Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
A |
G |
11: 119,909,594 (GRCm39) |
M114T |
probably benign |
Het |
Ablim3 |
A |
T |
18: 61,990,296 (GRCm39) |
|
probably null |
Het |
Adcy10 |
A |
G |
1: 165,340,709 (GRCm39) |
D238G |
probably benign |
Het |
Astn2 |
G |
T |
4: 65,500,023 (GRCm39) |
S955R |
possibly damaging |
Het |
Casc3 |
A |
G |
11: 98,712,297 (GRCm39) |
E112G |
probably damaging |
Het |
Cetn4 |
C |
T |
3: 37,364,094 (GRCm39) |
V39I |
probably benign |
Het |
Commd4 |
A |
G |
9: 57,064,090 (GRCm39) |
V37A |
possibly damaging |
Het |
Dyrk2 |
T |
C |
10: 118,696,643 (GRCm39) |
Q205R |
possibly damaging |
Het |
Gal3st4 |
A |
G |
5: 138,264,042 (GRCm39) |
V319A |
possibly damaging |
Het |
Inpp5d |
G |
A |
1: 87,645,788 (GRCm39) |
A1058T |
probably benign |
Het |
Lpin3 |
A |
G |
2: 160,746,936 (GRCm39) |
Y781C |
probably damaging |
Het |
Lrat |
C |
T |
3: 82,810,527 (GRCm39) |
V165M |
probably damaging |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Nlrp6 |
T |
C |
7: 140,502,103 (GRCm39) |
S142P |
probably benign |
Het |
Oas1a |
T |
C |
5: 121,035,269 (GRCm39) |
T349A |
probably benign |
Het |
Or52e8 |
A |
T |
7: 104,624,435 (GRCm39) |
F252L |
possibly damaging |
Het |
Or5m3b |
T |
C |
2: 85,872,295 (GRCm39) |
V212A |
probably benign |
Het |
Or5v1 |
A |
T |
17: 37,810,330 (GRCm39) |
I263F |
probably damaging |
Het |
Or8c20 |
T |
A |
9: 38,261,158 (GRCm39) |
S260T |
probably benign |
Het |
Pakap |
C |
A |
4: 57,637,876 (GRCm39) |
P18Q |
probably null |
Het |
Pcdha2 |
T |
C |
18: 37,072,915 (GRCm39) |
V182A |
probably benign |
Het |
Phactr3 |
A |
G |
2: 177,784,254 (GRCm39) |
D26G |
probably benign |
Het |
Phrf1 |
G |
A |
7: 140,820,850 (GRCm39) |
R159H |
probably damaging |
Het |
R3hdm4 |
C |
T |
10: 79,748,292 (GRCm39) |
E162K |
possibly damaging |
Het |
Rab3ip |
T |
C |
10: 116,754,753 (GRCm39) |
T268A |
probably benign |
Het |
Rapgef3 |
T |
C |
15: 97,656,742 (GRCm39) |
D299G |
probably damaging |
Het |
Rem1 |
A |
G |
2: 152,469,977 (GRCm39) |
|
probably null |
Het |
Slc28a2b |
A |
G |
2: 122,317,350 (GRCm39) |
N36S |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,293,473 (GRCm39) |
M1286T |
probably benign |
Het |
Thsd7a |
T |
C |
6: 12,748,799 (GRCm39) |
T52A |
probably benign |
Het |
Tmem135 |
A |
T |
7: 88,793,872 (GRCm39) |
F390Y |
probably damaging |
Het |
Trio |
T |
C |
15: 27,856,280 (GRCm39) |
D696G |
probably benign |
Het |
Ttll11 |
T |
C |
2: 35,793,135 (GRCm39) |
*191W |
probably null |
Het |
Ubr4 |
A |
G |
4: 139,135,083 (GRCm39) |
D805G |
probably damaging |
Het |
Usp9y |
A |
G |
Y: 1,336,467 (GRCm39) |
I1469T |
possibly damaging |
Het |
Vmn2r78 |
G |
T |
7: 86,569,330 (GRCm39) |
L74F |
possibly damaging |
Het |
Wdfy3 |
T |
C |
5: 102,044,425 (GRCm39) |
E1860G |
probably benign |
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 |
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 |
R6976:Vmn1r70
|
UTSW |
7 |
10,367,971 (GRCm39) |
missense |
probably benign |
0.02 |
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 |
|
|