Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts13 |
C |
T |
2: 26,873,049 (GRCm39) |
A339V |
probably benign |
Het |
Adck2 |
T |
C |
6: 39,553,436 (GRCm39) |
V349A |
probably benign |
Het |
Akna |
G |
T |
4: 63,304,516 (GRCm39) |
T546K |
probably benign |
Het |
Albfm1 |
A |
G |
5: 90,727,497 (GRCm39) |
I372V |
possibly damaging |
Het |
Ankrd29 |
T |
C |
18: 12,393,993 (GRCm39) |
K274E |
probably damaging |
Het |
Apc2 |
A |
T |
10: 80,142,209 (GRCm39) |
N376I |
probably damaging |
Het |
Cadps |
A |
G |
14: 12,418,047 (GRCm38) |
|
probably benign |
Het |
Cbl |
T |
C |
9: 44,080,331 (GRCm39) |
T243A |
probably damaging |
Het |
Cep15 |
A |
G |
14: 12,287,326 (GRCm38) |
N29S |
probably benign |
Het |
Cfap52 |
T |
C |
11: 67,844,901 (GRCm39) |
E56G |
probably benign |
Het |
Chd5 |
C |
A |
4: 152,464,413 (GRCm39) |
P1561Q |
probably benign |
Het |
Dscam |
A |
G |
16: 96,602,472 (GRCm39) |
S657P |
probably damaging |
Het |
Ece1 |
T |
C |
4: 137,690,149 (GRCm39) |
F732L |
probably damaging |
Het |
Eno2 |
T |
C |
6: 124,740,082 (GRCm39) |
D199G |
probably damaging |
Het |
Enpp3 |
A |
G |
10: 24,650,841 (GRCm39) |
|
probably benign |
Het |
Fbxl15 |
G |
T |
19: 46,317,690 (GRCm39) |
C124F |
probably damaging |
Het |
Fermt3 |
T |
C |
19: 6,979,712 (GRCm39) |
S474G |
probably benign |
Het |
Fkbp6 |
T |
C |
5: 135,368,350 (GRCm39) |
E252G |
probably damaging |
Het |
Gm6625 |
A |
T |
8: 89,873,667 (GRCm39) |
|
noncoding transcript |
Het |
Gnl1 |
T |
C |
17: 36,298,504 (GRCm39) |
I416T |
probably benign |
Het |
Gp1bb |
C |
A |
16: 18,439,675 (GRCm39) |
A140S |
probably benign |
Het |
Grin2c |
A |
G |
11: 115,148,785 (GRCm39) |
V271A |
possibly damaging |
Het |
Heatr1 |
T |
A |
13: 12,430,940 (GRCm39) |
S1012T |
possibly damaging |
Het |
Ighv5-6 |
T |
A |
12: 113,589,523 (GRCm39) |
|
probably benign |
Het |
Itga10 |
A |
G |
3: 96,562,429 (GRCm39) |
E737G |
possibly damaging |
Het |
Lmod2 |
A |
C |
6: 24,603,631 (GRCm39) |
N202T |
probably damaging |
Het |
Lrp1 |
C |
T |
10: 127,380,428 (GRCm39) |
V3908I |
probably benign |
Het |
Lrrtm4 |
T |
C |
6: 79,998,633 (GRCm39) |
V15A |
probably benign |
Het |
Mup4 |
A |
T |
4: 59,959,263 (GRCm39) |
D77E |
probably benign |
Het |
Myh7b |
A |
T |
2: 155,474,823 (GRCm39) |
E1787V |
probably damaging |
Het |
Myh7b |
T |
A |
2: 155,467,874 (GRCm39) |
M804K |
possibly damaging |
Het |
Nup133 |
T |
C |
8: 124,675,822 (GRCm39) |
S32G |
probably benign |
Het |
Or13c7d |
T |
A |
4: 43,770,399 (GRCm39) |
N204I |
probably benign |
Het |
Or52h1 |
T |
C |
7: 103,829,334 (GRCm39) |
I94V |
probably damaging |
Het |
Or7d10 |
T |
C |
9: 19,832,348 (GRCm39) |
V281A |
possibly damaging |
Het |
Or8b8 |
A |
G |
9: 37,809,404 (GRCm39) |
K235E |
probably damaging |
Het |
Polr2m |
T |
C |
9: 71,390,911 (GRCm39) |
D97G |
possibly damaging |
Het |
Pou2f3 |
A |
G |
9: 43,054,100 (GRCm39) |
|
probably benign |
Het |
Rex1bd |
C |
A |
8: 70,958,552 (GRCm39) |
V72F |
possibly damaging |
Het |
Rgp1 |
A |
G |
4: 43,581,505 (GRCm39) |
T261A |
possibly damaging |
Het |
Satb2 |
A |
G |
1: 56,987,334 (GRCm39) |
F84L |
probably damaging |
Het |
Sec14l1 |
G |
A |
11: 117,043,973 (GRCm39) |
D494N |
probably benign |
Het |
Spn |
G |
A |
7: 126,736,432 (GRCm39) |
T25M |
probably damaging |
Het |
Trp73 |
G |
A |
4: 154,148,920 (GRCm39) |
|
probably benign |
Het |
Tsc22d2 |
A |
G |
3: 58,324,967 (GRCm39) |
T620A |
unknown |
Het |
Zfp276 |
T |
C |
8: 123,981,483 (GRCm39) |
L10P |
probably damaging |
Het |
|
Other mutations in Zfp93 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00660:Zfp93
|
APN |
7 |
23,975,117 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Zfp93
|
APN |
7 |
23,974,509 (GRCm39) |
missense |
possibly damaging |
0.86 |
FR4342:Zfp93
|
UTSW |
7 |
23,975,011 (GRCm39) |
missense |
possibly damaging |
0.92 |
FR4737:Zfp93
|
UTSW |
7 |
23,974,814 (GRCm39) |
small deletion |
probably benign |
|
R0099:Zfp93
|
UTSW |
7 |
23,974,900 (GRCm39) |
missense |
probably benign |
0.01 |
R0376:Zfp93
|
UTSW |
7 |
23,975,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Zfp93
|
UTSW |
7 |
23,975,521 (GRCm39) |
missense |
probably damaging |
0.99 |
R1466:Zfp93
|
UTSW |
7 |
23,975,521 (GRCm39) |
missense |
probably damaging |
0.99 |
R1511:Zfp93
|
UTSW |
7 |
23,975,156 (GRCm39) |
nonsense |
probably null |
|
R1628:Zfp93
|
UTSW |
7 |
23,974,282 (GRCm39) |
missense |
probably benign |
0.00 |
R4581:Zfp93
|
UTSW |
7 |
23,975,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R4977:Zfp93
|
UTSW |
7 |
23,974,836 (GRCm39) |
missense |
probably benign |
0.00 |
R5162:Zfp93
|
UTSW |
7 |
23,975,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R6031:Zfp93
|
UTSW |
7 |
23,975,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R6031:Zfp93
|
UTSW |
7 |
23,975,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R6284:Zfp93
|
UTSW |
7 |
23,975,054 (GRCm39) |
nonsense |
probably null |
|
R6471:Zfp93
|
UTSW |
7 |
23,972,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R6694:Zfp93
|
UTSW |
7 |
23,975,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R6969:Zfp93
|
UTSW |
7 |
23,974,806 (GRCm39) |
nonsense |
probably null |
|
R7543:Zfp93
|
UTSW |
7 |
23,974,533 (GRCm39) |
missense |
probably benign |
0.13 |
R7623:Zfp93
|
UTSW |
7 |
23,975,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:Zfp93
|
UTSW |
7 |
23,974,643 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7957:Zfp93
|
UTSW |
7 |
23,974,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R8157:Zfp93
|
UTSW |
7 |
23,975,885 (GRCm39) |
nonsense |
probably null |
|
R8194:Zfp93
|
UTSW |
7 |
23,975,479 (GRCm39) |
missense |
probably benign |
0.08 |
R9700:Zfp93
|
UTSW |
7 |
23,974,894 (GRCm39) |
missense |
probably damaging |
0.99 |
|