Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh16a1 |
G |
A |
7: 44,795,459 (GRCm39) |
P400L |
probably damaging |
Het |
Angptl3 |
T |
C |
4: 98,919,738 (GRCm39) |
|
probably null |
Het |
Atoh1 |
T |
C |
6: 64,706,334 (GRCm39) |
W10R |
probably damaging |
Het |
Brd8 |
C |
T |
18: 34,735,780 (GRCm39) |
S899N |
probably damaging |
Het |
Ccm2 |
A |
G |
11: 6,544,154 (GRCm39) |
T317A |
probably damaging |
Het |
Ccnt1 |
A |
T |
15: 98,465,484 (GRCm39) |
W12R |
probably damaging |
Het |
Celf1 |
T |
A |
2: 90,831,408 (GRCm39) |
L79H |
probably damaging |
Het |
Cmip |
T |
C |
8: 118,175,770 (GRCm39) |
V423A |
probably damaging |
Het |
Ddr1 |
T |
A |
17: 35,999,481 (GRCm39) |
I431F |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,080,149 (GRCm39) |
L2343P |
probably benign |
Het |
Duox1 |
A |
G |
2: 122,176,817 (GRCm39) |
D1446G |
probably benign |
Het |
Erich3 |
A |
G |
3: 154,419,599 (GRCm39) |
H231R |
possibly damaging |
Het |
Fam221b |
T |
A |
4: 43,666,450 (GRCm39) |
I54F |
probably benign |
Het |
Fcgbpl1 |
G |
A |
7: 27,839,281 (GRCm39) |
V365M |
probably damaging |
Het |
Galntl5 |
T |
C |
5: 25,394,839 (GRCm39) |
F69L |
possibly damaging |
Het |
Gba2 |
T |
G |
4: 43,567,918 (GRCm39) |
|
probably null |
Het |
Gbf1 |
C |
A |
19: 46,240,556 (GRCm39) |
P46Q |
probably damaging |
Het |
Gimap6 |
T |
G |
6: 48,679,635 (GRCm39) |
S134R |
probably damaging |
Het |
Gm5424 |
A |
C |
10: 61,907,377 (GRCm39) |
|
noncoding transcript |
Het |
Hexb |
T |
C |
13: 97,314,532 (GRCm39) |
K404E |
possibly damaging |
Het |
Hs3st3a1 |
G |
A |
11: 64,327,331 (GRCm39) |
V147M |
probably damaging |
Het |
Hsd17b4 |
T |
C |
18: 50,315,063 (GRCm39) |
V610A |
probably benign |
Het |
Loxl3 |
T |
A |
6: 83,025,628 (GRCm39) |
W329R |
probably damaging |
Het |
Lrrc52 |
A |
G |
1: 167,273,575 (GRCm39) |
F247S |
probably damaging |
Het |
Naa38 |
C |
T |
11: 69,287,045 (GRCm39) |
R42W |
probably damaging |
Het |
Nadsyn1 |
G |
A |
7: 143,357,753 (GRCm39) |
Q485* |
probably null |
Het |
Nid1 |
A |
G |
13: 13,663,743 (GRCm39) |
|
probably null |
Het |
Ofcc1 |
T |
C |
13: 40,362,251 (GRCm39) |
T224A |
probably benign |
Het |
Or5m11b |
T |
G |
2: 85,806,517 (GRCm39) |
I310S |
probably benign |
Het |
Palld |
A |
G |
8: 62,330,476 (GRCm39) |
Y134H |
possibly damaging |
Het |
Pfkfb4 |
C |
T |
9: 108,854,178 (GRCm39) |
R351W |
probably damaging |
Het |
Pfn3 |
T |
C |
13: 55,562,699 (GRCm39) |
D94G |
possibly damaging |
Het |
Pkhd1 |
G |
A |
1: 20,187,419 (GRCm39) |
R3630C |
probably damaging |
Het |
Por |
T |
A |
5: 135,744,829 (GRCm39) |
F31I |
probably benign |
Het |
Ppp1r12c |
T |
C |
7: 4,492,858 (GRCm39) |
E127G |
probably benign |
Het |
Ppp1r9a |
T |
A |
6: 5,156,229 (GRCm39) |
S1162T |
probably damaging |
Het |
Psen2 |
C |
A |
1: 180,057,488 (GRCm39) |
A297S |
probably benign |
Het |
Rpusd2 |
G |
A |
2: 118,869,119 (GRCm39) |
R514Q |
probably damaging |
Het |
Rxrg |
A |
G |
1: 167,462,029 (GRCm39) |
M235V |
probably damaging |
Het |
Sash1 |
T |
C |
10: 8,615,229 (GRCm39) |
M644V |
probably damaging |
Het |
Sf3b3 |
T |
C |
8: 111,550,075 (GRCm39) |
T648A |
probably benign |
Het |
Slco1a7 |
T |
A |
6: 141,684,739 (GRCm39) |
T239S |
probably benign |
Het |
Ssu72 |
T |
C |
4: 155,816,483 (GRCm39) |
I155T |
probably benign |
Het |
Tmem214 |
G |
A |
5: 31,030,090 (GRCm39) |
A296T |
probably benign |
Het |
Trav12-2 |
C |
A |
14: 53,853,859 (GRCm39) |
N2K |
probably damaging |
Het |
Tyrp1 |
C |
T |
4: 80,755,845 (GRCm39) |
Q205* |
probably null |
Het |
Ubr4 |
T |
A |
4: 139,180,052 (GRCm39) |
|
probably null |
Het |
Ush2a |
A |
G |
1: 187,995,588 (GRCm39) |
S120G |
probably benign |
Het |
Vmn2r100 |
T |
C |
17: 19,741,504 (GRCm39) |
|
probably benign |
Het |
Zer1 |
G |
T |
2: 29,994,928 (GRCm39) |
T489K |
probably benign |
Het |
Zfp955b |
G |
T |
17: 33,521,238 (GRCm39) |
G236* |
probably null |
Het |
|
Other mutations in Tas2r102 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00685:Tas2r102
|
APN |
6 |
132,739,488 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL01777:Tas2r102
|
APN |
6 |
132,739,815 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01956:Tas2r102
|
APN |
6 |
132,739,416 (GRCm39) |
nonsense |
probably null |
|
IGL02650:Tas2r102
|
APN |
6 |
132,739,173 (GRCm39) |
missense |
probably null |
0.00 |
R0483:Tas2r102
|
UTSW |
6 |
132,739,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Tas2r102
|
UTSW |
6 |
132,739,636 (GRCm39) |
missense |
probably damaging |
0.98 |
R0726:Tas2r102
|
UTSW |
6 |
132,739,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1777:Tas2r102
|
UTSW |
6 |
132,739,254 (GRCm39) |
missense |
probably benign |
0.08 |
R3615:Tas2r102
|
UTSW |
6 |
132,739,781 (GRCm39) |
nonsense |
probably null |
|
R3616:Tas2r102
|
UTSW |
6 |
132,739,781 (GRCm39) |
nonsense |
probably null |
|
R4556:Tas2r102
|
UTSW |
6 |
132,739,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R4633:Tas2r102
|
UTSW |
6 |
132,739,642 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4724:Tas2r102
|
UTSW |
6 |
132,739,520 (GRCm39) |
missense |
probably damaging |
0.97 |
R5268:Tas2r102
|
UTSW |
6 |
132,739,360 (GRCm39) |
missense |
probably damaging |
0.98 |
R5494:Tas2r102
|
UTSW |
6 |
132,740,106 (GRCm39) |
missense |
probably benign |
0.12 |
|