Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts12 |
T |
C |
15: 11,065,245 (GRCm39) |
|
probably null |
Het |
Adamts3 |
T |
C |
5: 89,850,802 (GRCm39) |
N579S |
probably benign |
Het |
Akr1c19 |
A |
G |
13: 4,289,098 (GRCm39) |
|
probably benign |
Het |
Ankrd39 |
T |
A |
1: 36,581,142 (GRCm39) |
H69L |
probably damaging |
Het |
Apcdd1 |
T |
A |
18: 63,085,186 (GRCm39) |
M461K |
possibly damaging |
Het |
Bpifa3 |
G |
A |
2: 153,979,502 (GRCm39) |
C209Y |
probably damaging |
Het |
Cep131 |
T |
C |
11: 119,957,989 (GRCm39) |
E779G |
probably benign |
Het |
Cep85 |
T |
C |
4: 133,879,566 (GRCm39) |
Q394R |
probably damaging |
Het |
Cep85 |
G |
T |
4: 133,879,567 (GRCm39) |
Q394K |
probably damaging |
Het |
Clcn6 |
T |
C |
4: 148,101,992 (GRCm39) |
Y364C |
probably benign |
Het |
Fetub |
G |
A |
16: 22,748,391 (GRCm39) |
M1I |
probably null |
Het |
Greb1 |
T |
C |
12: 16,751,202 (GRCm39) |
I1003V |
probably damaging |
Het |
Hsf3 |
A |
G |
X: 95,364,200 (GRCm39) |
|
probably benign |
Het |
Jcad |
A |
G |
18: 4,673,312 (GRCm39) |
N358S |
probably damaging |
Het |
Kndc1 |
T |
C |
7: 139,493,888 (GRCm39) |
|
probably benign |
Het |
Lama1 |
A |
T |
17: 68,059,769 (GRCm39) |
|
probably benign |
Het |
Mark2 |
A |
G |
19: 7,258,603 (GRCm39) |
V50A |
probably benign |
Het |
Mmp7 |
T |
C |
9: 7,692,229 (GRCm39) |
W35R |
probably damaging |
Het |
Ndc80 |
A |
G |
17: 71,806,320 (GRCm39) |
V578A |
probably benign |
Het |
Nfyc |
T |
C |
4: 120,638,721 (GRCm39) |
E42G |
probably damaging |
Het |
Or1j15 |
A |
G |
2: 36,459,233 (GRCm39) |
T208A |
probably benign |
Het |
Or52b4 |
A |
T |
7: 102,184,391 (GRCm39) |
I146F |
probably damaging |
Het |
Or5d37 |
T |
C |
2: 87,923,360 (GRCm39) |
K307E |
possibly damaging |
Het |
Or8g21 |
A |
T |
9: 38,906,396 (GRCm39) |
C112S |
probably benign |
Het |
Or9i16 |
A |
T |
19: 13,864,722 (GRCm39) |
L284* |
probably null |
Het |
Pcdha11 |
T |
C |
18: 37,318,061 (GRCm39) |
F925L |
probably damaging |
Het |
Pdcd1 |
T |
G |
1: 93,968,571 (GRCm39) |
R154S |
probably benign |
Het |
Pepd |
T |
A |
7: 34,623,865 (GRCm39) |
D87E |
probably benign |
Het |
Pfn4 |
A |
G |
12: 4,820,240 (GRCm39) |
T30A |
probably benign |
Het |
Pgpep1l |
A |
G |
7: 67,887,456 (GRCm39) |
M48T |
possibly damaging |
Het |
Pla2g15 |
A |
G |
8: 106,889,748 (GRCm39) |
N340S |
probably benign |
Het |
Plcb4 |
A |
G |
2: 135,844,547 (GRCm39) |
D155G |
probably damaging |
Het |
Plg |
G |
A |
17: 12,622,956 (GRCm39) |
G499S |
probably damaging |
Het |
Plin3 |
C |
T |
17: 56,587,799 (GRCm39) |
W305* |
probably null |
Het |
Polq |
C |
A |
16: 36,848,265 (GRCm39) |
L291I |
probably damaging |
Het |
Sanbr |
A |
G |
11: 23,532,865 (GRCm39) |
|
probably null |
Het |
Sdf2l1 |
T |
A |
16: 16,950,014 (GRCm39) |
H54L |
probably damaging |
Het |
Slc38a2 |
C |
T |
15: 96,590,936 (GRCm39) |
D276N |
possibly damaging |
Het |
Syk |
A |
G |
13: 52,797,097 (GRCm39) |
T576A |
probably benign |
Het |
Uso1 |
T |
C |
5: 92,329,278 (GRCm39) |
F389L |
probably damaging |
Het |
Wwc2 |
T |
A |
8: 48,321,668 (GRCm39) |
Y482F |
unknown |
Het |
|
Other mutations in Tas2r119 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00577:Tas2r119
|
APN |
15 |
32,177,599 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01548:Tas2r119
|
APN |
15 |
32,178,123 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01826:Tas2r119
|
APN |
15 |
32,177,548 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02432:Tas2r119
|
APN |
15 |
32,177,853 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02585:Tas2r119
|
APN |
15 |
32,177,679 (GRCm39) |
missense |
probably benign |
0.04 |
R2248:Tas2r119
|
UTSW |
15 |
32,178,297 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2432:Tas2r119
|
UTSW |
15 |
32,178,165 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5098:Tas2r119
|
UTSW |
15 |
32,178,228 (GRCm39) |
missense |
probably benign |
0.03 |
R5624:Tas2r119
|
UTSW |
15 |
32,178,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R5819:Tas2r119
|
UTSW |
15 |
32,177,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R5901:Tas2r119
|
UTSW |
15 |
32,177,932 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6363:Tas2r119
|
UTSW |
15 |
32,178,034 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6495:Tas2r119
|
UTSW |
15 |
32,177,676 (GRCm39) |
missense |
probably benign |
|
R6521:Tas2r119
|
UTSW |
15 |
32,178,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Tas2r119
|
UTSW |
15 |
32,178,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Tas2r119
|
UTSW |
15 |
32,178,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R9015:Tas2r119
|
UTSW |
15 |
32,178,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R9193:Tas2r119
|
UTSW |
15 |
32,177,932 (GRCm39) |
missense |
probably benign |
0.02 |
X0063:Tas2r119
|
UTSW |
15 |
32,178,301 (GRCm39) |
missense |
possibly damaging |
0.95 |
|