Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110038F14Rik |
G |
A |
15: 76,834,475 (GRCm39) |
V124I |
probably damaging |
Het |
Acaca |
A |
G |
11: 84,206,678 (GRCm39) |
K1513E |
probably damaging |
Het |
Acacb |
T |
A |
5: 114,363,931 (GRCm39) |
F1464Y |
probably benign |
Het |
Adgrg6 |
G |
A |
10: 14,286,274 (GRCm39) |
A1114V |
possibly damaging |
Het |
Agl |
A |
G |
3: 116,566,438 (GRCm39) |
I975T |
possibly damaging |
Het |
Akap7 |
T |
C |
10: 25,147,451 (GRCm39) |
H93R |
probably damaging |
Het |
Arhgef11 |
T |
C |
3: 87,640,481 (GRCm39) |
W1213R |
probably benign |
Het |
Ccar1 |
T |
A |
10: 62,592,428 (GRCm39) |
E708V |
probably damaging |
Het |
Cfap206 |
C |
T |
4: 34,721,562 (GRCm39) |
S162N |
probably damaging |
Het |
Cilp |
T |
C |
9: 65,186,265 (GRCm39) |
S787P |
possibly damaging |
Het |
Col6a3 |
G |
A |
1: 90,730,014 (GRCm39) |
T1157I |
probably damaging |
Het |
D630003M21Rik |
T |
C |
2: 158,038,308 (GRCm39) |
Y1046C |
probably benign |
Het |
Dock3 |
A |
G |
9: 106,772,862 (GRCm39) |
S464P |
probably benign |
Het |
Dusp19 |
A |
G |
2: 80,454,618 (GRCm39) |
T113A |
probably benign |
Het |
Dync1h1 |
A |
C |
12: 110,615,538 (GRCm39) |
Y2957S |
probably benign |
Het |
Epdr1 |
T |
C |
13: 19,778,814 (GRCm39) |
Y94C |
probably damaging |
Het |
Fcho1 |
A |
T |
8: 72,165,191 (GRCm39) |
L422Q |
probably benign |
Het |
Gca |
T |
A |
2: 62,520,787 (GRCm39) |
Y210* |
probably null |
Het |
Gpnmb |
T |
C |
6: 49,032,615 (GRCm39) |
V513A |
probably benign |
Het |
Irx4 |
A |
G |
13: 73,415,786 (GRCm39) |
T192A |
probably damaging |
Het |
Isca1 |
T |
C |
13: 59,906,785 (GRCm39) |
T54A |
probably benign |
Het |
Kif12 |
GGGGC |
GGGGCCTCCACCCGGCGGGC |
4: 63,089,660 (GRCm39) |
|
probably benign |
Het |
L3mbtl1 |
T |
C |
2: 162,812,100 (GRCm39) |
V715A |
probably benign |
Het |
Lama1 |
G |
A |
17: 68,045,865 (GRCm39) |
D257N |
probably damaging |
Het |
Lgr5 |
T |
C |
10: 115,314,439 (GRCm39) |
H166R |
probably damaging |
Het |
M6pr |
A |
G |
6: 122,289,218 (GRCm39) |
R9G |
probably benign |
Het |
Nmt2 |
T |
G |
2: 3,315,731 (GRCm39) |
S240R |
probably benign |
Het |
Npas3 |
A |
G |
12: 54,114,857 (GRCm39) |
E593G |
possibly damaging |
Het |
Or8k30 |
G |
A |
2: 86,339,513 (GRCm39) |
A237T |
possibly damaging |
Het |
Pank4 |
T |
C |
4: 155,059,103 (GRCm39) |
M412T |
probably damaging |
Het |
Psd |
A |
G |
19: 46,303,186 (GRCm39) |
V100A |
possibly damaging |
Het |
Rab11fip3 |
T |
C |
17: 26,235,087 (GRCm39) |
T28A |
probably damaging |
Het |
Rnpepl1 |
A |
T |
1: 92,847,468 (GRCm39) |
D685V |
probably benign |
Het |
Rrad |
T |
C |
8: 105,357,283 (GRCm39) |
E88G |
probably benign |
Het |
Sdk2 |
T |
A |
11: 113,733,906 (GRCm39) |
M846L |
probably benign |
Het |
Sparcl1 |
A |
T |
5: 104,242,581 (GRCm39) |
V36E |
possibly damaging |
Het |
Spmip5 |
A |
T |
19: 58,777,545 (GRCm39) |
H80Q |
probably damaging |
Het |
Srrm4 |
C |
T |
5: 116,605,628 (GRCm39) |
E210K |
unknown |
Het |
Stk25 |
A |
T |
1: 93,551,145 (GRCm39) |
|
probably null |
Het |
Tacr3 |
A |
T |
3: 134,635,810 (GRCm39) |
Y338F |
probably damaging |
Het |
Tap2 |
A |
T |
17: 34,428,184 (GRCm39) |
Q286L |
probably benign |
Het |
Tedc1 |
C |
T |
12: 113,126,808 (GRCm39) |
R357* |
probably null |
Het |
Tubgcp5 |
C |
A |
7: 55,458,277 (GRCm39) |
A396E |
possibly damaging |
Het |
Ube2o |
T |
C |
11: 116,430,960 (GRCm39) |
D980G |
probably damaging |
Het |
Vmn2r58 |
T |
A |
7: 41,513,935 (GRCm39) |
H236L |
probably benign |
Het |
Zfp521 |
T |
C |
18: 13,950,303 (GRCm39) |
H1217R |
probably damaging |
Het |
Zfyve1 |
A |
T |
12: 83,601,779 (GRCm39) |
F110I |
probably benign |
Het |
|
Other mutations in Vmn1r86 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00492:Vmn1r86
|
APN |
7 |
12,836,468 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01124:Vmn1r86
|
APN |
7 |
12,836,856 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01291:Vmn1r86
|
APN |
7 |
12,836,433 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02347:Vmn1r86
|
APN |
7 |
12,836,574 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02457:Vmn1r86
|
APN |
7 |
12,836,707 (GRCm39) |
missense |
probably benign |
|
IGL02983:Vmn1r86
|
APN |
7 |
12,836,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R0304:Vmn1r86
|
UTSW |
7 |
12,836,707 (GRCm39) |
missense |
probably benign |
|
R0525:Vmn1r86
|
UTSW |
7 |
12,836,088 (GRCm39) |
missense |
probably benign |
0.13 |
R1958:Vmn1r86
|
UTSW |
7 |
12,836,621 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2227:Vmn1r86
|
UTSW |
7 |
12,836,847 (GRCm39) |
missense |
probably benign |
0.00 |
R3149:Vmn1r86
|
UTSW |
7 |
12,836,358 (GRCm39) |
nonsense |
probably null |
|
R3896:Vmn1r86
|
UTSW |
7 |
12,836,093 (GRCm39) |
missense |
probably benign |
0.18 |
R4735:Vmn1r86
|
UTSW |
7 |
12,836,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R5219:Vmn1r86
|
UTSW |
7 |
12,836,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R6003:Vmn1r86
|
UTSW |
7 |
12,836,125 (GRCm39) |
nonsense |
probably null |
|
R6457:Vmn1r86
|
UTSW |
7 |
12,836,279 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7442:Vmn1r86
|
UTSW |
7 |
12,835,983 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7622:Vmn1r86
|
UTSW |
7 |
12,836,685 (GRCm39) |
missense |
probably benign |
0.07 |
R8436:Vmn1r86
|
UTSW |
7 |
12,836,771 (GRCm39) |
missense |
probably benign |
0.25 |
R9141:Vmn1r86
|
UTSW |
7 |
12,836,789 (GRCm39) |
nonsense |
probably null |
|
R9374:Vmn1r86
|
UTSW |
7 |
12,836,781 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9398:Vmn1r86
|
UTSW |
7 |
12,836,261 (GRCm39) |
missense |
probably damaging |
0.98 |
R9551:Vmn1r86
|
UTSW |
7 |
12,836,781 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9552:Vmn1r86
|
UTSW |
7 |
12,836,781 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9606:Vmn1r86
|
UTSW |
7 |
12,836,741 (GRCm39) |
missense |
probably damaging |
1.00 |
|