Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700109H08Rik |
A |
G |
5: 3,632,240 (GRCm39) |
D190G |
probably benign |
Het |
Abhd11 |
A |
G |
5: 135,040,760 (GRCm39) |
I271V |
possibly damaging |
Het |
Akap6 |
T |
G |
12: 53,188,999 (GRCm39) |
S2138A |
probably benign |
Het |
Amn |
C |
A |
12: 111,241,440 (GRCm39) |
P235H |
probably damaging |
Het |
Arf2 |
A |
T |
11: 103,859,975 (GRCm39) |
M18L |
probably benign |
Het |
Asic2 |
A |
T |
11: 81,043,233 (GRCm39) |
F20Y |
possibly damaging |
Het |
Bok |
T |
C |
1: 93,622,664 (GRCm39) |
|
probably null |
Het |
Cachd1 |
T |
A |
4: 100,860,045 (GRCm39) |
|
probably benign |
Het |
Casp8 |
A |
G |
1: 58,883,617 (GRCm39) |
N308S |
probably benign |
Het |
Cavin3 |
G |
T |
7: 105,131,154 (GRCm39) |
H71Q |
possibly damaging |
Het |
Ccdc87 |
A |
G |
19: 4,891,646 (GRCm39) |
I713V |
probably benign |
Het |
Clcn6 |
A |
T |
4: 148,093,354 (GRCm39) |
|
probably null |
Het |
Cmas |
T |
C |
6: 142,716,927 (GRCm39) |
I273T |
possibly damaging |
Het |
Ctxn3 |
A |
T |
18: 57,610,378 (GRCm39) |
D65V |
probably damaging |
Het |
D130040H23Rik |
C |
A |
8: 69,755,705 (GRCm39) |
N387K |
probably benign |
Het |
Depp1 |
T |
A |
6: 116,629,122 (GRCm39) |
L155Q |
possibly damaging |
Het |
Dnah9 |
T |
C |
11: 65,818,816 (GRCm39) |
K3174R |
possibly damaging |
Het |
Ecpas |
C |
T |
4: 58,828,632 (GRCm39) |
V934I |
probably damaging |
Het |
Efcab14 |
A |
G |
4: 115,603,793 (GRCm39) |
N157S |
probably damaging |
Het |
Ets1 |
G |
A |
9: 32,641,474 (GRCm39) |
G109D |
probably damaging |
Het |
Fbln5 |
G |
A |
12: 101,734,754 (GRCm39) |
R173C |
probably damaging |
Het |
Fchsd1 |
G |
A |
18: 38,096,035 (GRCm39) |
P525L |
probably benign |
Het |
Gmppa |
G |
A |
1: 75,416,025 (GRCm39) |
V156I |
probably damaging |
Het |
Gtpbp1 |
A |
G |
15: 79,603,482 (GRCm39) |
D182G |
|
Het |
Ift140 |
T |
A |
17: 25,254,809 (GRCm39) |
S430T |
probably benign |
Het |
Kat7 |
G |
C |
11: 95,185,392 (GRCm39) |
C161W |
probably damaging |
Het |
Lipk |
T |
A |
19: 33,996,184 (GRCm39) |
M32K |
probably damaging |
Het |
Lum |
A |
T |
10: 97,404,351 (GRCm39) |
D82V |
possibly damaging |
Het |
Macf1 |
C |
A |
4: 123,248,944 (GRCm39) |
A7196S |
probably damaging |
Het |
Mroh2b |
T |
A |
15: 4,964,782 (GRCm39) |
S926T |
probably damaging |
Het |
Nbn |
G |
T |
4: 15,981,555 (GRCm39) |
R549I |
probably damaging |
Het |
Nfu1 |
T |
C |
6: 86,996,400 (GRCm39) |
I117T |
probably damaging |
Het |
Or51f1 |
T |
C |
7: 102,506,139 (GRCm39) |
T117A |
probably benign |
Het |
Or7a39 |
A |
G |
10: 78,715,155 (GRCm39) |
T50A |
probably benign |
Het |
Parp1 |
T |
C |
1: 180,422,275 (GRCm39) |
L778P |
probably damaging |
Het |
Pbld2 |
G |
T |
10: 62,888,069 (GRCm39) |
V125F |
probably benign |
Het |
Prkag2 |
A |
G |
5: 25,085,680 (GRCm39) |
|
probably null |
Het |
Prss54 |
A |
G |
8: 96,286,351 (GRCm39) |
F241L |
probably benign |
Het |
Rnf121 |
T |
C |
7: 101,678,316 (GRCm39) |
D177G |
probably damaging |
Het |
Slc12a7 |
G |
A |
13: 73,933,241 (GRCm39) |
V100I |
probably benign |
Het |
Slc28a1 |
C |
T |
7: 80,774,719 (GRCm39) |
L189F |
possibly damaging |
Het |
Slc35a3 |
T |
C |
3: 116,488,219 (GRCm39) |
Q16R |
probably damaging |
Het |
Snap91 |
A |
G |
9: 86,686,577 (GRCm39) |
F354L |
probably damaging |
Het |
Steap2 |
A |
G |
5: 5,723,539 (GRCm39) |
I447T |
probably benign |
Het |
Tas1r2 |
A |
G |
4: 139,387,318 (GRCm39) |
D259G |
probably benign |
Het |
Tgm3 |
T |
C |
2: 129,886,452 (GRCm39) |
S558P |
probably benign |
Het |
Tuba3a |
A |
G |
6: 125,258,018 (GRCm39) |
V324A |
probably damaging |
Het |
Vmn1r238 |
T |
G |
18: 3,123,232 (GRCm39) |
I61L |
possibly damaging |
Het |
Vmn1r52 |
A |
G |
6: 90,156,451 (GRCm39) |
T252A |
probably benign |
Het |
Vmp1 |
A |
G |
11: 86,492,885 (GRCm39) |
V308A |
probably damaging |
Het |
Wdfy4 |
A |
C |
14: 32,874,611 (GRCm39) |
V159G |
|
Het |
Zfp180 |
A |
G |
7: 23,804,687 (GRCm39) |
T369A |
possibly damaging |
Het |
Zfp827 |
A |
G |
8: 79,755,316 (GRCm39) |
M1V |
probably null |
Het |
Zmym4 |
A |
G |
4: 126,787,198 (GRCm39) |
I1031T |
probably damaging |
Het |
|
Other mutations in Tagap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01554:Tagap
|
APN |
17 |
8,151,780 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02589:Tagap
|
APN |
17 |
8,152,504 (GRCm39) |
missense |
possibly damaging |
0.87 |
BB003:Tagap
|
UTSW |
17 |
8,145,770 (GRCm39) |
critical splice donor site |
probably null |
|
BB013:Tagap
|
UTSW |
17 |
8,145,770 (GRCm39) |
critical splice donor site |
probably null |
|
R1750:Tagap
|
UTSW |
17 |
8,148,742 (GRCm39) |
missense |
probably benign |
0.06 |
R1791:Tagap
|
UTSW |
17 |
8,152,377 (GRCm39) |
missense |
probably benign |
0.04 |
R1791:Tagap
|
UTSW |
17 |
8,150,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R2509:Tagap
|
UTSW |
17 |
8,147,586 (GRCm39) |
missense |
probably benign |
0.00 |
R4093:Tagap
|
UTSW |
17 |
8,148,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R4627:Tagap
|
UTSW |
17 |
8,145,773 (GRCm39) |
splice site |
probably null |
|
R4747:Tagap
|
UTSW |
17 |
8,151,030 (GRCm39) |
missense |
probably benign |
|
R5222:Tagap
|
UTSW |
17 |
8,152,474 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5222:Tagap
|
UTSW |
17 |
8,152,473 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5866:Tagap
|
UTSW |
17 |
8,152,285 (GRCm39) |
missense |
probably damaging |
0.98 |
R6392:Tagap
|
UTSW |
17 |
8,152,893 (GRCm39) |
missense |
probably damaging |
0.99 |
R6638:Tagap
|
UTSW |
17 |
8,145,906 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6649:Tagap
|
UTSW |
17 |
8,152,546 (GRCm39) |
missense |
probably benign |
0.36 |
R6653:Tagap
|
UTSW |
17 |
8,152,546 (GRCm39) |
missense |
probably benign |
0.36 |
R7478:Tagap
|
UTSW |
17 |
8,152,422 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7509:Tagap
|
UTSW |
17 |
8,147,568 (GRCm39) |
missense |
probably damaging |
0.99 |
R7926:Tagap
|
UTSW |
17 |
8,145,770 (GRCm39) |
critical splice donor site |
probably null |
|
R8549:Tagap
|
UTSW |
17 |
8,152,797 (GRCm39) |
missense |
probably benign |
0.36 |
R9103:Tagap
|
UTSW |
17 |
8,152,335 (GRCm39) |
missense |
probably benign |
0.01 |
R9106:Tagap
|
UTSW |
17 |
8,150,280 (GRCm39) |
missense |
probably damaging |
1.00 |
|