Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb3 |
G |
T |
1: 25,586,613 (GRCm39) |
T360K |
probably damaging |
Het |
AW551984 |
T |
C |
9: 39,508,449 (GRCm39) |
K356E |
probably benign |
Het |
Bpifb2 |
T |
A |
2: 153,723,113 (GRCm39) |
V123E |
probably damaging |
Het |
Cacna1a |
T |
G |
8: 85,276,143 (GRCm39) |
F532V |
probably damaging |
Het |
Cct8 |
C |
A |
16: 87,284,576 (GRCm39) |
E204* |
probably null |
Het |
Cd163 |
T |
A |
6: 124,294,577 (GRCm39) |
|
probably null |
Het |
Cep152 |
C |
A |
2: 125,429,868 (GRCm39) |
A685S |
possibly damaging |
Het |
Chdh |
A |
G |
14: 29,758,798 (GRCm39) |
D581G |
probably benign |
Het |
Cnpy3 |
A |
C |
17: 47,058,391 (GRCm39) |
Y77* |
probably null |
Het |
Col5a3 |
T |
C |
9: 20,704,870 (GRCm39) |
E762G |
unknown |
Het |
Creb3 |
A |
G |
4: 43,563,247 (GRCm39) |
T115A |
probably benign |
Het |
Dlat |
G |
T |
9: 50,555,781 (GRCm39) |
A412E |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,367,514 (GRCm39) |
N1789S |
probably damaging |
Het |
Dzank1 |
C |
T |
2: 144,333,724 (GRCm39) |
E370K |
probably benign |
Het |
Eif3m |
A |
T |
2: 104,837,184 (GRCm39) |
|
probably null |
Het |
Gimap8 |
A |
T |
6: 48,635,920 (GRCm39) |
M562L |
probably benign |
Het |
Gprc6a |
T |
A |
10: 51,507,553 (GRCm39) |
|
probably benign |
Het |
Gsr |
T |
G |
8: 34,170,347 (GRCm39) |
|
probably null |
Het |
Gstcd |
A |
G |
3: 132,688,860 (GRCm39) |
V630A |
probably damaging |
Het |
Hip1r |
T |
C |
5: 124,128,043 (GRCm39) |
I116T |
probably benign |
Het |
Hivep3 |
A |
G |
4: 119,989,000 (GRCm39) |
E1817G |
probably damaging |
Het |
Inpp5f |
A |
C |
7: 128,265,449 (GRCm39) |
T135P |
probably damaging |
Het |
Ism2 |
A |
G |
12: 87,331,801 (GRCm39) |
|
silent |
Het |
Itga11 |
A |
G |
9: 62,673,070 (GRCm39) |
D784G |
probably damaging |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Itpr2 |
T |
C |
6: 146,298,456 (GRCm39) |
E10G |
probably damaging |
Het |
Knl1 |
A |
T |
2: 118,899,618 (GRCm39) |
K440* |
probably null |
Het |
Lonp2 |
T |
C |
8: 87,439,943 (GRCm39) |
S648P |
probably damaging |
Het |
Lrba |
T |
C |
3: 86,267,175 (GRCm39) |
S1622P |
probably benign |
Het |
Lrp2 |
G |
T |
2: 69,318,310 (GRCm39) |
A2047D |
probably damaging |
Het |
Mcm3 |
G |
A |
1: 20,873,801 (GRCm39) |
T773I |
probably benign |
Het |
Mki67 |
A |
G |
7: 135,297,198 (GRCm39) |
V2612A |
probably benign |
Het |
Mnx1 |
C |
A |
5: 29,683,129 (GRCm39) |
G49W |
probably damaging |
Het |
Muc5b |
T |
A |
7: 141,402,816 (GRCm39) |
Y673* |
probably null |
Het |
Myo15a |
A |
G |
11: 60,370,756 (GRCm39) |
H1172R |
probably benign |
Het |
Myo1g |
T |
C |
11: 6,466,080 (GRCm39) |
K363R |
probably null |
Het |
Ncoa4 |
T |
A |
14: 31,898,598 (GRCm39) |
C473S |
probably benign |
Het |
Nefh |
T |
C |
11: 4,889,656 (GRCm39) |
T988A |
unknown |
Het |
Nwd2 |
T |
A |
5: 63,961,803 (GRCm39) |
D462E |
probably benign |
Het |
Or2av9 |
T |
C |
11: 58,380,913 (GRCm39) |
T223A |
probably benign |
Het |
Pira13 |
G |
T |
7: 3,825,680 (GRCm39) |
Y396* |
probably null |
Het |
Plec |
T |
C |
15: 76,065,267 (GRCm39) |
E1466G |
unknown |
Het |
Prl3d2 |
G |
T |
13: 27,306,379 (GRCm39) |
M35I |
probably benign |
Het |
Reln |
T |
A |
5: 22,357,461 (GRCm39) |
I202F |
probably benign |
Het |
Rhot1 |
T |
A |
11: 80,116,428 (GRCm39) |
D78E |
probably benign |
Het |
Rsph3b |
T |
C |
17: 7,172,528 (GRCm39) |
|
probably null |
Het |
Scn10a |
C |
T |
9: 119,438,717 (GRCm39) |
M1717I |
probably damaging |
Het |
Sema6a |
T |
A |
18: 47,382,363 (GRCm39) |
H728L |
possibly damaging |
Het |
Slc26a3 |
G |
T |
12: 31,507,079 (GRCm39) |
A345S |
possibly damaging |
Het |
Slc35d2 |
A |
G |
13: 64,247,097 (GRCm39) |
V261A |
possibly damaging |
Het |
Slc49a3 |
T |
C |
5: 108,589,945 (GRCm39) |
T486A |
probably damaging |
Het |
Ssmem1 |
A |
G |
6: 30,519,513 (GRCm39) |
D66G |
probably damaging |
Het |
Sult2a8 |
A |
T |
7: 14,159,402 (GRCm39) |
N72K |
probably benign |
Het |
Tbx10 |
T |
C |
19: 4,046,921 (GRCm39) |
L108P |
probably damaging |
Het |
Tex14 |
T |
C |
11: 87,427,691 (GRCm39) |
S48P |
probably damaging |
Het |
Tmie |
A |
G |
9: 110,696,596 (GRCm39) |
L95P |
probably damaging |
Het |
Tom1l2 |
C |
G |
11: 60,161,259 (GRCm39) |
R84P |
probably damaging |
Het |
Trpm3 |
T |
A |
19: 22,866,799 (GRCm39) |
D543E |
possibly damaging |
Het |
Vps8 |
A |
T |
16: 21,261,189 (GRCm39) |
S110C |
probably damaging |
Het |
Zfp791 |
T |
A |
8: 85,837,597 (GRCm39) |
N89I |
probably damaging |
Het |
|
Other mutations in Vipr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00691:Vipr2
|
APN |
12 |
116,102,368 (GRCm39) |
splice site |
probably null |
|
IGL02233:Vipr2
|
APN |
12 |
116,058,356 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02691:Vipr2
|
APN |
12 |
116,099,849 (GRCm39) |
missense |
probably benign |
0.11 |
PIT4377001:Vipr2
|
UTSW |
12 |
116,058,418 (GRCm39) |
missense |
probably benign |
0.01 |
R0135:Vipr2
|
UTSW |
12 |
116,106,447 (GRCm39) |
missense |
probably benign |
0.00 |
R0207:Vipr2
|
UTSW |
12 |
116,106,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R1389:Vipr2
|
UTSW |
12 |
116,100,950 (GRCm39) |
missense |
probably benign |
0.01 |
R1560:Vipr2
|
UTSW |
12 |
116,058,401 (GRCm39) |
missense |
probably benign |
0.18 |
R1575:Vipr2
|
UTSW |
12 |
116,107,892 (GRCm39) |
missense |
probably benign |
|
R1696:Vipr2
|
UTSW |
12 |
116,102,777 (GRCm39) |
missense |
probably benign |
0.13 |
R1970:Vipr2
|
UTSW |
12 |
116,099,826 (GRCm39) |
missense |
probably benign |
0.01 |
R2010:Vipr2
|
UTSW |
12 |
116,086,430 (GRCm39) |
critical splice donor site |
probably null |
|
R3873:Vipr2
|
UTSW |
12 |
116,099,724 (GRCm39) |
unclassified |
probably benign |
|
R4953:Vipr2
|
UTSW |
12 |
116,107,876 (GRCm39) |
missense |
probably benign |
0.07 |
R6041:Vipr2
|
UTSW |
12 |
116,106,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R6337:Vipr2
|
UTSW |
12 |
116,086,363 (GRCm39) |
nonsense |
probably null |
|
R6902:Vipr2
|
UTSW |
12 |
116,102,819 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6946:Vipr2
|
UTSW |
12 |
116,102,819 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7763:Vipr2
|
UTSW |
12 |
116,086,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R9339:Vipr2
|
UTSW |
12 |
116,058,344 (GRCm39) |
missense |
probably damaging |
0.96 |
R9523:Vipr2
|
UTSW |
12 |
116,093,788 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Vipr2
|
UTSW |
12 |
116,106,565 (GRCm39) |
splice site |
probably null |
|
X0067:Vipr2
|
UTSW |
12 |
116,102,792 (GRCm39) |
missense |
probably damaging |
1.00 |
|