Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
T |
C |
19: 8,982,043 (GRCm39) |
I1109T |
possibly damaging |
Het |
Aipl1 |
C |
A |
11: 71,927,584 (GRCm39) |
D44Y |
probably benign |
Het |
Aldh8a1 |
C |
T |
10: 21,271,465 (GRCm39) |
T397M |
probably damaging |
Het |
Btbd16 |
T |
C |
7: 130,398,825 (GRCm39) |
S278P |
probably damaging |
Het |
Ccdc110 |
G |
A |
8: 46,395,830 (GRCm39) |
E574K |
probably damaging |
Het |
Cd19 |
T |
A |
7: 126,013,478 (GRCm39) |
K104* |
probably null |
Het |
Cenpe |
A |
G |
3: 134,952,783 (GRCm39) |
E1491G |
probably benign |
Het |
Col12a1 |
A |
T |
9: 79,537,831 (GRCm39) |
S2546T |
possibly damaging |
Het |
Col18a1 |
T |
C |
10: 76,948,418 (GRCm39) |
T365A |
unknown |
Het |
Ctif |
G |
T |
18: 75,653,176 (GRCm39) |
D360E |
probably benign |
Het |
Fat4 |
G |
A |
3: 38,946,203 (GRCm39) |
E1699K |
probably damaging |
Het |
Fbxo39 |
G |
A |
11: 72,208,526 (GRCm39) |
V293M |
probably damaging |
Het |
Fcgbpl1 |
T |
C |
7: 27,852,766 (GRCm39) |
I1351T |
possibly damaging |
Het |
Fhip1a |
A |
T |
3: 85,595,847 (GRCm39) |
I346N |
probably damaging |
Het |
Havcr2 |
A |
G |
11: 46,366,722 (GRCm39) |
K221E |
possibly damaging |
Het |
Hdac5 |
T |
C |
11: 102,097,294 (GRCm39) |
T209A |
probably benign |
Het |
Herc1 |
A |
G |
9: 66,341,073 (GRCm39) |
Q1730R |
probably damaging |
Het |
Ifi202b |
T |
C |
1: 173,804,923 (GRCm39) |
T10A |
probably benign |
Het |
Il18rap |
T |
C |
1: 40,564,428 (GRCm39) |
S153P |
probably benign |
Het |
Klk1b21 |
C |
T |
7: 43,753,787 (GRCm39) |
R24* |
probably null |
Het |
Kras |
ACTTCTTCTTCTTCTTCTTC |
ACTTCTTCTTCTTCTTC |
6: 145,166,360 (GRCm39) |
|
probably benign |
Het |
Ldlrad4 |
A |
G |
18: 68,383,643 (GRCm39) |
E113G |
possibly damaging |
Het |
Lhcgr |
AT |
ATT |
17: 89,049,677 (GRCm39) |
615 |
probably null |
Het |
Macf1 |
T |
C |
4: 123,291,206 (GRCm39) |
E3895G |
possibly damaging |
Het |
Mug1 |
T |
C |
6: 121,818,117 (GRCm39) |
S143P |
probably benign |
Het |
Nudcd2 |
A |
T |
11: 40,624,529 (GRCm39) |
|
probably benign |
Het |
Nup85 |
A |
G |
11: 115,468,759 (GRCm39) |
T201A |
probably benign |
Het |
Plppr2 |
A |
G |
9: 21,852,105 (GRCm39) |
E64G |
probably damaging |
Het |
Plvap |
A |
G |
8: 71,960,625 (GRCm39) |
S264P |
probably benign |
Het |
Polm |
T |
C |
11: 5,787,906 (GRCm39) |
|
probably benign |
Het |
Polr2d |
T |
A |
18: 31,928,365 (GRCm39) |
H93Q |
probably damaging |
Het |
Ptprt |
T |
C |
2: 162,120,005 (GRCm39) |
E154G |
probably damaging |
Het |
Rasal2 |
C |
A |
1: 157,071,154 (GRCm39) |
G67C |
probably damaging |
Het |
Sdk2 |
A |
G |
11: 113,763,683 (GRCm39) |
V329A |
possibly damaging |
Het |
Sorl1 |
A |
G |
9: 41,979,229 (GRCm39) |
V423A |
probably damaging |
Het |
Spef2 |
A |
G |
15: 9,601,598 (GRCm39) |
S1555P |
unknown |
Het |
Srgap3 |
A |
C |
6: 112,793,628 (GRCm39) |
L116R |
probably damaging |
Het |
St6galnac3 |
C |
T |
3: 153,117,217 (GRCm39) |
V169M |
probably damaging |
Het |
Stx16 |
T |
A |
2: 173,935,284 (GRCm39) |
M206K |
possibly damaging |
Het |
Txnip |
A |
G |
3: 96,466,929 (GRCm39) |
D201G |
possibly damaging |
Het |
Ubr4 |
T |
C |
4: 139,130,112 (GRCm39) |
V718A |
probably damaging |
Het |
Vav3 |
A |
C |
3: 109,416,164 (GRCm39) |
D261A |
probably benign |
Het |
Vcam1 |
A |
C |
3: 115,918,128 (GRCm39) |
L278V |
possibly damaging |
Het |
Vta1 |
C |
A |
10: 14,543,697 (GRCm39) |
A226S |
probably damaging |
Het |
Zfp217 |
G |
A |
2: 169,961,571 (GRCm39) |
S252F |
possibly damaging |
Het |
Zfp777 |
G |
A |
6: 48,006,075 (GRCm39) |
Q440* |
probably null |
Het |
|
Other mutations in Odad2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00693:Odad2
|
APN |
18 |
7,211,504 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00822:Odad2
|
APN |
18 |
7,181,817 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01345:Odad2
|
APN |
18 |
7,266,947 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01593:Odad2
|
APN |
18 |
7,127,345 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01645:Odad2
|
APN |
18 |
7,268,491 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01863:Odad2
|
APN |
18 |
7,222,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01955:Odad2
|
APN |
18 |
7,127,291 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02013:Odad2
|
APN |
18 |
7,265,157 (GRCm39) |
splice site |
probably benign |
|
IGL02142:Odad2
|
APN |
18 |
7,214,601 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02399:Odad2
|
APN |
18 |
7,285,719 (GRCm39) |
missense |
probably benign |
|
IGL02439:Odad2
|
APN |
18 |
7,268,444 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02452:Odad2
|
APN |
18 |
7,129,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02632:Odad2
|
APN |
18 |
7,214,727 (GRCm39) |
splice site |
probably benign |
|
IGL03344:Odad2
|
APN |
18 |
7,129,434 (GRCm39) |
nonsense |
probably null |
|
R0062:Odad2
|
UTSW |
18 |
7,129,593 (GRCm39) |
splice site |
probably benign |
|
R0062:Odad2
|
UTSW |
18 |
7,129,593 (GRCm39) |
splice site |
probably benign |
|
R0242:Odad2
|
UTSW |
18 |
7,211,516 (GRCm39) |
missense |
probably damaging |
0.96 |
R0242:Odad2
|
UTSW |
18 |
7,211,516 (GRCm39) |
missense |
probably damaging |
0.96 |
R0365:Odad2
|
UTSW |
18 |
7,217,800 (GRCm39) |
missense |
probably benign |
0.01 |
R0377:Odad2
|
UTSW |
18 |
7,127,415 (GRCm39) |
missense |
probably benign |
0.04 |
R0466:Odad2
|
UTSW |
18 |
7,286,758 (GRCm39) |
missense |
probably benign |
0.10 |
R0517:Odad2
|
UTSW |
18 |
7,223,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Odad2
|
UTSW |
18 |
7,222,676 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0841:Odad2
|
UTSW |
18 |
7,268,436 (GRCm39) |
missense |
probably damaging |
0.99 |
R1145:Odad2
|
UTSW |
18 |
7,268,436 (GRCm39) |
missense |
probably damaging |
0.99 |
R1145:Odad2
|
UTSW |
18 |
7,268,436 (GRCm39) |
missense |
probably damaging |
0.99 |
R1435:Odad2
|
UTSW |
18 |
7,222,646 (GRCm39) |
missense |
probably benign |
0.01 |
R1487:Odad2
|
UTSW |
18 |
7,273,245 (GRCm39) |
missense |
probably damaging |
0.98 |
R1634:Odad2
|
UTSW |
18 |
7,286,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R1677:Odad2
|
UTSW |
18 |
7,222,554 (GRCm39) |
missense |
probably benign |
0.01 |
R1778:Odad2
|
UTSW |
18 |
7,127,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R1792:Odad2
|
UTSW |
18 |
7,286,743 (GRCm39) |
missense |
probably benign |
0.00 |
R1809:Odad2
|
UTSW |
18 |
7,211,630 (GRCm39) |
missense |
probably benign |
0.08 |
R1842:Odad2
|
UTSW |
18 |
7,223,551 (GRCm39) |
missense |
probably benign |
0.04 |
R2144:Odad2
|
UTSW |
18 |
7,127,229 (GRCm39) |
missense |
probably damaging |
0.96 |
R2206:Odad2
|
UTSW |
18 |
7,223,676 (GRCm39) |
missense |
probably benign |
0.25 |
R2273:Odad2
|
UTSW |
18 |
7,223,676 (GRCm39) |
missense |
probably benign |
0.25 |
R2275:Odad2
|
UTSW |
18 |
7,223,676 (GRCm39) |
missense |
probably benign |
0.25 |
R2918:Odad2
|
UTSW |
18 |
7,222,625 (GRCm39) |
missense |
probably benign |
0.04 |
R3421:Odad2
|
UTSW |
18 |
7,223,523 (GRCm39) |
splice site |
probably benign |
|
R3422:Odad2
|
UTSW |
18 |
7,223,523 (GRCm39) |
splice site |
probably benign |
|
R4165:Odad2
|
UTSW |
18 |
7,217,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R4225:Odad2
|
UTSW |
18 |
7,181,732 (GRCm39) |
critical splice donor site |
probably null |
|
R4660:Odad2
|
UTSW |
18 |
7,211,609 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4745:Odad2
|
UTSW |
18 |
7,286,763 (GRCm39) |
missense |
probably benign |
0.28 |
R4812:Odad2
|
UTSW |
18 |
7,288,634 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4831:Odad2
|
UTSW |
18 |
7,222,564 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4923:Odad2
|
UTSW |
18 |
7,181,787 (GRCm39) |
missense |
probably damaging |
0.97 |
R4995:Odad2
|
UTSW |
18 |
7,223,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R5024:Odad2
|
UTSW |
18 |
7,088,555 (GRCm39) |
missense |
probably benign |
0.02 |
R5335:Odad2
|
UTSW |
18 |
7,294,566 (GRCm39) |
missense |
probably benign |
0.06 |
R5434:Odad2
|
UTSW |
18 |
7,222,550 (GRCm39) |
missense |
probably benign |
0.03 |
R5552:Odad2
|
UTSW |
18 |
7,285,360 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5719:Odad2
|
UTSW |
18 |
7,211,496 (GRCm39) |
missense |
probably benign |
0.00 |
R5736:Odad2
|
UTSW |
18 |
7,268,416 (GRCm39) |
missense |
probably benign |
0.01 |
R5792:Odad2
|
UTSW |
18 |
7,217,965 (GRCm39) |
missense |
probably benign |
0.00 |
R5848:Odad2
|
UTSW |
18 |
7,268,507 (GRCm39) |
splice site |
probably null |
|
R5957:Odad2
|
UTSW |
18 |
7,285,706 (GRCm39) |
missense |
probably benign |
0.01 |
R6001:Odad2
|
UTSW |
18 |
7,286,838 (GRCm39) |
missense |
probably benign |
0.03 |
R6309:Odad2
|
UTSW |
18 |
7,214,617 (GRCm39) |
missense |
probably benign |
0.04 |
R6559:Odad2
|
UTSW |
18 |
7,223,664 (GRCm39) |
missense |
probably damaging |
0.99 |
R6574:Odad2
|
UTSW |
18 |
7,129,394 (GRCm39) |
splice site |
probably null |
|
R6581:Odad2
|
UTSW |
18 |
7,129,560 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6736:Odad2
|
UTSW |
18 |
7,223,586 (GRCm39) |
missense |
probably damaging |
0.98 |
R6842:Odad2
|
UTSW |
18 |
7,268,401 (GRCm39) |
missense |
probably benign |
0.00 |
R6968:Odad2
|
UTSW |
18 |
7,273,155 (GRCm39) |
splice site |
probably null |
|
R6974:Odad2
|
UTSW |
18 |
7,294,479 (GRCm39) |
missense |
probably benign |
0.37 |
R7024:Odad2
|
UTSW |
18 |
7,211,593 (GRCm39) |
missense |
probably benign |
0.43 |
R7299:Odad2
|
UTSW |
18 |
7,222,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R7578:Odad2
|
UTSW |
18 |
7,211,593 (GRCm39) |
missense |
probably benign |
0.43 |
R7737:Odad2
|
UTSW |
18 |
7,217,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R7878:Odad2
|
UTSW |
18 |
7,217,801 (GRCm39) |
missense |
probably benign |
0.01 |
R8025:Odad2
|
UTSW |
18 |
7,127,224 (GRCm39) |
missense |
probably benign |
0.43 |
R8989:Odad2
|
UTSW |
18 |
7,268,464 (GRCm39) |
missense |
probably benign |
0.24 |
R8998:Odad2
|
UTSW |
18 |
7,211,574 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8999:Odad2
|
UTSW |
18 |
7,211,574 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9006:Odad2
|
UTSW |
18 |
7,294,516 (GRCm39) |
missense |
probably benign |
0.00 |
R9091:Odad2
|
UTSW |
18 |
7,217,846 (GRCm39) |
nonsense |
probably null |
|
R9106:Odad2
|
UTSW |
18 |
7,294,527 (GRCm39) |
missense |
probably benign |
0.18 |
R9153:Odad2
|
UTSW |
18 |
7,286,733 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9229:Odad2
|
UTSW |
18 |
7,127,324 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9254:Odad2
|
UTSW |
18 |
7,265,089 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9270:Odad2
|
UTSW |
18 |
7,217,846 (GRCm39) |
nonsense |
probably null |
|
R9379:Odad2
|
UTSW |
18 |
7,265,089 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9626:Odad2
|
UTSW |
18 |
7,211,422 (GRCm39) |
nonsense |
probably null |
|
R9708:Odad2
|
UTSW |
18 |
7,288,633 (GRCm39) |
missense |
probably benign |
0.02 |
Z1088:Odad2
|
UTSW |
18 |
7,266,919 (GRCm39) |
missense |
probably benign |
|
Z1176:Odad2
|
UTSW |
18 |
7,216,973 (GRCm39) |
nonsense |
probably null |
|
Z1176:Odad2
|
UTSW |
18 |
7,129,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|