Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam1b |
A |
G |
5: 121,638,856 (GRCm39) |
S730P |
possibly damaging |
Het |
Apoc4 |
C |
T |
7: 19,412,109 (GRCm39) |
C113Y |
probably damaging |
Het |
Arhgdia |
A |
G |
11: 120,471,202 (GRCm39) |
|
probably benign |
Het |
Ccdc171 |
A |
G |
4: 83,573,815 (GRCm39) |
T459A |
possibly damaging |
Het |
Ccdc190 |
A |
C |
1: 169,761,393 (GRCm39) |
K165T |
probably damaging |
Het |
Dop1b |
T |
C |
16: 93,567,128 (GRCm39) |
V1185A |
probably benign |
Het |
Ednrb |
C |
T |
14: 104,060,625 (GRCm39) |
V223I |
probably benign |
Het |
Ermp1 |
T |
C |
19: 29,623,538 (GRCm39) |
I151V |
possibly damaging |
Het |
Gm15737 |
T |
A |
6: 92,856,802 (GRCm39) |
|
probably benign |
Het |
Herc3 |
A |
G |
6: 58,837,371 (GRCm39) |
H348R |
possibly damaging |
Het |
Immp2l |
G |
T |
12: 41,675,590 (GRCm39) |
A95S |
probably damaging |
Het |
Invs |
A |
G |
4: 48,425,997 (GRCm39) |
Y928C |
probably damaging |
Het |
Itprid1 |
A |
G |
6: 55,874,680 (GRCm39) |
H210R |
probably benign |
Het |
Or1l4 |
A |
G |
2: 37,091,523 (GRCm39) |
E90G |
probably benign |
Het |
Or7g17 |
A |
T |
9: 18,768,352 (GRCm39) |
I135L |
probably benign |
Het |
Or8c15 |
A |
C |
9: 38,120,345 (GRCm39) |
|
probably benign |
Het |
Pkd1l2 |
G |
T |
8: 117,783,126 (GRCm39) |
S731R |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,392,747 (GRCm39) |
M1694T |
possibly damaging |
Het |
Pld2 |
C |
A |
11: 70,433,606 (GRCm39) |
R212S |
probably damaging |
Het |
Plekhg6 |
A |
G |
6: 125,355,793 (GRCm39) |
F4L |
probably benign |
Het |
Rps6ka6 |
T |
C |
X: 110,317,214 (GRCm39) |
Q634R |
probably benign |
Het |
Slc1a3 |
T |
C |
15: 8,671,822 (GRCm39) |
E378G |
probably benign |
Het |
Tmem184b |
T |
C |
15: 79,262,729 (GRCm39) |
T43A |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,577,132 (GRCm39) |
V24587A |
probably damaging |
Het |
Uba7 |
T |
A |
9: 107,854,547 (GRCm39) |
L262Q |
probably damaging |
Het |
Zfp954 |
G |
T |
7: 7,118,397 (GRCm39) |
H382Q |
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 |
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 |
R3888:Ano3
|
UTSW |
2 |
110,715,345 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|