ak9
|
UTSW |
10 |
41,303,234 (GRCm39) |
missense |
unknown |
|
R4707:Ak9
|
UTSW |
10 |
41,221,456 (GRCm39) |
missense |
probably benign |
0.36 |
R4908:Ak9
|
UTSW |
10 |
41,296,678 (GRCm39) |
missense |
unknown |
|
R4952:Ak9
|
UTSW |
10 |
41,296,585 (GRCm39) |
missense |
probably benign |
0.07 |
R5162:Ak9
|
UTSW |
10 |
41,233,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R5446:Ak9
|
UTSW |
10 |
41,296,505 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5494:Ak9
|
UTSW |
10 |
41,223,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Ak9
|
UTSW |
10 |
41,216,887 (GRCm39) |
missense |
probably benign |
0.23 |
R5849:Ak9
|
UTSW |
10 |
41,224,045 (GRCm39) |
missense |
probably benign |
0.31 |
R5858:Ak9
|
UTSW |
10 |
41,299,023 (GRCm39) |
missense |
unknown |
|
R5920:Ak9
|
UTSW |
10 |
41,296,672 (GRCm39) |
missense |
probably benign |
0.30 |
R5952:Ak9
|
UTSW |
10 |
41,233,559 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5955:Ak9
|
UTSW |
10 |
41,234,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R6050:Ak9
|
UTSW |
10 |
41,265,108 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6087:Ak9
|
UTSW |
10 |
41,258,828 (GRCm39) |
missense |
probably benign |
0.01 |
R6190:Ak9
|
UTSW |
10 |
41,298,404 (GRCm39) |
missense |
unknown |
|
R6190:Ak9
|
UTSW |
10 |
41,298,403 (GRCm39) |
missense |
unknown |
|
R6197:Ak9
|
UTSW |
10 |
41,193,826 (GRCm39) |
missense |
probably damaging |
0.98 |
R6220:Ak9
|
UTSW |
10 |
41,246,095 (GRCm39) |
missense |
unknown |
|
R6250:Ak9
|
UTSW |
10 |
41,265,030 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6315:Ak9
|
UTSW |
10 |
41,282,837 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6331:Ak9
|
UTSW |
10 |
41,258,825 (GRCm39) |
missense |
probably damaging |
0.99 |
R6812:Ak9
|
UTSW |
10 |
41,243,163 (GRCm39) |
missense |
unknown |
|
R6847:Ak9
|
UTSW |
10 |
41,233,797 (GRCm39) |
splice site |
probably null |
|
R7128:Ak9
|
UTSW |
10 |
41,300,713 (GRCm39) |
missense |
unknown |
|
R7253:Ak9
|
UTSW |
10 |
41,308,480 (GRCm39) |
missense |
unknown |
|
R7286:Ak9
|
UTSW |
10 |
41,283,367 (GRCm39) |
missense |
|
|
R7401:Ak9
|
UTSW |
10 |
41,299,000 (GRCm39) |
missense |
unknown |
|
R7698:Ak9
|
UTSW |
10 |
41,224,072 (GRCm39) |
missense |
|
|
R7758:Ak9
|
UTSW |
10 |
41,223,128 (GRCm39) |
missense |
|
|
R7806:Ak9
|
UTSW |
10 |
41,309,080 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7894:Ak9
|
UTSW |
10 |
41,296,535 (GRCm39) |
missense |
unknown |
|
R7929:Ak9
|
UTSW |
10 |
41,259,944 (GRCm39) |
missense |
|
|
R7941:Ak9
|
UTSW |
10 |
41,285,133 (GRCm39) |
missense |
unknown |
|
R8032:Ak9
|
UTSW |
10 |
41,300,616 (GRCm39) |
missense |
unknown |
|
R8143:Ak9
|
UTSW |
10 |
41,213,588 (GRCm39) |
nonsense |
probably null |
|
R8298:Ak9
|
UTSW |
10 |
41,265,054 (GRCm39) |
missense |
|
|
R8301:Ak9
|
UTSW |
10 |
41,300,712 (GRCm39) |
missense |
|
|
R8355:Ak9
|
UTSW |
10 |
41,275,700 (GRCm39) |
missense |
|
|
R8703:Ak9
|
UTSW |
10 |
41,201,120 (GRCm39) |
missense |
|
|
R8728:Ak9
|
UTSW |
10 |
41,282,959 (GRCm39) |
missense |
|
|
R8757:Ak9
|
UTSW |
10 |
41,299,036 (GRCm39) |
missense |
unknown |
|
R8798:Ak9
|
UTSW |
10 |
41,258,847 (GRCm39) |
missense |
|
|
R8868:Ak9
|
UTSW |
10 |
41,258,869 (GRCm39) |
nonsense |
probably null |
|
R8868:Ak9
|
UTSW |
10 |
41,193,842 (GRCm39) |
critical splice donor site |
probably null |
|
R9088:Ak9
|
UTSW |
10 |
41,282,870 (GRCm39) |
missense |
|
|
R9090:Ak9
|
UTSW |
10 |
41,300,623 (GRCm39) |
missense |
unknown |
|
R9165:Ak9
|
UTSW |
10 |
41,309,235 (GRCm39) |
missense |
unknown |
|
R9195:Ak9
|
UTSW |
10 |
41,283,479 (GRCm39) |
missense |
|
|
R9271:Ak9
|
UTSW |
10 |
41,300,623 (GRCm39) |
missense |
unknown |
|
R9297:Ak9
|
UTSW |
10 |
41,299,081 (GRCm39) |
missense |
unknown |
|
R9302:Ak9
|
UTSW |
10 |
41,196,486 (GRCm39) |
missense |
|
|
R9309:Ak9
|
UTSW |
10 |
41,192,364 (GRCm39) |
critical splice donor site |
probably null |
|
R9318:Ak9
|
UTSW |
10 |
41,299,081 (GRCm39) |
missense |
unknown |
|
R9393:Ak9
|
UTSW |
10 |
41,285,068 (GRCm39) |
missense |
unknown |
|
R9541:Ak9
|
UTSW |
10 |
41,243,173 (GRCm39) |
missense |
|
|
R9579:Ak9
|
UTSW |
10 |
41,213,576 (GRCm39) |
missense |
|
|
R9618:Ak9
|
UTSW |
10 |
41,203,627 (GRCm39) |
missense |
|
|
R9697:Ak9
|
UTSW |
10 |
41,298,968 (GRCm39) |
nonsense |
probably null |
|
R9753:Ak9
|
UTSW |
10 |
41,259,496 (GRCm39) |
missense |
|
|
Z1176:Ak9
|
UTSW |
10 |
41,299,019 (GRCm39) |
missense |
unknown |
|
Z1176:Ak9
|
UTSW |
10 |
41,224,247 (GRCm39) |
missense |
|
|
|