Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578I06Rik |
C |
T |
14: 64,210,658 (GRCm39) |
R190H |
probably benign |
Het |
Arsi |
T |
C |
18: 61,050,388 (GRCm39) |
W424R |
probably damaging |
Het |
Atad2 |
A |
G |
15: 57,980,252 (GRCm39) |
S411P |
probably damaging |
Het |
Cdhr2 |
G |
A |
13: 54,861,818 (GRCm39) |
V72I |
probably damaging |
Het |
Celf4 |
T |
C |
18: 25,624,258 (GRCm39) |
I414V |
probably damaging |
Het |
Cfap43 |
G |
A |
19: 47,770,844 (GRCm39) |
T689I |
probably benign |
Het |
Cpne9 |
C |
T |
6: 113,259,984 (GRCm39) |
|
probably benign |
Het |
Cyp3a11 |
A |
T |
5: 145,806,005 (GRCm39) |
S121T |
probably benign |
Het |
Dip2c |
C |
A |
13: 9,659,092 (GRCm39) |
Q864K |
probably damaging |
Het |
Fbxo3 |
A |
G |
2: 103,881,510 (GRCm39) |
T281A |
probably damaging |
Het |
Gm5148 |
T |
A |
3: 37,768,758 (GRCm39) |
H154L |
unknown |
Het |
Gsdma2 |
T |
A |
11: 98,542,758 (GRCm39) |
|
probably null |
Het |
Hfm1 |
T |
C |
5: 107,052,663 (GRCm39) |
I273M |
possibly damaging |
Het |
Hspa4l |
A |
G |
3: 40,700,435 (GRCm39) |
E14G |
probably benign |
Het |
Inava |
G |
T |
1: 136,142,088 (GRCm39) |
N670K |
probably benign |
Het |
Lgals12 |
T |
G |
19: 7,584,081 (GRCm39) |
E5D |
possibly damaging |
Het |
Lsg1 |
T |
G |
16: 30,392,061 (GRCm39) |
I237L |
probably benign |
Het |
Mettl14 |
T |
C |
3: 123,177,254 (GRCm39) |
E49G |
probably damaging |
Het |
Nbeal1 |
A |
G |
1: 60,370,107 (GRCm39) |
I2675V |
probably benign |
Het |
Or2y1e |
A |
T |
11: 49,218,304 (GRCm39) |
Q22L |
probably benign |
Het |
Or4b1b |
A |
T |
2: 90,112,406 (GRCm39) |
V171E |
probably damaging |
Het |
Or5k15 |
T |
G |
16: 58,710,143 (GRCm39) |
S147R |
probably benign |
Het |
Padi1 |
A |
T |
4: 140,542,089 (GRCm39) |
L611Q |
probably damaging |
Het |
Pcdhac2 |
A |
G |
18: 37,277,764 (GRCm39) |
D248G |
probably damaging |
Het |
Plekhm1 |
C |
A |
11: 103,261,760 (GRCm39) |
R940L |
probably damaging |
Het |
Rasa3 |
A |
G |
8: 13,664,532 (GRCm39) |
|
probably null |
Het |
Rspo2 |
C |
A |
15: 42,939,307 (GRCm39) |
R161L |
probably benign |
Het |
Sacs |
A |
G |
14: 61,443,786 (GRCm39) |
Y1944C |
probably damaging |
Het |
Slc7a10 |
G |
T |
7: 34,898,140 (GRCm39) |
M297I |
probably damaging |
Het |
Spata31e3 |
A |
C |
13: 50,404,141 (GRCm39) |
S54A |
probably benign |
Het |
Ssh2 |
A |
G |
11: 77,299,009 (GRCm39) |
T112A |
possibly damaging |
Het |
Ttc7 |
A |
T |
17: 87,628,829 (GRCm39) |
|
probably null |
Het |
Vmn2r112 |
A |
G |
17: 22,837,393 (GRCm39) |
K618R |
probably damaging |
Het |
Vmp1 |
T |
A |
11: 86,552,014 (GRCm39) |
I117L |
probably benign |
Het |
Vsnl1 |
A |
T |
12: 11,382,056 (GRCm39) |
Y108* |
probably null |
Het |
Wdr31 |
A |
G |
4: 62,375,675 (GRCm39) |
|
probably null |
Het |
Zfp329 |
A |
G |
7: 12,541,840 (GRCm39) |
V284A |
probably benign |
Het |
Zfp551 |
G |
A |
7: 12,150,318 (GRCm39) |
H364Y |
possibly damaging |
Het |
|
Other mutations in Vmn1r64 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Vmn1r64
|
APN |
7 |
5,886,827 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01070:Vmn1r64
|
APN |
7 |
5,886,941 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01817:Vmn1r64
|
APN |
7 |
5,887,222 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02026:Vmn1r64
|
APN |
7 |
5,886,649 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02657:Vmn1r64
|
APN |
7 |
5,886,727 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03352:Vmn1r64
|
APN |
7 |
5,887,070 (GRCm39) |
missense |
probably benign |
0.12 |
R0200:Vmn1r64
|
UTSW |
7 |
5,886,817 (GRCm39) |
missense |
probably benign |
0.38 |
R0540:Vmn1r64
|
UTSW |
7 |
5,887,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R0655:Vmn1r64
|
UTSW |
7 |
5,887,207 (GRCm39) |
missense |
probably benign |
0.25 |
R1212:Vmn1r64
|
UTSW |
7 |
5,887,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Vmn1r64
|
UTSW |
7 |
5,886,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R2034:Vmn1r64
|
UTSW |
7 |
5,886,988 (GRCm39) |
missense |
probably benign |
0.09 |
R2221:Vmn1r64
|
UTSW |
7 |
5,887,448 (GRCm39) |
missense |
probably benign |
0.00 |
R2240:Vmn1r64
|
UTSW |
7 |
5,887,369 (GRCm39) |
nonsense |
probably null |
|
R2305:Vmn1r64
|
UTSW |
7 |
5,887,535 (GRCm39) |
missense |
probably benign |
0.04 |
R3019:Vmn1r64
|
UTSW |
7 |
5,887,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Vmn1r64
|
UTSW |
7 |
5,887,357 (GRCm39) |
missense |
probably damaging |
0.99 |
R4996:Vmn1r64
|
UTSW |
7 |
5,887,052 (GRCm39) |
missense |
probably benign |
0.03 |
R5682:Vmn1r64
|
UTSW |
7 |
5,886,622 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5730:Vmn1r64
|
UTSW |
7 |
5,887,522 (GRCm39) |
missense |
probably benign |
0.01 |
R7397:Vmn1r64
|
UTSW |
7 |
5,887,013 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9697:Vmn1r64
|
UTSW |
7 |
5,886,859 (GRCm39) |
missense |
probably benign |
0.04 |
X0063:Vmn1r64
|
UTSW |
7 |
5,887,349 (GRCm39) |
missense |
probably benign |
0.00 |
|