Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Abca7 |
T |
C |
10: 79,835,427 (GRCm39) |
|
probably null |
Het |
Abca8a |
C |
T |
11: 109,980,735 (GRCm39) |
|
probably null |
Het |
Ablim3 |
A |
G |
18: 61,952,982 (GRCm39) |
Y361H |
probably benign |
Het |
Acan |
C |
T |
7: 78,748,289 (GRCm39) |
T1020I |
probably benign |
Het |
Baat |
A |
G |
4: 49,499,652 (GRCm39) |
L218P |
probably damaging |
Het |
Bcl11b |
C |
A |
12: 107,955,975 (GRCm39) |
C58F |
probably damaging |
Het |
Cand2 |
G |
T |
6: 115,766,474 (GRCm39) |
A360S |
probably damaging |
Het |
Cdh2 |
A |
G |
18: 16,783,372 (GRCm39) |
V62A |
possibly damaging |
Het |
Cep44 |
C |
T |
8: 56,985,831 (GRCm39) |
V354I |
probably benign |
Het |
Col3a1 |
G |
A |
1: 45,368,244 (GRCm39) |
R309Q |
unknown |
Het |
Col3a1 |
G |
A |
1: 45,383,967 (GRCm39) |
|
probably benign |
Het |
Coq5 |
A |
G |
5: 115,433,839 (GRCm39) |
|
probably null |
Het |
Crtac1 |
A |
G |
19: 42,322,347 (GRCm39) |
I131T |
possibly damaging |
Het |
Decr1 |
C |
T |
4: 15,924,270 (GRCm39) |
V217M |
probably damaging |
Het |
Dnajc13 |
A |
G |
9: 104,051,724 (GRCm39) |
V1706A |
probably benign |
Het |
Dop1a |
A |
G |
9: 86,369,357 (GRCm39) |
I63M |
probably damaging |
Het |
F830045P16Rik |
T |
C |
2: 129,314,635 (GRCm39) |
D214G |
probably benign |
Het |
Fam216a |
T |
A |
5: 122,505,584 (GRCm39) |
|
probably null |
Het |
Fdxacb1 |
A |
C |
9: 50,683,387 (GRCm39) |
H248P |
possibly damaging |
Het |
Gnai1 |
A |
T |
5: 18,496,596 (GRCm39) |
V109E |
probably benign |
Het |
Helz2 |
A |
T |
2: 180,872,550 (GRCm39) |
|
probably null |
Het |
Itgam |
T |
C |
7: 127,715,489 (GRCm39) |
|
probably null |
Het |
Kcnh1 |
A |
G |
1: 192,187,836 (GRCm39) |
S766G |
probably benign |
Het |
Klra1 |
C |
A |
6: 130,352,241 (GRCm39) |
C167F |
probably damaging |
Het |
Krtap9-3 |
T |
A |
11: 99,488,808 (GRCm39) |
T25S |
probably benign |
Het |
Mapk6 |
T |
C |
9: 75,295,626 (GRCm39) |
Y624C |
probably damaging |
Het |
Or10ag2 |
A |
G |
2: 87,249,187 (GRCm39) |
Y263C |
probably damaging |
Het |
Or1ad8 |
T |
G |
11: 50,898,381 (GRCm39) |
I194S |
probably damaging |
Het |
Or2y1g |
T |
C |
11: 49,171,209 (GRCm39) |
V78A |
probably damaging |
Het |
Or52e4 |
C |
T |
7: 104,705,660 (GRCm39) |
S69L |
probably damaging |
Het |
Or9m2 |
T |
A |
2: 87,821,107 (GRCm39) |
Y217* |
probably null |
Het |
P3h2 |
A |
G |
16: 25,803,699 (GRCm39) |
S356P |
possibly damaging |
Het |
Rln3 |
T |
G |
8: 84,769,866 (GRCm39) |
K94N |
probably damaging |
Het |
Skint5 |
T |
C |
4: 113,620,711 (GRCm39) |
I668V |
unknown |
Het |
Slitrk5 |
C |
A |
14: 111,916,852 (GRCm39) |
Q159K |
probably damaging |
Het |
Trim3 |
G |
T |
7: 105,268,716 (GRCm39) |
N79K |
probably damaging |
Het |
Tyw1 |
T |
A |
5: 130,296,756 (GRCm39) |
C101* |
probably null |
Het |
Ulk2 |
T |
C |
11: 61,672,537 (GRCm39) |
T934A |
probably benign |
Het |
Unc5b |
T |
C |
10: 60,608,072 (GRCm39) |
Y687C |
probably benign |
Het |
Vmn1r195 |
C |
T |
13: 22,462,556 (GRCm39) |
R9* |
probably null |
Het |
Zfc3h1 |
T |
G |
10: 115,254,597 (GRCm39) |
L1397R |
probably damaging |
Het |
Zfp296 |
T |
C |
7: 19,311,332 (GRCm39) |
V9A |
probably benign |
Het |
Zfp423 |
T |
A |
8: 88,509,091 (GRCm39) |
S397C |
probably damaging |
Het |
|
Other mutations in Pde12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02085:Pde12
|
APN |
14 |
26,387,619 (GRCm39) |
unclassified |
probably benign |
|
IGL02306:Pde12
|
APN |
14 |
26,389,533 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02630:Pde12
|
APN |
14 |
26,387,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02830:Pde12
|
APN |
14 |
26,389,740 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03268:Pde12
|
APN |
14 |
26,389,614 (GRCm39) |
missense |
probably benign |
0.32 |
R1727:Pde12
|
UTSW |
14 |
26,390,022 (GRCm39) |
missense |
probably benign |
0.02 |
R2057:Pde12
|
UTSW |
14 |
26,390,035 (GRCm39) |
missense |
probably benign |
|
R2059:Pde12
|
UTSW |
14 |
26,390,035 (GRCm39) |
missense |
probably benign |
|
R2510:Pde12
|
UTSW |
14 |
26,386,681 (GRCm39) |
makesense |
probably null |
|
R4174:Pde12
|
UTSW |
14 |
26,390,144 (GRCm39) |
missense |
probably benign |
0.00 |
R5121:Pde12
|
UTSW |
14 |
26,390,577 (GRCm39) |
nonsense |
probably null |
|
R5387:Pde12
|
UTSW |
14 |
26,387,608 (GRCm39) |
missense |
probably benign |
0.00 |
R5847:Pde12
|
UTSW |
14 |
26,386,786 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5987:Pde12
|
UTSW |
14 |
26,390,253 (GRCm39) |
missense |
probably benign |
0.02 |
R7495:Pde12
|
UTSW |
14 |
26,389,994 (GRCm39) |
missense |
probably benign |
0.19 |
R8021:Pde12
|
UTSW |
14 |
26,386,854 (GRCm39) |
nonsense |
probably null |
|
R8865:Pde12
|
UTSW |
14 |
26,390,280 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8898:Pde12
|
UTSW |
14 |
26,390,577 (GRCm39) |
missense |
probably benign |
0.22 |
R9300:Pde12
|
UTSW |
14 |
26,386,931 (GRCm39) |
missense |
probably damaging |
0.98 |
R9331:Pde12
|
UTSW |
14 |
26,389,828 (GRCm39) |
missense |
probably benign |
|
R9604:Pde12
|
UTSW |
14 |
26,390,008 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9739:Pde12
|
UTSW |
14 |
26,386,757 (GRCm39) |
missense |
possibly damaging |
0.66 |
|