Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930011G23Rik |
G |
A |
5: 99,377,241 (GRCm39) |
P402L |
probably damaging |
Het |
A930011G23Rik |
A |
G |
5: 99,377,236 (GRCm39) |
S404P |
probably damaging |
Het |
Acss1 |
A |
T |
2: 150,480,387 (GRCm39) |
V228E |
probably damaging |
Het |
Ampd1 |
T |
A |
3: 102,992,693 (GRCm39) |
M145K |
probably damaging |
Het |
Ankhd1 |
G |
A |
18: 36,781,599 (GRCm39) |
S2217N |
probably benign |
Het |
Asph |
T |
A |
4: 9,598,759 (GRCm39) |
D211V |
probably damaging |
Het |
Cd55b |
A |
T |
1: 130,316,413 (GRCm39) |
W379R |
probably damaging |
Het |
Derl3 |
A |
G |
10: 75,730,950 (GRCm39) |
T201A |
probably damaging |
Het |
Efcab6 |
A |
G |
15: 83,783,898 (GRCm39) |
L1008P |
probably damaging |
Het |
Eif4g3 |
A |
G |
4: 137,853,522 (GRCm39) |
I363V |
probably benign |
Het |
Heatr5a |
A |
G |
12: 51,961,804 (GRCm39) |
F1058L |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,522,583 (GRCm39) |
M3439K |
probably benign |
Het |
Ift140 |
C |
A |
17: 25,253,009 (GRCm39) |
|
probably benign |
Het |
Itgad |
A |
G |
7: 127,792,888 (GRCm39) |
Y832C |
probably damaging |
Het |
Itgb2 |
T |
A |
10: 77,385,833 (GRCm39) |
D265E |
possibly damaging |
Het |
Kif19a |
A |
T |
11: 114,676,393 (GRCm39) |
E449V |
probably damaging |
Het |
Krt40 |
T |
C |
11: 99,429,461 (GRCm39) |
E291G |
probably damaging |
Het |
Lama2 |
T |
C |
10: 26,980,124 (GRCm39) |
N1897S |
probably damaging |
Het |
Lepr |
A |
G |
4: 101,639,835 (GRCm39) |
Y767C |
probably damaging |
Het |
Lrrtm4 |
A |
G |
6: 80,786,031 (GRCm39) |
H546R |
probably benign |
Het |
Marchf6 |
A |
G |
15: 31,486,266 (GRCm39) |
S362P |
probably benign |
Het |
Med12l |
A |
G |
3: 59,001,067 (GRCm39) |
Y734C |
probably damaging |
Het |
Mrps18a |
C |
T |
17: 46,433,725 (GRCm39) |
R74C |
probably damaging |
Het |
Mvk |
A |
G |
5: 114,588,880 (GRCm39) |
E174G |
probably benign |
Het |
Naip2 |
A |
G |
13: 100,296,722 (GRCm39) |
S1105P |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 89,221,624 (GRCm39) |
M468V |
probably benign |
Het |
Obscn |
T |
C |
11: 58,984,175 (GRCm39) |
E1760G |
probably damaging |
Het |
Pcsk5 |
C |
A |
19: 17,652,832 (GRCm39) |
G285W |
probably damaging |
Het |
Pgpep1l |
A |
G |
7: 67,886,721 (GRCm39) |
I196T |
probably benign |
Het |
Phf14 |
T |
C |
6: 11,987,611 (GRCm39) |
M630T |
probably benign |
Het |
Plod2 |
T |
C |
9: 92,477,442 (GRCm39) |
|
probably benign |
Het |
Poldip2 |
G |
A |
11: 78,403,162 (GRCm39) |
A9T |
probably benign |
Het |
Pou2f1 |
A |
G |
1: 165,703,396 (GRCm39) |
S718P |
probably damaging |
Het |
Pramel34 |
G |
A |
5: 93,786,503 (GRCm39) |
P89S |
possibly damaging |
Het |
Ptpre |
A |
T |
7: 135,269,296 (GRCm39) |
Y246F |
probably damaging |
Het |
Pudp |
T |
C |
18: 50,701,403 (GRCm39) |
H110R |
probably benign |
Het |
Scaf4 |
C |
T |
16: 90,042,403 (GRCm39) |
G646E |
unknown |
Het |
Sec16a |
T |
A |
2: 26,318,149 (GRCm39) |
|
probably benign |
Het |
Serpina5 |
A |
G |
12: 104,070,116 (GRCm39) |
T338A |
probably benign |
Het |
Shisa5 |
T |
G |
9: 108,885,080 (GRCm39) |
F118V |
probably damaging |
Het |
Slc6a21 |
G |
A |
7: 44,936,061 (GRCm39) |
|
probably benign |
Het |
Sprtn |
T |
A |
8: 125,630,126 (GRCm39) |
V473E |
probably benign |
Het |
Styxl1 |
A |
G |
5: 135,787,996 (GRCm39) |
I165T |
probably damaging |
Het |
Tal2 |
T |
A |
4: 53,785,906 (GRCm39) |
I29N |
probably damaging |
Het |
Tas2r134 |
T |
C |
2: 51,517,839 (GRCm39) |
I106T |
probably damaging |
Het |
Tmem259 |
G |
A |
10: 79,814,973 (GRCm39) |
T217I |
probably damaging |
Het |
Trpc6 |
T |
C |
9: 8,655,339 (GRCm39) |
I723T |
probably damaging |
Het |
Vmn2r103 |
G |
T |
17: 20,032,510 (GRCm39) |
M761I |
probably benign |
Het |
Ybey |
A |
T |
10: 76,304,160 (GRCm39) |
I14N |
probably damaging |
Het |
|
Other mutations in Vmn1r211 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Vmn1r211
|
APN |
13 |
23,036,272 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01583:Vmn1r211
|
APN |
13 |
23,036,571 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02794:Vmn1r211
|
APN |
13 |
23,036,379 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02794:Vmn1r211
|
APN |
13 |
23,036,377 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02794:Vmn1r211
|
APN |
13 |
23,036,376 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03292:Vmn1r211
|
APN |
13 |
23,036,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Vmn1r211
|
UTSW |
13 |
23,036,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1682:Vmn1r211
|
UTSW |
13 |
23,035,813 (GRCm39) |
missense |
probably damaging |
0.97 |
R1868:Vmn1r211
|
UTSW |
13 |
23,035,779 (GRCm39) |
missense |
probably benign |
0.07 |
R2002:Vmn1r211
|
UTSW |
13 |
23,035,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R2037:Vmn1r211
|
UTSW |
13 |
23,036,134 (GRCm39) |
missense |
probably damaging |
0.98 |
R2655:Vmn1r211
|
UTSW |
13 |
23,036,586 (GRCm39) |
missense |
probably benign |
0.42 |
R4837:Vmn1r211
|
UTSW |
13 |
23,036,296 (GRCm39) |
missense |
probably benign |
0.41 |
R6284:Vmn1r211
|
UTSW |
13 |
23,036,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R6701:Vmn1r211
|
UTSW |
13 |
23,035,779 (GRCm39) |
missense |
probably benign |
0.07 |
R6715:Vmn1r211
|
UTSW |
13 |
23,035,949 (GRCm39) |
missense |
probably benign |
0.00 |
R7058:Vmn1r211
|
UTSW |
13 |
23,036,063 (GRCm39) |
missense |
probably benign |
0.15 |
R7465:Vmn1r211
|
UTSW |
13 |
23,036,086 (GRCm39) |
missense |
probably benign |
0.13 |
R8085:Vmn1r211
|
UTSW |
13 |
23,035,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8720:Vmn1r211
|
UTSW |
13 |
23,036,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R8730:Vmn1r211
|
UTSW |
13 |
23,035,838 (GRCm39) |
nonsense |
probably null |
|
R9120:Vmn1r211
|
UTSW |
13 |
23,035,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R9725:Vmn1r211
|
UTSW |
13 |
23,036,506 (GRCm39) |
missense |
probably benign |
0.03 |
|