Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cand1 |
C |
A |
10: 119,047,040 (GRCm39) |
V817L |
probably benign |
Het |
Cdc16 |
T |
G |
8: 13,817,575 (GRCm39) |
Y295* |
probably null |
Het |
Cdk12 |
T |
A |
11: 98,113,491 (GRCm39) |
N758K |
unknown |
Het |
Cep295 |
A |
G |
9: 15,234,148 (GRCm39) |
L2216S |
probably benign |
Het |
Chpf2 |
A |
G |
5: 24,797,259 (GRCm39) |
E735G |
probably damaging |
Het |
Chrdl2 |
A |
G |
7: 99,683,848 (GRCm39) |
T432A |
probably damaging |
Het |
Cyp4a12b |
T |
A |
4: 115,295,246 (GRCm39) |
|
probably null |
Het |
D130043K22Rik |
T |
G |
13: 25,051,157 (GRCm39) |
D464E |
probably damaging |
Het |
Dst |
G |
T |
1: 34,345,705 (GRCm39) |
A7622S |
probably damaging |
Het |
Fdx1 |
A |
T |
9: 51,859,949 (GRCm39) |
I127N |
probably damaging |
Het |
Fem1a |
A |
G |
17: 56,565,355 (GRCm39) |
I483V |
possibly damaging |
Het |
Gcc2 |
C |
A |
10: 58,094,070 (GRCm39) |
D51E |
probably benign |
Het |
Glrb |
A |
G |
3: 80,769,088 (GRCm39) |
S178P |
probably damaging |
Het |
Inpp4b |
A |
G |
8: 82,583,379 (GRCm39) |
Q161R |
probably damaging |
Het |
Lrrc45 |
T |
C |
11: 120,611,436 (GRCm39) |
|
probably benign |
Het |
Myh3 |
T |
C |
11: 66,981,681 (GRCm39) |
Y757H |
probably damaging |
Het |
Myo1h |
A |
C |
5: 114,453,132 (GRCm39) |
|
probably benign |
Het |
Nudt13 |
T |
A |
14: 20,356,418 (GRCm39) |
S114R |
probably damaging |
Het |
Omg |
T |
C |
11: 79,393,540 (GRCm39) |
N106S |
possibly damaging |
Het |
Pbrm1 |
T |
C |
14: 30,809,576 (GRCm39) |
V1163A |
probably damaging |
Het |
Pi4k2b |
T |
A |
5: 52,918,292 (GRCm39) |
Y350* |
probably null |
Het |
Prr29 |
C |
A |
11: 106,266,033 (GRCm39) |
T32K |
possibly damaging |
Het |
Psd4 |
C |
T |
2: 24,284,298 (GRCm39) |
A54V |
probably benign |
Het |
Shroom3 |
T |
C |
5: 93,098,924 (GRCm39) |
L1387P |
probably damaging |
Het |
Stk35 |
A |
G |
2: 129,643,912 (GRCm39) |
T299A |
probably damaging |
Het |
Thsd7b |
G |
A |
1: 130,092,814 (GRCm39) |
S1238N |
probably benign |
Het |
Utp11 |
T |
C |
4: 124,576,250 (GRCm39) |
K131R |
probably benign |
Het |
Vps50 |
C |
T |
6: 3,532,177 (GRCm39) |
Q227* |
probably null |
Het |
Zan |
T |
C |
5: 137,462,375 (GRCm39) |
T935A |
unknown |
Het |
|
Other mutations in Scd3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00507:Scd3
|
APN |
19 |
44,224,273 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02207:Scd3
|
APN |
19 |
44,204,028 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0054:Scd3
|
UTSW |
19 |
44,204,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R1820:Scd3
|
UTSW |
19 |
44,230,245 (GRCm39) |
missense |
probably benign |
0.00 |
R1847:Scd3
|
UTSW |
19 |
44,224,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R1944:Scd3
|
UTSW |
19 |
44,224,219 (GRCm39) |
missense |
probably benign |
0.16 |
R1945:Scd3
|
UTSW |
19 |
44,224,219 (GRCm39) |
missense |
probably benign |
0.16 |
R3834:Scd3
|
UTSW |
19 |
44,230,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R4551:Scd3
|
UTSW |
19 |
44,203,878 (GRCm39) |
missense |
probably benign |
0.00 |
R5797:Scd3
|
UTSW |
19 |
44,203,950 (GRCm39) |
missense |
probably benign |
0.10 |
R7921:Scd3
|
UTSW |
19 |
44,224,331 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7978:Scd3
|
UTSW |
19 |
44,222,688 (GRCm39) |
nonsense |
probably null |
|
R8247:Scd3
|
UTSW |
19 |
44,227,003 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8886:Scd3
|
UTSW |
19 |
44,230,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R9057:Scd3
|
UTSW |
19 |
44,224,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R9527:Scd3
|
UTSW |
19 |
44,226,816 (GRCm39) |
missense |
probably benign |
0.06 |
X0026:Scd3
|
UTSW |
19 |
44,222,757 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Scd3
|
UTSW |
19 |
44,224,315 (GRCm39) |
missense |
probably damaging |
1.00 |
|