Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alg10b |
T |
C |
15: 90,112,592 (GRCm39) |
|
probably benign |
Het |
Ambn |
T |
C |
5: 88,608,554 (GRCm39) |
|
probably benign |
Het |
Asap2 |
A |
G |
12: 21,297,296 (GRCm39) |
D585G |
probably null |
Het |
Chaf1a |
G |
T |
17: 56,366,336 (GRCm39) |
|
probably benign |
Het |
Ddhd1 |
A |
G |
14: 45,854,008 (GRCm39) |
S443P |
probably damaging |
Het |
Dlk2 |
A |
G |
17: 46,613,390 (GRCm39) |
E215G |
probably damaging |
Het |
Efhd2 |
T |
C |
4: 141,587,176 (GRCm39) |
N202S |
probably benign |
Het |
Gkap1 |
A |
T |
13: 58,384,853 (GRCm39) |
I308K |
probably damaging |
Het |
Gm9848 |
T |
A |
13: 113,244,774 (GRCm39) |
|
noncoding transcript |
Het |
Hmcn1 |
G |
A |
1: 150,594,991 (GRCm39) |
T1826I |
probably damaging |
Het |
Htr5a |
T |
C |
5: 28,047,742 (GRCm39) |
V99A |
probably benign |
Het |
Inha |
T |
G |
1: 75,486,572 (GRCm39) |
F289C |
probably damaging |
Het |
Kcna3 |
T |
C |
3: 106,945,294 (GRCm39) |
V519A |
probably benign |
Het |
Kcnma1 |
A |
T |
14: 23,364,390 (GRCm39) |
|
probably benign |
Het |
Kctd1 |
A |
G |
18: 15,195,747 (GRCm39) |
V292A |
possibly damaging |
Het |
Magea13 |
T |
A |
X: 57,964,829 (GRCm39) |
I196N |
probably damaging |
Het |
Map2k4 |
A |
G |
11: 65,647,089 (GRCm39) |
|
probably benign |
Het |
Mfap2 |
G |
T |
4: 140,742,856 (GRCm39) |
A175S |
possibly damaging |
Het |
Milr1 |
G |
A |
11: 106,656,071 (GRCm39) |
A114T |
possibly damaging |
Het |
Mogs |
G |
T |
6: 83,095,558 (GRCm39) |
V792F |
probably damaging |
Het |
Nt5dc3 |
T |
A |
10: 86,661,089 (GRCm39) |
M418K |
possibly damaging |
Het |
Or5b12 |
A |
G |
19: 12,897,490 (GRCm39) |
L61P |
probably damaging |
Het |
Or7d10 |
A |
G |
9: 19,832,054 (GRCm39) |
E183G |
probably benign |
Het |
Or8h8 |
A |
T |
2: 86,753,293 (GRCm39) |
N194K |
probably benign |
Het |
Osbpl10 |
G |
A |
9: 115,061,190 (GRCm39) |
W756* |
probably null |
Het |
Pgam5 |
A |
G |
5: 110,413,391 (GRCm39) |
Y235H |
probably damaging |
Het |
Pgm5 |
G |
T |
19: 24,793,842 (GRCm39) |
A274E |
probably damaging |
Het |
Prex1 |
C |
A |
2: 166,411,260 (GRCm39) |
|
probably benign |
Het |
Prps1l1 |
A |
T |
12: 35,035,377 (GRCm39) |
N164I |
probably benign |
Het |
Ralbp1 |
C |
A |
17: 66,171,277 (GRCm39) |
R232L |
probably damaging |
Het |
Rnaseh2a |
C |
T |
8: 85,691,752 (GRCm39) |
|
probably benign |
Het |
Stard9 |
A |
T |
2: 120,529,200 (GRCm39) |
H1819L |
possibly damaging |
Het |
Stom |
T |
A |
2: 35,226,889 (GRCm39) |
I15F |
probably benign |
Het |
Tasor2 |
A |
C |
13: 3,625,067 (GRCm39) |
S946A |
possibly damaging |
Het |
Tph1 |
T |
G |
7: 46,314,662 (GRCm39) |
T22P |
probably damaging |
Het |
Uqcrfs1 |
A |
G |
13: 30,724,904 (GRCm39) |
I212T |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,546,550 (GRCm39) |
I3442T |
probably benign |
Het |
Vinac1 |
C |
A |
2: 128,880,622 (GRCm39) |
V435L |
probably benign |
Het |
Vmn2r75 |
T |
C |
7: 85,814,774 (GRCm39) |
I240V |
probably benign |
Het |
Wdr17 |
T |
C |
8: 55,125,585 (GRCm39) |
T432A |
probably damaging |
Het |
|
Other mutations in Vmn2r113 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01386:Vmn2r113
|
APN |
17 |
23,175,024 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01743:Vmn2r113
|
APN |
17 |
23,177,285 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02224:Vmn2r113
|
APN |
17 |
23,174,960 (GRCm39) |
nonsense |
probably null |
|
IGL02498:Vmn2r113
|
APN |
17 |
23,177,349 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02969:Vmn2r113
|
APN |
17 |
23,177,591 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03010:Vmn2r113
|
APN |
17 |
23,175,038 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03240:Vmn2r113
|
APN |
17 |
23,174,931 (GRCm39) |
missense |
probably benign |
0.19 |
R1853:Vmn2r113
|
UTSW |
17 |
23,164,501 (GRCm39) |
missense |
probably benign |
|
R2058:Vmn2r113
|
UTSW |
17 |
23,177,223 (GRCm39) |
nonsense |
probably null |
|
R3010:Vmn2r113
|
UTSW |
17 |
23,177,105 (GRCm39) |
missense |
probably damaging |
0.97 |
R4942:Vmn2r113
|
UTSW |
17 |
23,177,321 (GRCm39) |
missense |
probably damaging |
0.97 |
R5072:Vmn2r113
|
UTSW |
17 |
23,177,329 (GRCm39) |
nonsense |
probably null |
|
R5755:Vmn2r113
|
UTSW |
17 |
23,176,955 (GRCm39) |
missense |
probably benign |
0.00 |
R6513:Vmn2r113
|
UTSW |
17 |
23,177,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R7164:Vmn2r113
|
UTSW |
17 |
23,167,137 (GRCm39) |
missense |
probably benign |
|
R7936:Vmn2r113
|
UTSW |
17 |
23,176,917 (GRCm39) |
missense |
probably benign |
0.05 |
R8087:Vmn2r113
|
UTSW |
17 |
23,177,711 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8193:Vmn2r113
|
UTSW |
17 |
23,164,501 (GRCm39) |
missense |
probably benign |
0.06 |
R8196:Vmn2r113
|
UTSW |
17 |
23,176,938 (GRCm39) |
missense |
probably damaging |
0.99 |
R8414:Vmn2r113
|
UTSW |
17 |
23,177,753 (GRCm39) |
nonsense |
probably null |
|
R8490:Vmn2r113
|
UTSW |
17 |
23,177,372 (GRCm39) |
missense |
probably benign |
0.18 |
|