Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700020N01Rik |
T |
C |
10: 21,497,578 (GRCm39) |
L73P |
probably damaging |
Het |
4933412E24Rik |
T |
G |
15: 59,887,524 (GRCm39) |
R305S |
probably damaging |
Het |
Adamts19 |
T |
A |
18: 58,970,920 (GRCm39) |
V168E |
probably damaging |
Het |
Ankrd34b |
T |
A |
13: 92,576,097 (GRCm39) |
L443Q |
probably damaging |
Het |
Arhgef2 |
A |
T |
3: 88,546,739 (GRCm39) |
H553L |
probably benign |
Het |
Atxn1 |
G |
T |
13: 45,720,505 (GRCm39) |
N463K |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,932,099 (GRCm39) |
|
probably null |
Het |
C4bp |
A |
G |
1: 130,564,482 (GRCm39) |
S401P |
probably damaging |
Het |
Cd5 |
T |
A |
19: 10,697,609 (GRCm39) |
R457W |
probably damaging |
Het |
Chek2 |
T |
G |
5: 110,996,302 (GRCm39) |
Y127D |
probably damaging |
Het |
Clec4a1 |
G |
A |
6: 122,898,960 (GRCm39) |
V10M |
probably damaging |
Het |
Cltc |
A |
G |
11: 86,603,457 (GRCm39) |
Y790H |
probably damaging |
Het |
Cops2 |
T |
C |
2: 125,701,028 (GRCm39) |
|
probably benign |
Het |
Cyb5d2 |
A |
G |
11: 72,679,929 (GRCm39) |
F122S |
probably damaging |
Het |
Daam1 |
T |
A |
12: 71,998,689 (GRCm39) |
L548H |
unknown |
Het |
Dcp1a |
A |
G |
14: 30,244,883 (GRCm39) |
T570A |
possibly damaging |
Het |
Dsg1a |
A |
C |
18: 20,465,090 (GRCm39) |
N427T |
probably benign |
Het |
Ear14 |
A |
T |
14: 51,441,564 (GRCm39) |
D140V |
probably damaging |
Het |
Epha4 |
A |
C |
1: 77,483,547 (GRCm39) |
F154C |
probably damaging |
Het |
Ets2 |
G |
A |
16: 95,507,321 (GRCm39) |
V12M |
probably damaging |
Het |
Fbxo40 |
G |
A |
16: 36,789,670 (GRCm39) |
T480I |
probably damaging |
Het |
Fdps |
A |
T |
3: 89,001,048 (GRCm39) |
Y322N |
probably damaging |
Het |
Gca |
T |
C |
2: 62,516,700 (GRCm39) |
M132T |
probably benign |
Het |
Ifi203 |
T |
G |
1: 173,765,496 (GRCm39) |
K26T |
probably damaging |
Het |
Itga10 |
A |
G |
3: 96,562,116 (GRCm39) |
R668G |
probably damaging |
Het |
Itgal |
T |
C |
7: 126,929,638 (GRCm39) |
I1185T |
unknown |
Het |
Kcnj13 |
A |
T |
1: 87,314,189 (GRCm39) |
N344K |
probably damaging |
Het |
Kdm5a |
A |
T |
6: 120,358,516 (GRCm39) |
L186F |
probably benign |
Het |
Klhl8 |
T |
C |
5: 104,010,954 (GRCm39) |
N624D |
probably benign |
Het |
Klrb1 |
G |
T |
6: 128,689,222 (GRCm39) |
T83K |
possibly damaging |
Het |
Krt77 |
TGCCGCCGCCGCCGCCGCCGCCGCCGC |
TGCCGCCGCCGCCGCCGCCGCCGC |
15: 101,768,407 (GRCm39) |
|
probably benign |
Het |
Ltb |
G |
T |
17: 35,413,655 (GRCm39) |
R53L |
probably benign |
Het |
Mterf3 |
A |
G |
13: 67,055,222 (GRCm39) |
V69A |
|
Het |
Mvb12a |
A |
G |
8: 71,997,888 (GRCm39) |
K101E |
probably damaging |
Het |
Nbeal2 |
T |
A |
9: 110,464,409 (GRCm39) |
Q1110L |
possibly damaging |
Het |
Neb |
T |
A |
2: 52,198,775 (GRCm39) |
T389S |
possibly damaging |
Het |
Nol4 |
A |
G |
18: 23,173,069 (GRCm39) |
F11L |
probably damaging |
Het |
Or10p22 |
T |
C |
10: 128,826,708 (GRCm39) |
L309P |
possibly damaging |
Het |
Or2a54 |
A |
G |
6: 43,093,440 (GRCm39) |
I255V |
probably benign |
Het |
Or2h15 |
A |
G |
17: 38,441,484 (GRCm39) |
S200P |
probably damaging |
Het |
Or52e8b |
C |
T |
7: 104,673,885 (GRCm39) |
G97R |
probably benign |
Het |
Pde2a |
T |
A |
7: 101,153,880 (GRCm39) |
Y487N |
possibly damaging |
Het |
Pde4a |
C |
T |
9: 21,077,404 (GRCm39) |
P61S |
possibly damaging |
Het |
Pramel16 |
T |
A |
4: 143,675,690 (GRCm39) |
T379S |
probably benign |
Het |
Prr5l |
A |
G |
2: 101,571,630 (GRCm39) |
|
probably null |
Het |
Ptpn6 |
G |
A |
6: 124,705,614 (GRCm39) |
T179I |
possibly damaging |
Het |
Ralyl |
T |
C |
3: 14,104,836 (GRCm39) |
S34P |
probably benign |
Het |
Rftn1 |
G |
T |
17: 50,354,408 (GRCm39) |
A318D |
probably damaging |
Het |
Robo2 |
A |
T |
16: 73,812,814 (GRCm39) |
C293* |
probably null |
Het |
Rtn4 |
T |
G |
11: 29,655,536 (GRCm39) |
D169E |
probably damaging |
Het |
Slc22a22 |
A |
T |
15: 57,122,506 (GRCm39) |
V157E |
probably damaging |
Het |
Sytl2 |
A |
G |
7: 90,034,283 (GRCm39) |
T498A |
probably benign |
Het |
Tgm6 |
G |
A |
2: 129,979,358 (GRCm39) |
V163I |
probably benign |
Het |
Tnpo3 |
A |
T |
6: 29,582,302 (GRCm39) |
C187S |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,616,485 (GRCm39) |
|
probably null |
Het |
Tut4 |
G |
A |
4: 108,336,905 (GRCm39) |
A210T |
possibly damaging |
Het |
Vangl2 |
C |
A |
1: 171,837,513 (GRCm39) |
V99F |
possibly damaging |
Het |
Vmn1r167 |
C |
T |
7: 23,204,215 (GRCm39) |
C267Y |
probably damaging |
Het |
Vsig10l |
T |
C |
7: 43,113,531 (GRCm39) |
V161A |
possibly damaging |
Het |
Xrcc5 |
G |
A |
1: 72,364,244 (GRCm39) |
R232Q |
possibly damaging |
Het |
Xrcc6 |
C |
G |
15: 81,913,463 (GRCm39) |
F365L |
probably damaging |
Het |
Zdhhc13 |
A |
G |
7: 48,465,257 (GRCm39) |
Y389C |
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 |
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 |
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 |
|