Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh18a1 |
C |
T |
19: 40,562,296 (GRCm39) |
V243I |
probably benign |
Het |
Ankrd11 |
A |
T |
8: 123,622,347 (GRCm39) |
S481T |
probably damaging |
Het |
Atg2b |
A |
G |
12: 105,618,475 (GRCm39) |
I859T |
possibly damaging |
Het |
B4galt3 |
G |
A |
1: 171,100,253 (GRCm39) |
R141Q |
possibly damaging |
Het |
Bace1 |
T |
C |
9: 45,768,491 (GRCm39) |
V262A |
probably damaging |
Het |
BC106179 |
A |
T |
16: 23,043,055 (GRCm39) |
I47N |
noncoding transcript |
Het |
Brpf1 |
C |
T |
6: 113,286,999 (GRCm39) |
P76S |
probably benign |
Het |
Cdk1 |
A |
G |
10: 69,176,426 (GRCm39) |
V227A |
probably benign |
Het |
Ceacam20 |
T |
C |
7: 19,705,618 (GRCm39) |
V203A |
probably benign |
Het |
Cfap251 |
T |
A |
5: 123,440,486 (GRCm39) |
Y1091N |
probably damaging |
Het |
Cma2 |
T |
C |
14: 56,210,727 (GRCm39) |
V194A |
probably benign |
Het |
Cnnm4 |
A |
G |
1: 36,545,617 (GRCm39) |
D749G |
probably benign |
Het |
Cyp11b2 |
T |
C |
15: 74,728,059 (GRCm39) |
T8A |
probably benign |
Het |
Dlk2 |
A |
G |
17: 46,613,384 (GRCm39) |
H170R |
probably benign |
Het |
Esyt1 |
C |
T |
10: 128,347,647 (GRCm39) |
R987Q |
possibly damaging |
Het |
Ganc |
T |
C |
2: 120,276,933 (GRCm39) |
I665T |
probably damaging |
Het |
Gas6 |
T |
C |
8: 13,520,276 (GRCm39) |
T471A |
probably benign |
Het |
Grik2 |
A |
G |
10: 49,449,744 (GRCm39) |
F153L |
probably benign |
Het |
Heatr5b |
A |
G |
17: 79,109,130 (GRCm39) |
V1043A |
possibly damaging |
Het |
Ipo5 |
A |
G |
14: 121,157,414 (GRCm39) |
D84G |
probably benign |
Het |
Irak4 |
T |
A |
15: 94,459,110 (GRCm39) |
|
probably null |
Het |
Lrp4 |
T |
A |
2: 91,305,086 (GRCm39) |
C238S |
probably damaging |
Het |
Mau2 |
A |
T |
8: 70,485,827 (GRCm39) |
|
probably null |
Het |
Mdn1 |
T |
C |
4: 32,707,477 (GRCm39) |
F1589L |
probably benign |
Het |
Mlxip |
T |
G |
5: 123,585,596 (GRCm39) |
S662A |
probably benign |
Het |
Mn1 |
A |
T |
5: 111,566,546 (GRCm39) |
N172I |
probably damaging |
Het |
Mup2 |
A |
C |
4: 60,138,454 (GRCm39) |
D79E |
probably benign |
Het |
Nab2 |
C |
A |
10: 127,498,645 (GRCm39) |
V475L |
probably benign |
Het |
Nlrp3 |
A |
G |
11: 59,439,614 (GRCm39) |
E397G |
probably damaging |
Het |
Odf2l |
A |
G |
3: 144,833,799 (GRCm39) |
E153G |
probably damaging |
Het |
Or13p10 |
T |
C |
4: 118,523,113 (GRCm39) |
L133P |
probably damaging |
Het |
Or51f5 |
G |
T |
7: 102,424,099 (GRCm39) |
D123Y |
probably damaging |
Het |
Or5d36 |
T |
A |
2: 87,901,381 (GRCm39) |
Y115F |
probably benign |
Het |
Or5l13 |
T |
C |
2: 87,779,788 (GRCm39) |
N263S |
probably benign |
Het |
Pkdrej |
T |
A |
15: 85,701,640 (GRCm39) |
H1432L |
probably benign |
Het |
Plec |
C |
T |
15: 76,063,374 (GRCm39) |
R2232H |
possibly damaging |
Het |
Polk |
T |
C |
13: 96,632,023 (GRCm39) |
M317V |
possibly damaging |
Het |
Ppp4r3a |
A |
G |
12: 101,008,164 (GRCm39) |
S758P |
probably benign |
Het |
Pramel26 |
A |
T |
4: 143,536,893 (GRCm39) |
D479E |
possibly damaging |
Het |
Prdm9 |
A |
G |
17: 15,765,035 (GRCm39) |
S582P |
possibly damaging |
Het |
R3hcc1l |
T |
A |
19: 42,564,616 (GRCm39) |
L643H |
probably damaging |
Het |
Rassf8 |
G |
A |
6: 145,765,783 (GRCm39) |
V38M |
unknown |
Het |
Reln |
G |
A |
5: 22,136,475 (GRCm39) |
Q2518* |
probably null |
Het |
Sel1l3 |
A |
G |
5: 53,345,296 (GRCm39) |
|
probably null |
Het |
Serpina3m |
A |
T |
12: 104,358,960 (GRCm39) |
D324V |
possibly damaging |
Het |
Slc12a6 |
T |
A |
2: 112,169,870 (GRCm39) |
|
probably null |
Het |
Slc25a3 |
A |
G |
10: 90,954,053 (GRCm39) |
W219R |
probably damaging |
Het |
Sort1 |
T |
A |
3: 108,241,951 (GRCm39) |
V299E |
probably benign |
Het |
Stx6 |
A |
G |
1: 155,073,889 (GRCm39) |
D233G |
possibly damaging |
Het |
Tefm |
A |
G |
11: 80,031,230 (GRCm39) |
V2A |
|
Het |
Tfdp2 |
T |
C |
9: 96,192,666 (GRCm39) |
S190P |
possibly damaging |
Het |
Tmprss7 |
A |
T |
16: 45,478,461 (GRCm39) |
I755N |
probably damaging |
Het |
Trpm8 |
A |
G |
1: 88,253,390 (GRCm39) |
|
probably null |
Het |
Ube2q2l |
A |
G |
6: 136,377,882 (GRCm39) |
I316T |
probably damaging |
Het |
Utp20 |
A |
G |
10: 88,614,234 (GRCm39) |
L1240P |
probably damaging |
Het |
Vmn1r159 |
G |
T |
7: 22,542,608 (GRCm39) |
Y141* |
probably null |
Het |
Vmn2r56 |
T |
A |
7: 12,444,960 (GRCm39) |
Y431F |
probably benign |
Het |
|
Other mutations in Ugt2a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0131:Ugt2a2
|
UTSW |
5 |
87,622,720 (GRCm39) |
nonsense |
probably null |
|
R0132:Ugt2a2
|
UTSW |
5 |
87,622,720 (GRCm39) |
nonsense |
probably null |
|
R0233:Ugt2a2
|
UTSW |
5 |
87,622,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Ugt2a2
|
UTSW |
5 |
87,612,007 (GRCm39) |
missense |
probably benign |
0.38 |
R0732:Ugt2a2
|
UTSW |
5 |
87,608,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R0841:Ugt2a2
|
UTSW |
5 |
87,622,648 (GRCm39) |
missense |
probably benign |
0.00 |
R1168:Ugt2a2
|
UTSW |
5 |
87,613,427 (GRCm39) |
splice site |
probably null |
|
R1433:Ugt2a2
|
UTSW |
5 |
87,611,965 (GRCm39) |
missense |
probably damaging |
0.98 |
R1552:Ugt2a2
|
UTSW |
5 |
87,609,880 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1795:Ugt2a2
|
UTSW |
5 |
87,622,315 (GRCm39) |
missense |
probably benign |
|
R1986:Ugt2a2
|
UTSW |
5 |
87,608,438 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2967:Ugt2a2
|
UTSW |
5 |
87,622,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R3053:Ugt2a2
|
UTSW |
5 |
87,622,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R4641:Ugt2a2
|
UTSW |
5 |
87,610,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Ugt2a2
|
UTSW |
5 |
87,622,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R5098:Ugt2a2
|
UTSW |
5 |
87,612,040 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5725:Ugt2a2
|
UTSW |
5 |
87,622,755 (GRCm39) |
missense |
probably damaging |
0.98 |
R6243:Ugt2a2
|
UTSW |
5 |
87,610,818 (GRCm39) |
missense |
probably benign |
0.13 |
R6502:Ugt2a2
|
UTSW |
5 |
87,608,318 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6650:Ugt2a2
|
UTSW |
5 |
87,622,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R7097:Ugt2a2
|
UTSW |
5 |
87,608,255 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7122:Ugt2a2
|
UTSW |
5 |
87,608,255 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7134:Ugt2a2
|
UTSW |
5 |
87,608,435 (GRCm39) |
missense |
probably benign |
0.12 |
R7205:Ugt2a2
|
UTSW |
5 |
87,608,468 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7476:Ugt2a2
|
UTSW |
5 |
87,622,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Ugt2a2
|
UTSW |
5 |
87,622,500 (GRCm39) |
missense |
probably damaging |
0.98 |
R8694:Ugt2a2
|
UTSW |
5 |
87,612,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8902:Ugt2a2
|
UTSW |
5 |
87,608,270 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9119:Ugt2a2
|
UTSW |
5 |
87,610,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R9233:Ugt2a2
|
UTSW |
5 |
87,613,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R9301:Ugt2a2
|
UTSW |
5 |
87,608,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R9302:Ugt2a2
|
UTSW |
5 |
87,609,940 (GRCm39) |
nonsense |
probably null |
|
R9556:Ugt2a2
|
UTSW |
5 |
87,609,821 (GRCm39) |
missense |
probably damaging |
1.00 |
|