Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310034C09Rik |
T |
C |
16: 88,556,151 (GRCm39) |
Y122H |
probably damaging |
Het |
Abhd14b |
T |
A |
9: 106,327,240 (GRCm39) |
H7Q |
probably benign |
Het |
Acod1 |
C |
T |
14: 103,286,780 (GRCm39) |
R28W |
possibly damaging |
Het |
Agap2 |
A |
G |
10: 126,924,194 (GRCm39) |
T803A |
unknown |
Het |
Angptl7 |
T |
C |
4: 148,581,741 (GRCm39) |
E215G |
probably damaging |
Het |
Ankrd34c |
T |
A |
9: 89,611,951 (GRCm39) |
D130V |
probably damaging |
Het |
BC028528 |
A |
G |
3: 95,792,298 (GRCm39) |
V144A |
probably benign |
Het |
Cab39l |
T |
C |
14: 59,776,640 (GRCm39) |
F274L |
probably damaging |
Het |
Cdsn |
T |
C |
17: 35,866,415 (GRCm39) |
S315P |
possibly damaging |
Het |
Celsr3 |
CGGGG |
CGGGGG |
9: 108,718,471 (GRCm39) |
|
probably null |
Het |
Cep97 |
A |
T |
16: 55,735,394 (GRCm39) |
L540* |
probably null |
Het |
Chrna2 |
G |
T |
14: 66,387,017 (GRCm39) |
E388* |
probably null |
Het |
Ckap4 |
A |
G |
10: 84,364,460 (GRCm39) |
V201A |
probably damaging |
Het |
Clec4b1 |
A |
G |
6: 123,042,922 (GRCm39) |
K47R |
probably benign |
Het |
Clvs2 |
A |
T |
10: 33,404,484 (GRCm39) |
I244N |
possibly damaging |
Het |
Cmtr1 |
G |
A |
17: 29,893,151 (GRCm39) |
E57K |
probably benign |
Het |
Cxxc1 |
T |
A |
18: 74,353,910 (GRCm39) |
D565E |
possibly damaging |
Het |
Dtx3l |
T |
A |
16: 35,754,073 (GRCm39) |
M178L |
probably benign |
Het |
Eml2 |
A |
G |
7: 18,930,161 (GRCm39) |
D294G |
possibly damaging |
Het |
Flt3 |
A |
G |
5: 147,269,698 (GRCm39) |
|
probably null |
Het |
Frs3 |
T |
A |
17: 48,014,777 (GRCm39) |
L490Q |
probably damaging |
Het |
Gm6882 |
G |
A |
7: 21,161,559 (GRCm39) |
T103I |
possibly damaging |
Het |
Gsdmd |
C |
T |
15: 75,736,270 (GRCm39) |
T133I |
probably benign |
Het |
Hhipl2 |
C |
A |
1: 183,209,540 (GRCm39) |
C331* |
probably null |
Het |
Ifnar1 |
C |
A |
16: 91,302,224 (GRCm39) |
D566E |
possibly damaging |
Het |
Ighv1-34 |
A |
T |
12: 114,814,939 (GRCm39) |
N74K |
probably benign |
Het |
Itk |
T |
C |
11: 46,233,222 (GRCm39) |
|
probably null |
Het |
Kdm7a |
T |
C |
6: 39,122,461 (GRCm39) |
D801G |
probably benign |
Het |
Marchf1 |
T |
C |
8: 66,871,641 (GRCm39) |
L139P |
probably damaging |
Het |
Metap1d |
T |
C |
2: 71,345,982 (GRCm39) |
V181A |
probably damaging |
Het |
Mfsd8 |
G |
A |
3: 40,789,628 (GRCm39) |
R140C |
probably damaging |
Het |
Mrps25 |
T |
C |
6: 92,152,745 (GRCm39) |
T92A |
probably benign |
Het |
Mucl3 |
T |
C |
17: 35,948,486 (GRCm39) |
H371R |
possibly damaging |
Het |
Ntng2 |
C |
A |
2: 29,138,050 (GRCm39) |
M1I |
probably null |
Het |
Or51b17 |
C |
T |
7: 103,542,256 (GRCm39) |
G229R |
probably benign |
Het |
Or51q1 |
A |
C |
7: 103,628,581 (GRCm39) |
M61L |
probably damaging |
Het |
Or8b57 |
T |
C |
9: 40,003,695 (GRCm39) |
K189R |
probably benign |
Het |
Pla2g12a |
A |
G |
3: 129,672,465 (GRCm39) |
D33G |
probably damaging |
Het |
Prlhr |
A |
G |
19: 60,456,284 (GRCm39) |
V94A |
possibly damaging |
Het |
Ralgapb |
T |
A |
2: 158,292,192 (GRCm39) |
S793T |
probably benign |
Het |
Rapgef6 |
T |
A |
11: 54,522,127 (GRCm39) |
L455* |
probably null |
Het |
Sbf2 |
T |
C |
7: 110,040,669 (GRCm39) |
H386R |
probably benign |
Het |
Sec23ip |
C |
A |
7: 128,365,749 (GRCm39) |
N539K |
probably damaging |
Het |
Shisa4 |
A |
G |
1: 135,300,907 (GRCm39) |
L121P |
probably damaging |
Het |
Slc28a2b |
C |
T |
2: 122,355,617 (GRCm39) |
T603I |
probably benign |
Het |
Stard9 |
T |
A |
2: 120,510,306 (GRCm39) |
F296I |
probably damaging |
Het |
Strn3 |
T |
C |
12: 51,707,955 (GRCm39) |
K147E |
probably damaging |
Het |
Taf5l |
T |
C |
8: 124,724,841 (GRCm39) |
N326S |
probably benign |
Het |
Tfb2m |
T |
A |
1: 179,369,914 (GRCm39) |
I170L |
probably benign |
Het |
Tfec |
T |
C |
6: 16,845,422 (GRCm39) |
N79S |
possibly damaging |
Het |
Tnn |
C |
T |
1: 159,946,053 (GRCm39) |
G922R |
probably damaging |
Het |
Tox3 |
T |
C |
8: 91,074,507 (GRCm39) |
Y24C |
probably damaging |
Het |
Vmn2r80 |
A |
G |
10: 78,984,707 (GRCm39) |
I20V |
probably benign |
Het |
Wdr97 |
T |
C |
15: 76,245,684 (GRCm39) |
V1307A |
|
Het |
|
Other mutations in Vmn2r6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01547:Vmn2r6
|
APN |
3 |
64,445,525 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01968:Vmn2r6
|
APN |
3 |
64,463,766 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02009:Vmn2r6
|
APN |
3 |
64,445,323 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02039:Vmn2r6
|
APN |
3 |
64,463,610 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02652:Vmn2r6
|
APN |
3 |
64,463,749 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02737:Vmn2r6
|
APN |
3 |
64,463,911 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02808:Vmn2r6
|
APN |
3 |
64,463,917 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03066:Vmn2r6
|
APN |
3 |
64,472,574 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03331:Vmn2r6
|
APN |
3 |
64,445,428 (GRCm39) |
missense |
probably damaging |
1.00 |
BB010:Vmn2r6
|
UTSW |
3 |
64,467,224 (GRCm39) |
missense |
probably benign |
0.02 |
BB020:Vmn2r6
|
UTSW |
3 |
64,467,224 (GRCm39) |
missense |
probably benign |
0.02 |
R0010:Vmn2r6
|
UTSW |
3 |
64,466,966 (GRCm39) |
nonsense |
probably null |
|
R0206:Vmn2r6
|
UTSW |
3 |
64,447,333 (GRCm39) |
missense |
probably benign |
|
R0206:Vmn2r6
|
UTSW |
3 |
64,447,333 (GRCm39) |
missense |
probably benign |
|
R0208:Vmn2r6
|
UTSW |
3 |
64,447,333 (GRCm39) |
missense |
probably benign |
|
R0427:Vmn2r6
|
UTSW |
3 |
64,467,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R0466:Vmn2r6
|
UTSW |
3 |
64,463,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R1018:Vmn2r6
|
UTSW |
3 |
64,464,261 (GRCm39) |
missense |
probably benign |
0.00 |
R1104:Vmn2r6
|
UTSW |
3 |
64,445,487 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1186:Vmn2r6
|
UTSW |
3 |
64,472,488 (GRCm39) |
missense |
probably benign |
0.01 |
R1245:Vmn2r6
|
UTSW |
3 |
64,464,211 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1295:Vmn2r6
|
UTSW |
3 |
64,445,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1473:Vmn2r6
|
UTSW |
3 |
64,445,579 (GRCm39) |
nonsense |
probably null |
|
R1498:Vmn2r6
|
UTSW |
3 |
64,463,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R1925:Vmn2r6
|
UTSW |
3 |
64,463,698 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2044:Vmn2r6
|
UTSW |
3 |
64,445,262 (GRCm39) |
missense |
probably damaging |
0.96 |
R2069:Vmn2r6
|
UTSW |
3 |
64,463,519 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2253:Vmn2r6
|
UTSW |
3 |
64,467,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R2261:Vmn2r6
|
UTSW |
3 |
64,464,090 (GRCm39) |
missense |
probably benign |
0.24 |
R2262:Vmn2r6
|
UTSW |
3 |
64,464,090 (GRCm39) |
missense |
probably benign |
0.24 |
R2350:Vmn2r6
|
UTSW |
3 |
64,463,773 (GRCm39) |
missense |
probably benign |
0.01 |
R2680:Vmn2r6
|
UTSW |
3 |
64,445,707 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2846:Vmn2r6
|
UTSW |
3 |
64,464,211 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2860:Vmn2r6
|
UTSW |
3 |
64,454,760 (GRCm39) |
missense |
probably benign |
0.00 |
R2861:Vmn2r6
|
UTSW |
3 |
64,454,760 (GRCm39) |
missense |
probably benign |
0.00 |
R3766:Vmn2r6
|
UTSW |
3 |
64,463,929 (GRCm39) |
missense |
probably benign |
0.19 |
R3870:Vmn2r6
|
UTSW |
3 |
64,464,042 (GRCm39) |
missense |
probably damaging |
0.96 |
R4018:Vmn2r6
|
UTSW |
3 |
64,463,893 (GRCm39) |
missense |
probably benign |
0.05 |
R4024:Vmn2r6
|
UTSW |
3 |
64,445,671 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4026:Vmn2r6
|
UTSW |
3 |
64,445,671 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4227:Vmn2r6
|
UTSW |
3 |
64,445,369 (GRCm39) |
missense |
probably damaging |
0.99 |
R4526:Vmn2r6
|
UTSW |
3 |
64,445,145 (GRCm39) |
missense |
probably benign |
0.32 |
R4570:Vmn2r6
|
UTSW |
3 |
64,467,068 (GRCm39) |
missense |
probably benign |
0.31 |
R4894:Vmn2r6
|
UTSW |
3 |
64,454,829 (GRCm39) |
missense |
probably benign |
|
R4934:Vmn2r6
|
UTSW |
3 |
64,463,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R5057:Vmn2r6
|
UTSW |
3 |
64,445,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R5059:Vmn2r6
|
UTSW |
3 |
64,445,044 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5148:Vmn2r6
|
UTSW |
3 |
64,464,015 (GRCm39) |
missense |
probably damaging |
0.99 |
R5155:Vmn2r6
|
UTSW |
3 |
64,445,935 (GRCm39) |
missense |
probably benign |
0.44 |
R5179:Vmn2r6
|
UTSW |
3 |
64,445,411 (GRCm39) |
missense |
probably benign |
0.00 |
R5256:Vmn2r6
|
UTSW |
3 |
64,464,263 (GRCm39) |
missense |
probably benign |
0.33 |
R5861:Vmn2r6
|
UTSW |
3 |
64,463,454 (GRCm39) |
missense |
probably benign |
0.00 |
R5950:Vmn2r6
|
UTSW |
3 |
64,472,652 (GRCm39) |
missense |
probably benign |
0.05 |
R6081:Vmn2r6
|
UTSW |
3 |
64,463,953 (GRCm39) |
missense |
probably benign |
0.25 |
R6173:Vmn2r6
|
UTSW |
3 |
64,467,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Vmn2r6
|
UTSW |
3 |
64,445,424 (GRCm39) |
missense |
probably benign |
0.04 |
R6240:Vmn2r6
|
UTSW |
3 |
64,464,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R6433:Vmn2r6
|
UTSW |
3 |
64,454,801 (GRCm39) |
nonsense |
probably null |
|
R6645:Vmn2r6
|
UTSW |
3 |
64,464,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R6791:Vmn2r6
|
UTSW |
3 |
64,445,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R7265:Vmn2r6
|
UTSW |
3 |
64,464,195 (GRCm39) |
missense |
probably benign |
0.00 |
R7503:Vmn2r6
|
UTSW |
3 |
64,447,372 (GRCm39) |
nonsense |
probably null |
|
R7562:Vmn2r6
|
UTSW |
3 |
64,463,941 (GRCm39) |
missense |
probably benign |
0.00 |
R7584:Vmn2r6
|
UTSW |
3 |
64,472,683 (GRCm39) |
missense |
probably benign |
0.07 |
R7611:Vmn2r6
|
UTSW |
3 |
64,472,563 (GRCm39) |
missense |
probably damaging |
0.98 |
R7759:Vmn2r6
|
UTSW |
3 |
64,463,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R7834:Vmn2r6
|
UTSW |
3 |
64,445,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R7933:Vmn2r6
|
UTSW |
3 |
64,467,224 (GRCm39) |
missense |
probably benign |
0.02 |
R7982:Vmn2r6
|
UTSW |
3 |
64,467,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R8024:Vmn2r6
|
UTSW |
3 |
64,467,245 (GRCm39) |
missense |
probably benign |
0.40 |
R8074:Vmn2r6
|
UTSW |
3 |
64,455,064 (GRCm39) |
intron |
probably benign |
|
R8169:Vmn2r6
|
UTSW |
3 |
64,447,310 (GRCm39) |
missense |
probably benign |
0.01 |
R8736:Vmn2r6
|
UTSW |
3 |
64,467,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Vmn2r6
|
UTSW |
3 |
64,463,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Vmn2r6
|
UTSW |
3 |
64,464,277 (GRCm39) |
missense |
probably benign |
0.12 |
R9206:Vmn2r6
|
UTSW |
3 |
64,467,032 (GRCm39) |
missense |
probably damaging |
0.97 |
R9295:Vmn2r6
|
UTSW |
3 |
64,463,484 (GRCm39) |
missense |
probably benign |
0.00 |
R9332:Vmn2r6
|
UTSW |
3 |
64,454,671 (GRCm39) |
missense |
probably benign |
0.01 |
R9616:Vmn2r6
|
UTSW |
3 |
64,445,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R9663:Vmn2r6
|
UTSW |
3 |
64,463,549 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9685:Vmn2r6
|
UTSW |
3 |
64,464,081 (GRCm39) |
missense |
probably benign |
0.19 |
X0020:Vmn2r6
|
UTSW |
3 |
64,445,871 (GRCm39) |
missense |
probably benign |
|
X0066:Vmn2r6
|
UTSW |
3 |
64,454,799 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Vmn2r6
|
UTSW |
3 |
64,463,746 (GRCm39) |
missense |
probably damaging |
0.98 |
|