Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
C |
A |
5: 8,856,018 (GRCm39) |
A42E |
probably damaging |
Het |
Agmo |
T |
A |
12: 37,451,985 (GRCm39) |
F247L |
probably damaging |
Het |
Arap1 |
C |
A |
7: 101,049,332 (GRCm39) |
|
probably null |
Het |
Arid1a |
T |
C |
4: 133,408,585 (GRCm39) |
D1974G |
unknown |
Het |
Asxl3 |
C |
T |
18: 22,656,070 (GRCm39) |
A1360V |
possibly damaging |
Het |
Celsr1 |
T |
A |
15: 85,825,337 (GRCm39) |
T1599S |
possibly damaging |
Het |
Chrdl2 |
T |
C |
7: 99,670,190 (GRCm39) |
|
probably null |
Het |
Csmd3 |
T |
C |
15: 47,701,794 (GRCm39) |
|
probably benign |
Het |
Dis3l |
C |
T |
9: 64,222,055 (GRCm39) |
E452K |
probably benign |
Het |
Dnajc2 |
A |
T |
5: 21,981,788 (GRCm39) |
H45Q |
probably damaging |
Het |
Eps8 |
G |
A |
6: 137,499,840 (GRCm39) |
P213L |
probably benign |
Het |
Erbb3 |
T |
A |
10: 128,407,227 (GRCm39) |
R978* |
probably null |
Het |
Exoc2 |
A |
T |
13: 31,111,403 (GRCm39) |
C142S |
probably benign |
Het |
Fam184b |
T |
C |
5: 45,695,039 (GRCm39) |
E735G |
probably damaging |
Het |
Fancm |
T |
C |
12: 65,123,864 (GRCm39) |
V174A |
probably damaging |
Het |
Fat4 |
T |
C |
3: 38,942,364 (GRCm39) |
L419P |
probably damaging |
Het |
Fsip2 |
G |
T |
2: 82,814,736 (GRCm39) |
V3490L |
probably benign |
Het |
Ftcd |
A |
T |
10: 76,417,255 (GRCm39) |
R255* |
probably null |
Het |
Galc |
T |
C |
12: 98,179,391 (GRCm39) |
N506S |
possibly damaging |
Het |
Gm20441 |
G |
T |
10: 75,608,644 (GRCm39) |
A26E |
probably damaging |
Het |
Gm21969 |
T |
G |
4: 139,367,999 (GRCm39) |
|
probably null |
Het |
Ifitm3 |
T |
A |
7: 140,589,787 (GRCm39) |
M89L |
possibly damaging |
Het |
Ift25 |
T |
A |
4: 107,132,449 (GRCm39) |
S79T |
probably benign |
Het |
Inmt |
T |
C |
6: 55,150,355 (GRCm39) |
E94G |
probably damaging |
Het |
Insrr |
G |
A |
3: 87,716,719 (GRCm39) |
G649D |
probably benign |
Het |
Ivd |
T |
C |
2: 118,692,572 (GRCm39) |
L24P |
probably benign |
Het |
Kcnc1 |
A |
G |
7: 46,084,593 (GRCm39) |
N506D |
probably benign |
Het |
Krt39 |
T |
A |
11: 99,411,723 (GRCm39) |
D121V |
probably benign |
Het |
Lcp1 |
A |
G |
14: 75,461,536 (GRCm39) |
I510V |
probably benign |
Het |
Mkx |
C |
T |
18: 7,002,418 (GRCm39) |
V43M |
probably damaging |
Het |
Mmp2 |
A |
G |
8: 93,579,235 (GRCm39) |
N108S |
possibly damaging |
Het |
Mob1b |
T |
C |
5: 88,903,947 (GRCm39) |
|
probably benign |
Het |
Morc3 |
A |
G |
16: 93,661,844 (GRCm39) |
|
probably benign |
Het |
Myh13 |
T |
G |
11: 67,260,204 (GRCm39) |
S1881A |
probably benign |
Het |
Nalcn |
T |
C |
14: 123,558,717 (GRCm39) |
E843G |
probably benign |
Het |
Ngef |
A |
G |
1: 87,408,301 (GRCm39) |
|
probably benign |
Het |
Or14c40 |
T |
A |
7: 86,313,344 (GRCm39) |
I158N |
probably damaging |
Het |
Osm |
A |
G |
11: 4,189,507 (GRCm39) |
Y97C |
probably damaging |
Het |
Pclo |
T |
A |
5: 14,816,792 (GRCm39) |
L4556Q |
unknown |
Het |
Pcyox1l |
T |
C |
18: 61,830,780 (GRCm39) |
D364G |
probably benign |
Het |
Plekha6 |
T |
A |
1: 133,211,031 (GRCm39) |
V467E |
probably benign |
Het |
Qrsl1 |
A |
T |
10: 43,758,158 (GRCm39) |
S312T |
probably damaging |
Het |
Ripk1 |
T |
A |
13: 34,194,572 (GRCm39) |
L70Q |
probably damaging |
Het |
Rnaseh1 |
A |
T |
12: 28,705,662 (GRCm39) |
Y162F |
probably damaging |
Het |
Ror2 |
T |
A |
13: 53,275,703 (GRCm39) |
T195S |
probably damaging |
Het |
Sh3bp2 |
T |
C |
5: 34,709,006 (GRCm39) |
L33P |
probably damaging |
Het |
Skil |
T |
A |
3: 31,151,968 (GRCm39) |
C163* |
probably null |
Het |
Slc25a37 |
A |
T |
14: 69,486,883 (GRCm39) |
N133K |
probably benign |
Het |
Slitrk3 |
A |
C |
3: 72,958,046 (GRCm39) |
V242G |
probably damaging |
Het |
Sra1 |
A |
G |
18: 36,801,845 (GRCm39) |
S82P |
probably benign |
Het |
Synj2 |
A |
G |
17: 6,088,199 (GRCm39) |
N1417D |
probably benign |
Het |
Tasor2 |
T |
C |
13: 3,624,661 (GRCm39) |
E1763G |
probably benign |
Het |
Ttc21b |
T |
C |
2: 66,018,624 (GRCm39) |
N1261S |
probably benign |
Het |
Vmn2r69 |
A |
G |
7: 85,055,889 (GRCm39) |
S750P |
probably damaging |
Het |
Wdr95 |
A |
G |
5: 149,519,786 (GRCm39) |
T568A |
probably benign |
Het |
Zfp319 |
T |
A |
8: 96,055,721 (GRCm39) |
I161F |
possibly damaging |
Het |
|
Other mutations in Tas2r122 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01712:Tas2r122
|
APN |
6 |
132,688,725 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02605:Tas2r122
|
APN |
6 |
132,688,572 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02646:Tas2r122
|
APN |
6 |
132,688,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02716:Tas2r122
|
APN |
6 |
132,688,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R0318:Tas2r122
|
UTSW |
6 |
132,688,795 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0462:Tas2r122
|
UTSW |
6 |
132,688,141 (GRCm39) |
missense |
probably benign |
0.06 |
R0532:Tas2r122
|
UTSW |
6 |
132,688,791 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0538:Tas2r122
|
UTSW |
6 |
132,688,778 (GRCm39) |
missense |
probably benign |
0.06 |
R0570:Tas2r122
|
UTSW |
6 |
132,688,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R1863:Tas2r122
|
UTSW |
6 |
132,688,065 (GRCm39) |
nonsense |
probably null |
|
R1966:Tas2r122
|
UTSW |
6 |
132,688,157 (GRCm39) |
nonsense |
probably null |
|
R2001:Tas2r122
|
UTSW |
6 |
132,688,585 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3500:Tas2r122
|
UTSW |
6 |
132,688,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R3871:Tas2r122
|
UTSW |
6 |
132,688,543 (GRCm39) |
missense |
probably benign |
0.00 |
R4174:Tas2r122
|
UTSW |
6 |
132,688,839 (GRCm39) |
missense |
probably damaging |
0.96 |
R5533:Tas2r122
|
UTSW |
6 |
132,688,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R5567:Tas2r122
|
UTSW |
6 |
132,688,335 (GRCm39) |
missense |
probably benign |
0.28 |
R6455:Tas2r122
|
UTSW |
6 |
132,688,626 (GRCm39) |
nonsense |
probably null |
|
R6716:Tas2r122
|
UTSW |
6 |
132,688,860 (GRCm39) |
missense |
probably damaging |
0.98 |
R8812:Tas2r122
|
UTSW |
6 |
132,688,702 (GRCm39) |
missense |
probably benign |
0.09 |
R9139:Tas2r122
|
UTSW |
6 |
132,688,779 (GRCm39) |
missense |
probably benign |
0.33 |
R9720:Tas2r122
|
UTSW |
6 |
132,688,634 (GRCm39) |
missense |
probably benign |
0.01 |
|