Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933407L21Rik |
T |
A |
1: 85,868,273 (GRCm39) |
|
probably null |
Het |
Acbd6 |
A |
G |
1: 155,500,643 (GRCm39) |
D201G |
probably damaging |
Het |
Adam17 |
G |
A |
12: 21,375,588 (GRCm39) |
R744C |
probably damaging |
Het |
Adss2 |
A |
G |
1: 177,595,335 (GRCm39) |
Y402H |
probably damaging |
Het |
B930094E09Rik |
G |
A |
18: 31,742,742 (GRCm39) |
S59N |
unknown |
Het |
Cmya5 |
T |
G |
13: 93,230,164 (GRCm39) |
R1641S |
probably benign |
Het |
Cps1 |
C |
A |
1: 67,204,659 (GRCm39) |
T493K |
possibly damaging |
Het |
Dmxl1 |
T |
A |
18: 50,011,326 (GRCm39) |
M1161K |
probably damaging |
Het |
Etl4 |
C |
T |
2: 20,534,772 (GRCm39) |
Q76* |
probably null |
Het |
Fn1 |
T |
C |
1: 71,679,465 (GRCm39) |
Y511C |
probably damaging |
Het |
Foxd2 |
T |
C |
4: 114,765,483 (GRCm39) |
H179R |
unknown |
Het |
Frem1 |
T |
C |
4: 82,831,844 (GRCm39) |
R1991G |
probably benign |
Het |
Gimap7 |
G |
A |
6: 48,700,779 (GRCm39) |
E122K |
probably benign |
Het |
Hps3 |
A |
G |
3: 20,057,387 (GRCm39) |
|
probably null |
Het |
Kctd2 |
A |
T |
11: 115,318,345 (GRCm39) |
K209N |
probably damaging |
Het |
Lcor |
T |
A |
19: 41,546,795 (GRCm39) |
S126R |
probably damaging |
Het |
Lct |
T |
C |
1: 128,231,963 (GRCm39) |
M629V |
probably damaging |
Het |
Lrp5 |
G |
A |
19: 3,662,330 (GRCm39) |
R173C |
probably damaging |
Het |
Muc5ac |
T |
C |
7: 141,344,961 (GRCm39) |
V144A |
possibly damaging |
Het |
Mypn |
T |
C |
10: 63,028,289 (GRCm39) |
Y258C |
probably damaging |
Het |
Ntf3 |
T |
C |
6: 126,079,405 (GRCm39) |
M21V |
probably benign |
Het |
Or4a71 |
T |
A |
2: 89,358,076 (GRCm39) |
H226L |
possibly damaging |
Het |
Or5b97 |
A |
T |
19: 12,878,497 (GRCm39) |
C216S |
probably benign |
Het |
Or6c1 |
A |
T |
10: 129,518,088 (GRCm39) |
D173E |
probably benign |
Het |
Or6c1 |
G |
A |
10: 129,518,087 (GRCm39) |
H174Y |
possibly damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rbm45 |
A |
G |
2: 76,205,768 (GRCm39) |
S207G |
probably benign |
Het |
Robo3 |
G |
A |
9: 37,333,477 (GRCm39) |
Q723* |
probably null |
Het |
Rreb1 |
G |
T |
13: 38,077,941 (GRCm39) |
R51L |
probably damaging |
Het |
Slc12a6 |
T |
A |
2: 112,097,375 (GRCm39) |
L70Q |
possibly damaging |
Het |
Slc15a2 |
A |
G |
16: 36,602,666 (GRCm39) |
F65S |
probably damaging |
Het |
Slitrk5 |
T |
A |
14: 111,917,229 (GRCm39) |
C284* |
probably null |
Het |
Smim17 |
G |
T |
7: 6,432,279 (GRCm39) |
G74C |
probably damaging |
Het |
Snapc4 |
G |
A |
2: 26,255,510 (GRCm39) |
Q1005* |
probably null |
Het |
Suv39h2 |
G |
A |
2: 3,465,845 (GRCm39) |
T170I |
probably benign |
Het |
Thrb |
A |
G |
14: 18,033,551 (GRCm38) |
K424R |
probably damaging |
Het |
Tm4sf4 |
C |
T |
3: 57,345,166 (GRCm39) |
Q191* |
probably null |
Het |
Trak1 |
G |
T |
9: 121,271,863 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
G |
2: 76,540,618 (GRCm39) |
S25796P |
probably damaging |
Het |
Ugp2 |
T |
C |
11: 21,303,366 (GRCm39) |
R80G |
probably benign |
Het |
Utp15 |
C |
T |
13: 98,395,674 (GRCm39) |
V103I |
probably benign |
Het |
Wdr3 |
A |
T |
3: 100,061,222 (GRCm39) |
S249T |
probably benign |
Het |
Zeb1 |
T |
A |
18: 5,748,743 (GRCm39) |
D86E |
probably damaging |
Het |
|
Other mutations in Ano3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00502:Ano3
|
APN |
2 |
110,601,395 (GRCm39) |
splice site |
probably benign |
|
IGL01066:Ano3
|
APN |
2 |
110,491,790 (GRCm39) |
missense |
probably null |
0.00 |
IGL01696:Ano3
|
APN |
2 |
110,498,082 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01729:Ano3
|
APN |
2 |
110,611,739 (GRCm39) |
splice site |
probably null |
|
IGL01785:Ano3
|
APN |
2 |
110,513,060 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01786:Ano3
|
APN |
2 |
110,513,060 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01992:Ano3
|
APN |
2 |
110,488,564 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02098:Ano3
|
APN |
2 |
110,496,786 (GRCm39) |
nonsense |
probably null |
|
IGL02333:Ano3
|
APN |
2 |
110,527,544 (GRCm39) |
splice site |
probably benign |
|
IGL02346:Ano3
|
APN |
2 |
110,601,271 (GRCm39) |
splice site |
probably benign |
|
IGL02352:Ano3
|
APN |
2 |
110,715,288 (GRCm39) |
nonsense |
probably null |
|
IGL02359:Ano3
|
APN |
2 |
110,715,288 (GRCm39) |
nonsense |
probably null |
|
IGL02544:Ano3
|
APN |
2 |
110,488,594 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02750:Ano3
|
APN |
2 |
110,496,329 (GRCm39) |
splice site |
probably benign |
|
IGL02861:Ano3
|
APN |
2 |
110,569,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02948:Ano3
|
APN |
2 |
110,527,363 (GRCm39) |
splice site |
probably benign |
|
IGL03327:Ano3
|
APN |
2 |
110,527,523 (GRCm39) |
missense |
possibly damaging |
0.62 |
3-1:Ano3
|
UTSW |
2 |
110,527,469 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02988:Ano3
|
UTSW |
2 |
110,605,355 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03147:Ano3
|
UTSW |
2 |
110,527,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R0349:Ano3
|
UTSW |
2 |
110,491,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R0426:Ano3
|
UTSW |
2 |
110,491,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R0523:Ano3
|
UTSW |
2 |
110,715,200 (GRCm39) |
missense |
probably benign |
0.13 |
R0557:Ano3
|
UTSW |
2 |
110,693,297 (GRCm39) |
splice site |
probably null |
|
R0611:Ano3
|
UTSW |
2 |
110,715,346 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0891:Ano3
|
UTSW |
2 |
110,528,321 (GRCm39) |
missense |
probably benign |
0.03 |
R1459:Ano3
|
UTSW |
2 |
110,711,174 (GRCm39) |
missense |
probably benign |
0.00 |
R1460:Ano3
|
UTSW |
2 |
110,513,103 (GRCm39) |
missense |
probably damaging |
0.97 |
R1773:Ano3
|
UTSW |
2 |
110,591,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Ano3
|
UTSW |
2 |
110,715,217 (GRCm39) |
missense |
probably benign |
0.00 |
R1919:Ano3
|
UTSW |
2 |
110,715,352 (GRCm39) |
missense |
probably benign |
|
R2185:Ano3
|
UTSW |
2 |
110,605,390 (GRCm39) |
missense |
probably benign |
0.01 |
R2280:Ano3
|
UTSW |
2 |
110,513,104 (GRCm39) |
missense |
probably benign |
0.22 |
R2281:Ano3
|
UTSW |
2 |
110,513,104 (GRCm39) |
missense |
probably benign |
0.22 |
R2348:Ano3
|
UTSW |
2 |
110,614,088 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2425:Ano3
|
UTSW |
2 |
110,693,188 (GRCm39) |
missense |
probably benign |
|
R2697:Ano3
|
UTSW |
2 |
110,625,305 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3923:Ano3
|
UTSW |
2 |
110,601,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R4352:Ano3
|
UTSW |
2 |
110,576,239 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4447:Ano3
|
UTSW |
2 |
110,591,923 (GRCm39) |
splice site |
probably null |
|
R4790:Ano3
|
UTSW |
2 |
110,715,264 (GRCm39) |
missense |
probably benign |
|
R4832:Ano3
|
UTSW |
2 |
110,498,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R4916:Ano3
|
UTSW |
2 |
110,601,365 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5113:Ano3
|
UTSW |
2 |
110,491,825 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5486:Ano3
|
UTSW |
2 |
110,576,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R5498:Ano3
|
UTSW |
2 |
110,527,448 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5589:Ano3
|
UTSW |
2 |
110,715,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R5627:Ano3
|
UTSW |
2 |
110,587,298 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5741:Ano3
|
UTSW |
2 |
110,488,618 (GRCm39) |
missense |
probably benign |
0.11 |
R5767:Ano3
|
UTSW |
2 |
110,491,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5883:Ano3
|
UTSW |
2 |
110,711,209 (GRCm39) |
missense |
probably null |
0.15 |
R5899:Ano3
|
UTSW |
2 |
110,693,232 (GRCm39) |
missense |
probably benign |
0.39 |
R5916:Ano3
|
UTSW |
2 |
110,512,181 (GRCm39) |
missense |
probably benign |
0.29 |
R6158:Ano3
|
UTSW |
2 |
110,496,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R6315:Ano3
|
UTSW |
2 |
110,527,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R6401:Ano3
|
UTSW |
2 |
110,605,459 (GRCm39) |
missense |
probably benign |
0.01 |
R6481:Ano3
|
UTSW |
2 |
110,625,372 (GRCm39) |
missense |
probably benign |
0.16 |
R6482:Ano3
|
UTSW |
2 |
110,527,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R6587:Ano3
|
UTSW |
2 |
110,628,249 (GRCm39) |
splice site |
probably null |
|
R6811:Ano3
|
UTSW |
2 |
110,711,212 (GRCm39) |
missense |
probably benign |
0.03 |
R7048:Ano3
|
UTSW |
2 |
110,513,116 (GRCm39) |
nonsense |
probably null |
|
R7145:Ano3
|
UTSW |
2 |
110,693,205 (GRCm39) |
missense |
probably benign |
0.31 |
R7207:Ano3
|
UTSW |
2 |
110,611,768 (GRCm39) |
missense |
probably damaging |
0.96 |
R7215:Ano3
|
UTSW |
2 |
110,496,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R7366:Ano3
|
UTSW |
2 |
110,587,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R7371:Ano3
|
UTSW |
2 |
110,715,194 (GRCm39) |
critical splice donor site |
probably null |
|
R7568:Ano3
|
UTSW |
2 |
110,780,638 (GRCm39) |
start gained |
probably benign |
|
R7636:Ano3
|
UTSW |
2 |
110,513,048 (GRCm39) |
nonsense |
probably null |
|
R7888:Ano3
|
UTSW |
2 |
110,496,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R7992:Ano3
|
UTSW |
2 |
110,605,367 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8024:Ano3
|
UTSW |
2 |
110,498,128 (GRCm39) |
missense |
probably damaging |
0.99 |
R8074:Ano3
|
UTSW |
2 |
110,780,577 (GRCm39) |
start gained |
probably benign |
|
R8111:Ano3
|
UTSW |
2 |
110,614,058 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8177:Ano3
|
UTSW |
2 |
110,496,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R8297:Ano3
|
UTSW |
2 |
110,491,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R8485:Ano3
|
UTSW |
2 |
110,498,200 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8509:Ano3
|
UTSW |
2 |
110,496,180 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8870:Ano3
|
UTSW |
2 |
110,614,074 (GRCm39) |
missense |
probably benign |
0.12 |
R9071:Ano3
|
UTSW |
2 |
110,625,418 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9072:Ano3
|
UTSW |
2 |
110,576,243 (GRCm39) |
missense |
probably benign |
0.06 |
R9073:Ano3
|
UTSW |
2 |
110,576,243 (GRCm39) |
missense |
probably benign |
0.06 |
R9315:Ano3
|
UTSW |
2 |
110,528,287 (GRCm39) |
missense |
probably damaging |
0.97 |
R9376:Ano3
|
UTSW |
2 |
110,496,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R9588:Ano3
|
UTSW |
2 |
110,528,342 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9697:Ano3
|
UTSW |
2 |
110,496,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R9716:Ano3
|
UTSW |
2 |
110,601,376 (GRCm39) |
missense |
probably damaging |
0.97 |
R9748:Ano3
|
UTSW |
2 |
110,488,640 (GRCm39) |
missense |
probably damaging |
1.00 |
RF012:Ano3
|
UTSW |
2 |
110,527,868 (GRCm39) |
missense |
possibly damaging |
0.83 |
RF013:Ano3
|
UTSW |
2 |
110,527,381 (GRCm39) |
missense |
probably benign |
0.30 |
X0058:Ano3
|
UTSW |
2 |
110,527,763 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Ano3
|
UTSW |
2 |
110,576,192 (GRCm39) |
missense |
probably damaging |
1.00 |
|