Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg1 |
A |
G |
9: 54,535,745 (GRCm39) |
I130T |
possibly damaging |
Het |
Adam24 |
T |
A |
8: 41,133,039 (GRCm39) |
L169* |
probably null |
Het |
Als2 |
A |
T |
1: 59,246,971 (GRCm39) |
I556N |
probably damaging |
Het |
Ankrd44 |
A |
T |
1: 54,688,599 (GRCm39) |
N212K |
|
Het |
Anpep |
T |
C |
7: 79,490,736 (GRCm39) |
D260G |
probably benign |
Het |
Arhgap17 |
A |
T |
7: 122,884,581 (GRCm39) |
|
probably null |
Het |
Atad2 |
C |
T |
15: 57,980,689 (GRCm39) |
R383Q |
probably damaging |
Het |
Atp11b |
T |
A |
3: 35,874,099 (GRCm39) |
M696K |
probably benign |
Het |
Atp13a2 |
A |
G |
4: 140,726,462 (GRCm39) |
T350A |
probably damaging |
Het |
Atp8b2 |
T |
C |
3: 89,850,979 (GRCm39) |
D29G |
possibly damaging |
Het |
Baz2a |
C |
T |
10: 127,960,326 (GRCm39) |
R1514W |
probably damaging |
Het |
Cep250 |
T |
A |
2: 155,815,375 (GRCm39) |
L631* |
probably null |
Het |
Cimip2a |
G |
A |
2: 25,110,252 (GRCm39) |
V55I |
probably damaging |
Het |
Clec4a3 |
T |
C |
6: 122,941,251 (GRCm39) |
I82T |
probably benign |
Het |
Csmd3 |
T |
A |
15: 47,454,170 (GRCm39) |
I2648F |
|
Het |
Cul5 |
A |
G |
9: 53,555,826 (GRCm39) |
F247L |
probably benign |
Het |
Dnajc24 |
A |
T |
2: 105,800,807 (GRCm39) |
M101K |
probably damaging |
Het |
Dnhd1 |
T |
A |
7: 105,344,200 (GRCm39) |
V1848E |
probably damaging |
Het |
Dspp |
A |
G |
5: 104,321,932 (GRCm39) |
T14A |
probably benign |
Het |
Gm7298 |
T |
G |
6: 121,762,855 (GRCm39) |
I1392S |
probably damaging |
Het |
Gm9955 |
A |
T |
18: 24,842,220 (GRCm39) |
S62R |
unknown |
Het |
Gtsf1 |
T |
G |
15: 103,328,388 (GRCm39) |
N130T |
probably benign |
Het |
Heatr5a |
C |
A |
12: 51,971,925 (GRCm39) |
S755I |
probably damaging |
Het |
Hrc |
A |
G |
7: 44,985,685 (GRCm39) |
T279A |
possibly damaging |
Het |
Hvcn1 |
T |
C |
5: 122,371,573 (GRCm39) |
W38R |
probably damaging |
Het |
Hyal6 |
A |
G |
6: 24,734,834 (GRCm39) |
S256G |
probably benign |
Het |
Insyn2b |
G |
T |
11: 34,352,359 (GRCm39) |
V134F |
probably damaging |
Het |
Ipo13 |
A |
G |
4: 117,761,081 (GRCm39) |
S546P |
possibly damaging |
Het |
Katnip |
T |
C |
7: 125,465,499 (GRCm39) |
V1317A |
probably benign |
Het |
Kif24 |
A |
G |
4: 41,395,085 (GRCm39) |
V730A |
probably benign |
Het |
L3mbtl2 |
T |
C |
15: 81,555,275 (GRCm39) |
V176A |
probably benign |
Het |
Lgi1 |
T |
C |
19: 38,294,733 (GRCm39) |
Y502H |
probably damaging |
Het |
Liph |
T |
A |
16: 21,795,078 (GRCm39) |
D178V |
probably damaging |
Het |
Maea |
T |
C |
5: 33,515,854 (GRCm39) |
V47A |
probably damaging |
Het |
Mak16 |
A |
C |
8: 31,656,602 (GRCm39) |
S42A |
probably benign |
Het |
Mamdc4 |
T |
C |
2: 25,458,977 (GRCm39) |
I269V |
probably benign |
Het |
Mapk8ip3 |
A |
T |
17: 25,120,728 (GRCm39) |
M812K |
probably benign |
Het |
Muc4 |
T |
A |
16: 32,752,788 (GRCm38) |
S889T |
unknown |
Het |
Npy6r |
A |
G |
18: 44,409,551 (GRCm39) |
N324S |
probably damaging |
Het |
Ntrk3 |
T |
G |
7: 78,005,895 (GRCm39) |
T489P |
possibly damaging |
Het |
Or52a5b |
G |
A |
7: 103,417,182 (GRCm39) |
Q141* |
probably null |
Het |
Or5h19 |
T |
A |
16: 58,856,296 (GRCm39) |
D268V |
probably benign |
Het |
Or5t17 |
G |
A |
2: 86,832,879 (GRCm39) |
V189I |
probably benign |
Het |
Otof |
G |
C |
5: 30,540,878 (GRCm39) |
T887S |
possibly damaging |
Het |
Papola |
T |
C |
12: 105,773,443 (GRCm39) |
V154A |
probably damaging |
Het |
Pde4dip |
T |
C |
3: 97,622,946 (GRCm39) |
H1421R |
probably benign |
Het |
Plpp5 |
T |
C |
8: 26,210,606 (GRCm39) |
S66P |
probably benign |
Het |
Ppp6r3 |
T |
A |
19: 3,568,337 (GRCm39) |
I154L |
probably benign |
Het |
Prr18 |
A |
C |
17: 8,560,741 (GRCm39) |
D299A |
possibly damaging |
Het |
Psmb1 |
G |
A |
17: 15,697,521 (GRCm39) |
S198F |
possibly damaging |
Het |
Qars1 |
T |
C |
9: 108,392,322 (GRCm39) |
V723A |
possibly damaging |
Het |
Rab6a |
A |
T |
7: 100,285,959 (GRCm39) |
R185* |
probably null |
Het |
Scn2a |
C |
T |
2: 65,579,197 (GRCm39) |
Q1511* |
probably null |
Het |
Serpinb3d |
T |
A |
1: 107,008,506 (GRCm39) |
I120F |
possibly damaging |
Het |
Serpini2 |
T |
C |
3: 75,165,455 (GRCm39) |
T175A |
probably damaging |
Het |
Skic2 |
T |
C |
17: 35,058,440 (GRCm39) |
T1226A |
probably benign |
Het |
Slc17a6 |
A |
G |
7: 51,317,259 (GRCm39) |
I427V |
possibly damaging |
Het |
Slc2a2 |
C |
T |
3: 28,773,631 (GRCm39) |
A312V |
possibly damaging |
Het |
Snx33 |
C |
T |
9: 56,833,151 (GRCm39) |
R306H |
probably damaging |
Het |
Spcs1 |
G |
A |
14: 30,722,438 (GRCm39) |
S127F |
possibly damaging |
Het |
Speg |
T |
C |
1: 75,399,027 (GRCm39) |
V2158A |
possibly damaging |
Het |
Sptbn4 |
T |
A |
7: 27,117,481 (GRCm39) |
I423F |
probably damaging |
Het |
Synj2 |
T |
A |
17: 6,076,754 (GRCm39) |
I930N |
possibly damaging |
Het |
Tcf3 |
C |
A |
10: 80,257,433 (GRCm39) |
V11F |
unknown |
Het |
Tead1 |
A |
T |
7: 112,441,144 (GRCm39) |
Q91L |
probably benign |
Het |
Tgm5 |
T |
A |
2: 120,916,249 (GRCm39) |
|
probably benign |
Het |
Tgoln1 |
C |
T |
6: 72,593,028 (GRCm39) |
G151S |
probably benign |
Het |
Tnfrsf11a |
C |
A |
1: 105,755,264 (GRCm39) |
N445K |
probably benign |
Het |
Ttn |
G |
C |
2: 76,540,514 (GRCm39) |
F34157L |
probably benign |
Het |
Vmn2r91 |
C |
A |
17: 18,356,424 (GRCm39) |
P697Q |
probably damaging |
Het |
Zeb2 |
G |
A |
2: 44,887,006 (GRCm39) |
L684F |
probably damaging |
Het |
Zfp661 |
T |
C |
2: 127,419,456 (GRCm39) |
D228G |
probably benign |
Het |
Zfp738 |
T |
C |
13: 67,821,147 (GRCm39) |
K77E |
probably damaging |
Het |
Zkscan1 |
T |
A |
5: 138,099,192 (GRCm39) |
D378E |
probably damaging |
Het |
Zswim9 |
T |
A |
7: 12,993,924 (GRCm39) |
D744V |
possibly damaging |
Het |
|
Other mutations in Tas2r140 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Tas2r140
|
APN |
6 |
40,468,274 (GRCm39) |
missense |
probably benign |
0.20 |
IGL00951:Tas2r140
|
APN |
6 |
40,468,913 (GRCm39) |
nonsense |
probably null |
|
IGL00980:Tas2r140
|
APN |
6 |
40,468,352 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02055:Tas2r140
|
APN |
6 |
40,468,493 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03101:Tas2r140
|
APN |
6 |
40,468,764 (GRCm39) |
missense |
probably benign |
0.03 |
R0149:Tas2r140
|
UTSW |
6 |
40,468,232 (GRCm39) |
missense |
probably benign |
0.08 |
R0244:Tas2r140
|
UTSW |
6 |
133,032,290 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0361:Tas2r140
|
UTSW |
6 |
40,468,232 (GRCm39) |
missense |
probably benign |
0.08 |
R0666:Tas2r140
|
UTSW |
6 |
133,032,405 (GRCm39) |
missense |
probably benign |
0.22 |
R0755:Tas2r140
|
UTSW |
6 |
40,468,344 (GRCm39) |
missense |
probably damaging |
0.99 |
R1174:Tas2r140
|
UTSW |
6 |
133,031,834 (GRCm39) |
missense |
probably benign |
0.27 |
R1237:Tas2r140
|
UTSW |
6 |
133,032,171 (GRCm39) |
missense |
probably benign |
0.04 |
R1553:Tas2r140
|
UTSW |
6 |
133,032,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R2030:Tas2r140
|
UTSW |
6 |
133,032,213 (GRCm39) |
missense |
probably benign |
0.23 |
R2030:Tas2r140
|
UTSW |
6 |
40,469,154 (GRCm39) |
missense |
possibly damaging |
0.58 |
R3123:Tas2r140
|
UTSW |
6 |
133,032,204 (GRCm39) |
missense |
probably benign |
0.05 |
R3124:Tas2r140
|
UTSW |
6 |
133,032,204 (GRCm39) |
missense |
probably benign |
0.05 |
R4233:Tas2r140
|
UTSW |
6 |
133,031,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R4234:Tas2r140
|
UTSW |
6 |
133,031,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R4236:Tas2r140
|
UTSW |
6 |
133,031,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R4525:Tas2r140
|
UTSW |
6 |
133,032,207 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4803:Tas2r140
|
UTSW |
6 |
133,032,743 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4840:Tas2r140
|
UTSW |
6 |
133,032,528 (GRCm39) |
missense |
probably benign |
0.01 |
R4885:Tas2r140
|
UTSW |
6 |
40,468,334 (GRCm39) |
missense |
probably damaging |
0.98 |
R5092:Tas2r140
|
UTSW |
6 |
40,468,200 (GRCm39) |
missense |
probably benign |
|
R5182:Tas2r140
|
UTSW |
6 |
40,468,866 (GRCm39) |
missense |
probably benign |
0.01 |
R5317:Tas2r140
|
UTSW |
6 |
133,032,543 (GRCm39) |
missense |
probably benign |
0.06 |
R5937:Tas2r140
|
UTSW |
6 |
133,032,236 (GRCm39) |
missense |
probably benign |
0.01 |
R5952:Tas2r140
|
UTSW |
6 |
40,468,476 (GRCm39) |
missense |
probably benign |
0.43 |
R6142:Tas2r140
|
UTSW |
6 |
133,032,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R7127:Tas2r140
|
UTSW |
6 |
133,031,922 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7143:Tas2r140
|
UTSW |
6 |
133,032,482 (GRCm39) |
missense |
probably benign |
0.00 |
R7494:Tas2r140
|
UTSW |
6 |
40,468,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R7513:Tas2r140
|
UTSW |
6 |
40,469,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R7875:Tas2r140
|
UTSW |
6 |
40,469,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R7979:Tas2r140
|
UTSW |
6 |
40,468,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R8804:Tas2r140
|
UTSW |
6 |
133,032,326 (GRCm39) |
missense |
probably damaging |
0.98 |
R9029:Tas2r140
|
UTSW |
6 |
133,032,181 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9055:Tas2r140
|
UTSW |
6 |
133,032,380 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9257:Tas2r140
|
UTSW |
6 |
40,468,592 (GRCm39) |
missense |
probably damaging |
0.98 |
R9385:Tas2r140
|
UTSW |
6 |
133,032,241 (GRCm39) |
missense |
probably benign |
0.03 |
R9530:Tas2r140
|
UTSW |
6 |
133,032,494 (GRCm39) |
missense |
probably benign |
0.00 |
R9760:Tas2r140
|
UTSW |
6 |
40,469,036 (GRCm39) |
missense |
probably benign |
0.41 |
X0022:Tas2r140
|
UTSW |
6 |
40,468,275 (GRCm39) |
missense |
possibly damaging |
0.63 |
|