Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam17 |
A |
G |
12: 21,382,089 (GRCm39) |
C591R |
probably damaging |
Het |
Bace2 |
G |
A |
16: 97,223,180 (GRCm39) |
R368Q |
probably damaging |
Het |
Calm5 |
C |
A |
13: 3,904,402 (GRCm39) |
S32* |
probably null |
Het |
Ccdc198 |
T |
A |
14: 49,471,955 (GRCm39) |
M152L |
probably benign |
Het |
Cln3 |
G |
T |
7: 126,171,730 (GRCm39) |
S346R |
probably damaging |
Het |
G6pd2 |
G |
A |
5: 61,967,686 (GRCm39) |
R487H |
possibly damaging |
Het |
Glipr2 |
A |
T |
4: 43,977,600 (GRCm39) |
N77Y |
probably damaging |
Het |
Huwe1 |
A |
T |
X: 150,646,955 (GRCm39) |
I682F |
probably damaging |
Het |
Kbtbd2 |
A |
G |
6: 56,766,264 (GRCm39) |
V37A |
probably benign |
Het |
Kdm7a |
C |
T |
6: 39,129,757 (GRCm39) |
R473Q |
probably damaging |
Het |
Lrrc71 |
T |
A |
3: 87,652,715 (GRCm39) |
|
probably benign |
Het |
Mcm3 |
G |
T |
1: 20,879,869 (GRCm39) |
R543S |
probably benign |
Het |
Mgat4a |
T |
C |
1: 37,505,660 (GRCm39) |
D43G |
probably damaging |
Het |
Mphosph8 |
T |
C |
14: 56,928,457 (GRCm39) |
Y703H |
probably benign |
Het |
Ncf2 |
T |
C |
1: 152,683,976 (GRCm39) |
|
probably benign |
Het |
Nek6 |
T |
G |
2: 38,475,305 (GRCm39) |
V282G |
probably damaging |
Het |
Nhlrc1 |
T |
C |
13: 47,167,666 (GRCm39) |
D197G |
possibly damaging |
Het |
Nup93 |
G |
T |
8: 95,034,520 (GRCm39) |
V612F |
probably damaging |
Het |
Or5be3 |
C |
T |
2: 86,864,028 (GRCm39) |
C179Y |
probably damaging |
Het |
Or9i14 |
A |
G |
19: 13,792,646 (GRCm39) |
F103L |
probably benign |
Het |
Pafah1b2 |
T |
C |
9: 45,887,404 (GRCm39) |
K36E |
probably damaging |
Het |
Paqr9 |
A |
G |
9: 95,442,997 (GRCm39) |
E329G |
probably benign |
Het |
Pclo |
A |
G |
5: 14,571,383 (GRCm39) |
Q256R |
probably damaging |
Het |
Pctp |
A |
T |
11: 89,879,578 (GRCm39) |
D94E |
probably benign |
Het |
Pde8a |
T |
A |
7: 80,958,568 (GRCm39) |
Y315* |
probably null |
Het |
Pex14 |
A |
T |
4: 149,126,225 (GRCm39) |
V41D |
probably damaging |
Het |
Ptgir |
A |
G |
7: 16,640,794 (GRCm39) |
M29V |
possibly damaging |
Het |
Rasal2 |
T |
C |
1: 157,003,561 (GRCm39) |
K366R |
probably damaging |
Het |
Rprd1a |
A |
C |
18: 24,640,160 (GRCm39) |
|
probably null |
Het |
Senp8 |
A |
C |
9: 59,657,546 (GRCm39) |
M1R |
probably null |
Het |
Slc49a4 |
T |
C |
16: 35,518,312 (GRCm39) |
Y467C |
probably damaging |
Het |
Slco1b2 |
A |
G |
6: 141,616,893 (GRCm39) |
T409A |
probably benign |
Het |
Strc |
T |
C |
2: 121,196,286 (GRCm39) |
T1581A |
probably benign |
Het |
Tmem117 |
T |
C |
15: 94,536,035 (GRCm39) |
I23T |
possibly damaging |
Het |
Ttc13 |
A |
G |
8: 125,402,016 (GRCm39) |
L657P |
probably damaging |
Het |
Ube4b |
A |
G |
4: 149,443,622 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn1r125 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00503:Vmn1r125
|
APN |
7 |
21,006,106 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
PIT4466001:Vmn1r125
|
UTSW |
7 |
21,006,818 (GRCm39) |
missense |
probably benign |
0.00 |
R1921:Vmn1r125
|
UTSW |
7 |
21,006,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R4661:Vmn1r125
|
UTSW |
7 |
21,006,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R6058:Vmn1r125
|
UTSW |
7 |
21,006,144 (GRCm39) |
frame shift |
probably null |
|
R6083:Vmn1r125
|
UTSW |
7 |
21,006,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R6172:Vmn1r125
|
UTSW |
7 |
21,006,275 (GRCm39) |
missense |
probably benign |
0.25 |
R6674:Vmn1r125
|
UTSW |
7 |
21,006,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R7135:Vmn1r125
|
UTSW |
7 |
21,006,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R7257:Vmn1r125
|
UTSW |
7 |
21,006,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R8197:Vmn1r125
|
UTSW |
7 |
21,006,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R9007:Vmn1r125
|
UTSW |
7 |
21,006,503 (GRCm39) |
missense |
probably benign |
0.17 |
R9447:Vmn1r125
|
UTSW |
7 |
21,006,627 (GRCm39) |
missense |
probably benign |
0.05 |
R9477:Vmn1r125
|
UTSW |
7 |
21,006,261 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9646:Vmn1r125
|
UTSW |
7 |
21,006,261 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1177:Vmn1r125
|
UTSW |
7 |
21,006,676 (GRCm39) |
missense |
possibly damaging |
0.89 |
|