Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
A |
T |
9: 57,166,019 (GRCm39) |
H118Q |
probably damaging |
Het |
Adgrl3 |
T |
G |
5: 81,796,560 (GRCm39) |
V623G |
probably damaging |
Het |
B9d2 |
A |
G |
7: 25,385,442 (GRCm39) |
D84G |
probably damaging |
Het |
Clec1a |
A |
T |
6: 129,405,827 (GRCm39) |
L268H |
probably damaging |
Het |
Copa |
A |
T |
1: 171,939,491 (GRCm39) |
N576I |
possibly damaging |
Het |
Cyp11b1 |
T |
C |
15: 74,712,798 (GRCm39) |
T88A |
probably benign |
Het |
Dis3l2 |
T |
C |
1: 86,785,063 (GRCm39) |
I318T |
probably benign |
Het |
Dmtf1 |
T |
C |
5: 9,180,654 (GRCm39) |
|
probably benign |
Het |
Dnah17 |
C |
A |
11: 117,932,310 (GRCm39) |
A3639S |
probably damaging |
Het |
Dnajc8 |
T |
A |
4: 132,272,031 (GRCm39) |
I89N |
probably damaging |
Het |
Dync2h1 |
T |
A |
9: 7,102,549 (GRCm39) |
H377L |
probably benign |
Het |
Erfe |
T |
A |
1: 91,298,054 (GRCm39) |
I212N |
probably benign |
Het |
Fam117b |
A |
G |
1: 59,992,094 (GRCm39) |
T248A |
probably damaging |
Het |
Fbxo10 |
A |
T |
4: 45,044,849 (GRCm39) |
N595K |
probably damaging |
Het |
Fzd10 |
T |
A |
5: 128,678,646 (GRCm39) |
M122K |
probably damaging |
Het |
Gpr15 |
C |
T |
16: 58,538,144 (GRCm39) |
R315H |
probably benign |
Het |
Gvin2 |
G |
A |
7: 105,551,187 (GRCm39) |
Q622* |
probably null |
Het |
H6pd |
T |
C |
4: 150,066,508 (GRCm39) |
D626G |
probably damaging |
Het |
Hexd |
A |
G |
11: 121,113,107 (GRCm39) |
D514G |
probably damaging |
Het |
Hoxd4 |
T |
C |
2: 74,558,836 (GRCm39) |
S220P |
possibly damaging |
Het |
Invs |
A |
G |
4: 48,396,260 (GRCm39) |
H311R |
possibly damaging |
Het |
Ip6k1 |
A |
G |
9: 107,901,634 (GRCm39) |
T70A |
probably damaging |
Het |
Lipt2 |
T |
C |
7: 99,809,578 (GRCm39) |
C222R |
probably damaging |
Het |
Lrrc3 |
T |
A |
10: 77,736,866 (GRCm39) |
D190V |
probably damaging |
Het |
Marchf10 |
T |
C |
11: 105,280,603 (GRCm39) |
T561A |
probably benign |
Het |
Mcm10 |
G |
A |
2: 5,005,746 (GRCm39) |
T463I |
probably benign |
Het |
Mideas |
A |
G |
12: 84,203,233 (GRCm39) |
S890P |
probably damaging |
Het |
Mmel1 |
T |
C |
4: 154,966,134 (GRCm39) |
L52P |
probably damaging |
Het |
Nipbl |
T |
C |
15: 8,332,969 (GRCm39) |
N2218S |
probably benign |
Het |
Nr4a3 |
C |
T |
4: 48,051,486 (GRCm39) |
P80L |
probably benign |
Het |
Nrip1 |
C |
T |
16: 76,089,476 (GRCm39) |
G694R |
possibly damaging |
Het |
Oit3 |
A |
T |
10: 59,271,767 (GRCm39) |
C197S |
probably damaging |
Het |
Or5al1 |
C |
T |
2: 85,990,196 (GRCm39) |
V173M |
probably benign |
Het |
Or8b1b |
A |
G |
9: 38,375,543 (GRCm39) |
I69V |
probably benign |
Het |
Otol1 |
A |
G |
3: 69,935,433 (GRCm39) |
E475G |
possibly damaging |
Het |
Pes1 |
T |
C |
11: 3,923,330 (GRCm39) |
F168L |
probably damaging |
Het |
Plch1 |
C |
T |
3: 63,615,155 (GRCm39) |
R780H |
possibly damaging |
Het |
Pxdn |
C |
G |
12: 30,065,504 (GRCm39) |
P1275A |
probably damaging |
Het |
Sgcz |
T |
C |
8: 37,993,443 (GRCm39) |
E218G |
probably damaging |
Het |
Slc27a5 |
A |
T |
7: 12,725,135 (GRCm39) |
N437K |
probably damaging |
Het |
Sult2b1 |
A |
G |
7: 45,384,612 (GRCm39) |
S155P |
probably damaging |
Het |
Tgfbrap1 |
T |
C |
1: 43,091,056 (GRCm39) |
M690V |
probably benign |
Het |
Tmem151a |
A |
T |
19: 5,133,119 (GRCm39) |
L29Q |
probably damaging |
Het |
Tmprss2 |
A |
G |
16: 97,369,637 (GRCm39) |
I379T |
probably damaging |
Het |
Vmn2r73 |
A |
C |
7: 85,507,446 (GRCm39) |
V622G |
probably benign |
Het |
Wdr72 |
A |
G |
9: 74,117,928 (GRCm39) |
H880R |
probably benign |
Het |
Zfhx3 |
A |
G |
8: 109,678,024 (GRCm39) |
T3025A |
possibly damaging |
Het |
|
Other mutations in Vmn1r168 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01761:Vmn1r168
|
APN |
7 |
23,241,070 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02621:Vmn1r168
|
APN |
7 |
23,240,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02650:Vmn1r168
|
APN |
7 |
23,240,916 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4466001:Vmn1r168
|
UTSW |
7 |
23,240,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R0320:Vmn1r168
|
UTSW |
7 |
23,240,767 (GRCm39) |
missense |
probably benign |
0.12 |
R1595:Vmn1r168
|
UTSW |
7 |
23,240,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1618:Vmn1r168
|
UTSW |
7 |
23,240,725 (GRCm39) |
missense |
probably benign |
0.02 |
R1808:Vmn1r168
|
UTSW |
7 |
23,240,184 (GRCm39) |
missense |
probably benign |
0.05 |
R2418:Vmn1r168
|
UTSW |
7 |
23,240,824 (GRCm39) |
missense |
probably benign |
0.05 |
R2419:Vmn1r168
|
UTSW |
7 |
23,240,824 (GRCm39) |
missense |
probably benign |
0.05 |
R4846:Vmn1r168
|
UTSW |
7 |
23,240,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Vmn1r168
|
UTSW |
7 |
23,240,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R5269:Vmn1r168
|
UTSW |
7 |
23,240,839 (GRCm39) |
missense |
probably benign |
0.40 |
R6265:Vmn1r168
|
UTSW |
7 |
23,240,961 (GRCm39) |
missense |
probably benign |
|
R6353:Vmn1r168
|
UTSW |
7 |
23,240,944 (GRCm39) |
missense |
probably benign |
0.02 |
R6768:Vmn1r168
|
UTSW |
7 |
23,240,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Vmn1r168
|
UTSW |
7 |
23,240,487 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8749:Vmn1r168
|
UTSW |
7 |
23,240,428 (GRCm39) |
missense |
probably benign |
0.10 |
R9749:Vmn1r168
|
UTSW |
7 |
23,240,237 (GRCm39) |
missense |
probably damaging |
0.98 |
R9768:Vmn1r168
|
UTSW |
7 |
23,240,509 (GRCm39) |
missense |
probably benign |
0.02 |
|