Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730049H05Rik |
A |
C |
6: 92,811,420 (GRCm39) |
|
probably benign |
Het |
Cbarp |
A |
G |
10: 79,971,348 (GRCm39) |
L159P |
probably damaging |
Het |
Ccnd2 |
A |
G |
6: 127,107,422 (GRCm39) |
I249T |
probably damaging |
Het |
Cerk |
G |
T |
15: 86,039,311 (GRCm39) |
C193* |
probably null |
Het |
Chrna2 |
A |
G |
14: 66,387,216 (GRCm39) |
E454G |
probably benign |
Het |
Clnk |
T |
C |
5: 38,925,412 (GRCm39) |
T130A |
probably benign |
Het |
Dcbld2 |
T |
C |
16: 58,285,701 (GRCm39) |
L620P |
probably damaging |
Het |
Dhx29 |
T |
A |
13: 113,095,499 (GRCm39) |
V942E |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,971,675 (GRCm39) |
|
probably benign |
Het |
Dnai1 |
G |
A |
4: 41,604,229 (GRCm39) |
C212Y |
probably damaging |
Het |
Dpep1 |
A |
G |
8: 123,925,518 (GRCm39) |
D57G |
possibly damaging |
Het |
Gfm2 |
G |
A |
13: 97,311,532 (GRCm39) |
V701I |
probably benign |
Het |
Grm1 |
C |
T |
10: 10,595,622 (GRCm39) |
A669T |
probably benign |
Het |
Hsd3b3 |
C |
T |
3: 98,649,492 (GRCm39) |
G277D |
probably damaging |
Het |
Hsf5 |
A |
G |
11: 87,522,508 (GRCm39) |
Y367C |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lipo4 |
C |
T |
19: 33,480,619 (GRCm39) |
V250I |
probably benign |
Het |
Lrrc14 |
T |
C |
15: 76,597,765 (GRCm39) |
V165A |
probably benign |
Het |
Map3k9 |
A |
G |
12: 81,819,691 (GRCm39) |
F188L |
probably damaging |
Het |
Mpo |
A |
G |
11: 87,691,866 (GRCm39) |
Y433C |
probably damaging |
Het |
Nsd2 |
A |
G |
5: 34,003,461 (GRCm39) |
K185E |
probably benign |
Het |
Or6n2 |
T |
A |
1: 173,897,147 (GRCm39) |
F94L |
probably damaging |
Het |
Oxct1 |
T |
A |
15: 4,066,601 (GRCm39) |
N72K |
possibly damaging |
Het |
Ptpn12 |
A |
G |
5: 21,206,321 (GRCm39) |
I324T |
probably benign |
Het |
Sez6 |
T |
C |
11: 77,867,708 (GRCm39) |
I875T |
probably damaging |
Het |
Tpr |
T |
A |
1: 150,311,655 (GRCm39) |
V1811E |
probably damaging |
Het |
Trpc4 |
A |
G |
3: 54,225,516 (GRCm39) |
D871G |
probably damaging |
Het |
Upf2 |
A |
G |
2: 6,051,821 (GRCm39) |
E1161G |
unknown |
Het |
|
Other mutations in Zp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Zp2
|
APN |
7 |
119,732,623 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00707:Zp2
|
APN |
7 |
119,732,636 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00916:Zp2
|
APN |
7 |
119,737,397 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01554:Zp2
|
APN |
7 |
119,737,548 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01845:Zp2
|
APN |
7 |
119,737,414 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02111:Zp2
|
APN |
7 |
119,731,641 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02145:Zp2
|
APN |
7 |
119,739,074 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02155:Zp2
|
APN |
7 |
119,743,340 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02178:Zp2
|
APN |
7 |
119,732,973 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02646:Zp2
|
APN |
7 |
119,734,564 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03220:Zp2
|
APN |
7 |
119,736,450 (GRCm39) |
missense |
possibly damaging |
0.90 |
PIT4687001:Zp2
|
UTSW |
7 |
119,741,102 (GRCm39) |
missense |
probably benign |
0.00 |
R0138:Zp2
|
UTSW |
7 |
119,736,423 (GRCm39) |
missense |
probably damaging |
0.96 |
R0197:Zp2
|
UTSW |
7 |
119,742,799 (GRCm39) |
splice site |
probably benign |
|
R0519:Zp2
|
UTSW |
7 |
119,737,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Zp2
|
UTSW |
7 |
119,734,693 (GRCm39) |
splice site |
probably benign |
|
R0879:Zp2
|
UTSW |
7 |
119,734,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Zp2
|
UTSW |
7 |
119,742,799 (GRCm39) |
splice site |
probably benign |
|
R1160:Zp2
|
UTSW |
7 |
119,735,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R1235:Zp2
|
UTSW |
7 |
119,737,566 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1753:Zp2
|
UTSW |
7 |
119,737,328 (GRCm39) |
missense |
probably benign |
|
R1883:Zp2
|
UTSW |
7 |
119,732,624 (GRCm39) |
missense |
probably benign |
0.02 |
R1995:Zp2
|
UTSW |
7 |
119,734,388 (GRCm39) |
missense |
probably damaging |
0.97 |
R2196:Zp2
|
UTSW |
7 |
119,737,529 (GRCm39) |
missense |
probably benign |
|
R2850:Zp2
|
UTSW |
7 |
119,737,529 (GRCm39) |
missense |
probably benign |
|
R3715:Zp2
|
UTSW |
7 |
119,741,057 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4082:Zp2
|
UTSW |
7 |
119,734,475 (GRCm39) |
missense |
probably benign |
0.01 |
R4731:Zp2
|
UTSW |
7 |
119,737,343 (GRCm39) |
missense |
probably damaging |
0.96 |
R4732:Zp2
|
UTSW |
7 |
119,737,343 (GRCm39) |
missense |
probably damaging |
0.96 |
R4733:Zp2
|
UTSW |
7 |
119,737,343 (GRCm39) |
missense |
probably damaging |
0.96 |
R4754:Zp2
|
UTSW |
7 |
119,737,541 (GRCm39) |
missense |
probably benign |
0.01 |
R4863:Zp2
|
UTSW |
7 |
119,734,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5274:Zp2
|
UTSW |
7 |
119,737,315 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5392:Zp2
|
UTSW |
7 |
119,734,987 (GRCm39) |
nonsense |
probably null |
|
R5877:Zp2
|
UTSW |
7 |
119,732,562 (GRCm39) |
missense |
probably null |
0.94 |
R6390:Zp2
|
UTSW |
7 |
119,740,453 (GRCm39) |
missense |
probably benign |
0.23 |
R6404:Zp2
|
UTSW |
7 |
119,734,765 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6546:Zp2
|
UTSW |
7 |
119,731,748 (GRCm39) |
missense |
probably benign |
0.00 |
R6622:Zp2
|
UTSW |
7 |
119,741,136 (GRCm39) |
missense |
probably benign |
|
R6622:Zp2
|
UTSW |
7 |
119,731,748 (GRCm39) |
missense |
probably benign |
0.00 |
R6707:Zp2
|
UTSW |
7 |
119,733,145 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7274:Zp2
|
UTSW |
7 |
119,731,614 (GRCm39) |
makesense |
probably null |
|
R7275:Zp2
|
UTSW |
7 |
119,734,576 (GRCm39) |
splice site |
probably null |
|
R7541:Zp2
|
UTSW |
7 |
119,735,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R7585:Zp2
|
UTSW |
7 |
119,733,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R7709:Zp2
|
UTSW |
7 |
119,734,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R7742:Zp2
|
UTSW |
7 |
119,731,731 (GRCm39) |
missense |
unknown |
|
R7767:Zp2
|
UTSW |
7 |
119,736,392 (GRCm39) |
missense |
probably benign |
0.01 |
R7771:Zp2
|
UTSW |
7 |
119,742,865 (GRCm39) |
missense |
probably damaging |
0.96 |
R8391:Zp2
|
UTSW |
7 |
119,726,179 (GRCm39) |
missense |
probably benign |
0.00 |
R8872:Zp2
|
UTSW |
7 |
119,733,025 (GRCm39) |
missense |
probably benign |
0.14 |
R8880:Zp2
|
UTSW |
7 |
119,742,835 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9673:Zp2
|
UTSW |
7 |
119,733,238 (GRCm39) |
missense |
probably damaging |
1.00 |
X0017:Zp2
|
UTSW |
7 |
119,732,608 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Zp2
|
UTSW |
7 |
119,732,590 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Zp2
|
UTSW |
7 |
119,734,402 (GRCm39) |
missense |
not run |
|
Z1177:Zp2
|
UTSW |
7 |
119,734,432 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zp2
|
UTSW |
7 |
119,734,402 (GRCm39) |
missense |
not run |
|
|