Other mutations in this stock |
Total: 23 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
C |
9: 124,057,789 (GRCm39) |
|
probably benign |
Het |
4930556J24Rik |
A |
T |
11: 3,888,178 (GRCm39) |
|
probably null |
Het |
Acoxl |
T |
C |
2: 127,928,264 (GRCm39) |
|
probably benign |
Het |
Ahi1 |
G |
C |
10: 20,848,009 (GRCm39) |
R472S |
probably damaging |
Het |
Akap10 |
A |
G |
11: 61,763,846 (GRCm39) |
L662P |
possibly damaging |
Het |
Arhgef10 |
C |
T |
8: 14,978,925 (GRCm39) |
T64M |
possibly damaging |
Het |
Ccr4 |
C |
T |
9: 114,321,906 (GRCm39) |
G53D |
probably damaging |
Het |
Cdc25a |
T |
C |
9: 109,713,176 (GRCm39) |
|
probably benign |
Het |
Clec4n |
A |
C |
6: 123,221,499 (GRCm39) |
Q114H |
probably damaging |
Het |
Cmya5 |
A |
G |
13: 93,210,983 (GRCm39) |
|
probably benign |
Het |
Depdc1a |
T |
C |
3: 159,228,184 (GRCm39) |
V312A |
probably damaging |
Het |
Ephb6 |
C |
T |
6: 41,594,219 (GRCm39) |
P583L |
probably damaging |
Het |
Klra8 |
A |
T |
6: 130,099,007 (GRCm39) |
D185E |
possibly damaging |
Het |
Meis2 |
T |
A |
2: 115,694,961 (GRCm39) |
Q394L |
probably benign |
Het |
Or2t47 |
G |
A |
11: 58,442,348 (GRCm39) |
T239I |
probably damaging |
Het |
Pzp |
C |
T |
6: 128,467,052 (GRCm39) |
G1107D |
probably damaging |
Het |
Ralgapa2 |
C |
T |
2: 146,188,731 (GRCm39) |
W1350* |
probably null |
Het |
Scand1 |
C |
A |
2: 156,153,865 (GRCm39) |
R135L |
probably damaging |
Het |
Spopl |
A |
T |
2: 23,401,455 (GRCm39) |
M351K |
probably benign |
Het |
Tmed4 |
T |
C |
11: 6,223,727 (GRCm39) |
|
probably benign |
Het |
Ube2e2 |
A |
G |
14: 18,630,297 (GRCm38) |
|
probably null |
Het |
Ubxn4 |
G |
A |
1: 128,190,641 (GRCm39) |
E256K |
probably benign |
Het |
Wrap53 |
A |
T |
11: 69,453,031 (GRCm39) |
D425E |
probably damaging |
Het |
|
Other mutations in Usp51 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02232:Usp51
|
APN |
X |
151,791,669 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02511:Usp51
|
APN |
X |
151,791,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R1563:Usp51
|
UTSW |
X |
151,790,988 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Usp51
|
UTSW |
X |
151,791,219 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Usp51
|
UTSW |
X |
151,791,218 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Usp51
|
UTSW |
X |
151,792,295 (GRCm39) |
missense |
probably damaging |
1.00 |
|