Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc8 |
T |
C |
7: 45,772,364 (GRCm39) |
Y805C |
probably damaging |
Het |
Aoc1l3 |
T |
A |
6: 48,964,512 (GRCm39) |
D173E |
probably benign |
Het |
Cabp7 |
T |
A |
11: 4,688,886 (GRCm39) |
I195F |
probably damaging |
Het |
Camsap1 |
T |
C |
2: 25,835,201 (GRCm39) |
N317S |
probably damaging |
Het |
Ccdc127 |
T |
G |
13: 74,500,994 (GRCm39) |
L4V |
probably damaging |
Het |
Ccdc7a |
T |
C |
8: 129,774,100 (GRCm39) |
E145G |
probably damaging |
Het |
Cdh10 |
T |
A |
15: 19,013,287 (GRCm39) |
V629D |
probably damaging |
Het |
Cdh23 |
A |
C |
10: 60,214,530 (GRCm39) |
L1497R |
probably damaging |
Het |
Chsy3 |
A |
G |
18: 59,542,875 (GRCm39) |
K671R |
probably benign |
Het |
Clca4b |
T |
C |
3: 144,621,367 (GRCm39) |
Y569C |
probably damaging |
Het |
Cnga1 |
T |
C |
5: 72,786,696 (GRCm39) |
|
probably benign |
Het |
Cyp51 |
T |
A |
5: 4,150,188 (GRCm39) |
E178D |
probably damaging |
Het |
Defa30 |
T |
A |
8: 21,625,471 (GRCm39) |
N78K |
probably benign |
Het |
Disp1 |
C |
A |
1: 182,869,030 (GRCm39) |
R1130L |
probably damaging |
Het |
Dnah14 |
G |
T |
1: 181,450,568 (GRCm39) |
C727F |
probably benign |
Het |
Egf |
A |
T |
3: 129,548,607 (GRCm39) |
W3R |
unknown |
Het |
Egfem1 |
G |
A |
3: 29,136,364 (GRCm39) |
|
probably null |
Het |
Epb41l1 |
G |
T |
2: 156,368,812 (GRCm39) |
V682L |
possibly damaging |
Het |
Etv1 |
A |
G |
12: 38,834,369 (GRCm39) |
|
probably null |
Het |
Faap100 |
A |
G |
11: 120,268,200 (GRCm39) |
F191S |
possibly damaging |
Het |
Fmo1 |
T |
A |
1: 162,667,263 (GRCm39) |
D184V |
possibly damaging |
Het |
Ghrl |
A |
G |
6: 113,696,344 (GRCm39) |
L16P |
probably damaging |
Het |
Gria4 |
T |
A |
9: 4,420,278 (GRCm39) |
L861F |
probably damaging |
Het |
Gsr |
T |
A |
8: 34,185,090 (GRCm39) |
M428K |
probably damaging |
Het |
Hspa5 |
C |
T |
2: 34,663,204 (GRCm39) |
P127L |
probably damaging |
Het |
Kbtbd12 |
A |
G |
6: 88,595,497 (GRCm39) |
M111T |
possibly damaging |
Het |
Krtap21-1 |
G |
T |
16: 89,200,623 (GRCm39) |
Y6* |
probably null |
Het |
Lin9 |
A |
G |
1: 180,494,935 (GRCm39) |
D219G |
probably damaging |
Het |
Lrrc38 |
A |
G |
4: 143,076,739 (GRCm39) |
M1V |
probably null |
Het |
Macc1 |
T |
G |
12: 119,410,773 (GRCm39) |
F514V |
probably benign |
Het |
Madcam1 |
C |
T |
10: 79,504,139 (GRCm39) |
R242C |
probably benign |
Het |
Mfhas1 |
T |
C |
8: 36,131,944 (GRCm39) |
S1037P |
probably benign |
Het |
Micall2 |
C |
T |
5: 139,694,699 (GRCm39) |
|
probably benign |
Het |
Mtr |
C |
A |
13: 12,205,095 (GRCm39) |
A1122S |
possibly damaging |
Het |
Muc6 |
T |
A |
7: 141,226,456 (GRCm39) |
|
probably benign |
Het |
Myh15 |
T |
A |
16: 48,929,662 (GRCm39) |
C529* |
probably null |
Het |
Napsa |
T |
C |
7: 44,234,509 (GRCm39) |
V247A |
probably damaging |
Het |
Nr2c2 |
A |
G |
6: 92,135,338 (GRCm39) |
T309A |
probably damaging |
Het |
Or1e26 |
A |
T |
11: 73,480,558 (GRCm39) |
I2K |
probably benign |
Het |
Or1q1 |
T |
A |
2: 36,887,173 (GRCm39) |
V117E |
probably benign |
Het |
Or2n1b |
A |
T |
17: 38,459,691 (GRCm39) |
M71L |
probably benign |
Het |
Osgepl1 |
A |
T |
1: 53,360,710 (GRCm39) |
I384F |
possibly damaging |
Het |
Otud4 |
C |
T |
8: 80,377,671 (GRCm39) |
L111F |
possibly damaging |
Het |
Pds5b |
A |
G |
5: 150,673,385 (GRCm39) |
Y481C |
probably damaging |
Het |
Pdzrn4 |
T |
A |
15: 92,668,303 (GRCm39) |
Y818* |
probably null |
Het |
Pin1rt1 |
T |
C |
2: 104,544,767 (GRCm39) |
S122G |
probably benign |
Het |
Pkdcc |
A |
T |
17: 83,531,687 (GRCm39) |
Y487F |
probably damaging |
Het |
Plxna4 |
C |
T |
6: 32,493,440 (GRCm39) |
C392Y |
probably damaging |
Het |
Psd4 |
T |
G |
2: 24,284,985 (GRCm39) |
M283R |
probably benign |
Het |
Ralgds |
G |
T |
2: 28,430,741 (GRCm39) |
G68W |
probably damaging |
Het |
Rmdn2 |
T |
A |
17: 79,928,808 (GRCm39) |
I20N |
probably damaging |
Het |
Sestd1 |
A |
G |
2: 77,022,910 (GRCm39) |
V486A |
probably benign |
Het |
Skic8 |
T |
A |
9: 54,626,539 (GRCm39) |
D275V |
probably damaging |
Het |
Spmap2 |
G |
T |
10: 79,422,796 (GRCm39) |
D35E |
probably benign |
Het |
Tango6 |
A |
G |
8: 107,533,748 (GRCm39) |
H958R |
possibly damaging |
Het |
Taok3 |
C |
T |
5: 117,411,771 (GRCm39) |
R857C |
probably damaging |
Het |
Tasor |
A |
T |
14: 27,194,392 (GRCm39) |
L1197F |
probably damaging |
Het |
Trio |
T |
C |
15: 27,832,137 (GRCm39) |
E1245G |
probably damaging |
Het |
Usp19 |
C |
T |
9: 108,374,334 (GRCm39) |
H763Y |
possibly damaging |
Het |
Vmn1r185 |
A |
G |
7: 26,310,651 (GRCm39) |
S285P |
probably damaging |
Het |
Vwa3b |
G |
A |
1: 37,212,959 (GRCm39) |
E152K |
probably benign |
Het |
Xrcc5 |
G |
A |
1: 72,433,875 (GRCm39) |
M731I |
probably benign |
Het |
Zfp619 |
G |
A |
7: 39,186,787 (GRCm39) |
S939N |
possibly damaging |
Het |
Zfp874a |
C |
A |
13: 67,590,418 (GRCm39) |
C422F |
probably damaging |
Het |
Zfp948 |
A |
G |
17: 21,808,719 (GRCm39) |
D637G |
possibly damaging |
Het |
|
Other mutations in Vmn1r45 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00264:Vmn1r45
|
APN |
6 |
89,910,646 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02010:Vmn1r45
|
APN |
6 |
89,910,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02124:Vmn1r45
|
APN |
6 |
89,910,035 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02413:Vmn1r45
|
APN |
6 |
89,910,503 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0123:Vmn1r45
|
UTSW |
6 |
89,910,492 (GRCm39) |
nonsense |
probably null |
|
R0225:Vmn1r45
|
UTSW |
6 |
89,910,492 (GRCm39) |
nonsense |
probably null |
|
R1513:Vmn1r45
|
UTSW |
6 |
89,910,058 (GRCm39) |
missense |
probably damaging |
0.97 |
R2154:Vmn1r45
|
UTSW |
6 |
89,910,965 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3082:Vmn1r45
|
UTSW |
6 |
89,910,724 (GRCm39) |
missense |
probably benign |
0.03 |
R3781:Vmn1r45
|
UTSW |
6 |
89,910,799 (GRCm39) |
missense |
probably benign |
|
R4982:Vmn1r45
|
UTSW |
6 |
89,910,847 (GRCm39) |
missense |
probably damaging |
0.99 |
R5086:Vmn1r45
|
UTSW |
6 |
89,910,082 (GRCm39) |
missense |
probably benign |
0.06 |
R5327:Vmn1r45
|
UTSW |
6 |
89,910,123 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5470:Vmn1r45
|
UTSW |
6 |
89,910,698 (GRCm39) |
missense |
probably benign |
0.04 |
R6681:Vmn1r45
|
UTSW |
6 |
89,910,985 (GRCm39) |
start gained |
probably benign |
|
R7050:Vmn1r45
|
UTSW |
6 |
89,910,703 (GRCm39) |
missense |
probably damaging |
0.97 |
R7171:Vmn1r45
|
UTSW |
6 |
89,910,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R7236:Vmn1r45
|
UTSW |
6 |
89,910,133 (GRCm39) |
missense |
probably benign |
0.15 |
R7401:Vmn1r45
|
UTSW |
6 |
89,910,416 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7417:Vmn1r45
|
UTSW |
6 |
89,910,035 (GRCm39) |
missense |
probably benign |
0.03 |
R8068:Vmn1r45
|
UTSW |
6 |
89,910,261 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8223:Vmn1r45
|
UTSW |
6 |
89,910,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R8942:Vmn1r45
|
UTSW |
6 |
89,910,876 (GRCm39) |
missense |
probably benign |
0.00 |
RF019:Vmn1r45
|
UTSW |
6 |
89,910,091 (GRCm39) |
missense |
probably damaging |
0.99 |
X0026:Vmn1r45
|
UTSW |
6 |
89,910,724 (GRCm39) |
missense |
probably benign |
0.00 |
|