Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap9 |
T |
C |
5: 4,010,734 (GRCm39) |
V497A |
probably benign |
Het |
Alx3 |
T |
C |
3: 107,507,980 (GRCm39) |
F163S |
possibly damaging |
Het |
Ankmy1 |
T |
C |
1: 92,798,014 (GRCm39) |
R997G |
probably benign |
Het |
Arfgef2 |
T |
C |
2: 166,702,604 (GRCm39) |
S848P |
probably benign |
Het |
Atp11b |
A |
G |
3: 35,891,156 (GRCm39) |
I810V |
probably benign |
Het |
C1ql4 |
T |
G |
15: 98,982,718 (GRCm39) |
I212L |
probably benign |
Het |
Cep63 |
T |
C |
9: 102,475,387 (GRCm39) |
Y443C |
probably benign |
Het |
Cfap45 |
C |
T |
1: 172,372,696 (GRCm39) |
Q464* |
probably null |
Het |
Clcn3 |
T |
C |
8: 61,376,039 (GRCm39) |
K618R |
probably damaging |
Het |
Dmpk |
C |
G |
7: 18,821,944 (GRCm39) |
L301V |
probably benign |
Het |
Dnaaf4 |
T |
C |
9: 72,879,713 (GRCm39) |
S418P |
probably damaging |
Het |
Hook1 |
A |
G |
4: 95,881,367 (GRCm39) |
D113G |
probably damaging |
Het |
Ift122 |
A |
G |
6: 115,897,340 (GRCm39) |
E914G |
probably damaging |
Het |
Insr |
A |
G |
8: 3,248,059 (GRCm39) |
|
probably null |
Het |
Itpr2 |
A |
T |
6: 146,045,605 (GRCm39) |
|
probably null |
Het |
Myo6 |
C |
T |
9: 80,183,656 (GRCm39) |
Q684* |
probably null |
Het |
Nrde2 |
T |
A |
12: 100,096,756 (GRCm39) |
I1015F |
possibly damaging |
Het |
Or12e9 |
T |
A |
2: 87,202,446 (GRCm39) |
V190E |
probably damaging |
Het |
Or2d4 |
G |
A |
7: 106,544,187 (GRCm39) |
T7I |
possibly damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pappa |
A |
T |
4: 65,074,076 (GRCm39) |
N210I |
probably damaging |
Het |
Pax4 |
G |
A |
6: 28,445,138 (GRCm39) |
P179L |
probably damaging |
Het |
Pcx |
G |
A |
19: 4,668,532 (GRCm39) |
D656N |
probably damaging |
Het |
Pms1 |
T |
A |
1: 53,245,916 (GRCm39) |
H541L |
probably benign |
Het |
Pten |
C |
T |
19: 32,777,291 (GRCm39) |
P95L |
probably damaging |
Het |
Rsrc2 |
G |
A |
5: 123,877,562 (GRCm39) |
R140* |
probably null |
Het |
Shc3 |
T |
C |
13: 51,670,601 (GRCm39) |
M49V |
probably damaging |
Het |
Snap91 |
C |
G |
9: 86,697,497 (GRCm39) |
K288N |
probably damaging |
Het |
Spag17 |
C |
T |
3: 99,970,787 (GRCm39) |
Q1324* |
probably null |
Het |
Tasor |
A |
G |
14: 27,151,183 (GRCm39) |
E53G |
probably benign |
Het |
Tfr2 |
A |
G |
5: 137,569,242 (GRCm39) |
|
probably benign |
Het |
Tgfbrap1 |
A |
T |
1: 43,114,803 (GRCm39) |
I99K |
probably damaging |
Het |
Tmem38a |
T |
A |
8: 73,333,878 (GRCm39) |
V119E |
probably damaging |
Het |
Tmtc4 |
T |
G |
14: 123,182,969 (GRCm39) |
D243A |
probably benign |
Het |
Tnc |
A |
T |
4: 63,889,515 (GRCm39) |
S1755T |
probably damaging |
Het |
Trim67 |
T |
C |
8: 125,551,589 (GRCm39) |
S590P |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,590,287 (GRCm39) |
T12814S |
probably damaging |
Het |
Uspl1 |
T |
A |
5: 149,150,923 (GRCm39) |
S708T |
probably benign |
Het |
Vmn2r69 |
A |
T |
7: 85,055,717 (GRCm39) |
F807Y |
probably damaging |
Het |
Vmn2r97 |
C |
T |
17: 19,148,615 (GRCm39) |
P170L |
probably damaging |
Het |
Zfp612 |
C |
T |
8: 110,816,532 (GRCm39) |
Q580* |
probably null |
Het |
|
Other mutations in H2-M10.2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00771:H2-M10.2
|
APN |
17 |
36,597,288 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01490:H2-M10.2
|
APN |
17 |
36,596,377 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02347:H2-M10.2
|
APN |
17 |
36,596,505 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02884:H2-M10.2
|
APN |
17 |
36,595,568 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03244:H2-M10.2
|
APN |
17 |
36,596,463 (GRCm39) |
missense |
probably benign |
0.33 |
R0383:H2-M10.2
|
UTSW |
17 |
36,595,253 (GRCm39) |
missense |
probably benign |
0.04 |
R1756:H2-M10.2
|
UTSW |
17 |
36,597,015 (GRCm39) |
splice site |
probably benign |
|
R1803:H2-M10.2
|
UTSW |
17 |
36,596,763 (GRCm39) |
missense |
probably benign |
|
R2496:H2-M10.2
|
UTSW |
17 |
36,596,771 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3816:H2-M10.2
|
UTSW |
17 |
36,597,254 (GRCm39) |
nonsense |
probably null |
|
R4597:H2-M10.2
|
UTSW |
17 |
36,596,285 (GRCm39) |
missense |
probably benign |
0.07 |
R4832:H2-M10.2
|
UTSW |
17 |
36,595,219 (GRCm39) |
missense |
probably damaging |
0.99 |
R5325:H2-M10.2
|
UTSW |
17 |
36,596,471 (GRCm39) |
missense |
probably benign |
0.00 |
R7443:H2-M10.2
|
UTSW |
17 |
36,596,945 (GRCm39) |
missense |
probably benign |
|
R8064:H2-M10.2
|
UTSW |
17 |
36,595,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R8894:H2-M10.2
|
UTSW |
17 |
36,595,555 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9420:H2-M10.2
|
UTSW |
17 |
36,595,643 (GRCm39) |
missense |
probably benign |
0.01 |
R9489:H2-M10.2
|
UTSW |
17 |
36,596,936 (GRCm39) |
missense |
probably benign |
0.04 |
|