Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
G |
C |
8: 41,207,257 (GRCm39) |
Q174H |
probably benign |
Het |
Adipor2 |
A |
T |
6: 119,338,866 (GRCm39) |
M129K |
possibly damaging |
Het |
Arhgap29 |
T |
A |
3: 121,807,894 (GRCm39) |
M616K |
probably damaging |
Het |
Calcrl |
A |
T |
2: 84,181,609 (GRCm39) |
F180I |
probably damaging |
Het |
Cdh4 |
T |
C |
2: 179,537,560 (GRCm39) |
V864A |
probably damaging |
Het |
Cep78 |
A |
G |
19: 15,938,436 (GRCm39) |
F504S |
probably benign |
Het |
Coasy |
A |
G |
11: 100,975,211 (GRCm39) |
|
probably null |
Het |
Dnah3 |
T |
C |
7: 119,530,696 (GRCm39) |
N751S |
probably benign |
Het |
Ecpas |
C |
T |
4: 58,814,027 (GRCm39) |
E1360K |
possibly damaging |
Het |
Ecpas |
T |
A |
4: 58,822,111 (GRCm39) |
D1152V |
probably damaging |
Het |
Eea1 |
T |
A |
10: 95,855,857 (GRCm39) |
N631K |
probably benign |
Het |
Fam149b |
A |
G |
14: 20,401,394 (GRCm39) |
K27R |
probably damaging |
Het |
Fbxw26 |
A |
G |
9: 109,574,221 (GRCm39) |
W42R |
probably damaging |
Het |
Gas6 |
A |
G |
8: 13,520,217 (GRCm39) |
|
probably null |
Het |
Gfral |
C |
T |
9: 76,104,328 (GRCm39) |
R228Q |
probably benign |
Het |
Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
Gmppa |
T |
C |
1: 75,418,899 (GRCm39) |
V324A |
possibly damaging |
Het |
Gstm2 |
C |
T |
3: 107,891,444 (GRCm39) |
|
probably null |
Het |
Kcng3 |
A |
G |
17: 83,895,639 (GRCm39) |
S276P |
probably benign |
Het |
Lrrd1 |
T |
C |
5: 3,901,254 (GRCm39) |
S520P |
probably benign |
Het |
Lrrn2 |
A |
G |
1: 132,865,505 (GRCm39) |
N190S |
probably benign |
Het |
Lrwd1 |
G |
C |
5: 136,159,887 (GRCm39) |
A392G |
probably benign |
Het |
Mab21l2 |
A |
G |
3: 86,454,044 (GRCm39) |
Y319H |
probably damaging |
Het |
Ndufv3 |
A |
G |
17: 31,746,382 (GRCm39) |
N91D |
probably benign |
Het |
Nfatc2 |
T |
A |
2: 168,378,313 (GRCm39) |
M451L |
probably benign |
Het |
Or10g9b |
A |
T |
9: 39,918,030 (GRCm39) |
S72T |
probably damaging |
Het |
Pcdhgb2 |
G |
T |
18: 37,825,393 (GRCm39) |
V795F |
possibly damaging |
Het |
Pdcd11 |
T |
A |
19: 47,099,430 (GRCm39) |
M843K |
possibly damaging |
Het |
Pla2g4c |
T |
A |
7: 13,073,617 (GRCm39) |
N221K |
probably benign |
Het |
Ppox |
T |
C |
1: 171,104,885 (GRCm39) |
Y422C |
probably damaging |
Het |
Retreg3 |
A |
G |
11: 100,991,769 (GRCm39) |
S55P |
probably damaging |
Het |
Rnf103 |
C |
A |
6: 71,485,909 (GRCm39) |
T180K |
probably damaging |
Het |
Tbl3 |
A |
T |
17: 24,923,408 (GRCm39) |
L307H |
probably damaging |
Het |
Tex26 |
A |
T |
5: 149,363,240 (GRCm39) |
|
probably null |
Het |
Tln2 |
A |
T |
9: 67,293,887 (GRCm39) |
I247K |
probably damaging |
Het |
Txlnb |
T |
C |
10: 17,674,876 (GRCm39) |
S10P |
probably benign |
Het |
Vwde |
C |
A |
6: 13,195,985 (GRCm39) |
E347* |
probably null |
Het |
Wasf1 |
G |
A |
10: 40,802,570 (GRCm39) |
R75Q |
probably damaging |
Het |
Zfp647 |
G |
T |
15: 76,802,206 (GRCm39) |
A2E |
unknown |
Het |
|
Other mutations in Zfp14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00790:Zfp14
|
APN |
7 |
29,738,312 (GRCm39) |
nonsense |
probably null |
|
IGL01018:Zfp14
|
APN |
7 |
29,737,526 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01060:Zfp14
|
APN |
7 |
29,737,510 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03223:Zfp14
|
APN |
7 |
29,737,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Zfp14
|
UTSW |
7 |
29,737,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R0052:Zfp14
|
UTSW |
7 |
29,737,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R1860:Zfp14
|
UTSW |
7 |
29,738,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R2852:Zfp14
|
UTSW |
7 |
29,738,596 (GRCm39) |
missense |
probably benign |
0.01 |
R2887:Zfp14
|
UTSW |
7 |
29,738,190 (GRCm39) |
missense |
probably damaging |
0.98 |
R4585:Zfp14
|
UTSW |
7 |
29,738,341 (GRCm39) |
missense |
probably damaging |
0.99 |
R4586:Zfp14
|
UTSW |
7 |
29,738,341 (GRCm39) |
missense |
probably damaging |
0.99 |
R4625:Zfp14
|
UTSW |
7 |
29,738,020 (GRCm39) |
nonsense |
probably null |
|
R4988:Zfp14
|
UTSW |
7 |
29,737,482 (GRCm39) |
missense |
probably benign |
|
R6709:Zfp14
|
UTSW |
7 |
29,737,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R7799:Zfp14
|
UTSW |
7 |
29,738,368 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8375:Zfp14
|
UTSW |
7 |
29,738,579 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8784:Zfp14
|
UTSW |
7 |
29,742,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R8997:Zfp14
|
UTSW |
7 |
29,737,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R9721:Zfp14
|
UTSW |
7 |
29,738,609 (GRCm39) |
missense |
probably benign |
0.00 |
X0017:Zfp14
|
UTSW |
7 |
29,738,082 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1186:Zfp14
|
UTSW |
7 |
29,738,577 (GRCm39) |
missense |
probably damaging |
0.98 |
|