Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,353,834 (GRCm39) |
T3719A |
probably damaging |
Het |
Acaca |
A |
G |
11: 84,151,457 (GRCm39) |
K785R |
probably damaging |
Het |
Acsm3 |
G |
A |
7: 119,377,677 (GRCm39) |
V401M |
probably damaging |
Het |
Aff4 |
G |
T |
11: 53,306,296 (GRCm39) |
R1146L |
probably damaging |
Het |
Alms1 |
C |
A |
6: 85,673,683 (GRCm39) |
P3562T |
probably damaging |
Het |
Arsj |
A |
G |
3: 126,232,463 (GRCm39) |
E403G |
probably benign |
Het |
Baiap2l1 |
C |
T |
5: 144,212,723 (GRCm39) |
V431I |
probably benign |
Het |
Cecr2 |
T |
A |
6: 120,735,560 (GRCm39) |
M904K |
probably benign |
Het |
Cenpe |
A |
T |
3: 134,943,300 (GRCm39) |
T775S |
probably benign |
Het |
Dennd1b |
G |
A |
1: 138,950,848 (GRCm39) |
E30K |
possibly damaging |
Het |
Dnah5 |
A |
G |
15: 28,326,815 (GRCm39) |
D2008G |
probably damaging |
Het |
Dnm2 |
T |
C |
9: 21,392,672 (GRCm39) |
V460A |
probably damaging |
Het |
Ell2 |
G |
T |
13: 75,910,110 (GRCm39) |
L285F |
probably benign |
Het |
Erg |
A |
G |
16: 95,162,141 (GRCm39) |
S322P |
probably damaging |
Het |
Extl3 |
A |
G |
14: 65,314,529 (GRCm39) |
F218L |
probably benign |
Het |
Fzd9 |
T |
C |
5: 135,279,420 (GRCm39) |
E155G |
probably damaging |
Het |
Ghr |
A |
G |
15: 3,362,837 (GRCm39) |
W212R |
probably damaging |
Het |
Gulp1 |
A |
G |
1: 44,783,708 (GRCm39) |
|
probably benign |
Het |
Hdgfl2 |
C |
T |
17: 56,404,281 (GRCm39) |
R332C |
possibly damaging |
Het |
Lratd1 |
A |
T |
12: 14,199,929 (GRCm39) |
I266N |
probably damaging |
Het |
Nsd2 |
T |
C |
5: 34,018,530 (GRCm39) |
|
probably benign |
Het |
Or4c12 |
A |
G |
2: 89,774,282 (GRCm39) |
F59S |
probably damaging |
Het |
Or5a3 |
T |
C |
19: 12,400,165 (GRCm39) |
I164T |
possibly damaging |
Het |
Or5b121 |
C |
T |
19: 13,507,616 (GRCm39) |
T237I |
probably benign |
Het |
Phf11b |
A |
C |
14: 59,578,740 (GRCm39) |
S9A |
probably benign |
Het |
Psd4 |
T |
C |
2: 24,295,407 (GRCm39) |
S854P |
probably damaging |
Het |
Reln |
C |
T |
5: 22,174,315 (GRCm39) |
D1963N |
probably damaging |
Het |
Rpe65 |
T |
A |
3: 159,306,042 (GRCm39) |
|
probably benign |
Het |
Sdccag8 |
T |
C |
1: 176,672,811 (GRCm39) |
S235P |
probably damaging |
Het |
Sgip1 |
G |
T |
4: 102,786,110 (GRCm39) |
|
probably null |
Het |
Skint5 |
G |
A |
4: 113,800,019 (GRCm39) |
P36L |
probably damaging |
Het |
Slc26a3 |
G |
T |
12: 31,502,490 (GRCm39) |
|
probably benign |
Het |
Snx13 |
T |
A |
12: 35,174,479 (GRCm39) |
C669* |
probably null |
Het |
Svil |
A |
T |
18: 5,062,385 (GRCm39) |
T902S |
probably damaging |
Het |
Syne2 |
T |
C |
12: 76,088,149 (GRCm39) |
S4989P |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,640,283 (GRCm39) |
T13775M |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,165,351 (GRCm39) |
|
probably benign |
Het |
Ush1c |
C |
T |
7: 45,858,380 (GRCm39) |
R636H |
possibly damaging |
Het |
Usp17lc |
A |
T |
7: 103,067,651 (GRCm39) |
R315S |
probably benign |
Het |
Wsb2 |
T |
G |
5: 117,509,229 (GRCm39) |
I170S |
probably damaging |
Het |
Zfp800 |
G |
A |
6: 28,242,983 (GRCm39) |
L661F |
possibly damaging |
Het |
|
Other mutations in Vmn1r236 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01953:Vmn1r236
|
APN |
17 |
21,507,473 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02252:Vmn1r236
|
APN |
17 |
21,507,101 (GRCm39) |
missense |
probably benign |
0.41 |
IGL03030:Vmn1r236
|
APN |
17 |
21,507,108 (GRCm39) |
nonsense |
probably null |
|
IGL03117:Vmn1r236
|
APN |
17 |
21,507,508 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03342:Vmn1r236
|
APN |
17 |
21,507,236 (GRCm39) |
missense |
probably benign |
0.37 |
R0569:Vmn1r236
|
UTSW |
17 |
21,507,172 (GRCm39) |
missense |
probably benign |
0.05 |
R1747:Vmn1r236
|
UTSW |
17 |
21,507,179 (GRCm39) |
missense |
probably benign |
0.31 |
R1872:Vmn1r236
|
UTSW |
17 |
21,507,673 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1876:Vmn1r236
|
UTSW |
17 |
21,506,900 (GRCm39) |
missense |
probably benign |
|
R3692:Vmn1r236
|
UTSW |
17 |
21,507,068 (GRCm39) |
missense |
probably benign |
0.09 |
R4822:Vmn1r236
|
UTSW |
17 |
21,507,202 (GRCm39) |
missense |
probably damaging |
0.99 |
R6918:Vmn1r236
|
UTSW |
17 |
21,507,878 (GRCm39) |
missense |
probably benign |
0.37 |
R7089:Vmn1r236
|
UTSW |
17 |
21,507,204 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7895:Vmn1r236
|
UTSW |
17 |
21,507,728 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7965:Vmn1r236
|
UTSW |
17 |
21,507,696 (GRCm39) |
nonsense |
probably null |
|
R8906:Vmn1r236
|
UTSW |
17 |
21,507,356 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9300:Vmn1r236
|
UTSW |
17 |
21,506,945 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9410:Vmn1r236
|
UTSW |
17 |
21,507,756 (GRCm39) |
nonsense |
probably null |
|
R9535:Vmn1r236
|
UTSW |
17 |
21,507,418 (GRCm39) |
missense |
probably benign |
0.01 |
R9617:Vmn1r236
|
UTSW |
17 |
21,507,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Vmn1r236
|
UTSW |
17 |
21,507,043 (GRCm39) |
missense |
probably benign |
|
R9679:Vmn1r236
|
UTSW |
17 |
21,507,286 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9797:Vmn1r236
|
UTSW |
17 |
21,506,969 (GRCm39) |
missense |
probably benign |
0.00 |
|