Other mutations in this stock |
Total: 23 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700093K21Rik |
T |
C |
11: 23,467,270 (GRCm39) |
E121G |
possibly damaging |
Het |
Abtb3 |
A |
T |
10: 85,465,155 (GRCm39) |
H665L |
probably damaging |
Het |
Adgrg1 |
G |
A |
8: 95,733,468 (GRCm39) |
V307I |
possibly damaging |
Het |
Cilp |
A |
G |
9: 65,176,869 (GRCm39) |
T42A |
probably benign |
Het |
Col6a3 |
T |
A |
1: 90,722,047 (GRCm39) |
K1493M |
probably null |
Het |
Col6a6 |
A |
G |
9: 105,659,289 (GRCm39) |
V552A |
possibly damaging |
Het |
Cradd |
T |
C |
10: 95,158,586 (GRCm39) |
T54A |
probably benign |
Het |
Elfn2 |
A |
G |
15: 78,557,344 (GRCm39) |
I401T |
probably benign |
Het |
G530012D18Rik |
CAGAGAGA |
CAGAGAGAGA |
1: 85,504,945 (GRCm39) |
|
probably null |
Het |
Hoxc6 |
A |
G |
15: 102,919,279 (GRCm39) |
I172V |
probably damaging |
Het |
Knl1 |
T |
C |
2: 118,901,635 (GRCm39) |
L1112P |
possibly damaging |
Het |
Lipo4 |
T |
A |
19: 33,480,595 (GRCm39) |
I258F |
probably benign |
Het |
Morf4l1 |
A |
G |
9: 89,976,557 (GRCm39) |
V257A |
probably benign |
Het |
Or51a8 |
A |
T |
7: 102,549,819 (GRCm39) |
M82L |
probably benign |
Het |
Rnpepl1 |
T |
A |
1: 92,844,609 (GRCm39) |
M367K |
probably damaging |
Het |
Robo2 |
A |
G |
16: 73,831,996 (GRCm39) |
L228P |
probably damaging |
Het |
Samd9l |
T |
A |
6: 3,376,939 (GRCm39) |
E107D |
probably benign |
Het |
Shc1 |
A |
G |
3: 89,332,126 (GRCm39) |
I194V |
probably benign |
Het |
Slc25a46 |
A |
G |
18: 31,716,668 (GRCm39) |
I278T |
probably benign |
Het |
Tmem178 |
T |
A |
17: 81,308,429 (GRCm39) |
C275S |
possibly damaging |
Het |
Tpsg1 |
A |
T |
17: 25,592,768 (GRCm39) |
Q40L |
possibly damaging |
Het |
Trank1 |
A |
G |
9: 111,196,038 (GRCm39) |
E1354G |
possibly damaging |
Het |
Vstm5 |
T |
C |
9: 15,168,849 (GRCm39) |
S138P |
probably damaging |
Het |
|
Other mutations in Vit |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Vit
|
APN |
17 |
78,909,336 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00929:Vit
|
APN |
17 |
78,886,830 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01447:Vit
|
APN |
17 |
78,932,633 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02000:Vit
|
APN |
17 |
78,912,915 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02230:Vit
|
APN |
17 |
78,927,056 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02245:Vit
|
APN |
17 |
78,932,480 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02315:Vit
|
APN |
17 |
78,930,087 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03133:Vit
|
APN |
17 |
78,873,500 (GRCm39) |
missense |
probably benign |
|
R0025:Vit
|
UTSW |
17 |
78,907,264 (GRCm39) |
missense |
probably benign |
0.00 |
R0025:Vit
|
UTSW |
17 |
78,907,264 (GRCm39) |
missense |
probably benign |
0.00 |
R0520:Vit
|
UTSW |
17 |
78,932,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R0550:Vit
|
UTSW |
17 |
78,932,222 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0565:Vit
|
UTSW |
17 |
78,932,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R0856:Vit
|
UTSW |
17 |
78,927,086 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1327:Vit
|
UTSW |
17 |
78,932,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R1690:Vit
|
UTSW |
17 |
78,932,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R1802:Vit
|
UTSW |
17 |
78,912,940 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1822:Vit
|
UTSW |
17 |
78,930,265 (GRCm39) |
missense |
probably benign |
0.01 |
R1826:Vit
|
UTSW |
17 |
78,842,105 (GRCm39) |
missense |
probably benign |
0.22 |
R1827:Vit
|
UTSW |
17 |
78,853,875 (GRCm39) |
critical splice donor site |
probably null |
|
R1862:Vit
|
UTSW |
17 |
78,930,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R2235:Vit
|
UTSW |
17 |
78,912,867 (GRCm39) |
missense |
probably benign |
0.01 |
R2571:Vit
|
UTSW |
17 |
78,894,174 (GRCm39) |
missense |
probably benign |
|
R4011:Vit
|
UTSW |
17 |
78,842,121 (GRCm39) |
splice site |
probably benign |
|
R4190:Vit
|
UTSW |
17 |
78,894,255 (GRCm39) |
missense |
probably benign |
0.13 |
R4191:Vit
|
UTSW |
17 |
78,894,255 (GRCm39) |
missense |
probably benign |
0.13 |
R4192:Vit
|
UTSW |
17 |
78,894,255 (GRCm39) |
missense |
probably benign |
0.13 |
R4193:Vit
|
UTSW |
17 |
78,894,255 (GRCm39) |
missense |
probably benign |
0.13 |
R4635:Vit
|
UTSW |
17 |
78,881,641 (GRCm39) |
missense |
probably benign |
0.01 |
R4705:Vit
|
UTSW |
17 |
78,932,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R4841:Vit
|
UTSW |
17 |
78,909,308 (GRCm39) |
missense |
probably benign |
|
R4842:Vit
|
UTSW |
17 |
78,909,308 (GRCm39) |
missense |
probably benign |
|
R4884:Vit
|
UTSW |
17 |
78,932,182 (GRCm39) |
missense |
probably damaging |
0.99 |
R4923:Vit
|
UTSW |
17 |
78,894,270 (GRCm39) |
missense |
probably benign |
0.03 |
R5128:Vit
|
UTSW |
17 |
78,932,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R5272:Vit
|
UTSW |
17 |
78,894,264 (GRCm39) |
missense |
probably benign |
|
R5779:Vit
|
UTSW |
17 |
78,853,855 (GRCm39) |
missense |
probably benign |
|
R6596:Vit
|
UTSW |
17 |
78,930,274 (GRCm39) |
missense |
probably benign |
0.35 |
R6658:Vit
|
UTSW |
17 |
78,930,232 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6792:Vit
|
UTSW |
17 |
78,886,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R6894:Vit
|
UTSW |
17 |
78,934,187 (GRCm39) |
nonsense |
probably null |
|
R7032:Vit
|
UTSW |
17 |
78,932,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R7061:Vit
|
UTSW |
17 |
78,932,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Vit
|
UTSW |
17 |
78,932,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R7106:Vit
|
UTSW |
17 |
78,894,228 (GRCm39) |
missense |
probably benign |
|
R7292:Vit
|
UTSW |
17 |
78,912,927 (GRCm39) |
missense |
probably benign |
0.03 |
R7413:Vit
|
UTSW |
17 |
78,932,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Vit
|
UTSW |
17 |
78,853,828 (GRCm39) |
missense |
probably benign |
0.00 |
R8385:Vit
|
UTSW |
17 |
78,927,066 (GRCm39) |
missense |
probably benign |
0.01 |
R9106:Vit
|
UTSW |
17 |
78,934,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R9314:Vit
|
UTSW |
17 |
78,927,044 (GRCm39) |
missense |
probably benign |
0.02 |
R9433:Vit
|
UTSW |
17 |
78,932,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R9588:Vit
|
UTSW |
17 |
78,930,079 (GRCm39) |
missense |
probably damaging |
0.98 |
R9772:Vit
|
UTSW |
17 |
78,932,398 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Vit
|
UTSW |
17 |
78,873,593 (GRCm39) |
missense |
probably benign |
|
X0064:Vit
|
UTSW |
17 |
78,932,314 (GRCm39) |
missense |
probably damaging |
1.00 |
|