Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts15 |
A |
G |
9: 30,813,775 (GRCm39) |
S797P |
probably damaging |
Het |
Akap9 |
T |
C |
5: 4,011,783 (GRCm39) |
Y829H |
probably damaging |
Het |
Anp32a |
A |
G |
9: 62,279,375 (GRCm39) |
D74G |
probably damaging |
Het |
B3gat1 |
T |
C |
9: 26,663,112 (GRCm39) |
I13T |
probably damaging |
Het |
Cbfa2t3 |
A |
T |
8: 123,374,448 (GRCm39) |
V99D |
probably damaging |
Het |
Celsr2 |
C |
T |
3: 108,309,799 (GRCm39) |
C1600Y |
probably damaging |
Het |
Ddx31 |
T |
A |
2: 28,749,078 (GRCm39) |
N291K |
probably damaging |
Het |
Dennd1a |
T |
G |
2: 37,742,446 (GRCm39) |
M3L |
probably benign |
Het |
Dnah12 |
C |
T |
14: 26,488,147 (GRCm39) |
P1017L |
probably damaging |
Het |
Dnajc6 |
A |
T |
4: 101,456,364 (GRCm39) |
D86V |
probably damaging |
Het |
Evx2 |
T |
G |
2: 74,488,195 (GRCm39) |
K208N |
probably damaging |
Het |
F13a1 |
A |
G |
13: 37,052,785 (GRCm39) |
V718A |
probably damaging |
Het |
Fcho2 |
T |
C |
13: 98,862,706 (GRCm39) |
D757G |
probably benign |
Het |
Fmnl2 |
A |
G |
2: 52,995,549 (GRCm39) |
E424G |
probably damaging |
Het |
Fryl |
C |
T |
5: 73,232,094 (GRCm39) |
W424* |
probably null |
Het |
Gata3 |
G |
T |
2: 9,879,579 (GRCm39) |
Y97* |
probably null |
Het |
Gm15446 |
T |
A |
5: 110,090,323 (GRCm39) |
C192S |
probably damaging |
Het |
Hdac10 |
A |
T |
15: 89,009,521 (GRCm39) |
D470E |
probably benign |
Het |
Ier2 |
A |
G |
8: 85,389,055 (GRCm39) |
L109P |
probably benign |
Het |
Iftap |
T |
C |
2: 101,440,916 (GRCm39) |
E29G |
probably damaging |
Het |
Kcnh2 |
T |
C |
5: 24,527,217 (GRCm39) |
T559A |
probably benign |
Het |
Khk |
C |
T |
5: 31,087,938 (GRCm39) |
A204V |
probably damaging |
Het |
Kndc1 |
T |
A |
7: 139,507,321 (GRCm39) |
M1169K |
possibly damaging |
Het |
Krtap31-1 |
A |
G |
11: 99,798,919 (GRCm39) |
S41G |
probably benign |
Het |
Nabp1 |
T |
C |
1: 51,512,162 (GRCm39) |
|
probably null |
Het |
Nphp3 |
A |
G |
9: 103,913,039 (GRCm39) |
D939G |
probably benign |
Het |
Or5e1 |
A |
T |
7: 108,354,309 (GRCm39) |
N82I |
probably damaging |
Het |
Plcg2 |
T |
C |
8: 118,340,974 (GRCm39) |
I1089T |
possibly damaging |
Het |
Ptk2 |
A |
T |
15: 73,134,424 (GRCm39) |
D558E |
probably damaging |
Het |
Serpinb6d |
A |
G |
13: 33,853,112 (GRCm39) |
D168G |
probably benign |
Het |
Shisa8 |
G |
A |
15: 82,092,756 (GRCm39) |
P189L |
probably damaging |
Het |
Shkbp1 |
A |
G |
7: 27,054,204 (GRCm39) |
V89A |
probably benign |
Het |
Slc40a1 |
C |
T |
1: 45,950,457 (GRCm39) |
A332T |
probably damaging |
Het |
Slc44a3 |
A |
T |
3: 121,291,496 (GRCm39) |
Y373* |
probably null |
Het |
Slf2 |
T |
C |
19: 44,937,440 (GRCm39) |
V722A |
probably benign |
Het |
Spanxn4 |
A |
G |
12: 62,734,624 (GRCm39) |
|
noncoding transcript |
Het |
Stag3 |
T |
A |
5: 138,296,901 (GRCm39) |
|
probably null |
Het |
Tanc1 |
T |
C |
2: 59,628,038 (GRCm39) |
I612T |
possibly damaging |
Het |
Thbs2 |
T |
A |
17: 14,906,043 (GRCm39) |
M286L |
probably benign |
Het |
Top1 |
T |
A |
2: 160,545,515 (GRCm39) |
N294K |
probably benign |
Het |
Tpr |
T |
G |
1: 150,302,644 (GRCm39) |
L1381V |
probably damaging |
Het |
Trpm8 |
T |
G |
1: 88,254,154 (GRCm39) |
S126A |
probably benign |
Het |
Ttc41 |
A |
G |
10: 86,611,857 (GRCm39) |
Y1075C |
probably damaging |
Het |
Vmn1r67 |
T |
C |
7: 10,180,907 (GRCm39) |
V57A |
possibly damaging |
Het |
Zbtb5 |
T |
C |
4: 44,993,500 (GRCm39) |
H628R |
probably damaging |
Het |
Zfp810 |
T |
C |
9: 22,190,216 (GRCm39) |
I231V |
probably benign |
Het |
|
Other mutations in Ubox5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00538:Ubox5
|
APN |
2 |
130,441,808 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01947:Ubox5
|
APN |
2 |
130,442,579 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01978:Ubox5
|
APN |
2 |
130,442,372 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02252:Ubox5
|
APN |
2 |
130,441,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02994:Ubox5
|
APN |
2 |
130,442,237 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03150:Ubox5
|
APN |
2 |
130,442,060 (GRCm39) |
missense |
probably benign |
0.44 |
PIT4403001:Ubox5
|
UTSW |
2 |
130,442,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R0792:Ubox5
|
UTSW |
2 |
130,442,630 (GRCm39) |
missense |
probably damaging |
0.99 |
R1344:Ubox5
|
UTSW |
2 |
130,442,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1418:Ubox5
|
UTSW |
2 |
130,442,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1436:Ubox5
|
UTSW |
2 |
130,439,213 (GRCm39) |
unclassified |
probably benign |
|
R1650:Ubox5
|
UTSW |
2 |
130,442,345 (GRCm39) |
missense |
probably benign |
0.03 |
R1772:Ubox5
|
UTSW |
2 |
130,433,794 (GRCm39) |
missense |
probably benign |
0.24 |
R2495:Ubox5
|
UTSW |
2 |
130,441,441 (GRCm39) |
nonsense |
probably null |
|
R4767:Ubox5
|
UTSW |
2 |
130,433,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R5107:Ubox5
|
UTSW |
2 |
130,441,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R8271:Ubox5
|
UTSW |
2 |
130,441,629 (GRCm39) |
missense |
probably benign |
|
R8290:Ubox5
|
UTSW |
2 |
130,442,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R9330:Ubox5
|
UTSW |
2 |
130,442,165 (GRCm39) |
missense |
probably benign |
0.00 |
R9599:Ubox5
|
UTSW |
2 |
130,441,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|