Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429P17Rik |
A |
G |
13: 48,114,446 (GRCm39) |
|
noncoding transcript |
Het |
Agap2 |
T |
C |
10: 126,918,827 (GRCm39) |
|
probably benign |
Het |
Bicra |
G |
A |
7: 15,721,678 (GRCm39) |
T613I |
probably benign |
Het |
Cd163 |
T |
C |
6: 124,284,277 (GRCm39) |
S150P |
possibly damaging |
Het |
Cfap107 |
G |
A |
4: 144,165,098 (GRCm39) |
T26M |
probably damaging |
Het |
F830045P16Rik |
T |
G |
2: 129,314,614 (GRCm39) |
Q221P |
probably damaging |
Het |
Fam135b |
T |
A |
15: 71,328,784 (GRCm39) |
M1172L |
probably benign |
Het |
Fbxo2 |
G |
T |
4: 148,249,581 (GRCm39) |
|
probably null |
Het |
Frem1 |
C |
T |
4: 82,877,533 (GRCm39) |
|
probably benign |
Het |
Galnt17 |
C |
T |
5: 131,114,734 (GRCm39) |
|
probably null |
Het |
Gipc2 |
A |
G |
3: 151,833,771 (GRCm39) |
I170T |
probably damaging |
Het |
Gm2399 |
C |
T |
13: 12,717,417 (GRCm39) |
|
noncoding transcript |
Het |
Hdac10 |
T |
A |
15: 89,010,194 (GRCm39) |
M283L |
probably benign |
Het |
Icam5 |
A |
G |
9: 20,946,095 (GRCm39) |
E309G |
possibly damaging |
Het |
Ift70a1 |
A |
G |
2: 75,810,277 (GRCm39) |
V602A |
probably benign |
Het |
Igkv3-5 |
T |
A |
6: 70,640,865 (GRCm39) |
S115R |
probably benign |
Het |
Impg2 |
A |
G |
16: 56,025,568 (GRCm39) |
R67G |
probably damaging |
Het |
Kansl1l |
T |
C |
1: 66,840,232 (GRCm39) |
Y356C |
probably damaging |
Het |
Ly75 |
T |
C |
2: 60,168,655 (GRCm39) |
D751G |
probably damaging |
Het |
Lyst |
A |
G |
13: 13,917,831 (GRCm39) |
D3297G |
probably damaging |
Het |
Mall |
A |
G |
2: 127,571,699 (GRCm39) |
F30L |
probably benign |
Het |
Map1b |
C |
T |
13: 99,571,512 (GRCm39) |
G403D |
probably damaging |
Het |
Mmp11 |
T |
C |
10: 75,762,730 (GRCm39) |
Y241C |
probably damaging |
Het |
Niban1 |
C |
A |
1: 151,579,555 (GRCm39) |
R425S |
probably damaging |
Het |
Or4a72 |
A |
G |
2: 89,405,557 (GRCm39) |
V171A |
probably benign |
Het |
Pcnt |
C |
T |
10: 76,228,609 (GRCm39) |
A1519T |
probably damaging |
Het |
Pcsk2 |
A |
G |
2: 143,529,490 (GRCm39) |
M96V |
probably benign |
Het |
Piwil4 |
T |
C |
9: 14,614,391 (GRCm39) |
D124G |
probably damaging |
Het |
Plb1 |
A |
T |
5: 32,471,041 (GRCm39) |
I538F |
probably damaging |
Het |
Polq |
A |
G |
16: 36,883,200 (GRCm39) |
D1788G |
probably damaging |
Het |
Pus7 |
A |
G |
5: 23,980,962 (GRCm39) |
S134P |
probably damaging |
Het |
Sec61a2 |
G |
A |
2: 5,891,363 (GRCm39) |
S56L |
possibly damaging |
Het |
Sel1l |
G |
T |
12: 91,810,033 (GRCm39) |
D26E |
probably benign |
Het |
Slc25a48 |
G |
A |
13: 56,612,758 (GRCm39) |
|
probably benign |
Het |
Tnfrsf13b |
G |
A |
11: 61,032,146 (GRCm39) |
V59I |
possibly damaging |
Het |
Usp6nl |
G |
A |
2: 6,445,879 (GRCm39) |
V619M |
probably benign |
Het |
Vmn1r67 |
A |
G |
7: 10,180,767 (GRCm39) |
I10M |
possibly damaging |
Het |
Vmn2r71 |
A |
G |
7: 85,264,782 (GRCm39) |
D38G |
probably damaging |
Het |
|
Other mutations in Tas2r126 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00915:Tas2r126
|
APN |
6 |
42,412,283 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01327:Tas2r126
|
APN |
6 |
42,411,684 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02153:Tas2r126
|
APN |
6 |
42,411,598 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02291:Tas2r126
|
APN |
6 |
42,412,221 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03365:Tas2r126
|
APN |
6 |
42,412,391 (GRCm39) |
missense |
probably benign |
0.36 |
R0091:Tas2r126
|
UTSW |
6 |
42,412,036 (GRCm39) |
missense |
probably benign |
|
R0486:Tas2r126
|
UTSW |
6 |
42,412,225 (GRCm39) |
missense |
probably benign |
0.01 |
R0611:Tas2r126
|
UTSW |
6 |
42,412,025 (GRCm39) |
missense |
probably damaging |
0.99 |
R1527:Tas2r126
|
UTSW |
6 |
42,412,070 (GRCm39) |
missense |
probably benign |
0.03 |
R1529:Tas2r126
|
UTSW |
6 |
42,411,502 (GRCm39) |
missense |
probably benign |
0.00 |
R1883:Tas2r126
|
UTSW |
6 |
42,411,961 (GRCm39) |
missense |
probably benign |
|
R1884:Tas2r126
|
UTSW |
6 |
42,411,961 (GRCm39) |
missense |
probably benign |
|
R2039:Tas2r126
|
UTSW |
6 |
42,411,557 (GRCm39) |
missense |
probably benign |
0.22 |
R4863:Tas2r126
|
UTSW |
6 |
42,412,324 (GRCm39) |
missense |
probably benign |
0.02 |
R5975:Tas2r126
|
UTSW |
6 |
42,411,934 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7127:Tas2r126
|
UTSW |
6 |
42,411,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R7351:Tas2r126
|
UTSW |
6 |
42,412,240 (GRCm39) |
missense |
probably benign |
0.02 |
R7714:Tas2r126
|
UTSW |
6 |
42,412,031 (GRCm39) |
missense |
probably benign |
0.12 |
R9154:Tas2r126
|
UTSW |
6 |
42,412,174 (GRCm39) |
missense |
probably benign |
0.25 |
R9336:Tas2r126
|
UTSW |
6 |
42,411,877 (GRCm39) |
missense |
probably benign |
0.45 |
R9516:Tas2r126
|
UTSW |
6 |
42,412,307 (GRCm39) |
missense |
probably null |
0.98 |
R9722:Tas2r126
|
UTSW |
6 |
42,412,082 (GRCm39) |
missense |
possibly damaging |
0.78 |
|