Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agxt2 |
A |
T |
15: 10,378,900 (GRCm39) |
N167I |
probably damaging |
Het |
Arel1 |
A |
G |
12: 84,981,017 (GRCm39) |
I330T |
probably benign |
Het |
Ate1 |
T |
C |
7: 129,996,389 (GRCm39) |
K484E |
possibly damaging |
Het |
Atl2 |
T |
C |
17: 80,183,469 (GRCm39) |
D42G |
probably benign |
Het |
Bltp1 |
T |
C |
3: 37,042,429 (GRCm39) |
I2805T |
probably damaging |
Het |
Cd209e |
C |
T |
8: 3,901,212 (GRCm39) |
W147* |
probably null |
Het |
Cdc40 |
G |
A |
10: 40,717,809 (GRCm39) |
Q365* |
probably null |
Het |
Cenpe |
A |
G |
3: 134,945,644 (GRCm39) |
T1053A |
probably benign |
Het |
Colgalt1 |
T |
C |
8: 72,076,306 (GRCm39) |
S586P |
probably damaging |
Het |
Crem |
A |
G |
18: 3,295,370 (GRCm39) |
I91T |
probably damaging |
Het |
Csrnp3 |
G |
A |
2: 65,852,987 (GRCm39) |
V460I |
possibly damaging |
Het |
Cul1 |
T |
A |
6: 47,474,246 (GRCm39) |
I136N |
possibly damaging |
Het |
Ddx19b |
A |
T |
8: 111,737,929 (GRCm39) |
I273N |
probably damaging |
Het |
Fap |
A |
G |
2: 62,348,817 (GRCm39) |
I505T |
probably damaging |
Het |
Fbxo44 |
A |
T |
4: 148,238,078 (GRCm39) |
Y216* |
probably null |
Het |
Fbxw10 |
T |
A |
11: 62,748,567 (GRCm39) |
M398K |
probably damaging |
Het |
Fut10 |
T |
C |
8: 31,726,514 (GRCm39) |
V423A |
possibly damaging |
Het |
Fyco1 |
A |
C |
9: 123,655,646 (GRCm39) |
D1037E |
probably benign |
Het |
Gabrg2 |
G |
A |
11: 41,867,377 (GRCm39) |
R81* |
probably null |
Het |
Gcn1 |
T |
C |
5: 115,717,220 (GRCm39) |
V204A |
probably benign |
Het |
Gnl1 |
T |
C |
17: 36,299,608 (GRCm39) |
L593P |
probably damaging |
Het |
Grm4 |
T |
C |
17: 27,653,754 (GRCm39) |
Q732R |
probably damaging |
Het |
Icam5 |
T |
C |
9: 20,948,415 (GRCm39) |
V741A |
possibly damaging |
Het |
Iqub |
C |
T |
6: 24,505,768 (GRCm39) |
E47K |
probably benign |
Het |
Kcnk3 |
A |
G |
5: 30,779,580 (GRCm39) |
K210R |
probably benign |
Het |
Kdm2b |
T |
A |
5: 123,125,851 (GRCm39) |
R12* |
probably null |
Het |
Kifbp |
T |
C |
10: 62,399,282 (GRCm39) |
|
probably benign |
Het |
Kndc1 |
C |
T |
7: 139,507,708 (GRCm39) |
S1222F |
possibly damaging |
Het |
Lgi1 |
C |
T |
19: 38,294,538 (GRCm39) |
H413Y |
probably damaging |
Het |
Lhx8 |
A |
G |
3: 154,033,653 (GRCm39) |
Y51H |
probably damaging |
Het |
Lim2 |
T |
C |
7: 43,083,055 (GRCm39) |
I80T |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,368,852 (GRCm39) |
F405L |
probably benign |
Het |
Mefv |
G |
A |
16: 3,528,764 (GRCm39) |
T559I |
probably damaging |
Het |
Nin |
A |
G |
12: 70,077,710 (GRCm39) |
W1739R |
probably damaging |
Het |
Or10h1 |
A |
T |
17: 33,418,718 (GRCm39) |
K232M |
probably damaging |
Het |
Or11j4 |
T |
C |
14: 50,630,269 (GRCm39) |
F19L |
probably damaging |
Het |
Or5t16 |
A |
G |
2: 86,818,710 (GRCm39) |
I270T |
probably benign |
Het |
Or8b3b |
C |
T |
9: 38,584,147 (GRCm39) |
V198I |
probably damaging |
Het |
Otop3 |
T |
C |
11: 115,231,886 (GRCm39) |
|
probably null |
Het |
Pate9 |
A |
T |
9: 36,446,254 (GRCm39) |
C53S |
probably damaging |
Het |
Pip5kl1 |
A |
G |
2: 32,469,082 (GRCm39) |
I247V |
probably benign |
Het |
Polr2d |
T |
A |
18: 31,922,226 (GRCm39) |
M1K |
probably null |
Het |
Prss53 |
T |
C |
7: 127,488,193 (GRCm39) |
T141A |
possibly damaging |
Het |
Rdh12 |
A |
G |
12: 79,268,802 (GRCm39) |
N293S |
probably benign |
Het |
Rnf146 |
G |
A |
10: 29,223,754 (GRCm39) |
T44I |
probably benign |
Het |
Rsbn1l |
A |
T |
5: 21,101,865 (GRCm39) |
C588S |
probably damaging |
Het |
Septin8 |
G |
A |
11: 53,426,862 (GRCm39) |
V208I |
probably damaging |
Het |
Sgo2a |
T |
G |
1: 58,058,822 (GRCm39) |
S1134A |
possibly damaging |
Het |
Sh3bp4 |
C |
T |
1: 89,073,297 (GRCm39) |
T715I |
probably benign |
Het |
Snrnp200 |
A |
G |
2: 127,078,517 (GRCm39) |
T1758A |
probably damaging |
Het |
Snx6 |
A |
T |
12: 54,812,423 (GRCm39) |
D70E |
probably benign |
Het |
Spag9 |
T |
C |
11: 93,983,695 (GRCm39) |
S341P |
probably damaging |
Het |
Sparcl1 |
T |
C |
5: 104,240,590 (GRCm39) |
D278G |
probably benign |
Het |
Spmap2l |
T |
A |
5: 77,185,200 (GRCm39) |
|
probably null |
Het |
Srbd1 |
T |
A |
17: 86,292,885 (GRCm39) |
S895C |
|
Het |
Stxbp5l |
ATTTT |
ATTTTT |
16: 37,036,414 (GRCm39) |
|
probably null |
Het |
Tas2r136 |
T |
C |
6: 132,754,323 (GRCm39) |
D268G |
probably benign |
Het |
Tas2r143 |
T |
A |
6: 42,377,888 (GRCm39) |
Y239* |
probably null |
Het |
Tbc1d17 |
C |
T |
7: 44,492,328 (GRCm39) |
G419D |
probably damaging |
Het |
Tff2 |
C |
T |
17: 31,362,113 (GRCm39) |
W68* |
probably null |
Het |
Thop1 |
T |
C |
10: 80,916,440 (GRCm39) |
C483R |
probably damaging |
Het |
Tmem245 |
A |
C |
4: 56,903,916 (GRCm39) |
|
probably null |
Het |
Tmem67 |
A |
G |
4: 12,055,038 (GRCm39) |
F655S |
probably damaging |
Het |
Trim36 |
T |
G |
18: 46,302,264 (GRCm39) |
S583R |
possibly damaging |
Het |
Ucp1 |
T |
C |
8: 84,017,216 (GRCm39) |
V2A |
probably benign |
Het |
Ugt1a6a |
T |
A |
1: 88,066,803 (GRCm39) |
M203K |
probably damaging |
Het |
Usp1 |
A |
G |
4: 98,819,347 (GRCm39) |
K270E |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,841,783 (GRCm39) |
F1935S |
probably damaging |
Het |
Zfp521 |
C |
A |
18: 13,979,137 (GRCm39) |
L425F |
probably damaging |
Het |
Zfp831 |
A |
T |
2: 174,485,978 (GRCm39) |
R218W |
probably damaging |
Het |
|
Other mutations in Zfp799 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01667:Zfp799
|
APN |
17 |
33,040,794 (GRCm39) |
missense |
possibly damaging |
0.73 |
P0016:Zfp799
|
UTSW |
17 |
33,038,331 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0116:Zfp799
|
UTSW |
17 |
33,040,009 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0326:Zfp799
|
UTSW |
17 |
33,039,700 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1487:Zfp799
|
UTSW |
17 |
33,039,651 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1863:Zfp799
|
UTSW |
17 |
33,038,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Zfp799
|
UTSW |
17 |
33,040,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Zfp799
|
UTSW |
17 |
33,041,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Zfp799
|
UTSW |
17 |
33,038,472 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2271:Zfp799
|
UTSW |
17 |
33,040,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R2697:Zfp799
|
UTSW |
17 |
33,039,214 (GRCm39) |
nonsense |
probably null |
|
R5134:Zfp799
|
UTSW |
17 |
33,039,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R5613:Zfp799
|
UTSW |
17 |
33,038,964 (GRCm39) |
missense |
probably damaging |
0.98 |
R5839:Zfp799
|
UTSW |
17 |
33,041,086 (GRCm39) |
missense |
probably null |
0.99 |
R6389:Zfp799
|
UTSW |
17 |
33,039,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R6414:Zfp799
|
UTSW |
17 |
33,039,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R6475:Zfp799
|
UTSW |
17 |
33,039,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R6593:Zfp799
|
UTSW |
17 |
33,038,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Zfp799
|
UTSW |
17 |
33,039,210 (GRCm39) |
missense |
probably benign |
0.19 |
R7543:Zfp799
|
UTSW |
17 |
33,039,534 (GRCm39) |
missense |
probably benign |
0.11 |
R7883:Zfp799
|
UTSW |
17 |
33,039,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R7889:Zfp799
|
UTSW |
17 |
33,038,473 (GRCm39) |
nonsense |
probably null |
|
R8090:Zfp799
|
UTSW |
17 |
33,039,949 (GRCm39) |
missense |
probably benign |
0.04 |
R8726:Zfp799
|
UTSW |
17 |
33,039,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R9030:Zfp799
|
UTSW |
17 |
33,039,565 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9052:Zfp799
|
UTSW |
17 |
33,039,786 (GRCm39) |
missense |
probably benign |
0.00 |
R9310:Zfp799
|
UTSW |
17 |
33,039,733 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9430:Zfp799
|
UTSW |
17 |
33,039,186 (GRCm39) |
missense |
probably damaging |
0.99 |
R9643:Zfp799
|
UTSW |
17 |
33,039,435 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Zfp799
|
UTSW |
17 |
33,039,190 (GRCm39) |
nonsense |
probably null |
|
Z1177:Zfp799
|
UTSW |
17 |
33,049,195 (GRCm39) |
start gained |
probably benign |
|
Z1177:Zfp799
|
UTSW |
17 |
33,049,193 (GRCm39) |
start gained |
probably benign |
|
|