Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
A |
G |
7: 78,738,045 (GRCm39) |
E250G |
probably damaging |
Het |
Adgra1 |
A |
G |
7: 139,455,512 (GRCm39) |
N380S |
probably benign |
Het |
Ap3d1 |
G |
A |
10: 80,563,001 (GRCm39) |
P160L |
probably damaging |
Het |
Atg9a |
C |
T |
1: 75,162,372 (GRCm39) |
V505M |
probably damaging |
Het |
Chsy3 |
A |
T |
18: 59,543,102 (GRCm39) |
I747F |
probably damaging |
Het |
Clec2g |
A |
G |
6: 128,958,269 (GRCm39) |
S100G |
probably benign |
Het |
Cmya5 |
G |
T |
13: 93,228,804 (GRCm39) |
P2095T |
probably damaging |
Het |
Espl1 |
T |
A |
15: 102,207,012 (GRCm39) |
L159M |
probably benign |
Het |
Fbxw8 |
T |
C |
5: 118,233,776 (GRCm39) |
D285G |
possibly damaging |
Het |
Fras1 |
C |
T |
5: 96,916,222 (GRCm39) |
R3419W |
probably damaging |
Het |
Galc |
T |
A |
12: 98,197,672 (GRCm39) |
|
probably null |
Het |
Ghdc |
T |
C |
11: 100,660,543 (GRCm39) |
E110G |
probably damaging |
Het |
Gm4787 |
G |
C |
12: 81,424,604 (GRCm39) |
T518S |
probably benign |
Het |
H2-T24 |
T |
C |
17: 36,325,562 (GRCm39) |
T309A |
probably benign |
Het |
Helb |
A |
C |
10: 119,937,391 (GRCm39) |
F618V |
probably damaging |
Het |
Hycc1 |
A |
C |
5: 24,170,220 (GRCm39) |
S376R |
possibly damaging |
Het |
Ifi211 |
A |
G |
1: 173,735,262 (GRCm39) |
F56L |
probably damaging |
Het |
Kntc1 |
T |
C |
5: 123,950,160 (GRCm39) |
F1988L |
probably damaging |
Het |
Mapk13 |
G |
A |
17: 28,997,465 (GRCm39) |
S361N |
probably benign |
Het |
Mapk3 |
A |
G |
7: 126,363,408 (GRCm39) |
I146V |
probably benign |
Het |
Megf6 |
G |
A |
4: 154,338,295 (GRCm39) |
|
probably null |
Het |
Mug1 |
G |
T |
6: 121,838,092 (GRCm39) |
V441F |
probably benign |
Het |
Mymk |
A |
G |
2: 26,952,226 (GRCm39) |
S173P |
probably benign |
Het |
Nox4 |
A |
G |
7: 87,023,616 (GRCm39) |
T501A |
possibly damaging |
Het |
Or13c7 |
C |
A |
4: 43,854,624 (GRCm39) |
S105Y |
possibly damaging |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or52n2 |
T |
C |
7: 104,542,104 (GRCm39) |
T244A |
possibly damaging |
Het |
Prkcb |
C |
A |
7: 121,888,678 (GRCm39) |
H37Q |
probably damaging |
Het |
Rabggtb |
A |
G |
3: 153,615,024 (GRCm39) |
F189L |
probably damaging |
Het |
Setd1b |
T |
C |
5: 123,281,471 (GRCm39) |
I75T |
unknown |
Het |
Slc10a5 |
T |
A |
3: 10,400,148 (GRCm39) |
R171* |
probably null |
Het |
Slc12a4 |
A |
G |
8: 106,680,484 (GRCm39) |
F211L |
probably damaging |
Het |
Slc1a5 |
T |
A |
7: 16,527,759 (GRCm39) |
W352R |
probably damaging |
Het |
Slc22a27 |
C |
G |
19: 7,843,303 (GRCm39) |
A359P |
probably damaging |
Het |
St8sia4 |
A |
G |
1: 95,555,460 (GRCm39) |
M190T |
probably damaging |
Het |
Tmeff2 |
A |
G |
1: 51,018,476 (GRCm39) |
M153V |
probably benign |
Het |
Trappc12 |
T |
C |
12: 28,796,696 (GRCm39) |
T279A |
probably damaging |
Het |
Ubn1 |
G |
T |
16: 4,895,818 (GRCm39) |
A955S |
probably benign |
Het |
Usp24 |
T |
A |
4: 106,239,500 (GRCm39) |
H1147Q |
possibly damaging |
Het |
Vrk1 |
T |
A |
12: 106,039,865 (GRCm39) |
|
probably null |
Het |
Zdhhc25 |
T |
A |
15: 88,485,365 (GRCm39) |
Y233* |
probably null |
Het |
Zfp109 |
A |
G |
7: 23,928,179 (GRCm39) |
V418A |
probably benign |
Het |
|
Other mutations in Dcaf10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02431:Dcaf10
|
APN |
4 |
45,342,630 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02660:Dcaf10
|
APN |
4 |
45,372,769 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0048:Dcaf10
|
UTSW |
4 |
45,374,262 (GRCm39) |
nonsense |
probably null |
|
R0550:Dcaf10
|
UTSW |
4 |
45,372,753 (GRCm39) |
missense |
probably benign |
|
R0611:Dcaf10
|
UTSW |
4 |
45,373,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R2289:Dcaf10
|
UTSW |
4 |
45,359,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R2973:Dcaf10
|
UTSW |
4 |
45,373,957 (GRCm39) |
missense |
probably benign |
0.04 |
R3610:Dcaf10
|
UTSW |
4 |
45,372,962 (GRCm39) |
nonsense |
probably null |
|
R3735:Dcaf10
|
UTSW |
4 |
45,348,117 (GRCm39) |
missense |
probably benign |
0.01 |
R4655:Dcaf10
|
UTSW |
4 |
45,372,769 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4665:Dcaf10
|
UTSW |
4 |
45,372,769 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4690:Dcaf10
|
UTSW |
4 |
45,372,769 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4724:Dcaf10
|
UTSW |
4 |
45,372,769 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4725:Dcaf10
|
UTSW |
4 |
45,372,769 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4735:Dcaf10
|
UTSW |
4 |
45,372,769 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4743:Dcaf10
|
UTSW |
4 |
45,370,409 (GRCm39) |
missense |
probably damaging |
0.98 |
R5254:Dcaf10
|
UTSW |
4 |
45,370,415 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5855:Dcaf10
|
UTSW |
4 |
45,342,558 (GRCm39) |
missense |
probably benign |
0.18 |
R6833:Dcaf10
|
UTSW |
4 |
45,373,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R7132:Dcaf10
|
UTSW |
4 |
45,342,391 (GRCm39) |
missense |
probably benign |
|
R7345:Dcaf10
|
UTSW |
4 |
45,342,583 (GRCm39) |
missense |
probably damaging |
0.98 |
R7366:Dcaf10
|
UTSW |
4 |
45,373,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R7832:Dcaf10
|
UTSW |
4 |
45,348,196 (GRCm39) |
missense |
probably damaging |
1.00 |
|