Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam20 |
G |
A |
8: 41,249,671 (GRCm39) |
V594I |
possibly damaging |
Het |
Adgb |
A |
T |
10: 10,318,227 (GRCm39) |
|
probably null |
Het |
Adgrb3 |
A |
C |
1: 25,150,906 (GRCm39) |
L1109R |
probably damaging |
Het |
Angptl4 |
G |
A |
17: 33,996,008 (GRCm39) |
P323S |
possibly damaging |
Het |
Arhgap21 |
A |
T |
2: 20,864,717 (GRCm39) |
M1197K |
probably damaging |
Het |
Arhgef40 |
A |
G |
14: 52,239,742 (GRCm39) |
T1319A |
probably damaging |
Het |
C4bp |
A |
G |
1: 130,575,764 (GRCm39) |
|
probably null |
Het |
Cd200r1 |
T |
C |
16: 44,610,374 (GRCm39) |
S161P |
possibly damaging |
Het |
Ckap5 |
A |
G |
2: 91,445,495 (GRCm39) |
K1711E |
possibly damaging |
Het |
Cldn19 |
T |
C |
4: 119,114,094 (GRCm39) |
S79P |
possibly damaging |
Het |
Cplane1 |
T |
C |
15: 8,251,427 (GRCm39) |
S1900P |
probably benign |
Het |
Dnah17 |
T |
G |
11: 117,915,533 (GRCm39) |
N4334T |
probably damaging |
Het |
Dpm2 |
G |
A |
2: 32,462,412 (GRCm39) |
|
probably null |
Het |
Eef1a2 |
A |
T |
2: 180,794,626 (GRCm39) |
V191E |
probably damaging |
Het |
Gmds |
G |
A |
13: 32,411,248 (GRCm39) |
T62I |
probably damaging |
Het |
Hyal5 |
A |
T |
6: 24,876,630 (GRCm39) |
I168F |
probably damaging |
Het |
Idh3a |
T |
C |
9: 54,499,679 (GRCm39) |
V31A |
probably benign |
Het |
Inf2 |
C |
A |
12: 112,577,264 (GRCm39) |
A1036E |
unknown |
Het |
Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
Kidins220 |
T |
A |
12: 25,051,564 (GRCm39) |
|
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lrp1b |
A |
G |
2: 41,335,206 (GRCm39) |
C779R |
probably damaging |
Het |
Lrp2 |
A |
G |
2: 69,289,816 (GRCm39) |
|
probably null |
Het |
Lrp2 |
G |
A |
2: 69,379,391 (GRCm39) |
T107M |
probably damaging |
Het |
Lrpap1 |
T |
C |
5: 35,255,547 (GRCm39) |
E184G |
probably benign |
Het |
Mapre1 |
C |
T |
2: 153,588,201 (GRCm39) |
T8M |
possibly damaging |
Het |
Mms19 |
G |
A |
19: 41,954,695 (GRCm39) |
Q75* |
probably null |
Het |
Mtcl1 |
T |
C |
17: 66,649,949 (GRCm39) |
I1390V |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,411,289 (GRCm39) |
S1412G |
unknown |
Het |
Myh4 |
A |
T |
11: 67,148,009 (GRCm39) |
Q1686L |
probably benign |
Het |
Or1e25 |
A |
T |
11: 73,493,979 (GRCm39) |
D191V |
probably damaging |
Het |
Or9s13 |
A |
T |
1: 92,547,805 (GRCm39) |
D59V |
probably damaging |
Het |
Rcvrn |
A |
T |
11: 67,590,802 (GRCm39) |
I129F |
probably damaging |
Het |
Reg3b |
T |
A |
6: 78,348,216 (GRCm39) |
M10K |
possibly damaging |
Het |
Rimbp2 |
T |
A |
5: 128,850,529 (GRCm39) |
E918V |
probably damaging |
Het |
Rpl5 |
A |
G |
5: 108,051,667 (GRCm39) |
T154A |
probably benign |
Het |
Sall4 |
A |
C |
2: 168,598,162 (GRCm39) |
L195R |
probably damaging |
Het |
Sh3gl2 |
T |
C |
4: 85,297,618 (GRCm39) |
S199P |
possibly damaging |
Het |
Shank1 |
G |
T |
7: 43,994,416 (GRCm39) |
R859L |
unknown |
Het |
Thsd7b |
A |
G |
1: 130,117,919 (GRCm39) |
E1445G |
possibly damaging |
Het |
Tnfaip6 |
A |
G |
2: 51,942,339 (GRCm39) |
E216G |
probably benign |
Het |
Tram1 |
T |
C |
1: 13,639,827 (GRCm39) |
T307A |
probably benign |
Het |
Trpv5 |
A |
G |
6: 41,637,277 (GRCm39) |
V354A |
probably benign |
Het |
Tyro3 |
A |
G |
2: 119,643,774 (GRCm39) |
E745G |
probably damaging |
Het |
Vmn2r28 |
A |
T |
7: 5,491,357 (GRCm39) |
W297R |
probably damaging |
Het |
Vrk3 |
A |
T |
7: 44,412,460 (GRCm39) |
|
probably null |
Het |
Zfhx4 |
T |
C |
3: 5,465,845 (GRCm39) |
V2001A |
probably benign |
Het |
Zfp512b |
AG |
AGG |
2: 181,230,556 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Vmn1r68 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01892:Vmn1r68
|
APN |
7 |
10,261,334 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02051:Vmn1r68
|
APN |
7 |
10,261,948 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02112:Vmn1r68
|
APN |
7 |
10,261,787 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02619:Vmn1r68
|
APN |
7 |
10,261,603 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03033:Vmn1r68
|
APN |
7 |
10,262,074 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03184:Vmn1r68
|
APN |
7 |
10,261,799 (GRCm39) |
missense |
probably benign |
0.16 |
PIT4354001:Vmn1r68
|
UTSW |
7 |
10,261,958 (GRCm39) |
missense |
probably benign |
|
R0141:Vmn1r68
|
UTSW |
7 |
10,261,252 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0359:Vmn1r68
|
UTSW |
7 |
10,261,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R0634:Vmn1r68
|
UTSW |
7 |
10,261,162 (GRCm39) |
missense |
probably benign |
0.00 |
R1731:Vmn1r68
|
UTSW |
7 |
10,261,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R2021:Vmn1r68
|
UTSW |
7 |
10,261,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R2022:Vmn1r68
|
UTSW |
7 |
10,261,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R2243:Vmn1r68
|
UTSW |
7 |
10,262,089 (GRCm39) |
missense |
probably damaging |
0.98 |
R2262:Vmn1r68
|
UTSW |
7 |
10,261,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Vmn1r68
|
UTSW |
7 |
10,261,275 (GRCm39) |
missense |
probably benign |
0.23 |
R4843:Vmn1r68
|
UTSW |
7 |
10,261,904 (GRCm39) |
missense |
probably benign |
0.00 |
R5198:Vmn1r68
|
UTSW |
7 |
10,261,723 (GRCm39) |
missense |
probably benign |
0.00 |
R5835:Vmn1r68
|
UTSW |
7 |
10,261,747 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5906:Vmn1r68
|
UTSW |
7 |
10,261,550 (GRCm39) |
missense |
probably benign |
0.02 |
R6015:Vmn1r68
|
UTSW |
7 |
10,261,616 (GRCm39) |
missense |
probably benign |
0.31 |
R7073:Vmn1r68
|
UTSW |
7 |
10,261,778 (GRCm39) |
missense |
probably benign |
0.00 |
R7614:Vmn1r68
|
UTSW |
7 |
10,261,553 (GRCm39) |
missense |
probably benign |
0.05 |
R7699:Vmn1r68
|
UTSW |
7 |
10,261,559 (GRCm39) |
missense |
probably benign |
0.15 |
R7700:Vmn1r68
|
UTSW |
7 |
10,261,559 (GRCm39) |
missense |
probably benign |
0.15 |
R7912:Vmn1r68
|
UTSW |
7 |
10,261,237 (GRCm39) |
missense |
probably benign |
0.01 |
R8166:Vmn1r68
|
UTSW |
7 |
10,261,888 (GRCm39) |
missense |
probably benign |
0.10 |
R8426:Vmn1r68
|
UTSW |
7 |
10,261,382 (GRCm39) |
missense |
probably benign |
0.02 |
R9466:Vmn1r68
|
UTSW |
7 |
10,261,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R9466:Vmn1r68
|
UTSW |
7 |
10,261,317 (GRCm39) |
nonsense |
probably null |
|
|