Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5530400C23Rik |
A |
T |
6: 133,271,445 (GRCm39) |
D163V |
probably benign |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Ankrd17 |
G |
A |
5: 90,413,404 (GRCm39) |
A1170V |
probably damaging |
Het |
Ano1 |
A |
C |
7: 144,202,337 (GRCm39) |
|
probably benign |
Het |
Atl2 |
T |
C |
17: 80,168,890 (GRCm39) |
N37D |
probably damaging |
Het |
C2cd5 |
T |
C |
6: 143,028,969 (GRCm39) |
Y90C |
probably damaging |
Het |
Carm1 |
A |
G |
9: 21,498,655 (GRCm39) |
N499S |
probably benign |
Het |
Ccdc47 |
G |
A |
11: 106,099,039 (GRCm39) |
|
probably null |
Het |
Cd300lf |
G |
T |
11: 115,007,940 (GRCm39) |
L251M |
probably damaging |
Het |
Cfap74 |
A |
G |
4: 155,522,623 (GRCm39) |
S670G |
probably damaging |
Het |
Clec4a1 |
A |
G |
6: 122,909,196 (GRCm39) |
D188G |
probably damaging |
Het |
Col4a1 |
T |
C |
8: 11,295,760 (GRCm39) |
|
probably benign |
Het |
Csn2 |
T |
A |
5: 87,842,508 (GRCm39) |
H165L |
probably benign |
Het |
Cstdc1 |
G |
T |
2: 148,625,298 (GRCm39) |
L77F |
probably damaging |
Het |
Dlx3 |
T |
C |
11: 95,011,326 (GRCm39) |
V60A |
possibly damaging |
Het |
Elp1 |
A |
C |
4: 56,778,969 (GRCm39) |
I616S |
probably damaging |
Het |
Fam221a |
A |
G |
6: 49,353,049 (GRCm39) |
H21R |
probably damaging |
Het |
Foxj3 |
T |
A |
4: 119,477,340 (GRCm39) |
H349Q |
unknown |
Het |
Gm37240 |
G |
A |
3: 84,423,000 (GRCm39) |
T123I |
probably damaging |
Het |
Gpc1 |
A |
T |
1: 92,782,615 (GRCm39) |
T121S |
probably benign |
Het |
Insyn2b |
G |
A |
11: 34,352,788 (GRCm39) |
E277K |
probably damaging |
Het |
Itga2b |
A |
G |
11: 102,351,961 (GRCm39) |
V512A |
probably damaging |
Het |
Itgae |
A |
G |
11: 73,002,675 (GRCm39) |
Y144C |
probably damaging |
Het |
Izumo3 |
A |
T |
4: 92,035,037 (GRCm39) |
I60K |
possibly damaging |
Het |
Kif9 |
G |
A |
9: 110,319,012 (GRCm39) |
V159M |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 41,265,914 (GRCm39) |
D229G |
probably damaging |
Het |
Nkpd1 |
G |
A |
7: 19,257,193 (GRCm39) |
G324D |
probably damaging |
Het |
Nrp2 |
T |
A |
1: 62,808,221 (GRCm39) |
Y617N |
probably benign |
Het |
Ocm |
T |
C |
5: 143,960,674 (GRCm39) |
D91G |
probably damaging |
Het |
Or4l15 |
A |
G |
14: 50,197,986 (GRCm39) |
L181P |
possibly damaging |
Het |
Or52ad1 |
A |
G |
7: 102,995,454 (GRCm39) |
V227A |
probably damaging |
Het |
Or52n2b |
A |
G |
7: 104,565,834 (GRCm39) |
I223T |
probably damaging |
Het |
Or6c70 |
T |
C |
10: 129,710,422 (GRCm39) |
E68G |
probably damaging |
Het |
Pex5l |
G |
A |
3: 33,047,065 (GRCm39) |
A295V |
probably damaging |
Het |
Plekhg4 |
T |
A |
8: 106,108,030 (GRCm39) |
V1029E |
possibly damaging |
Het |
Pou2f2 |
G |
A |
7: 24,792,320 (GRCm39) |
P512S |
probably benign |
Het |
Prpf8 |
G |
A |
11: 75,397,236 (GRCm39) |
R2023Q |
possibly damaging |
Het |
Ptprd |
A |
T |
4: 76,047,050 (GRCm39) |
S399R |
probably damaging |
Het |
Qrich2 |
T |
C |
11: 116,337,976 (GRCm39) |
Y1889C |
probably damaging |
Het |
R3hdm4 |
C |
T |
10: 79,748,292 (GRCm39) |
E162K |
possibly damaging |
Het |
Ranbp6 |
G |
T |
19: 29,789,128 (GRCm39) |
T408K |
probably benign |
Het |
Scn7a |
G |
A |
2: 66,530,342 (GRCm39) |
R668C |
probably damaging |
Het |
Sertad4 |
T |
C |
1: 192,529,414 (GRCm39) |
N134S |
probably damaging |
Het |
Spg11 |
G |
T |
2: 121,891,481 (GRCm39) |
N1963K |
probably damaging |
Het |
Svil |
C |
T |
18: 5,057,345 (GRCm39) |
P598S |
probably damaging |
Het |
Top2a |
T |
C |
11: 98,909,738 (GRCm39) |
N120S |
probably damaging |
Het |
Trappc9 |
C |
T |
15: 72,930,066 (GRCm39) |
E97K |
possibly damaging |
Het |
Vmn2r99 |
G |
T |
17: 19,599,601 (GRCm39) |
M428I |
probably benign |
Het |
Zfp62 |
A |
T |
11: 49,107,439 (GRCm39) |
H510L |
probably damaging |
Het |
|
Other mutations in Vmn1r91 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01875:Vmn1r91
|
APN |
7 |
19,835,859 (GRCm39) |
nonsense |
probably null |
|
IGL02125:Vmn1r91
|
APN |
7 |
19,835,429 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02263:Vmn1r91
|
APN |
7 |
19,835,768 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02338:Vmn1r91
|
APN |
7 |
19,835,671 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02708:Vmn1r91
|
APN |
7 |
19,835,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1880:Vmn1r91
|
UTSW |
7 |
19,835,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R2679:Vmn1r91
|
UTSW |
7 |
19,835,983 (GRCm39) |
missense |
probably damaging |
0.97 |
R4730:Vmn1r91
|
UTSW |
7 |
19,835,695 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5633:Vmn1r91
|
UTSW |
7 |
19,835,870 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5979:Vmn1r91
|
UTSW |
7 |
19,835,990 (GRCm39) |
missense |
probably benign |
0.00 |
R6151:Vmn1r91
|
UTSW |
7 |
19,835,360 (GRCm39) |
missense |
probably benign |
|
R6177:Vmn1r91
|
UTSW |
7 |
19,835,404 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7397:Vmn1r91
|
UTSW |
7 |
19,835,695 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7589:Vmn1r91
|
UTSW |
7 |
19,835,802 (GRCm39) |
missense |
probably benign |
0.07 |
R7872:Vmn1r91
|
UTSW |
7 |
19,835,839 (GRCm39) |
missense |
probably benign |
0.26 |
R7886:Vmn1r91
|
UTSW |
7 |
19,835,490 (GRCm39) |
missense |
probably benign |
|
R7903:Vmn1r91
|
UTSW |
7 |
19,835,135 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7953:Vmn1r91
|
UTSW |
7 |
19,835,218 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8043:Vmn1r91
|
UTSW |
7 |
19,835,218 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8202:Vmn1r91
|
UTSW |
7 |
19,835,749 (GRCm39) |
missense |
probably damaging |
1.00 |
|