Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acbd5 |
A |
G |
2: 22,989,579 (GRCm39) |
N401D |
probably benign |
Het |
Agtpbp1 |
T |
A |
13: 59,644,829 (GRCm39) |
D679V |
possibly damaging |
Het |
Akap8 |
A |
G |
17: 32,524,622 (GRCm39) |
V558A |
probably benign |
Het |
Arrdc2 |
C |
T |
8: 71,290,171 (GRCm39) |
R170Q |
probably benign |
Het |
Atg10 |
A |
T |
13: 91,189,027 (GRCm39) |
H94Q |
probably damaging |
Het |
Atg4a-ps |
G |
A |
3: 103,552,837 (GRCm39) |
A168V |
probably damaging |
Het |
Crb2 |
G |
T |
2: 37,673,395 (GRCm39) |
R97L |
probably benign |
Het |
Dnaja1 |
C |
T |
4: 40,724,052 (GRCm39) |
A71V |
possibly damaging |
Het |
Dysf |
G |
A |
6: 84,163,491 (GRCm39) |
|
probably null |
Het |
G6pd2 |
A |
G |
5: 61,966,869 (GRCm39) |
R215G |
probably damaging |
Het |
Hcn3 |
A |
G |
3: 89,054,920 (GRCm39) |
S776P |
probably benign |
Het |
Ift140 |
C |
A |
17: 25,254,805 (GRCm39) |
N159K |
possibly damaging |
Het |
Mafa |
A |
G |
15: 75,619,147 (GRCm39) |
S209P |
probably benign |
Het |
Mug2 |
A |
G |
6: 122,051,683 (GRCm39) |
|
probably null |
Het |
Myh14 |
T |
C |
7: 44,265,687 (GRCm39) |
D1564G |
possibly damaging |
Het |
Ncor2 |
T |
A |
5: 125,102,824 (GRCm39) |
I1792F |
probably damaging |
Het |
Nod2 |
T |
C |
8: 89,379,519 (GRCm39) |
F7L |
probably benign |
Het |
Or10d5 |
A |
G |
9: 39,861,660 (GRCm39) |
S136P |
probably benign |
Het |
Or1m1 |
T |
A |
9: 18,666,775 (GRCm39) |
D52V |
probably damaging |
Het |
Or2aa1 |
T |
C |
11: 59,480,265 (GRCm39) |
T217A |
probably benign |
Het |
Pak3 |
T |
C |
X: 142,547,972 (GRCm39) |
V318A |
probably damaging |
Het |
Pik3ap1 |
T |
C |
19: 41,290,970 (GRCm39) |
T521A |
probably benign |
Het |
Pkdcc |
G |
C |
17: 83,523,378 (GRCm39) |
A162P |
probably benign |
Het |
Rassf4 |
A |
G |
6: 116,618,701 (GRCm39) |
V194A |
probably damaging |
Het |
Scp2d1 |
T |
A |
2: 144,665,868 (GRCm39) |
I69N |
probably damaging |
Het |
Spg11 |
A |
G |
2: 121,905,782 (GRCm39) |
S1288P |
probably damaging |
Het |
Sptb |
A |
G |
12: 76,645,532 (GRCm39) |
S2019P |
probably damaging |
Het |
Stxbp5l |
A |
T |
16: 37,021,004 (GRCm39) |
L630* |
probably null |
Het |
Trim41 |
TTCCTCCTCCTCCTCCTCCTCCTCCTCC |
TTCCTCCTCCTCCTCCTCCTCCTCC |
11: 48,707,084 (GRCm39) |
|
probably benign |
Het |
Trpc1 |
C |
T |
9: 95,605,182 (GRCm39) |
R159H |
probably damaging |
Het |
Zbtb14 |
C |
T |
17: 69,695,214 (GRCm39) |
P304L |
probably damaging |
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 |
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 |
R8151:Odad2
|
UTSW |
18 |
7,127,358 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|