Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
G |
A |
17: 24,603,434 (GRCm39) |
G542D |
possibly damaging |
Het |
Adh6b |
A |
G |
3: 138,063,450 (GRCm39) |
Y343C |
probably damaging |
Het |
Adsl |
T |
A |
15: 80,836,495 (GRCm39) |
|
probably null |
Het |
Apob |
T |
A |
12: 8,057,630 (GRCm39) |
|
probably null |
Het |
Atp6ap1l |
T |
A |
13: 91,047,017 (GRCm39) |
|
probably benign |
Het |
Cacnb3 |
A |
G |
15: 98,537,750 (GRCm39) |
D74G |
probably damaging |
Het |
Cfap251 |
A |
G |
5: 123,411,696 (GRCm39) |
|
probably benign |
Het |
Clca3a2 |
T |
A |
3: 144,512,104 (GRCm39) |
D544V |
probably damaging |
Het |
Col3a1 |
G |
A |
1: 45,372,756 (GRCm39) |
|
probably benign |
Het |
D7Ertd443e |
A |
G |
7: 133,951,397 (GRCm39) |
|
probably null |
Het |
Dscam |
T |
C |
16: 96,573,637 (GRCm39) |
D775G |
probably damaging |
Het |
Eif2b3 |
T |
A |
4: 116,879,408 (GRCm39) |
M16K |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,840,771 (GRCm39) |
Y281C |
probably damaging |
Het |
Epha2 |
T |
A |
4: 141,036,176 (GRCm39) |
L204Q |
possibly damaging |
Het |
Filip1l |
A |
C |
16: 57,391,025 (GRCm39) |
I538L |
possibly damaging |
Het |
Gcnt2 |
T |
A |
13: 41,071,831 (GRCm39) |
V158D |
probably damaging |
Het |
Gnaq |
A |
G |
19: 16,309,449 (GRCm39) |
N162S |
probably benign |
Het |
Haus5 |
A |
T |
7: 30,353,651 (GRCm39) |
N575K |
probably benign |
Het |
Hjurp |
A |
T |
1: 88,202,772 (GRCm39) |
Y71N |
possibly damaging |
Het |
Igsf5 |
A |
G |
16: 96,174,279 (GRCm39) |
D103G |
probably damaging |
Het |
Myo10 |
A |
G |
15: 25,726,569 (GRCm39) |
D297G |
possibly damaging |
Het |
Net1 |
C |
T |
13: 3,936,623 (GRCm39) |
R314H |
probably damaging |
Het |
Or4b1c |
C |
A |
2: 90,126,512 (GRCm39) |
R231L |
probably benign |
Het |
Or4k51 |
T |
A |
2: 111,584,897 (GRCm39) |
V101D |
probably damaging |
Het |
Pcsk4 |
C |
A |
10: 80,157,979 (GRCm39) |
Q586H |
probably null |
Het |
Pramel11 |
A |
T |
4: 143,623,706 (GRCm39) |
M156K |
probably benign |
Het |
Prss1 |
A |
G |
6: 41,440,131 (GRCm39) |
D156G |
possibly damaging |
Het |
Rnf133 |
A |
T |
6: 23,649,259 (GRCm39) |
N266K |
probably damaging |
Het |
Setd2 |
G |
T |
9: 110,446,595 (GRCm39) |
A2482S |
possibly damaging |
Het |
Sgo2a |
A |
T |
1: 58,055,726 (GRCm39) |
S637C |
probably damaging |
Het |
Slc2a5 |
C |
A |
4: 150,224,262 (GRCm39) |
S290* |
probably null |
Het |
Spata6 |
T |
G |
4: 111,625,992 (GRCm39) |
H120Q |
possibly damaging |
Het |
Stk11 |
G |
A |
10: 79,963,775 (GRCm39) |
V194I |
probably damaging |
Het |
Tkt |
T |
C |
14: 30,287,603 (GRCm39) |
V199A |
probably benign |
Het |
Traf3 |
G |
A |
12: 111,209,952 (GRCm39) |
V183M |
possibly damaging |
Het |
Trappc11 |
T |
C |
8: 47,966,437 (GRCm39) |
Y483C |
probably damaging |
Het |
Trappc9 |
T |
C |
15: 72,785,215 (GRCm39) |
|
probably benign |
Het |
Trim59 |
T |
C |
3: 68,945,067 (GRCm39) |
H91R |
probably benign |
Het |
Ttc21a |
A |
G |
9: 119,781,278 (GRCm39) |
S484G |
probably benign |
Het |
Usp13 |
A |
T |
3: 32,969,947 (GRCm39) |
H691L |
probably benign |
Het |
Vmn2r111 |
T |
A |
17: 22,790,124 (GRCm39) |
Q294L |
possibly damaging |
Het |
Vmn2r17 |
A |
G |
5: 109,575,774 (GRCm39) |
D215G |
possibly damaging |
Het |
Zfp280b |
A |
G |
10: 75,875,183 (GRCm39) |
D354G |
probably benign |
Het |
Zfp607a |
A |
G |
7: 27,578,523 (GRCm39) |
H531R |
probably damaging |
Het |
Zfp74 |
A |
T |
7: 29,634,158 (GRCm39) |
C517S |
probably damaging |
Het |
|
Other mutations in Vmn1r238 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Vmn1r238
|
APN |
18 |
3,123,243 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01385:Vmn1r238
|
APN |
18 |
3,122,770 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02716:Vmn1r238
|
APN |
18 |
3,123,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R1219:Vmn1r238
|
UTSW |
18 |
3,123,135 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1568:Vmn1r238
|
UTSW |
18 |
3,123,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1864:Vmn1r238
|
UTSW |
18 |
3,123,040 (GRCm39) |
nonsense |
probably null |
|
R3024:Vmn1r238
|
UTSW |
18 |
3,123,305 (GRCm39) |
missense |
probably benign |
0.13 |
R4291:Vmn1r238
|
UTSW |
18 |
3,123,214 (GRCm39) |
nonsense |
probably null |
|
R4304:Vmn1r238
|
UTSW |
18 |
3,123,040 (GRCm39) |
nonsense |
probably null |
|
R4586:Vmn1r238
|
UTSW |
18 |
3,123,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R4664:Vmn1r238
|
UTSW |
18 |
3,123,300 (GRCm39) |
missense |
probably damaging |
0.99 |
R5430:Vmn1r238
|
UTSW |
18 |
3,122,521 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5834:Vmn1r238
|
UTSW |
18 |
3,123,168 (GRCm39) |
missense |
probably benign |
|
R7186:Vmn1r238
|
UTSW |
18 |
3,122,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R7206:Vmn1r238
|
UTSW |
18 |
3,122,623 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7308:Vmn1r238
|
UTSW |
18 |
3,122,875 (GRCm39) |
missense |
probably benign |
0.09 |
R7346:Vmn1r238
|
UTSW |
18 |
3,123,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Vmn1r238
|
UTSW |
18 |
3,123,393 (GRCm39) |
missense |
probably benign |
0.10 |
R7571:Vmn1r238
|
UTSW |
18 |
3,122,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Vmn1r238
|
UTSW |
18 |
3,123,033 (GRCm39) |
missense |
probably benign |
0.03 |
R8085:Vmn1r238
|
UTSW |
18 |
3,123,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R8086:Vmn1r238
|
UTSW |
18 |
3,123,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8325:Vmn1r238
|
UTSW |
18 |
3,122,529 (GRCm39) |
missense |
probably benign |
0.00 |
R8423:Vmn1r238
|
UTSW |
18 |
3,123,365 (GRCm39) |
nonsense |
probably null |
|
R8747:Vmn1r238
|
UTSW |
18 |
3,123,232 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8930:Vmn1r238
|
UTSW |
18 |
3,123,127 (GRCm39) |
missense |
probably benign |
0.03 |
R8932:Vmn1r238
|
UTSW |
18 |
3,123,127 (GRCm39) |
missense |
probably benign |
0.03 |
R9279:Vmn1r238
|
UTSW |
18 |
3,122,994 (GRCm39) |
missense |
probably damaging |
0.99 |
R9382:Vmn1r238
|
UTSW |
18 |
3,122,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R9644:Vmn1r238
|
UTSW |
18 |
3,122,635 (GRCm39) |
missense |
probably benign |
0.10 |
R9725:Vmn1r238
|
UTSW |
18 |
3,122,577 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Vmn1r238
|
UTSW |
18 |
3,122,505 (GRCm39) |
missense |
probably benign |
0.00 |
|