Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bod1l |
T |
C |
5: 41,974,441 (GRCm39) |
E2291G |
probably damaging |
Het |
Cchcr1 |
T |
C |
17: 35,836,233 (GRCm39) |
V341A |
probably damaging |
Het |
Cimip3 |
AC |
A |
17: 47,744,348 (GRCm39) |
|
probably benign |
Het |
Dsg1c |
T |
C |
18: 20,399,253 (GRCm39) |
V119A |
possibly damaging |
Het |
Fap |
A |
G |
2: 62,386,448 (GRCm39) |
S58P |
probably damaging |
Het |
Flnc |
A |
T |
6: 29,459,426 (GRCm39) |
T2509S |
probably damaging |
Het |
Fnip2 |
A |
T |
3: 79,386,812 (GRCm39) |
D971E |
possibly damaging |
Het |
Gab2 |
A |
G |
7: 96,948,280 (GRCm39) |
Y290C |
probably damaging |
Het |
Gm7104 |
C |
T |
12: 88,251,364 (GRCm39) |
|
noncoding transcript |
Het |
Ints10 |
T |
A |
8: 69,266,272 (GRCm39) |
S478T |
probably damaging |
Het |
Iqca1l |
A |
T |
5: 24,750,440 (GRCm39) |
|
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Krt90 |
G |
A |
15: 101,471,218 (GRCm39) |
R15W |
probably damaging |
Het |
Lgr5 |
A |
G |
10: 115,423,368 (GRCm39) |
S11P |
possibly damaging |
Het |
Mycn |
T |
A |
12: 12,987,281 (GRCm39) |
N372I |
probably damaging |
Het |
Or2ag18 |
A |
T |
7: 106,405,072 (GRCm39) |
V199D |
probably damaging |
Het |
Or9a2 |
A |
G |
6: 41,749,083 (GRCm39) |
V50A |
probably benign |
Het |
Paxbp1 |
T |
A |
16: 90,839,569 (GRCm39) |
E117V |
probably damaging |
Het |
Phc2 |
T |
C |
4: 128,637,351 (GRCm39) |
|
probably null |
Het |
Prr5 |
T |
A |
15: 84,587,345 (GRCm39) |
V365E |
probably benign |
Het |
Rev3l |
A |
G |
10: 39,696,552 (GRCm39) |
I521M |
probably damaging |
Het |
Robo3 |
A |
T |
9: 37,330,591 (GRCm39) |
Y1002N |
probably damaging |
Het |
Svep1 |
A |
T |
4: 58,145,156 (GRCm39) |
|
probably null |
Het |
Thsd7a |
A |
G |
6: 12,331,548 (GRCm39) |
V1342A |
probably damaging |
Het |
Tmtc3 |
A |
C |
10: 100,284,888 (GRCm39) |
N582K |
probably damaging |
Het |
Tnfrsf11b |
G |
A |
15: 54,119,578 (GRCm39) |
|
probably benign |
Het |
Trim30a |
A |
G |
7: 104,060,348 (GRCm39) |
V476A |
probably damaging |
Het |
Ugt1a8 |
A |
G |
1: 88,015,770 (GRCm39) |
E61G |
possibly damaging |
Het |
Vmn1r75 |
A |
T |
7: 11,614,757 (GRCm39) |
N163I |
possibly damaging |
Het |
Vps35l |
A |
G |
7: 118,345,613 (GRCm39) |
T49A |
possibly damaging |
Het |
|
Other mutations in Zfp119a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00420:Zfp119a
|
APN |
17 |
56,172,792 (GRCm39) |
nonsense |
probably null |
|
R0421:Zfp119a
|
UTSW |
17 |
56,172,248 (GRCm39) |
nonsense |
probably null |
|
R1385:Zfp119a
|
UTSW |
17 |
56,172,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R1600:Zfp119a
|
UTSW |
17 |
56,175,355 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2310:Zfp119a
|
UTSW |
17 |
56,172,440 (GRCm39) |
missense |
probably benign |
0.00 |
R2924:Zfp119a
|
UTSW |
17 |
56,175,343 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4594:Zfp119a
|
UTSW |
17 |
56,173,325 (GRCm39) |
missense |
probably benign |
|
R5217:Zfp119a
|
UTSW |
17 |
56,172,425 (GRCm39) |
nonsense |
probably null |
|
R5321:Zfp119a
|
UTSW |
17 |
56,172,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R5392:Zfp119a
|
UTSW |
17 |
56,173,328 (GRCm39) |
missense |
probably benign |
0.03 |
R5678:Zfp119a
|
UTSW |
17 |
56,175,336 (GRCm39) |
missense |
probably benign |
0.03 |
R7033:Zfp119a
|
UTSW |
17 |
56,173,009 (GRCm39) |
missense |
probably benign |
0.04 |
R7355:Zfp119a
|
UTSW |
17 |
56,173,287 (GRCm39) |
nonsense |
probably null |
|
R7489:Zfp119a
|
UTSW |
17 |
56,173,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R8130:Zfp119a
|
UTSW |
17 |
56,172,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8940:Zfp119a
|
UTSW |
17 |
56,172,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R9542:Zfp119a
|
UTSW |
17 |
56,172,593 (GRCm39) |
nonsense |
probably null |
|
Z1176:Zfp119a
|
UTSW |
17 |
56,173,011 (GRCm39) |
missense |
possibly damaging |
0.61 |
|