Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alms1 |
T |
C |
6: 85,599,647 (GRCm39) |
V1960A |
possibly damaging |
Het |
Asph |
A |
T |
4: 9,475,471 (GRCm39) |
N537K |
probably damaging |
Het |
Bnip2 |
T |
C |
9: 69,908,116 (GRCm39) |
|
probably benign |
Het |
Cc2d2a |
C |
A |
5: 43,840,457 (GRCm39) |
Q104K |
probably benign |
Het |
Clec4a1 |
T |
C |
6: 122,905,033 (GRCm39) |
|
probably benign |
Het |
Dnajb8 |
T |
C |
6: 88,199,508 (GRCm39) |
S15P |
probably damaging |
Het |
Erp27 |
C |
A |
6: 136,896,987 (GRCm39) |
V72L |
probably damaging |
Het |
Gpr156 |
A |
G |
16: 37,799,395 (GRCm39) |
T131A |
probably damaging |
Het |
Grk1 |
T |
C |
8: 13,465,993 (GRCm39) |
V479A |
probably damaging |
Het |
H2bc1 |
T |
A |
13: 24,117,982 (GRCm39) |
D53V |
possibly damaging |
Het |
Hspg2 |
A |
G |
4: 137,289,237 (GRCm39) |
D3784G |
probably damaging |
Het |
Irf2 |
A |
T |
8: 47,260,260 (GRCm39) |
K26M |
probably damaging |
Het |
Irx6 |
C |
A |
8: 93,402,717 (GRCm39) |
C27* |
probably null |
Het |
Izumo1r |
C |
T |
9: 14,812,975 (GRCm39) |
C99Y |
probably damaging |
Het |
Klrb1a |
T |
A |
6: 128,595,072 (GRCm39) |
T132S |
probably benign |
Het |
Mmp13 |
C |
T |
9: 7,278,974 (GRCm39) |
|
probably benign |
Het |
Myo5b |
G |
A |
18: 74,831,348 (GRCm39) |
R766Q |
probably damaging |
Het |
Myt1 |
T |
C |
2: 181,437,532 (GRCm39) |
L81P |
probably damaging |
Het |
Nfat5 |
G |
A |
8: 108,094,191 (GRCm39) |
V793I |
probably damaging |
Het |
Nup210 |
A |
G |
6: 91,030,596 (GRCm39) |
V108A |
possibly damaging |
Het |
Omd |
T |
A |
13: 49,743,119 (GRCm39) |
Y56* |
probably null |
Het |
Or4b1d |
A |
G |
2: 89,969,268 (GRCm39) |
S72P |
probably damaging |
Het |
Pramel27 |
A |
G |
4: 143,579,363 (GRCm39) |
N316S |
probably benign |
Het |
Psmd9 |
A |
G |
5: 123,372,697 (GRCm39) |
E60G |
probably damaging |
Het |
Rab11fip1 |
T |
C |
8: 27,642,825 (GRCm39) |
E658G |
possibly damaging |
Het |
Smchd1 |
T |
A |
17: 71,701,720 (GRCm39) |
K1091* |
probably null |
Het |
Supt16 |
A |
T |
14: 52,419,764 (GRCm39) |
N111K |
possibly damaging |
Het |
Trrap |
A |
G |
5: 144,793,799 (GRCm39) |
T3666A |
probably benign |
Het |
Ttn |
T |
C |
2: 76,616,095 (GRCm39) |
D8289G |
probably damaging |
Het |
Ush2a |
T |
A |
1: 188,643,438 (GRCm39) |
S4267T |
probably benign |
Het |
Usp50 |
T |
A |
2: 126,551,386 (GRCm39) |
E31V |
probably benign |
Het |
|
Other mutations in Cd300ld |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01628:Cd300ld
|
APN |
11 |
114,876,999 (GRCm39) |
missense |
probably benign |
|
IGL02019:Cd300ld
|
APN |
11 |
114,878,227 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02738:Cd300ld
|
APN |
11 |
114,875,076 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03386:Cd300ld
|
APN |
11 |
114,874,998 (GRCm39) |
missense |
probably benign |
|
R2001:Cd300ld
|
UTSW |
11 |
114,878,156 (GRCm39) |
missense |
probably benign |
0.44 |
R2197:Cd300ld
|
UTSW |
11 |
114,875,058 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3039:Cd300ld
|
UTSW |
11 |
114,877,003 (GRCm39) |
missense |
probably benign |
|
R5540:Cd300ld
|
UTSW |
11 |
114,878,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R7096:Cd300ld
|
UTSW |
11 |
114,878,321 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7371:Cd300ld
|
UTSW |
11 |
114,878,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7548:Cd300ld
|
UTSW |
11 |
114,878,248 (GRCm39) |
missense |
probably benign |
0.02 |
R7710:Cd300ld
|
UTSW |
11 |
114,875,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R9211:Cd300ld
|
UTSW |
11 |
114,878,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R9396:Cd300ld
|
UTSW |
11 |
114,878,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|