Other mutations in this stock |
Total: 11 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cul4a |
A |
G |
8: 13,177,735 (GRCm39) |
K292E |
probably benign |
Het |
Fat2 |
T |
C |
11: 55,202,070 (GRCm39) |
T335A |
probably benign |
Het |
Hrh2 |
T |
C |
13: 54,368,840 (GRCm39) |
V272A |
possibly damaging |
Het |
Jak3 |
A |
G |
8: 72,136,681 (GRCm39) |
I663V |
probably damaging |
Het |
Kifc3 |
A |
G |
8: 95,864,644 (GRCm39) |
V22A |
probably damaging |
Het |
Nat8f1 |
A |
G |
6: 85,887,957 (GRCm39) |
M1T |
probably null |
Het |
Scn7a |
A |
T |
2: 66,506,388 (GRCm39) |
S1500R |
possibly damaging |
Het |
Stambp |
A |
T |
6: 83,547,419 (GRCm39) |
S23R |
probably damaging |
Het |
Tenm3 |
T |
C |
8: 48,729,456 (GRCm39) |
N1517D |
probably damaging |
Het |
Zfp663 |
A |
T |
2: 165,194,525 (GRCm39) |
F565I |
probably damaging |
Het |
Zscan26 |
C |
T |
13: 21,629,369 (GRCm39) |
R378H |
probably benign |
Het |
|
Other mutations in Zng1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01618:Zng1
|
APN |
19 |
24,918,140 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02351:Zng1
|
APN |
19 |
24,909,026 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02358:Zng1
|
APN |
19 |
24,909,026 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02628:Zng1
|
APN |
19 |
24,935,269 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03001:Zng1
|
APN |
19 |
24,900,002 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03053:Zng1
|
APN |
19 |
24,932,741 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03409:Zng1
|
APN |
19 |
24,900,130 (GRCm39) |
missense |
probably benign |
0.01 |
R0544:Zng1
|
UTSW |
19 |
24,926,575 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0655:Zng1
|
UTSW |
19 |
24,930,684 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0833:Zng1
|
UTSW |
19 |
24,918,203 (GRCm39) |
splice site |
probably benign |
|
R1296:Zng1
|
UTSW |
19 |
24,920,039 (GRCm39) |
splice site |
probably benign |
|
R1723:Zng1
|
UTSW |
19 |
24,925,458 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1888:Zng1
|
UTSW |
19 |
24,932,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Zng1
|
UTSW |
19 |
24,932,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R4526:Zng1
|
UTSW |
19 |
24,935,328 (GRCm39) |
missense |
probably benign |
0.20 |
R5092:Zng1
|
UTSW |
19 |
24,898,383 (GRCm39) |
critical splice donor site |
probably null |
|
R5238:Zng1
|
UTSW |
19 |
24,897,994 (GRCm39) |
missense |
probably damaging |
0.99 |
R5852:Zng1
|
UTSW |
19 |
24,932,769 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7248:Zng1
|
UTSW |
19 |
24,898,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R7699:Zng1
|
UTSW |
19 |
24,920,045 (GRCm39) |
critical splice donor site |
probably null |
|
R7700:Zng1
|
UTSW |
19 |
24,920,045 (GRCm39) |
critical splice donor site |
probably null |
|
R7733:Zng1
|
UTSW |
19 |
24,918,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R8363:Zng1
|
UTSW |
19 |
24,920,091 (GRCm39) |
missense |
probably benign |
0.01 |
R8825:Zng1
|
UTSW |
19 |
24,926,601 (GRCm39) |
missense |
probably benign |
0.23 |
R8931:Zng1
|
UTSW |
19 |
24,932,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R9118:Zng1
|
UTSW |
19 |
24,920,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R9467:Zng1
|
UTSW |
19 |
24,930,684 (GRCm39) |
missense |
possibly damaging |
0.90 |
|