Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss2 |
T |
A |
2: 155,397,929 (GRCm39) |
|
probably null |
Het |
Adamts4 |
G |
T |
1: 171,079,877 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
T |
A |
13: 81,669,116 (GRCm39) |
K2480M |
probably damaging |
Het |
Ankhd1 |
A |
C |
18: 36,781,307 (GRCm39) |
S2120R |
probably benign |
Het |
Ash1l |
T |
A |
3: 88,888,964 (GRCm39) |
V281E |
possibly damaging |
Het |
Bdh1 |
G |
A |
16: 31,256,847 (GRCm39) |
A35T |
probably benign |
Het |
Brpf3 |
A |
G |
17: 29,054,751 (GRCm39) |
M1098V |
probably damaging |
Het |
Cel |
G |
A |
2: 28,446,854 (GRCm39) |
S439F |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 118,162,378 (GRCm39) |
S64G |
probably benign |
Het |
Dpp7 |
T |
C |
2: 25,244,836 (GRCm39) |
|
probably null |
Het |
Fam83c |
T |
A |
2: 155,672,157 (GRCm39) |
Y426F |
possibly damaging |
Het |
Fasn |
A |
G |
11: 120,710,693 (GRCm39) |
I322T |
probably damaging |
Het |
Glod4 |
A |
G |
11: 76,134,406 (GRCm39) |
F22S |
probably damaging |
Het |
Gm3127 |
A |
G |
14: 15,432,190 (GRCm39) |
T231A |
possibly damaging |
Het |
Gm49383 |
A |
G |
12: 69,243,730 (GRCm39) |
S444P |
possibly damaging |
Het |
Gnaz |
T |
C |
10: 74,827,268 (GRCm39) |
S7P |
possibly damaging |
Het |
Grin2b |
C |
T |
6: 135,757,198 (GRCm39) |
S421N |
probably benign |
Het |
Grm1 |
T |
C |
10: 10,564,924 (GRCm39) |
D1128G |
probably benign |
Het |
Hoxb13 |
A |
G |
11: 96,087,044 (GRCm39) |
T284A |
probably benign |
Het |
Il9r |
G |
A |
11: 32,143,177 (GRCm39) |
Q260* |
probably null |
Het |
Lrrfip1 |
T |
A |
1: 91,042,737 (GRCm39) |
C381S |
probably benign |
Het |
Mitd1 |
A |
T |
1: 37,921,778 (GRCm39) |
D85E |
probably benign |
Het |
Muc4 |
G |
A |
16: 32,582,892 (GRCm39) |
D2556N |
possibly damaging |
Het |
Nlrc4 |
A |
G |
17: 74,752,934 (GRCm39) |
I483T |
probably damaging |
Het |
Or13e8 |
A |
G |
4: 43,697,170 (GRCm39) |
M1T |
probably null |
Het |
Or2ag17 |
A |
T |
7: 106,389,434 (GRCm39) |
M258K |
probably damaging |
Het |
Or8g4 |
A |
G |
9: 39,662,540 (GRCm39) |
N286S |
probably damaging |
Het |
Pcdhb7 |
C |
A |
18: 37,476,631 (GRCm39) |
A589E |
probably benign |
Het |
Pcdhgb5 |
G |
A |
18: 37,864,321 (GRCm39) |
E39K |
probably damaging |
Het |
Pja2 |
T |
C |
17: 64,615,954 (GRCm39) |
K314E |
probably damaging |
Het |
Plcb1 |
A |
G |
2: 135,104,159 (GRCm39) |
E276G |
possibly damaging |
Het |
Ppp2r5c |
A |
G |
12: 110,510,579 (GRCm39) |
E122G |
probably damaging |
Het |
Prrc2c |
A |
T |
1: 162,520,413 (GRCm39) |
N732K |
probably damaging |
Het |
Rb1cc1 |
T |
A |
1: 6,333,126 (GRCm39) |
D1348E |
probably benign |
Het |
Sh3rf1 |
G |
T |
8: 61,814,766 (GRCm39) |
E442* |
probably null |
Het |
Snapc1 |
A |
G |
12: 74,016,974 (GRCm39) |
D204G |
probably damaging |
Het |
Sry |
C |
T |
Y: 2,662,938 (GRCm39) |
D241N |
unknown |
Het |
Strn4 |
T |
A |
7: 16,564,279 (GRCm39) |
M303K |
probably benign |
Het |
Tas2r118 |
A |
G |
6: 23,969,470 (GRCm39) |
I197T |
probably benign |
Het |
Tnni3k |
A |
G |
3: 154,498,413 (GRCm39) |
Y809H |
probably benign |
Het |
Tnpo3 |
A |
T |
6: 29,572,594 (GRCm39) |
C419* |
probably null |
Het |
Trpm6 |
T |
C |
19: 18,760,527 (GRCm39) |
S143P |
probably benign |
Het |
Ttc23l |
A |
T |
15: 10,537,666 (GRCm39) |
C201* |
probably null |
Het |
Ubr4 |
A |
G |
4: 139,120,388 (GRCm39) |
N271S |
probably damaging |
Het |
Vmn2r27 |
C |
T |
6: 124,201,312 (GRCm39) |
W215* |
probably null |
Het |
Xirp1 |
A |
T |
9: 119,846,984 (GRCm39) |
M633K |
probably damaging |
Het |
Zfp174 |
T |
C |
16: 3,665,804 (GRCm39) |
I23T |
possibly damaging |
Het |
Zfp536 |
T |
A |
7: 37,179,828 (GRCm39) |
S926C |
probably damaging |
Het |
Zfp943 |
T |
C |
17: 22,209,922 (GRCm39) |
S65P |
possibly damaging |
Het |
|
Other mutations in Vmn1r70 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03092:Vmn1r70
|
APN |
7 |
10,368,186 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03250:Vmn1r70
|
APN |
7 |
10,368,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R0375:Vmn1r70
|
UTSW |
7 |
10,367,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R0482:Vmn1r70
|
UTSW |
7 |
10,368,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R0497:Vmn1r70
|
UTSW |
7 |
10,367,953 (GRCm39) |
missense |
probably benign |
0.19 |
R1964:Vmn1r70
|
UTSW |
7 |
10,367,737 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2067:Vmn1r70
|
UTSW |
7 |
10,368,264 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3807:Vmn1r70
|
UTSW |
7 |
10,367,715 (GRCm39) |
missense |
probably benign |
0.01 |
R4573:Vmn1r70
|
UTSW |
7 |
10,367,556 (GRCm39) |
splice site |
probably null |
|
R5070:Vmn1r70
|
UTSW |
7 |
10,368,325 (GRCm39) |
missense |
probably benign |
0.04 |
R5442:Vmn1r70
|
UTSW |
7 |
10,367,877 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5558:Vmn1r70
|
UTSW |
7 |
10,368,402 (GRCm39) |
missense |
probably benign |
0.01 |
R6036:Vmn1r70
|
UTSW |
7 |
10,367,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R6036:Vmn1r70
|
UTSW |
7 |
10,367,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R6189:Vmn1r70
|
UTSW |
7 |
10,367,598 (GRCm39) |
missense |
probably benign |
0.04 |
R7571:Vmn1r70
|
UTSW |
7 |
10,367,871 (GRCm39) |
missense |
probably benign |
0.00 |
R9236:Vmn1r70
|
UTSW |
7 |
10,368,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R9568:Vmn1r70
|
UTSW |
7 |
10,368,292 (GRCm39) |
missense |
probably benign |
0.03 |
R9673:Vmn1r70
|
UTSW |
7 |
10,368,364 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Vmn1r70
|
UTSW |
7 |
10,367,517 (GRCm39) |
missense |
probably benign |
|
|