Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc3 |
T |
C |
11: 94,241,817 (GRCm39) |
S1405G |
probably benign |
Het |
Acaca |
T |
C |
11: 84,171,261 (GRCm39) |
V1165A |
possibly damaging |
Het |
Acin1 |
C |
A |
14: 54,880,474 (GRCm39) |
|
probably benign |
Het |
Akr1b8 |
G |
A |
6: 34,340,312 (GRCm39) |
V159I |
probably benign |
Het |
Alms1 |
T |
C |
6: 85,597,504 (GRCm39) |
Y777H |
probably damaging |
Het |
Cblc |
C |
A |
7: 19,530,407 (GRCm39) |
G101C |
probably damaging |
Het |
Cdc42ep5 |
G |
A |
7: 4,154,614 (GRCm39) |
P58L |
possibly damaging |
Het |
Cic |
A |
G |
7: 24,987,908 (GRCm39) |
N1532S |
probably benign |
Het |
Cipc |
T |
A |
12: 86,999,714 (GRCm39) |
|
probably benign |
Het |
Clca4b |
T |
C |
3: 144,617,146 (GRCm39) |
I835V |
probably benign |
Het |
Cntrob |
C |
T |
11: 69,211,714 (GRCm39) |
G170D |
probably damaging |
Het |
Col14a1 |
A |
G |
15: 55,235,998 (GRCm39) |
Q304R |
unknown |
Het |
Csmd3 |
T |
C |
15: 47,777,364 (GRCm39) |
T1181A |
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,413,834 (GRCm39) |
F994L |
probably damaging |
Het |
Ddx42 |
C |
A |
11: 106,138,529 (GRCm39) |
A776D |
probably benign |
Het |
Disp2 |
G |
T |
2: 118,622,165 (GRCm39) |
E966* |
probably null |
Het |
Dmpk |
A |
T |
7: 18,822,139 (GRCm39) |
N366Y |
probably damaging |
Het |
Dmrt1 |
A |
G |
19: 25,580,674 (GRCm39) |
Y362C |
possibly damaging |
Het |
Dock10 |
C |
T |
1: 80,493,330 (GRCm39) |
G1880D |
possibly damaging |
Het |
Dzip1l |
A |
G |
9: 99,545,664 (GRCm39) |
R638G |
possibly damaging |
Het |
Dzip3 |
T |
A |
16: 48,746,332 (GRCm39) |
|
probably benign |
Het |
Ear-ps2 |
G |
A |
14: 44,284,517 (GRCm39) |
|
noncoding transcript |
Het |
Eno4 |
T |
C |
19: 58,934,068 (GRCm39) |
S90P |
probably damaging |
Het |
Epn2 |
C |
G |
11: 61,426,129 (GRCm39) |
A283P |
probably damaging |
Het |
Eya3 |
T |
A |
4: 132,397,543 (GRCm39) |
Y67* |
probably null |
Het |
Fat2 |
T |
C |
11: 55,175,841 (GRCm39) |
N1624S |
probably benign |
Het |
Fez1 |
T |
A |
9: 36,781,766 (GRCm39) |
|
probably null |
Het |
Fgfr1 |
T |
C |
8: 26,053,504 (GRCm39) |
S260P |
probably damaging |
Het |
Glb1 |
A |
G |
9: 114,293,220 (GRCm39) |
S532G |
probably benign |
Het |
Gm15455 |
A |
T |
1: 33,876,874 (GRCm39) |
|
noncoding transcript |
Het |
Grid2ip |
A |
G |
5: 143,377,131 (GRCm39) |
|
probably benign |
Het |
Guca2b |
C |
A |
4: 119,513,996 (GRCm39) |
G129V |
probably damaging |
Het |
Hes3 |
T |
C |
4: 152,372,124 (GRCm39) |
E65G |
probably damaging |
Het |
Itgbl1 |
T |
C |
14: 124,204,120 (GRCm39) |
C404R |
probably damaging |
Het |
Kansl1 |
C |
T |
11: 104,247,593 (GRCm39) |
V586I |
possibly damaging |
Het |
Krt18 |
A |
G |
15: 101,940,293 (GRCm39) |
D390G |
probably benign |
Het |
Laptm5 |
T |
C |
4: 130,660,982 (GRCm39) |
|
probably benign |
Het |
Lgals3bp |
C |
T |
11: 118,288,977 (GRCm39) |
E116K |
probably benign |
Het |
Lrrc39 |
C |
T |
3: 116,363,769 (GRCm39) |
S114F |
probably damaging |
Het |
Mfap3 |
T |
C |
11: 57,419,117 (GRCm39) |
|
probably null |
Het |
Nphp3 |
A |
G |
9: 103,899,931 (GRCm39) |
H481R |
probably benign |
Het |
Ntm |
T |
C |
9: 29,090,501 (GRCm39) |
T73A |
possibly damaging |
Het |
Or5m13b |
T |
A |
2: 85,749,215 (GRCm39) |
|
probably null |
Het |
Or8g4 |
T |
A |
9: 39,662,024 (GRCm39) |
M114K |
probably damaging |
Het |
Pbk |
G |
A |
14: 66,049,386 (GRCm39) |
C21Y |
probably benign |
Het |
Pglyrp1 |
A |
G |
7: 18,618,871 (GRCm39) |
E74G |
probably benign |
Het |
R3hdm1 |
G |
T |
1: 128,164,503 (GRCm39) |
|
probably benign |
Het |
Rap1gds1 |
T |
C |
3: 138,633,375 (GRCm39) |
T599A |
probably damaging |
Het |
Rigi |
A |
G |
4: 40,203,798 (GRCm39) |
|
probably benign |
Het |
Rims1 |
A |
T |
1: 22,358,836 (GRCm39) |
M1273K |
probably damaging |
Het |
Sbf1 |
G |
A |
15: 89,187,315 (GRCm39) |
R721* |
probably null |
Het |
Slc17a1 |
T |
C |
13: 24,064,700 (GRCm39) |
I388T |
probably damaging |
Het |
Sprn |
A |
C |
7: 139,733,469 (GRCm39) |
|
probably benign |
Het |
Tango6 |
T |
C |
8: 107,426,863 (GRCm39) |
V459A |
possibly damaging |
Het |
Tert |
C |
T |
13: 73,775,939 (GRCm39) |
T230I |
probably benign |
Het |
Thada |
T |
C |
17: 84,733,614 (GRCm39) |
D1011G |
possibly damaging |
Het |
Tln2 |
C |
T |
9: 67,302,743 (GRCm39) |
R76Q |
probably damaging |
Het |
Trip11 |
A |
T |
12: 101,851,549 (GRCm39) |
N838K |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,597,997 (GRCm39) |
W19639R |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,135,983 (GRCm39) |
S924T |
probably benign |
Het |
Upb1 |
A |
G |
10: 75,250,861 (GRCm39) |
E110G |
probably benign |
Het |
Vegfa |
C |
T |
17: 46,339,272 (GRCm39) |
|
probably null |
Het |
Vmn2r16 |
A |
T |
5: 109,487,168 (GRCm39) |
I130F |
probably benign |
Het |
Wscd2 |
T |
A |
5: 113,689,240 (GRCm39) |
V82E |
probably benign |
Het |
Zfp462 |
A |
G |
4: 55,008,612 (GRCm39) |
T193A |
probably benign |
Het |
Zfp467 |
A |
G |
6: 48,416,291 (GRCm39) |
|
probably benign |
Het |
Zfp619 |
T |
C |
7: 39,186,412 (GRCm39) |
L814P |
probably benign |
Het |
|
Other mutations in Vmn1r231 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00233:Vmn1r231
|
APN |
17 |
21,110,828 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02124:Vmn1r231
|
APN |
17 |
21,110,568 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02151:Vmn1r231
|
APN |
17 |
21,109,997 (GRCm39) |
missense |
probably benign |
0.06 |
R0066:Vmn1r231
|
UTSW |
17 |
21,109,998 (GRCm39) |
missense |
probably benign |
0.27 |
R0066:Vmn1r231
|
UTSW |
17 |
21,109,998 (GRCm39) |
missense |
probably benign |
0.27 |
R0396:Vmn1r231
|
UTSW |
17 |
21,110,661 (GRCm39) |
missense |
probably damaging |
0.98 |
R0427:Vmn1r231
|
UTSW |
17 |
21,110,490 (GRCm39) |
missense |
probably benign |
0.05 |
R0470:Vmn1r231
|
UTSW |
17 |
21,110,265 (GRCm39) |
nonsense |
probably null |
|
R0848:Vmn1r231
|
UTSW |
17 |
21,110,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R1692:Vmn1r231
|
UTSW |
17 |
21,110,871 (GRCm39) |
missense |
probably benign |
0.02 |
R1987:Vmn1r231
|
UTSW |
17 |
21,110,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Vmn1r231
|
UTSW |
17 |
21,110,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R2105:Vmn1r231
|
UTSW |
17 |
21,110,380 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4440:Vmn1r231
|
UTSW |
17 |
21,110,718 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4634:Vmn1r231
|
UTSW |
17 |
21,110,660 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4646:Vmn1r231
|
UTSW |
17 |
21,110,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Vmn1r231
|
UTSW |
17 |
21,110,489 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4938:Vmn1r231
|
UTSW |
17 |
21,110,613 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5544:Vmn1r231
|
UTSW |
17 |
21,110,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R5942:Vmn1r231
|
UTSW |
17 |
21,110,417 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6053:Vmn1r231
|
UTSW |
17 |
21,110,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R6692:Vmn1r231
|
UTSW |
17 |
21,110,745 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6712:Vmn1r231
|
UTSW |
17 |
21,109,992 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7131:Vmn1r231
|
UTSW |
17 |
21,110,140 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7854:Vmn1r231
|
UTSW |
17 |
21,110,894 (GRCm39) |
missense |
probably damaging |
0.98 |
R7918:Vmn1r231
|
UTSW |
17 |
21,110,236 (GRCm39) |
nonsense |
probably null |
|
R8187:Vmn1r231
|
UTSW |
17 |
21,110,893 (GRCm39) |
missense |
probably benign |
0.10 |
R8238:Vmn1r231
|
UTSW |
17 |
21,110,640 (GRCm39) |
missense |
probably benign |
0.08 |
R8313:Vmn1r231
|
UTSW |
17 |
21,110,289 (GRCm39) |
missense |
probably benign |
0.02 |
R8525:Vmn1r231
|
UTSW |
17 |
21,110,001 (GRCm39) |
missense |
probably benign |
0.06 |
R9276:Vmn1r231
|
UTSW |
17 |
21,110,560 (GRCm39) |
missense |
probably benign |
0.00 |
RF010:Vmn1r231
|
UTSW |
17 |
21,110,255 (GRCm39) |
missense |
probably damaging |
0.99 |
|