Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
A |
G |
15: 81,949,936 (GRCm39) |
I1278V |
possibly damaging |
Het |
Baz1b |
A |
G |
5: 135,266,821 (GRCm39) |
H1210R |
probably damaging |
Het |
Cdt1 |
C |
T |
8: 123,296,070 (GRCm39) |
S128L |
probably benign |
Het |
Cfap54 |
A |
T |
10: 92,800,398 (GRCm39) |
N1603K |
unknown |
Het |
Cfap99 |
A |
G |
5: 34,469,026 (GRCm39) |
N300S |
possibly damaging |
Het |
Chrdl2 |
G |
A |
7: 99,676,940 (GRCm39) |
|
probably null |
Het |
Cpb2 |
C |
A |
14: 75,510,015 (GRCm39) |
F258L |
probably damaging |
Het |
Csmd3 |
A |
T |
15: 47,868,218 (GRCm39) |
D767E |
probably damaging |
Het |
Dennd3 |
C |
T |
15: 73,434,198 (GRCm39) |
T956I |
probably damaging |
Het |
Emcn |
A |
G |
3: 137,129,228 (GRCm39) |
T245A |
possibly damaging |
Het |
Gm4353 |
A |
G |
7: 115,682,864 (GRCm39) |
V239A |
probably damaging |
Het |
Gm4884 |
G |
A |
7: 40,692,810 (GRCm39) |
A260T |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,446,421 (GRCm39) |
D205G |
possibly damaging |
Het |
Hectd4 |
A |
G |
5: 121,481,210 (GRCm39) |
S3005G |
probably benign |
Het |
Ifngr1 |
T |
C |
10: 19,479,553 (GRCm39) |
L148P |
probably damaging |
Het |
Irf2 |
C |
T |
8: 47,271,929 (GRCm39) |
T172M |
probably damaging |
Het |
Irs1 |
T |
C |
1: 82,267,970 (GRCm39) |
H82R |
possibly damaging |
Het |
Kcnc4 |
G |
T |
3: 107,366,084 (GRCm39) |
N41K |
probably damaging |
Het |
Lig3 |
C |
T |
11: 82,682,870 (GRCm39) |
A490V |
possibly damaging |
Het |
Megf6 |
G |
A |
4: 154,349,649 (GRCm39) |
E946K |
probably damaging |
Het |
Mpi |
A |
T |
9: 57,452,200 (GRCm39) |
Y359N |
probably damaging |
Het |
Nf1 |
A |
G |
11: 79,349,709 (GRCm39) |
S1365G |
probably damaging |
Het |
P3h3 |
C |
A |
6: 124,828,041 (GRCm39) |
|
probably null |
Het |
Pdk2 |
A |
T |
11: 94,930,259 (GRCm39) |
V59D |
probably damaging |
Het |
Ppip5k2 |
T |
C |
1: 97,683,613 (GRCm39) |
K168R |
probably benign |
Het |
Prg4 |
G |
T |
1: 150,331,318 (GRCm39) |
P452T |
unknown |
Het |
Prl2b1 |
T |
C |
13: 27,567,442 (GRCm39) |
N234S |
possibly damaging |
Het |
Rnd1 |
T |
A |
15: 98,574,455 (GRCm39) |
T41S |
possibly damaging |
Het |
Sall4 |
G |
A |
2: 168,597,830 (GRCm39) |
P337S |
probably damaging |
Het |
Slc1a2 |
G |
A |
2: 102,586,298 (GRCm39) |
A301T |
possibly damaging |
Het |
Sorcs3 |
C |
T |
19: 48,194,913 (GRCm39) |
R99W |
possibly damaging |
Het |
Svep1 |
G |
A |
4: 58,044,053 (GRCm39) |
T3531I |
possibly damaging |
Het |
Sycp2 |
T |
C |
2: 178,004,761 (GRCm39) |
D894G |
probably benign |
Het |
Syne1 |
T |
C |
10: 5,178,659 (GRCm39) |
N4605S |
probably benign |
Het |
Syt4 |
A |
C |
18: 31,573,472 (GRCm39) |
C348G |
possibly damaging |
Het |
Tceanc2 |
G |
A |
4: 107,034,778 (GRCm39) |
T28M |
probably damaging |
Het |
Tmco1 |
A |
G |
1: 167,136,254 (GRCm39) |
D5G |
|
Het |
Tnfsf12 |
T |
C |
11: 69,577,713 (GRCm39) |
K235E |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,220,450 (GRCm39) |
S2396P |
possibly damaging |
Het |
Vipas39 |
T |
A |
12: 87,304,191 (GRCm39) |
D125V |
probably damaging |
Het |
Vmn2r16 |
A |
G |
5: 109,511,649 (GRCm39) |
N619D |
probably damaging |
Het |
Vps13a |
A |
G |
19: 16,718,157 (GRCm39) |
V521A |
probably benign |
Het |
Wdr20rt |
T |
A |
12: 65,273,035 (GRCm39) |
L166Q |
probably damaging |
Het |
Zbtb11 |
T |
A |
16: 55,821,022 (GRCm39) |
C706* |
probably null |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
Zscan21 |
A |
T |
5: 138,116,178 (GRCm39) |
Y30F |
unknown |
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 |
ANU05:Vmn1r86
|
UTSW |
7 |
12,836,433 (GRCm39) |
missense |
probably benign |
0.14 |
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 |
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 |
|