Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg3 |
A |
T |
17: 57,190,751 (GRCm39) |
T440S |
probably damaging |
Het |
Akap12 |
T |
A |
10: 4,304,864 (GRCm39) |
V558E |
probably damaging |
Het |
Atg4c |
T |
C |
4: 99,146,624 (GRCm39) |
|
probably benign |
Het |
Atg7 |
T |
A |
6: 114,701,884 (GRCm39) |
N673K |
possibly damaging |
Het |
Brpf3 |
A |
G |
17: 29,040,279 (GRCm39) |
D900G |
probably benign |
Het |
C2cd5 |
T |
C |
6: 143,025,669 (GRCm39) |
Y176C |
probably damaging |
Het |
Cep70 |
A |
T |
9: 99,180,557 (GRCm39) |
I571F |
possibly damaging |
Het |
Cir1 |
C |
T |
2: 73,134,120 (GRCm39) |
G150R |
probably null |
Het |
Cyp46a1 |
T |
C |
12: 108,309,296 (GRCm39) |
V68A |
probably damaging |
Het |
Dlgap2 |
A |
G |
8: 14,881,579 (GRCm39) |
T883A |
possibly damaging |
Het |
Dnah2 |
C |
A |
11: 69,412,013 (GRCm39) |
K249N |
possibly damaging |
Het |
Dnajc11 |
A |
G |
4: 152,062,503 (GRCm39) |
K434R |
probably benign |
Het |
Eri3 |
A |
G |
4: 117,506,508 (GRCm39) |
Y279C |
probably damaging |
Het |
Hectd4 |
T |
A |
5: 121,503,116 (GRCm39) |
Y4362N |
possibly damaging |
Het |
Ilk |
A |
G |
7: 105,389,547 (GRCm39) |
K85E |
possibly damaging |
Het |
Insrr |
G |
T |
3: 87,721,498 (GRCm39) |
G1135* |
probably null |
Het |
Itgax |
T |
A |
7: 127,748,295 (GRCm39) |
M1108K |
probably benign |
Het |
Mpzl3 |
C |
T |
9: 44,979,514 (GRCm39) |
T155I |
probably benign |
Het |
Or4f57 |
A |
T |
2: 111,790,912 (GRCm39) |
C169S |
probably damaging |
Het |
Or6c212 |
A |
T |
10: 129,559,065 (GRCm39) |
M116K |
probably damaging |
Het |
Pkd1l2 |
G |
A |
8: 117,792,484 (GRCm39) |
T436I |
probably benign |
Het |
Polr2h |
A |
G |
16: 20,537,807 (GRCm39) |
Y68C |
probably damaging |
Het |
Pramel47 |
C |
T |
5: 95,489,258 (GRCm39) |
P234S |
probably benign |
Het |
Rhobtb3 |
A |
G |
13: 76,091,550 (GRCm39) |
S2P |
probably damaging |
Het |
Slc24a5 |
T |
C |
2: 124,925,147 (GRCm39) |
S263P |
probably damaging |
Het |
Spz1 |
T |
G |
13: 92,711,851 (GRCm39) |
K208N |
possibly damaging |
Het |
Tbpl2 |
C |
A |
2: 23,981,105 (GRCm39) |
C231F |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,938,440 (GRCm39) |
I869M |
probably damaging |
Het |
Tesk1 |
G |
A |
4: 43,447,027 (GRCm39) |
E472K |
possibly damaging |
Het |
Tesk1 |
C |
A |
4: 43,447,026 (GRCm39) |
C471* |
probably null |
Het |
Thoc2l |
C |
T |
5: 104,667,209 (GRCm39) |
T577I |
probably benign |
Het |
Tmem213 |
T |
A |
6: 38,092,601 (GRCm39) |
V111E |
probably damaging |
Het |
Tmem232 |
A |
T |
17: 65,563,558 (GRCm39) |
Y612N |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,729,707 (GRCm39) |
|
probably benign |
Het |
Vmn2r113 |
G |
A |
17: 23,177,591 (GRCm39) |
V792I |
probably benign |
Het |
Wdfy1 |
A |
G |
1: 79,691,588 (GRCm39) |
V273A |
probably benign |
Het |
Wwp1 |
A |
G |
4: 19,623,200 (GRCm39) |
S762P |
probably damaging |
Het |
|
Other mutations in 1700011L22Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03344:1700011L22Rik
|
APN |
8 |
79,975,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:1700011L22Rik
|
UTSW |
8 |
79,937,284 (GRCm39) |
nonsense |
probably null |
|
R0331:1700011L22Rik
|
UTSW |
8 |
79,956,021 (GRCm39) |
missense |
probably benign |
0.08 |
R0904:1700011L22Rik
|
UTSW |
8 |
79,975,118 (GRCm39) |
start gained |
probably benign |
|
R3801:1700011L22Rik
|
UTSW |
8 |
79,974,922 (GRCm39) |
missense |
probably benign |
0.06 |
R3804:1700011L22Rik
|
UTSW |
8 |
79,974,922 (GRCm39) |
missense |
probably benign |
0.06 |
R4606:1700011L22Rik
|
UTSW |
8 |
79,937,374 (GRCm39) |
missense |
probably benign |
0.00 |
R6045:1700011L22Rik
|
UTSW |
8 |
79,955,996 (GRCm39) |
missense |
probably benign |
0.00 |
R6993:1700011L22Rik
|
UTSW |
8 |
79,975,053 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7249:1700011L22Rik
|
UTSW |
8 |
79,974,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7442:1700011L22Rik
|
UTSW |
8 |
79,946,919 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:1700011L22Rik
|
UTSW |
8 |
79,937,380 (GRCm39) |
nonsense |
probably null |
|
Z1177:1700011L22Rik
|
UTSW |
8 |
79,974,925 (GRCm39) |
missense |
probably damaging |
1.00 |
|