Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim3 |
A |
G |
18: 61,957,018 (GRCm39) |
|
probably benign |
Het |
Adam24 |
T |
A |
8: 41,133,793 (GRCm39) |
C420* |
probably null |
Het |
Atp12a |
G |
A |
14: 56,610,893 (GRCm39) |
G346S |
probably damaging |
Het |
Bpifa3 |
A |
T |
2: 153,979,529 (GRCm39) |
Q218L |
probably damaging |
Het |
Cntrl |
T |
C |
2: 35,039,034 (GRCm39) |
|
probably benign |
Het |
Defb41 |
A |
G |
1: 18,335,248 (GRCm39) |
|
probably null |
Het |
Edc4 |
C |
A |
8: 106,617,637 (GRCm39) |
T1094K |
probably damaging |
Het |
Exoc4 |
T |
A |
6: 33,895,359 (GRCm39) |
I792N |
possibly damaging |
Het |
G3bp2 |
A |
T |
5: 92,211,187 (GRCm39) |
|
probably benign |
Het |
Herc6 |
T |
A |
6: 57,639,204 (GRCm39) |
N888K |
probably damaging |
Het |
Iqgap1 |
G |
A |
7: 80,373,576 (GRCm39) |
T1471M |
probably benign |
Het |
Kpna6 |
G |
T |
4: 129,541,896 (GRCm39) |
H500Q |
probably benign |
Het |
Krt78 |
G |
A |
15: 101,854,896 (GRCm39) |
Q972* |
probably null |
Het |
Krtap9-5 |
T |
A |
11: 99,839,589 (GRCm39) |
C97S |
unknown |
Het |
Mapk10 |
T |
A |
5: 103,139,723 (GRCm39) |
|
probably benign |
Het |
Mybphl |
A |
G |
3: 108,272,319 (GRCm39) |
T3A |
probably benign |
Het |
Nup155 |
A |
T |
15: 8,187,244 (GRCm39) |
H1391L |
probably damaging |
Het |
Oca2 |
A |
G |
7: 55,966,141 (GRCm39) |
I378V |
probably damaging |
Het |
Or7a39 |
T |
A |
10: 78,715,517 (GRCm39) |
C170* |
probably null |
Het |
Pax6 |
C |
A |
2: 105,510,646 (GRCm39) |
Q2K |
probably benign |
Het |
Plxna2 |
C |
A |
1: 194,462,818 (GRCm39) |
|
probably null |
Het |
Ppp1r13b |
A |
G |
12: 111,801,550 (GRCm39) |
L378P |
probably damaging |
Het |
Prkdc |
G |
A |
16: 15,570,646 (GRCm39) |
E2310K |
probably damaging |
Het |
Pth2r |
G |
A |
1: 65,411,507 (GRCm39) |
G348E |
possibly damaging |
Het |
Rarb |
T |
C |
14: 16,436,769 (GRCm38) |
I251V |
probably damaging |
Het |
Rasa2 |
A |
G |
9: 96,434,376 (GRCm39) |
L637P |
probably damaging |
Het |
Sucla2 |
C |
T |
14: 73,798,074 (GRCm39) |
|
probably benign |
Het |
Syt1 |
A |
T |
10: 108,472,523 (GRCm39) |
D120E |
probably benign |
Het |
Tedc2 |
T |
A |
17: 24,435,291 (GRCm39) |
E366V |
probably damaging |
Het |
Tedc2 |
C |
A |
17: 24,435,292 (GRCm39) |
E366* |
probably null |
Het |
Tmbim1 |
A |
G |
1: 74,329,905 (GRCm39) |
|
probably benign |
Het |
Tnfrsf25 |
G |
A |
4: 152,202,745 (GRCm39) |
C191Y |
probably damaging |
Het |
Tnn |
T |
C |
1: 159,952,968 (GRCm39) |
K691E |
probably damaging |
Het |
Trim7 |
T |
A |
11: 48,728,646 (GRCm39) |
V98E |
probably damaging |
Het |
Tspan3 |
A |
G |
9: 56,068,104 (GRCm39) |
F15L |
probably benign |
Het |
Uap1l1 |
A |
G |
2: 25,252,759 (GRCm39) |
L427S |
probably damaging |
Het |
Upf1 |
A |
C |
8: 70,791,053 (GRCm39) |
M574R |
probably damaging |
Het |
Ush2a |
T |
A |
1: 188,282,404 (GRCm39) |
V1931E |
probably benign |
Het |
|
Other mutations in Zfp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0684:Zfp3
|
UTSW |
11 |
70,662,395 (GRCm39) |
missense |
probably benign |
0.09 |
R1389:Zfp3
|
UTSW |
11 |
70,663,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R1940:Zfp3
|
UTSW |
11 |
70,662,202 (GRCm39) |
missense |
probably benign |
0.00 |
R1962:Zfp3
|
UTSW |
11 |
70,662,954 (GRCm39) |
nonsense |
probably null |
|
R4112:Zfp3
|
UTSW |
11 |
70,662,333 (GRCm39) |
missense |
probably benign |
0.14 |
R4637:Zfp3
|
UTSW |
11 |
70,662,181 (GRCm39) |
missense |
probably benign |
0.21 |
R6006:Zfp3
|
UTSW |
11 |
70,662,590 (GRCm39) |
missense |
probably benign |
0.00 |
R6333:Zfp3
|
UTSW |
11 |
70,662,266 (GRCm39) |
missense |
probably benign |
0.00 |
R7213:Zfp3
|
UTSW |
11 |
70,663,351 (GRCm39) |
missense |
probably benign |
0.24 |
R7378:Zfp3
|
UTSW |
11 |
70,662,899 (GRCm39) |
missense |
probably benign |
0.11 |
R8434:Zfp3
|
UTSW |
11 |
70,663,384 (GRCm39) |
missense |
probably benign |
0.08 |
R9094:Zfp3
|
UTSW |
11 |
70,663,241 (GRCm39) |
missense |
probably benign |
0.31 |
R9095:Zfp3
|
UTSW |
11 |
70,662,405 (GRCm39) |
missense |
probably benign |
0.20 |
R9404:Zfp3
|
UTSW |
11 |
70,663,366 (GRCm39) |
missense |
probably damaging |
0.98 |
R9622:Zfp3
|
UTSW |
11 |
70,662,739 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Zfp3
|
UTSW |
11 |
70,662,152 (GRCm39) |
missense |
probably benign |
|
Z1177:Zfp3
|
UTSW |
11 |
70,662,718 (GRCm39) |
missense |
probably damaging |
1.00 |
|