Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd11 |
T |
C |
8: 123,626,415 (GRCm39) |
I198V |
possibly damaging |
Het |
Arhgap12 |
T |
C |
18: 6,111,734 (GRCm39) |
D210G |
probably damaging |
Het |
Arpc2 |
T |
A |
1: 74,287,322 (GRCm39) |
N31K |
probably damaging |
Het |
Atp11a |
T |
A |
8: 12,866,990 (GRCm39) |
V139D |
possibly damaging |
Het |
Bicral |
T |
C |
17: 47,124,955 (GRCm39) |
K615E |
probably damaging |
Het |
Ccdc27 |
TTCCTCCTCCTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTC |
4: 154,120,763 (GRCm39) |
|
probably benign |
Het |
Chrnb1 |
T |
C |
11: 69,677,922 (GRCm39) |
M277V |
possibly damaging |
Het |
Csmd1 |
C |
T |
8: 15,960,464 (GRCm39) |
C3317Y |
probably damaging |
Het |
Ddx1 |
A |
T |
12: 13,281,504 (GRCm39) |
L353* |
probably null |
Het |
Degs2 |
T |
C |
12: 108,658,358 (GRCm39) |
K207R |
probably damaging |
Het |
Fam167a |
T |
C |
14: 63,689,769 (GRCm39) |
V22A |
probably benign |
Het |
Fam186a |
G |
A |
15: 99,831,566 (GRCm39) |
|
probably benign |
Het |
Gprc5b |
T |
C |
7: 118,583,749 (GRCm39) |
D40G |
probably benign |
Het |
Grsf1 |
G |
A |
5: 88,812,015 (GRCm39) |
P271S |
probably benign |
Het |
Inpp5j |
A |
G |
11: 3,451,134 (GRCm39) |
I505T |
probably damaging |
Het |
Lurap1l |
G |
A |
4: 80,872,095 (GRCm39) |
S196N |
probably benign |
Het |
Mapk8 |
T |
C |
14: 33,104,177 (GRCm39) |
D413G |
probably damaging |
Het |
Mapkbp1 |
A |
G |
2: 119,848,346 (GRCm39) |
D632G |
probably damaging |
Het |
Mcidas |
A |
G |
13: 113,130,906 (GRCm39) |
D77G |
probably damaging |
Het |
Mdga1 |
A |
G |
17: 30,188,964 (GRCm39) |
V33A |
unknown |
Het |
Me3 |
A |
G |
7: 89,501,038 (GRCm39) |
D583G |
probably benign |
Het |
Mndal |
T |
A |
1: 173,703,337 (GRCm39) |
T23S |
possibly damaging |
Het |
Myh13 |
T |
C |
11: 67,240,436 (GRCm39) |
M780T |
possibly damaging |
Het |
Nat10 |
A |
G |
2: 103,570,158 (GRCm39) |
L395P |
probably damaging |
Het |
Naxd |
T |
C |
8: 11,552,757 (GRCm39) |
V59A |
probably damaging |
Het |
Nbeal2 |
A |
T |
9: 110,465,743 (GRCm39) |
V876E |
probably benign |
Het |
Or11h4b |
C |
G |
14: 50,918,507 (GRCm39) |
E195Q |
probably benign |
Het |
Or1o2 |
T |
G |
17: 37,542,739 (GRCm39) |
H174P |
possibly damaging |
Het |
Or4a39 |
T |
C |
2: 89,236,935 (GRCm39) |
T163A |
probably benign |
Het |
Or51v8 |
T |
C |
7: 103,320,178 (GRCm39) |
Y20C |
possibly damaging |
Het |
Or8g50 |
A |
G |
9: 39,648,344 (GRCm39) |
T78A |
probably benign |
Het |
Pcdhgb8 |
G |
C |
18: 37,896,594 (GRCm39) |
D555H |
probably damaging |
Het |
Pcsk4 |
C |
T |
10: 80,160,845 (GRCm39) |
R327Q |
probably benign |
Het |
Pkhd1 |
C |
T |
1: 20,188,031 (GRCm39) |
V3426I |
probably benign |
Het |
Ranbp2 |
T |
C |
10: 58,301,488 (GRCm39) |
F687L |
possibly damaging |
Het |
Rb1 |
A |
G |
14: 73,435,966 (GRCm39) |
|
probably null |
Het |
Tfpi2 |
C |
A |
6: 3,963,926 (GRCm39) |
V51L |
probably damaging |
Het |
Tnn |
T |
C |
1: 159,924,925 (GRCm39) |
D1143G |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,541,586 (GRCm39) |
M25473T |
probably benign |
Het |
Vmn2r79 |
A |
G |
7: 86,651,099 (GRCm39) |
H166R |
possibly damaging |
Het |
Wdr25 |
T |
A |
12: 108,993,257 (GRCm39) |
F491Y |
probably benign |
Het |
Zfp972 |
G |
A |
2: 177,563,250 (GRCm39) |
Q56* |
probably null |
Het |
Zfp982 |
A |
G |
4: 147,597,150 (GRCm39) |
K169R |
probably benign |
Het |
|
Other mutations in Vmn1r201 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02792:Vmn1r201
|
APN |
13 |
22,659,014 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03137:Vmn1r201
|
APN |
13 |
22,658,974 (GRCm39) |
missense |
probably benign |
0.01 |
R0278:Vmn1r201
|
UTSW |
13 |
22,659,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R0381:Vmn1r201
|
UTSW |
13 |
22,659,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R0544:Vmn1r201
|
UTSW |
13 |
22,659,316 (GRCm39) |
missense |
probably benign |
0.04 |
R1411:Vmn1r201
|
UTSW |
13 |
22,658,849 (GRCm39) |
missense |
probably benign |
0.01 |
R1544:Vmn1r201
|
UTSW |
13 |
22,658,968 (GRCm39) |
missense |
probably benign |
0.20 |
R1850:Vmn1r201
|
UTSW |
13 |
22,658,801 (GRCm39) |
missense |
probably benign |
0.08 |
R1891:Vmn1r201
|
UTSW |
13 |
22,659,425 (GRCm39) |
missense |
probably benign |
0.01 |
R2071:Vmn1r201
|
UTSW |
13 |
22,658,995 (GRCm39) |
missense |
probably benign |
0.34 |
R4924:Vmn1r201
|
UTSW |
13 |
22,658,882 (GRCm39) |
missense |
probably benign |
0.00 |
R4989:Vmn1r201
|
UTSW |
13 |
22,659,622 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5028:Vmn1r201
|
UTSW |
13 |
22,659,530 (GRCm39) |
nonsense |
probably null |
|
R5318:Vmn1r201
|
UTSW |
13 |
22,659,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R5369:Vmn1r201
|
UTSW |
13 |
22,659,672 (GRCm39) |
missense |
probably benign |
0.00 |
R5682:Vmn1r201
|
UTSW |
13 |
22,659,355 (GRCm39) |
missense |
probably damaging |
0.99 |
R5699:Vmn1r201
|
UTSW |
13 |
22,659,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R6180:Vmn1r201
|
UTSW |
13 |
22,659,499 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6273:Vmn1r201
|
UTSW |
13 |
22,659,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R6295:Vmn1r201
|
UTSW |
13 |
22,659,533 (GRCm39) |
missense |
probably benign |
0.00 |
R6331:Vmn1r201
|
UTSW |
13 |
22,659,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R7296:Vmn1r201
|
UTSW |
13 |
22,659,509 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7758:Vmn1r201
|
UTSW |
13 |
22,658,989 (GRCm39) |
missense |
not run |
|
R7832:Vmn1r201
|
UTSW |
13 |
22,659,538 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7887:Vmn1r201
|
UTSW |
13 |
22,658,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R7976:Vmn1r201
|
UTSW |
13 |
22,658,875 (GRCm39) |
missense |
probably benign |
0.32 |
R8676:Vmn1r201
|
UTSW |
13 |
22,659,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R9228:Vmn1r201
|
UTSW |
13 |
22,659,670 (GRCm39) |
missense |
probably benign |
0.21 |
R9570:Vmn1r201
|
UTSW |
13 |
22,659,236 (GRCm39) |
missense |
probably damaging |
1.00 |
|