Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
G |
11: 110,218,651 (GRCm39) |
F72L |
probably benign |
Het |
Btrc |
G |
A |
19: 45,496,197 (GRCm39) |
V211M |
probably damaging |
Het |
Col6a5 |
A |
T |
9: 105,805,664 (GRCm39) |
Y1081N |
unknown |
Het |
Cryzl1 |
T |
C |
16: 91,504,118 (GRCm39) |
Y109C |
probably benign |
Het |
Dlec1 |
T |
A |
9: 118,941,669 (GRCm39) |
S352T |
probably benign |
Het |
Dzip3 |
T |
G |
16: 48,778,038 (GRCm39) |
T349P |
possibly damaging |
Het |
Endou |
A |
G |
15: 97,618,913 (GRCm39) |
V37A |
probably damaging |
Het |
Exosc1 |
A |
T |
19: 41,912,499 (GRCm39) |
C129* |
probably null |
Het |
Flywch1 |
C |
G |
17: 23,975,625 (GRCm39) |
R539P |
probably damaging |
Het |
Gm14410 |
G |
A |
2: 176,885,298 (GRCm39) |
T322I |
probably damaging |
Het |
Lcor |
G |
T |
19: 41,573,643 (GRCm39) |
W799C |
probably damaging |
Het |
Lpin2 |
G |
A |
17: 71,553,853 (GRCm39) |
V857M |
probably damaging |
Het |
Or52ae9 |
T |
C |
7: 103,389,862 (GRCm39) |
N195S |
probably damaging |
Het |
Patl1 |
A |
G |
19: 11,898,785 (GRCm39) |
Q160R |
probably damaging |
Het |
Phtf1 |
C |
T |
3: 103,910,827 (GRCm39) |
T606I |
probably benign |
Het |
Polr3a |
T |
C |
14: 24,505,009 (GRCm39) |
I1084V |
possibly damaging |
Het |
Scrt1 |
T |
C |
15: 76,403,370 (GRCm39) |
S207G |
unknown |
Het |
Slc15a5 |
G |
T |
6: 137,964,436 (GRCm39) |
N496K |
probably benign |
Het |
Slc34a1 |
A |
T |
13: 23,996,614 (GRCm39) |
I40F |
possibly damaging |
Het |
Tdrd12 |
A |
C |
7: 35,177,519 (GRCm39) |
V945G |
probably damaging |
Het |
Tdrkh |
C |
A |
3: 94,332,965 (GRCm39) |
L169I |
probably damaging |
Het |
Tmem59l |
A |
G |
8: 70,939,865 (GRCm39) |
C35R |
probably damaging |
Het |
Tpte |
A |
T |
8: 22,787,219 (GRCm39) |
R33* |
probably null |
Het |
Trpv2 |
T |
A |
11: 62,475,397 (GRCm39) |
L270H |
probably damaging |
Het |
Utp18 |
A |
G |
11: 93,757,260 (GRCm39) |
L468P |
probably damaging |
Het |
Uxs1 |
A |
G |
1: 43,844,805 (GRCm39) |
I51T |
probably damaging |
Het |
Vmn1r20 |
C |
T |
6: 57,409,427 (GRCm39) |
S251L |
probably benign |
Het |
Vmn1r24 |
A |
T |
6: 57,933,182 (GRCm39) |
L112* |
probably null |
Het |
Vmn1r5 |
T |
C |
6: 56,962,592 (GRCm39) |
L89P |
probably damaging |
Het |
Vmn2r10 |
G |
T |
5: 109,143,505 (GRCm39) |
A815E |
probably 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 |
R3910:Zfp119a
|
UTSW |
17 |
56,173,520 (GRCm39) |
missense |
probably benign |
|
R4594:Zfp119a
|
UTSW |
17 |
56,173,325 (GRCm39) |
missense |
probably benign |
|
R5217:Zfp119a
|
UTSW |
17 |
56,172,425 (GRCm39) |
nonsense |
probably null |
|
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 |
|