Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam5 |
T |
C |
8: 25,271,610 (GRCm39) |
N599S |
probably benign |
Het |
Adam6a |
A |
T |
12: 113,509,893 (GRCm39) |
*755Y |
probably null |
Het |
Adgrb3 |
G |
T |
1: 25,132,868 (GRCm39) |
T1166K |
probably benign |
Het |
Ano1 |
T |
C |
7: 144,198,479 (GRCm39) |
Y345C |
probably benign |
Het |
Ano1 |
A |
G |
7: 144,149,275 (GRCm39) |
V862A |
probably damaging |
Het |
Asap2 |
C |
T |
12: 21,279,264 (GRCm39) |
A382V |
probably damaging |
Het |
Asb18 |
A |
G |
1: 89,923,963 (GRCm39) |
V100A |
probably benign |
Het |
Bdnf |
G |
A |
2: 109,553,931 (GRCm39) |
A102T |
probably benign |
Het |
Ccser2 |
G |
A |
14: 36,660,626 (GRCm39) |
T509M |
probably damaging |
Het |
Cfap47 |
A |
G |
X: 78,532,764 (GRCm39) |
I767T |
possibly damaging |
Het |
Des |
G |
A |
1: 75,339,227 (GRCm39) |
A251T |
probably benign |
Het |
Dmd |
C |
T |
X: 84,153,590 (GRCm39) |
Q3224* |
probably null |
Het |
Endog |
G |
T |
2: 30,061,975 (GRCm39) |
|
probably null |
Het |
Ggt7 |
A |
G |
2: 155,342,691 (GRCm39) |
V269A |
probably damaging |
Het |
Gucy2c |
A |
G |
6: 136,686,739 (GRCm39) |
F808S |
probably damaging |
Het |
Hira |
A |
G |
16: 18,730,930 (GRCm39) |
T210A |
probably benign |
Het |
Ifitm5 |
C |
A |
7: 140,530,076 (GRCm39) |
R16L |
probably benign |
Het |
Igdcc4 |
T |
C |
9: 65,031,273 (GRCm39) |
C404R |
probably damaging |
Het |
Ints7 |
G |
A |
1: 191,347,890 (GRCm39) |
R754H |
probably benign |
Het |
Irf9 |
A |
G |
14: 55,845,058 (GRCm39) |
E258G |
probably damaging |
Het |
Megf11 |
T |
C |
9: 64,567,728 (GRCm39) |
C406R |
probably damaging |
Het |
Olfml1 |
A |
G |
7: 107,189,364 (GRCm39) |
N143S |
possibly damaging |
Het |
Or4m1 |
A |
G |
14: 50,557,713 (GRCm39) |
F193S |
possibly damaging |
Het |
Or6c66b |
T |
A |
10: 129,376,711 (GRCm39) |
F102I |
probably benign |
Het |
Or7g30 |
A |
G |
9: 19,352,266 (GRCm39) |
D19G |
probably benign |
Het |
Otof |
G |
T |
5: 30,562,527 (GRCm39) |
Q254K |
probably damaging |
Het |
Pate7 |
A |
T |
9: 35,688,044 (GRCm39) |
N65K |
possibly damaging |
Het |
Plcd3 |
A |
G |
11: 102,968,696 (GRCm39) |
F332L |
probably benign |
Het |
Plxnc1 |
T |
C |
10: 94,635,230 (GRCm39) |
D1332G |
probably damaging |
Het |
Rnasel |
A |
T |
1: 153,634,130 (GRCm39) |
D521V |
probably benign |
Het |
Sema5a |
T |
A |
15: 32,575,143 (GRCm39) |
V417D |
possibly damaging |
Het |
Senp6 |
G |
A |
9: 80,044,000 (GRCm39) |
R877Q |
probably benign |
Het |
Shroom2 |
A |
T |
X: 151,442,353 (GRCm39) |
D937E |
probably damaging |
Het |
Slc35a3 |
A |
G |
3: 116,488,262 (GRCm39) |
S142P |
probably damaging |
Het |
Srpx |
A |
T |
X: 9,905,298 (GRCm39) |
V398E |
probably damaging |
Het |
Stk10 |
A |
T |
11: 32,560,653 (GRCm39) |
K669N |
possibly damaging |
Het |
Sumf2 |
A |
G |
5: 129,878,811 (GRCm39) |
D49G |
probably damaging |
Het |
Syde1 |
T |
A |
10: 78,424,721 (GRCm39) |
E370D |
probably damaging |
Het |
Top2a |
G |
A |
11: 98,896,985 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
A |
2: 76,550,842 (GRCm39) |
T23190S |
probably damaging |
Het |
Ttyh3 |
C |
A |
5: 140,615,167 (GRCm39) |
C407F |
probably damaging |
Het |
Vmn2r27 |
G |
T |
6: 124,169,370 (GRCm39) |
H587N |
possibly damaging |
Het |
Vmn2r74 |
A |
G |
7: 85,606,692 (GRCm39) |
I218T |
possibly damaging |
Het |
Vsig10 |
A |
G |
5: 117,462,954 (GRCm39) |
N60S |
probably benign |
Het |
Zc3h7a |
A |
G |
16: 10,956,979 (GRCm39) |
S877P |
probably damaging |
Het |
Zfp979 |
G |
T |
4: 147,699,853 (GRCm39) |
T29N |
probably damaging |
Het |
Znfx1 |
G |
A |
2: 166,880,615 (GRCm39) |
R390C |
possibly damaging |
Het |
|
Other mutations in Tas2r115 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00565:Tas2r115
|
APN |
6 |
132,714,741 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01516:Tas2r115
|
APN |
6 |
132,714,576 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01637:Tas2r115
|
APN |
6 |
132,714,592 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02041:Tas2r115
|
APN |
6 |
132,714,430 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02178:Tas2r115
|
APN |
6 |
132,714,271 (GRCm39) |
missense |
probably benign |
0.11 |
R0467:Tas2r115
|
UTSW |
6 |
132,714,682 (GRCm39) |
missense |
probably benign |
0.02 |
R0553:Tas2r115
|
UTSW |
6 |
132,714,922 (GRCm39) |
missense |
probably benign |
0.18 |
R1425:Tas2r115
|
UTSW |
6 |
132,714,442 (GRCm39) |
missense |
probably benign |
0.02 |
R1770:Tas2r115
|
UTSW |
6 |
132,714,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Tas2r115
|
UTSW |
6 |
132,714,470 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2136:Tas2r115
|
UTSW |
6 |
132,714,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R2141:Tas2r115
|
UTSW |
6 |
132,714,321 (GRCm39) |
missense |
probably benign |
0.43 |
R2142:Tas2r115
|
UTSW |
6 |
132,714,321 (GRCm39) |
missense |
probably benign |
0.43 |
R4479:Tas2r115
|
UTSW |
6 |
132,714,495 (GRCm39) |
missense |
probably damaging |
0.98 |
R4687:Tas2r115
|
UTSW |
6 |
132,714,247 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4948:Tas2r115
|
UTSW |
6 |
132,714,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R5097:Tas2r115
|
UTSW |
6 |
132,714,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R5856:Tas2r115
|
UTSW |
6 |
132,714,501 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6927:Tas2r115
|
UTSW |
6 |
132,714,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R7473:Tas2r115
|
UTSW |
6 |
132,714,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R7688:Tas2r115
|
UTSW |
6 |
132,714,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R8415:Tas2r115
|
UTSW |
6 |
132,714,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R8495:Tas2r115
|
UTSW |
6 |
132,714,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R9032:Tas2r115
|
UTSW |
6 |
132,714,327 (GRCm39) |
missense |
probably benign |
0.37 |
R9085:Tas2r115
|
UTSW |
6 |
132,714,327 (GRCm39) |
missense |
probably benign |
0.37 |
R9318:Tas2r115
|
UTSW |
6 |
132,714,472 (GRCm39) |
missense |
probably benign |
0.01 |
R9665:Tas2r115
|
UTSW |
6 |
132,714,390 (GRCm39) |
missense |
probably benign |
0.31 |
R9751:Tas2r115
|
UTSW |
6 |
132,714,918 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1088:Tas2r115
|
UTSW |
6 |
132,714,044 (GRCm39) |
nonsense |
probably null |
|
Z1176:Tas2r115
|
UTSW |
6 |
132,714,819 (GRCm39) |
missense |
probably damaging |
1.00 |
|