Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
A |
14: 32,383,559 (GRCm39) |
Q802L |
probably benign |
Het |
Atp8b4 |
C |
A |
2: 126,217,677 (GRCm39) |
W613L |
probably damaging |
Het |
AW554918 |
C |
A |
18: 25,533,129 (GRCm39) |
T261K |
possibly damaging |
Het |
Cttnbp2 |
A |
G |
6: 18,389,204 (GRCm39) |
V1178A |
probably benign |
Het |
Ddx18 |
T |
C |
1: 121,489,878 (GRCm39) |
N177S |
probably benign |
Het |
Dhx29 |
A |
G |
13: 113,083,807 (GRCm39) |
K621E |
probably damaging |
Het |
Eef2 |
G |
T |
10: 81,013,692 (GRCm39) |
R66L |
probably damaging |
Het |
Ergic2 |
A |
G |
6: 148,108,179 (GRCm39) |
|
probably benign |
Het |
Fcna |
G |
C |
2: 25,517,505 (GRCm39) |
P49A |
probably damaging |
Het |
Hace1 |
T |
A |
10: 45,524,771 (GRCm39) |
D234E |
possibly damaging |
Het |
Ifi202b |
A |
G |
1: 173,791,479 (GRCm39) |
S400P |
probably benign |
Het |
Ighv1-23 |
C |
T |
12: 114,728,087 (GRCm39) |
V112I |
probably benign |
Het |
Il4i1 |
T |
C |
7: 44,486,082 (GRCm39) |
L22P |
probably damaging |
Het |
Il7 |
G |
T |
3: 7,641,093 (GRCm39) |
Q67K |
probably benign |
Het |
Inpp5d |
C |
A |
1: 87,595,779 (GRCm39) |
T175N |
possibly damaging |
Het |
Klk1b26 |
A |
G |
7: 43,666,297 (GRCm39) |
I247V |
probably benign |
Het |
Klrc1 |
A |
G |
6: 129,654,726 (GRCm39) |
|
probably null |
Het |
Lama1 |
T |
C |
17: 68,044,598 (GRCm39) |
C166R |
probably damaging |
Het |
Mrps5 |
A |
G |
2: 127,438,832 (GRCm39) |
D219G |
probably benign |
Het |
Mtus1 |
T |
C |
8: 41,501,100 (GRCm39) |
T806A |
probably damaging |
Het |
Naip2 |
G |
A |
13: 100,325,771 (GRCm39) |
R46* |
probably null |
Het |
Nos2 |
A |
T |
11: 78,848,414 (GRCm39) |
Y1107F |
probably benign |
Het |
Nsd3 |
T |
C |
8: 26,190,047 (GRCm39) |
I135T |
probably damaging |
Het |
Or13c7b |
C |
T |
4: 43,821,258 (GRCm39) |
M34I |
probably benign |
Het |
Or2d4 |
G |
T |
7: 106,543,383 (GRCm39) |
S275* |
probably null |
Het |
Or6c65 |
A |
G |
10: 129,604,301 (GRCm39) |
H312R |
probably benign |
Het |
Pla2g4f |
T |
C |
2: 120,133,587 (GRCm39) |
S579G |
probably benign |
Het |
Ppip5k1 |
A |
T |
2: 121,158,142 (GRCm39) |
S252R |
probably damaging |
Het |
Proc |
T |
A |
18: 32,256,738 (GRCm39) |
T310S |
probably benign |
Het |
Psg21 |
A |
T |
7: 18,386,305 (GRCm39) |
L227Q |
probably damaging |
Het |
Rusc2 |
T |
G |
4: 43,415,935 (GRCm39) |
S414A |
probably damaging |
Het |
Sec24a |
T |
A |
11: 51,620,285 (GRCm39) |
N456Y |
probably damaging |
Het |
Slc1a7 |
A |
G |
4: 107,868,191 (GRCm39) |
E497G |
probably benign |
Het |
Spag8 |
T |
A |
4: 43,651,606 (GRCm39) |
S423C |
probably damaging |
Het |
Spata13 |
A |
G |
14: 60,944,172 (GRCm39) |
T522A |
probably benign |
Het |
Top1mt |
T |
C |
15: 75,529,025 (GRCm39) |
N573S |
probably benign |
Het |
Trim69 |
T |
C |
2: 122,009,125 (GRCm39) |
V395A |
probably benign |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Tusc1 |
C |
A |
4: 93,223,173 (GRCm39) |
R162L |
probably damaging |
Het |
Unc13b |
T |
A |
4: 43,234,658 (GRCm39) |
|
probably benign |
Het |
Utp25 |
A |
C |
1: 192,810,810 (GRCm39) |
S64R |
possibly damaging |
Het |
Zfhx4 |
A |
G |
3: 5,468,883 (GRCm39) |
K3014E |
probably damaging |
Het |
|
Other mutations in Vmn1r2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00328:Vmn1r2
|
APN |
4 |
3,172,807 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4151001:Vmn1r2
|
UTSW |
4 |
3,172,623 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4354001:Vmn1r2
|
UTSW |
4 |
3,172,162 (GRCm39) |
missense |
probably benign |
0.23 |
R1836:Vmn1r2
|
UTSW |
4 |
3,172,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R1855:Vmn1r2
|
UTSW |
4 |
3,172,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R2319:Vmn1r2
|
UTSW |
4 |
3,172,083 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
R3824:Vmn1r2
|
UTSW |
4 |
3,172,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R5654:Vmn1r2
|
UTSW |
4 |
3,172,261 (GRCm39) |
missense |
probably benign |
0.17 |
R7084:Vmn1r2
|
UTSW |
4 |
3,172,134 (GRCm39) |
missense |
probably benign |
0.44 |
R7661:Vmn1r2
|
UTSW |
4 |
3,172,149 (GRCm39) |
missense |
probably benign |
0.00 |
R9134:Vmn1r2
|
UTSW |
4 |
3,172,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R9324:Vmn1r2
|
UTSW |
4 |
3,172,678 (GRCm39) |
missense |
probably damaging |
0.99 |
R9614:Vmn1r2
|
UTSW |
4 |
3,172,587 (GRCm39) |
missense |
probably damaging |
1.00 |
|