Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ccdc77 |
T |
A |
6: 120,308,809 (GRCm39) |
L335F |
probably benign |
Het |
Ccr3 |
T |
A |
9: 123,829,046 (GRCm39) |
F127Y |
probably damaging |
Het |
Cfap43 |
T |
C |
19: 47,785,579 (GRCm39) |
N437S |
probably benign |
Het |
Cfh |
A |
G |
1: 140,064,553 (GRCm39) |
V365A |
probably damaging |
Het |
Copg1 |
T |
A |
6: 87,874,945 (GRCm39) |
V380D |
probably damaging |
Het |
Cxxc1 |
T |
C |
18: 74,353,256 (GRCm39) |
I497T |
possibly damaging |
Het |
Disp3 |
G |
A |
4: 148,326,047 (GRCm39) |
T1237I |
possibly damaging |
Het |
Dnaaf9 |
A |
T |
2: 130,555,390 (GRCm39) |
F839L |
probably benign |
Het |
Dnah7a |
A |
T |
1: 53,675,246 (GRCm39) |
F360L |
probably benign |
Het |
Dnhd1 |
C |
T |
7: 105,363,252 (GRCm39) |
A3938V |
probably damaging |
Het |
Eif4g1 |
A |
G |
16: 20,502,818 (GRCm39) |
D1000G |
probably damaging |
Het |
Emsy |
A |
T |
7: 98,242,983 (GRCm39) |
V1052D |
probably damaging |
Het |
Ep400 |
A |
G |
5: 110,858,959 (GRCm39) |
|
probably benign |
Het |
Fa2h |
T |
C |
8: 112,082,779 (GRCm39) |
H146R |
probably damaging |
Het |
Gad1 |
G |
A |
2: 70,424,996 (GRCm39) |
C430Y |
probably benign |
Het |
Gtse1 |
T |
C |
15: 85,753,252 (GRCm39) |
S456P |
probably damaging |
Het |
Gucy2g |
T |
C |
19: 55,187,202 (GRCm39) |
T1073A |
probably damaging |
Het |
Hectd2 |
T |
G |
19: 36,562,897 (GRCm39) |
N3K |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,525,768 (GRCm39) |
C3318* |
probably null |
Het |
Lipo2 |
C |
T |
19: 33,726,824 (GRCm39) |
S71N |
probably benign |
Het |
Mynn |
G |
T |
3: 30,661,217 (GRCm39) |
D100Y |
probably damaging |
Het |
Myo16 |
G |
A |
8: 10,612,318 (GRCm39) |
|
probably null |
Het |
Npr2 |
G |
T |
4: 43,640,947 (GRCm39) |
K384N |
probably benign |
Het |
Nrde2 |
A |
G |
12: 100,098,492 (GRCm39) |
V725A |
possibly damaging |
Het |
Or11h23 |
T |
A |
14: 50,948,661 (GRCm39) |
S291R |
probably damaging |
Het |
Or2l13 |
A |
G |
16: 19,305,938 (GRCm39) |
M117V |
probably damaging |
Het |
Otud7a |
C |
T |
7: 63,335,266 (GRCm39) |
P101S |
possibly damaging |
Het |
Pcdhb7 |
T |
A |
18: 37,475,410 (GRCm39) |
L182Q |
probably benign |
Het |
Pdss1 |
A |
G |
2: 22,805,425 (GRCm39) |
|
probably null |
Het |
Ppargc1b |
T |
A |
18: 61,444,512 (GRCm39) |
H233L |
probably damaging |
Het |
Ppm1b |
A |
G |
17: 85,320,987 (GRCm39) |
|
probably null |
Het |
Prdm14 |
A |
T |
1: 13,195,949 (GRCm39) |
S37R |
possibly damaging |
Het |
Prss45 |
A |
G |
9: 110,667,497 (GRCm39) |
T39A |
probably benign |
Het |
Qars1 |
T |
C |
9: 108,392,161 (GRCm39) |
|
probably benign |
Het |
Rxfp2 |
T |
G |
5: 149,961,712 (GRCm39) |
H77Q |
probably benign |
Het |
Scd4 |
A |
G |
19: 44,329,685 (GRCm39) |
M219V |
probably benign |
Het |
Sec24b |
G |
T |
3: 129,834,985 (GRCm39) |
P71Q |
probably benign |
Het |
Snd1 |
T |
G |
6: 28,886,576 (GRCm39) |
V861G |
probably benign |
Het |
Sspo |
A |
G |
6: 48,441,876 (GRCm39) |
|
probably null |
Het |
Tbc1d31 |
T |
A |
15: 57,833,120 (GRCm39) |
I953N |
possibly damaging |
Het |
Tlr4 |
A |
G |
4: 66,757,732 (GRCm39) |
N175S |
probably benign |
Het |
Tspyl4 |
A |
G |
10: 34,174,518 (GRCm39) |
N337D |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,642,545 (GRCm39) |
L13330H |
probably damaging |
Het |
Usp33 |
T |
A |
3: 152,089,756 (GRCm39) |
Y765* |
probably null |
Het |
Vmn2r59 |
T |
A |
7: 41,696,529 (GRCm39) |
Y71F |
probably benign |
Het |
Zbed6 |
A |
G |
1: 133,585,576 (GRCm39) |
F587S |
probably benign |
Het |
Zfhx4 |
T |
C |
3: 5,467,161 (GRCm39) |
S2465P |
probably damaging |
Het |
|
Other mutations in Tas2r129 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02227:Tas2r129
|
APN |
6 |
132,928,357 (GRCm39) |
nonsense |
probably null |
|
R0389:Tas2r129
|
UTSW |
6 |
132,928,159 (GRCm39) |
missense |
probably benign |
0.26 |
R0443:Tas2r129
|
UTSW |
6 |
132,928,159 (GRCm39) |
missense |
probably benign |
0.26 |
R0487:Tas2r129
|
UTSW |
6 |
132,928,907 (GRCm39) |
missense |
probably benign |
0.31 |
R0487:Tas2r129
|
UTSW |
6 |
132,928,906 (GRCm39) |
missense |
probably benign |
0.26 |
R1253:Tas2r129
|
UTSW |
6 |
132,928,999 (GRCm39) |
missense |
probably benign |
0.11 |
R3124:Tas2r129
|
UTSW |
6 |
132,928,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R4493:Tas2r129
|
UTSW |
6 |
132,928,317 (GRCm39) |
missense |
probably benign |
0.31 |
R4494:Tas2r129
|
UTSW |
6 |
132,928,317 (GRCm39) |
missense |
probably benign |
0.31 |
R4591:Tas2r129
|
UTSW |
6 |
132,928,574 (GRCm39) |
missense |
probably benign |
0.10 |
R6156:Tas2r129
|
UTSW |
6 |
132,928,455 (GRCm39) |
missense |
probably benign |
0.31 |
R6495:Tas2r129
|
UTSW |
6 |
132,928,128 (GRCm39) |
missense |
probably benign |
0.00 |
R7600:Tas2r129
|
UTSW |
6 |
132,928,137 (GRCm39) |
nonsense |
probably null |
|
R7608:Tas2r129
|
UTSW |
6 |
132,928,156 (GRCm39) |
missense |
probably damaging |
0.98 |
R8498:Tas2r129
|
UTSW |
6 |
132,928,815 (GRCm39) |
missense |
probably benign |
0.01 |
R8870:Tas2r129
|
UTSW |
6 |
132,928,522 (GRCm39) |
missense |
probably damaging |
0.98 |
R9276:Tas2r129
|
UTSW |
6 |
132,928,576 (GRCm39) |
missense |
probably benign |
0.12 |
|