Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578I06Rik |
T |
C |
14: 64,223,629 (GRCm39) |
Y49C |
probably damaging |
Het |
Abca6 |
A |
T |
11: 110,093,210 (GRCm39) |
L1021* |
probably null |
Het |
Abcc9 |
A |
G |
6: 142,574,229 (GRCm39) |
S1003P |
possibly damaging |
Het |
Aldh4a1 |
A |
G |
4: 139,372,345 (GRCm39) |
I505V |
probably benign |
Het |
Brwd1 |
T |
C |
16: 95,803,693 (GRCm39) |
D2159G |
possibly damaging |
Het |
C1s2 |
T |
C |
6: 124,602,454 (GRCm39) |
I586V |
probably benign |
Het |
Cd300e |
C |
A |
11: 114,946,171 (GRCm39) |
D97Y |
probably damaging |
Het |
Celsr3 |
A |
G |
9: 108,723,596 (GRCm39) |
D2877G |
probably damaging |
Het |
Cep41 |
T |
C |
6: 30,655,841 (GRCm39) |
N328D |
probably benign |
Het |
Cldn15 |
G |
A |
5: 137,003,765 (GRCm39) |
V227M |
probably damaging |
Het |
Clec10a |
T |
G |
11: 70,060,155 (GRCm39) |
I98S |
probably damaging |
Het |
Cpne4 |
A |
G |
9: 104,749,963 (GRCm39) |
Q89R |
probably damaging |
Het |
Cryba2 |
C |
A |
1: 74,932,037 (GRCm39) |
A4S |
probably benign |
Het |
Csmd2 |
G |
A |
4: 128,442,613 (GRCm39) |
A3222T |
|
Het |
Dapk1 |
C |
A |
13: 60,898,991 (GRCm39) |
Y820* |
probably null |
Het |
Efcab5 |
G |
A |
11: 77,022,934 (GRCm39) |
T593I |
probably damaging |
Het |
Entrep3 |
C |
A |
3: 89,094,645 (GRCm39) |
A416D |
possibly damaging |
Het |
Gar1 |
A |
G |
3: 129,620,608 (GRCm39) |
Y160H |
probably damaging |
Het |
Gm21834 |
T |
A |
17: 58,048,863 (GRCm39) |
I118L |
probably benign |
Het |
Gtf2a1l |
G |
A |
17: 89,001,531 (GRCm39) |
G129D |
probably damaging |
Het |
Gzmb |
T |
A |
14: 56,497,712 (GRCm39) |
Y176F |
probably benign |
Het |
Helz2 |
T |
G |
2: 180,881,975 (GRCm39) |
K273Q |
probably benign |
Het |
Ifi207 |
T |
A |
1: 173,555,234 (GRCm39) |
E816V |
probably damaging |
Het |
Insr |
A |
C |
8: 3,235,106 (GRCm39) |
D694E |
probably benign |
Het |
Insyn2b |
G |
A |
11: 34,352,072 (GRCm39) |
R38Q |
probably damaging |
Het |
Ipcef1 |
A |
T |
10: 6,870,036 (GRCm39) |
C172* |
probably null |
Het |
Itgal |
T |
G |
7: 126,921,796 (GRCm39) |
|
probably null |
Het |
Laptm5 |
A |
T |
4: 130,655,990 (GRCm39) |
M103L |
|
Het |
Lypd4 |
A |
T |
7: 24,566,160 (GRCm39) |
C55S |
probably null |
Het |
Mccc1 |
A |
C |
3: 36,030,865 (GRCm39) |
H400Q |
possibly damaging |
Het |
Myl4 |
C |
T |
11: 104,474,887 (GRCm39) |
R79W |
probably damaging |
Het |
Myo18a |
A |
G |
11: 77,709,596 (GRCm39) |
T569A |
probably benign |
Het |
Or14a259 |
G |
C |
7: 86,013,194 (GRCm39) |
S117* |
probably null |
Het |
Or4c117 |
T |
A |
2: 88,955,629 (GRCm39) |
T149S |
probably benign |
Het |
Or5ak24 |
A |
G |
2: 85,261,060 (GRCm39) |
S38P |
probably damaging |
Het |
Otof |
T |
A |
5: 30,538,265 (GRCm39) |
D1153V |
probably damaging |
Het |
Pcdha12 |
A |
T |
18: 37,153,614 (GRCm39) |
D111V |
probably damaging |
Het |
Pomt2 |
G |
T |
12: 87,157,146 (GRCm39) |
F724L |
probably damaging |
Het |
Ros1 |
T |
A |
10: 51,994,491 (GRCm39) |
Y1284F |
probably damaging |
Het |
Skint6 |
T |
C |
4: 113,034,224 (GRCm39) |
K301R |
possibly damaging |
Het |
Slc30a5 |
T |
A |
13: 100,951,214 (GRCm39) |
R223* |
probably null |
Het |
Slc35a1 |
A |
T |
4: 34,675,181 (GRCm39) |
V119E |
probably damaging |
Het |
Slc6a11 |
A |
T |
6: 114,220,914 (GRCm39) |
I482F |
probably damaging |
Het |
Tektl1 |
T |
C |
10: 78,583,128 (GRCm39) |
T419A |
probably damaging |
Het |
Tgm1 |
A |
T |
14: 55,942,991 (GRCm39) |
C616* |
probably null |
Het |
Tiam2 |
T |
A |
17: 3,553,298 (GRCm39) |
I1125N |
probably damaging |
Het |
Tln2 |
T |
C |
9: 67,136,732 (GRCm39) |
D1251G |
probably damaging |
Het |
Tnfaip2 |
C |
G |
12: 111,412,161 (GRCm39) |
S187R |
probably benign |
Het |
Ush2a |
A |
G |
1: 188,644,045 (GRCm39) |
Y4469C |
probably damaging |
Het |
Vmn2r53 |
A |
G |
7: 12,335,124 (GRCm39) |
S179P |
probably damaging |
Het |
Zfp474 |
A |
C |
18: 52,771,502 (GRCm39) |
I52L |
probably benign |
Het |
|
Other mutations in Vmn1r229 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0682:Vmn1r229
|
UTSW |
17 |
21,034,950 (GRCm39) |
missense |
probably benign |
0.43 |
R1401:Vmn1r229
|
UTSW |
17 |
21,034,904 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1484:Vmn1r229
|
UTSW |
17 |
21,034,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1551:Vmn1r229
|
UTSW |
17 |
21,035,051 (GRCm39) |
missense |
probably benign |
0.36 |
R1568:Vmn1r229
|
UTSW |
17 |
21,035,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1793:Vmn1r229
|
UTSW |
17 |
21,034,974 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2157:Vmn1r229
|
UTSW |
17 |
21,035,638 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4458:Vmn1r229
|
UTSW |
17 |
21,034,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R4556:Vmn1r229
|
UTSW |
17 |
21,034,953 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4891:Vmn1r229
|
UTSW |
17 |
21,035,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R6310:Vmn1r229
|
UTSW |
17 |
21,034,976 (GRCm39) |
missense |
probably benign |
0.01 |
R6995:Vmn1r229
|
UTSW |
17 |
21,035,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R8109:Vmn1r229
|
UTSW |
17 |
21,035,268 (GRCm39) |
missense |
probably benign |
0.05 |
R8155:Vmn1r229
|
UTSW |
17 |
21,035,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R8232:Vmn1r229
|
UTSW |
17 |
21,035,309 (GRCm39) |
missense |
probably damaging |
0.96 |
R8828:Vmn1r229
|
UTSW |
17 |
21,034,990 (GRCm39) |
missense |
probably damaging |
0.97 |
R8943:Vmn1r229
|
UTSW |
17 |
21,035,418 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9147:Vmn1r229
|
UTSW |
17 |
21,034,758 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R9148:Vmn1r229
|
UTSW |
17 |
21,034,758 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R9621:Vmn1r229
|
UTSW |
17 |
21,035,315 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Vmn1r229
|
UTSW |
17 |
21,035,327 (GRCm39) |
missense |
probably damaging |
1.00 |
|