Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afdn |
A |
G |
17: 14,038,491 (GRCm39) |
E283G |
probably damaging |
Het |
Ahnak |
A |
G |
19: 8,982,297 (GRCm39) |
I1194V |
probably benign |
Het |
Aqr |
T |
A |
2: 113,943,127 (GRCm39) |
N1149Y |
probably damaging |
Het |
Bms1 |
T |
C |
6: 118,393,480 (GRCm39) |
I131V |
probably benign |
Het |
Cacna1s |
A |
C |
1: 136,046,118 (GRCm39) |
T1461P |
probably benign |
Het |
Chrnb3 |
T |
C |
8: 27,883,397 (GRCm39) |
S113P |
probably damaging |
Het |
Col1a2 |
C |
T |
6: 4,516,398 (GRCm39) |
R171C |
unknown |
Het |
Cramp1 |
A |
G |
17: 25,204,024 (GRCm39) |
V318A |
probably damaging |
Het |
Csf2ra |
A |
G |
19: 61,214,975 (GRCm39) |
V163A |
possibly damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Ctnnd2 |
A |
G |
15: 30,669,708 (GRCm39) |
D439G |
possibly damaging |
Het |
Dnah11 |
T |
A |
12: 117,991,180 (GRCm39) |
|
probably null |
Het |
Dyrk4 |
C |
A |
6: 126,857,194 (GRCm39) |
C495F |
probably damaging |
Het |
Gabra6 |
A |
G |
11: 42,198,244 (GRCm39) |
V402A |
probably benign |
Het |
Gba2 |
T |
C |
4: 43,568,538 (GRCm39) |
M643V |
possibly damaging |
Het |
Gbp9 |
A |
T |
5: 105,242,433 (GRCm39) |
|
probably benign |
Het |
Git1 |
T |
A |
11: 77,394,217 (GRCm39) |
D282E |
probably damaging |
Het |
Gm5799 |
T |
C |
14: 43,782,086 (GRCm39) |
I86T |
probably damaging |
Het |
Gm9894 |
T |
C |
13: 67,913,213 (GRCm39) |
|
noncoding transcript |
Het |
Gng12 |
A |
G |
6: 66,992,745 (GRCm39) |
K4R |
probably benign |
Het |
Hnrnpul1 |
A |
T |
7: 25,426,182 (GRCm39) |
D556E |
probably benign |
Het |
Kat6b |
T |
A |
14: 21,719,107 (GRCm39) |
L1153Q |
possibly damaging |
Het |
Ly75 |
A |
T |
2: 60,213,526 (GRCm39) |
L17Q |
probably null |
Het |
Mc5r |
T |
C |
18: 68,471,910 (GRCm39) |
F90L |
probably damaging |
Het |
Or1x2 |
C |
A |
11: 50,918,192 (GRCm39) |
A121D |
probably damaging |
Het |
Or5k8 |
A |
T |
16: 58,645,019 (GRCm39) |
S18T |
probably benign |
Het |
Or6b13 |
T |
C |
7: 139,782,500 (GRCm39) |
Y61C |
probably damaging |
Het |
Or7c70 |
A |
T |
10: 78,682,897 (GRCm39) |
M284K |
probably damaging |
Het |
Or8b9 |
A |
T |
9: 37,766,656 (GRCm39) |
I181L |
probably benign |
Het |
Pi4ka |
A |
T |
16: 17,143,293 (GRCm39) |
Y6N |
probably damaging |
Het |
Polr2g |
C |
A |
19: 8,775,820 (GRCm39) |
|
probably null |
Het |
Psme3 |
A |
G |
11: 101,208,480 (GRCm39) |
Q82R |
probably benign |
Het |
Rab11a |
G |
T |
9: 64,633,929 (GRCm39) |
T17K |
possibly damaging |
Het |
Rbm12 |
A |
T |
2: 155,940,017 (GRCm39) |
L85Q |
probably damaging |
Het |
Skap1 |
A |
T |
11: 96,599,512 (GRCm39) |
Y188F |
probably damaging |
Het |
Tmprss6 |
A |
T |
15: 78,326,536 (GRCm39) |
F34I |
probably damaging |
Het |
Trip12 |
A |
C |
1: 84,771,854 (GRCm39) |
I98S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,708,532 (GRCm39) |
|
probably benign |
Het |
Ube2t |
A |
T |
1: 134,899,079 (GRCm39) |
K21* |
probably null |
Het |
Vmn1r216 |
T |
C |
13: 23,283,647 (GRCm39) |
V110A |
possibly damaging |
Het |
Vmn2r109 |
A |
T |
17: 20,761,150 (GRCm39) |
F736I |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,845,158 (GRCm39) |
T2081A |
probably benign |
Het |
Zfp13 |
C |
T |
17: 23,795,072 (GRCm39) |
A493T |
probably benign |
Het |
|
Other mutations in Ginm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Ginm1
|
APN |
10 |
7,668,460 (GRCm39) |
unclassified |
probably benign |
|
IGL02606:Ginm1
|
APN |
10 |
7,646,163 (GRCm39) |
missense |
probably damaging |
0.98 |
Juniper
|
UTSW |
10 |
7,655,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Ginm1
|
UTSW |
10 |
7,651,138 (GRCm39) |
splice site |
probably benign |
|
R0010:Ginm1
|
UTSW |
10 |
7,651,138 (GRCm39) |
splice site |
probably benign |
|
R0052:Ginm1
|
UTSW |
10 |
7,655,070 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0052:Ginm1
|
UTSW |
10 |
7,655,070 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1901:Ginm1
|
UTSW |
10 |
7,650,980 (GRCm39) |
critical splice donor site |
probably null |
|
R2106:Ginm1
|
UTSW |
10 |
7,651,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R5374:Ginm1
|
UTSW |
10 |
7,655,078 (GRCm39) |
missense |
probably damaging |
0.99 |
R5929:Ginm1
|
UTSW |
10 |
7,649,814 (GRCm39) |
missense |
probably benign |
0.16 |
R6062:Ginm1
|
UTSW |
10 |
7,651,097 (GRCm39) |
missense |
probably benign |
0.00 |
R6102:Ginm1
|
UTSW |
10 |
7,644,260 (GRCm39) |
missense |
probably benign |
0.00 |
R6792:Ginm1
|
UTSW |
10 |
7,649,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Ginm1
|
UTSW |
10 |
7,653,614 (GRCm39) |
nonsense |
probably null |
|
R7417:Ginm1
|
UTSW |
10 |
7,649,844 (GRCm39) |
missense |
probably damaging |
0.99 |
R7663:Ginm1
|
UTSW |
10 |
7,651,126 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7757:Ginm1
|
UTSW |
10 |
7,655,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R8237:Ginm1
|
UTSW |
10 |
7,668,419 (GRCm39) |
missense |
unknown |
|
R8437:Ginm1
|
UTSW |
10 |
7,646,130 (GRCm39) |
missense |
probably benign |
|
R9004:Ginm1
|
UTSW |
10 |
7,651,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R9239:Ginm1
|
UTSW |
10 |
7,649,825 (GRCm39) |
missense |
possibly damaging |
0.93 |
|