Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp1 |
C |
T |
12: 30,945,934 (GRCm39) |
E140K |
possibly damaging |
Het |
Acsm4 |
T |
A |
7: 119,293,042 (GRCm39) |
D57E |
probably damaging |
Het |
Adamts9 |
A |
G |
6: 92,826,271 (GRCm39) |
|
probably null |
Het |
Aen |
T |
A |
7: 78,557,060 (GRCm39) |
Y303N |
probably damaging |
Het |
Alcam |
T |
C |
16: 52,116,115 (GRCm39) |
|
probably null |
Het |
Apol7b |
A |
G |
15: 77,309,746 (GRCm39) |
L17P |
probably damaging |
Het |
Cacna1c |
A |
T |
6: 118,629,754 (GRCm39) |
Y1058* |
probably null |
Het |
Camk2d |
T |
C |
3: 126,601,873 (GRCm39) |
V354A |
probably benign |
Het |
Carf |
T |
G |
1: 60,164,017 (GRCm39) |
M43R |
probably damaging |
Het |
Casp8 |
T |
A |
1: 58,863,283 (GRCm39) |
F81Y |
probably damaging |
Het |
Cd74 |
G |
A |
18: 60,937,064 (GRCm39) |
R20H |
probably benign |
Het |
Cers5 |
A |
T |
15: 99,643,812 (GRCm39) |
Y16* |
probably null |
Het |
Chuk |
A |
T |
19: 44,067,397 (GRCm39) |
M586K |
probably null |
Het |
D130043K22Rik |
C |
A |
13: 25,055,324 (GRCm39) |
P496Q |
probably damaging |
Het |
Dab2 |
A |
G |
15: 6,459,419 (GRCm39) |
R311G |
probably damaging |
Het |
Depp1 |
A |
T |
6: 116,629,223 (GRCm39) |
S189C |
possibly damaging |
Het |
Diaph1 |
A |
T |
18: 38,038,187 (GRCm39) |
I48N |
unknown |
Het |
Dnajc13 |
T |
C |
9: 104,057,320 (GRCm39) |
D1560G |
probably damaging |
Het |
Dsg2 |
T |
C |
18: 20,715,780 (GRCm39) |
S241P |
probably damaging |
Het |
Efcab5 |
T |
C |
11: 76,996,204 (GRCm39) |
D1119G |
probably benign |
Het |
Efr3a |
G |
T |
15: 65,740,906 (GRCm39) |
|
probably benign |
Het |
Evc2 |
A |
G |
5: 37,550,427 (GRCm39) |
K814E |
probably damaging |
Het |
Hic2 |
A |
G |
16: 17,076,686 (GRCm39) |
D505G |
probably benign |
Het |
Ing1 |
T |
A |
8: 11,607,010 (GRCm39) |
V34D |
probably damaging |
Het |
Inpp5k |
A |
G |
11: 75,528,317 (GRCm39) |
M172V |
probably benign |
Het |
Itgae |
T |
C |
11: 73,006,418 (GRCm39) |
V362A |
probably damaging |
Het |
Lama2 |
T |
A |
10: 27,063,750 (GRCm39) |
R1346S |
probably damaging |
Het |
Lrrc7 |
T |
C |
3: 157,882,943 (GRCm39) |
N450S |
probably damaging |
Het |
Lrrn3 |
T |
A |
12: 41,502,583 (GRCm39) |
Y578F |
possibly damaging |
Het |
Maml2 |
A |
T |
9: 13,617,797 (GRCm39) |
N381I |
probably damaging |
Het |
Mettl15 |
T |
G |
2: 108,923,266 (GRCm39) |
E385D |
probably benign |
Het |
Mthfr |
T |
A |
4: 148,139,900 (GRCm39) |
I623N |
possibly damaging |
Het |
Muc4 |
A |
C |
16: 32,574,448 (GRCm39) |
N966T |
probably benign |
Het |
Myoc |
A |
G |
1: 162,476,565 (GRCm39) |
Y423C |
probably damaging |
Het |
Ncoa2 |
A |
T |
1: 13,218,602 (GRCm39) |
M1409K |
probably benign |
Het |
Ncor2 |
T |
C |
5: 125,187,039 (GRCm39) |
|
probably benign |
Het |
Numb |
T |
C |
12: 83,844,033 (GRCm39) |
E395G |
probably damaging |
Het |
Oas1g |
A |
G |
5: 121,020,012 (GRCm39) |
F198S |
probably damaging |
Het |
Or2b28 |
T |
C |
13: 21,531,194 (GRCm39) |
V32A |
probably benign |
Het |
Or5k17 |
A |
G |
16: 58,746,049 (GRCm39) |
V295A |
probably benign |
Het |
Prdm13 |
T |
A |
4: 21,678,909 (GRCm39) |
Y527F |
probably damaging |
Het |
Prr14l |
A |
G |
5: 32,986,177 (GRCm39) |
L1106P |
probably damaging |
Het |
Ptbp1 |
T |
A |
10: 79,699,107 (GRCm39) |
I555N |
probably damaging |
Het |
Ptchd4 |
A |
T |
17: 42,814,606 (GRCm39) |
T836S |
possibly damaging |
Het |
Rlbp1 |
T |
C |
7: 79,033,686 (GRCm39) |
D3G |
probably benign |
Het |
Sdk2 |
T |
C |
11: 113,685,871 (GRCm39) |
E1883G |
probably damaging |
Het |
Serpinc1 |
A |
T |
1: 160,820,974 (GRCm39) |
K140N |
probably damaging |
Het |
Serpind1 |
A |
T |
16: 17,160,249 (GRCm39) |
Y382F |
probably damaging |
Het |
Slc28a3 |
T |
C |
13: 58,710,920 (GRCm39) |
E534G |
probably damaging |
Het |
Slco1a7 |
A |
G |
6: 141,711,429 (GRCm39) |
M94T |
probably benign |
Het |
Ttyh2 |
T |
A |
11: 114,601,005 (GRCm39) |
I418N |
probably benign |
Het |
Tubgcp4 |
C |
T |
2: 121,005,905 (GRCm39) |
Q98* |
probably null |
Het |
Vwa1 |
A |
T |
4: 155,857,358 (GRCm39) |
S147T |
probably damaging |
Het |
Xylt1 |
T |
C |
7: 117,191,179 (GRCm39) |
V325A |
possibly damaging |
Het |
Zfp335 |
T |
C |
2: 164,741,376 (GRCm39) |
H685R |
probably damaging |
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 |
|
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 |
R8222:Ugt2a2
|
UTSW |
5 |
87,608,369 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|