Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Anapc1 |
A |
G |
2: 128,476,598 (GRCm39) |
M1340T |
probably benign |
Het |
Arhgef15 |
A |
G |
11: 68,842,233 (GRCm39) |
L457P |
probably damaging |
Het |
Arih2 |
A |
T |
9: 108,486,986 (GRCm39) |
C317S |
probably damaging |
Het |
Asb14 |
A |
T |
14: 26,633,793 (GRCm39) |
T333S |
probably damaging |
Het |
Atp13a4 |
T |
C |
16: 29,227,821 (GRCm39) |
N1012S |
|
Het |
Capn9 |
C |
A |
8: 125,332,449 (GRCm39) |
D429E |
probably benign |
Het |
Celsr1 |
G |
T |
15: 85,917,286 (GRCm39) |
S229* |
probably null |
Het |
Cntrob |
C |
T |
11: 69,193,741 (GRCm39) |
R803Q |
possibly damaging |
Het |
Dnah8 |
A |
G |
17: 31,029,297 (GRCm39) |
I4089V |
probably benign |
Het |
Fam162b |
A |
G |
10: 51,466,155 (GRCm39) |
|
probably null |
Het |
Fhod3 |
A |
G |
18: 25,102,244 (GRCm39) |
D180G |
probably damaging |
Het |
Gtf3c4 |
A |
G |
2: 28,723,966 (GRCm39) |
S589P |
possibly damaging |
Het |
Jcad |
T |
C |
18: 4,673,912 (GRCm39) |
L558P |
probably damaging |
Het |
Kmt2d |
A |
G |
15: 98,737,586 (GRCm39) |
I5170T |
unknown |
Het |
Lamb3 |
T |
C |
1: 193,008,319 (GRCm39) |
F251L |
probably benign |
Het |
Lpxn |
T |
A |
19: 12,802,336 (GRCm39) |
D220E |
probably benign |
Het |
Mex3a |
T |
A |
3: 88,444,480 (GRCm39) |
F519I |
probably damaging |
Het |
Mfap1a |
T |
C |
2: 121,337,001 (GRCm39) |
M8V |
probably benign |
Het |
Mical3 |
T |
A |
6: 120,934,712 (GRCm39) |
D1789V |
probably damaging |
Het |
Mpdz |
G |
A |
4: 81,235,905 (GRCm39) |
Q1211* |
probably null |
Het |
Myd88 |
A |
G |
9: 119,167,070 (GRCm39) |
|
probably null |
Het |
Myof |
T |
A |
19: 37,941,412 (GRCm39) |
K799N |
probably damaging |
Het |
Naip2 |
T |
A |
13: 100,298,243 (GRCm39) |
S598C |
probably damaging |
Het |
Ndst4 |
C |
T |
3: 125,518,385 (GRCm39) |
S354L |
probably benign |
Het |
Ntn4 |
A |
G |
10: 93,480,488 (GRCm39) |
T71A |
probably benign |
Het |
Omd |
A |
C |
13: 49,745,837 (GRCm39) |
M416L |
probably benign |
Het |
Oog1 |
G |
C |
12: 87,655,086 (GRCm39) |
L411F |
probably damaging |
Het |
Or10a3m |
T |
A |
7: 108,313,042 (GRCm39) |
W161R |
probably damaging |
Het |
Or1e32 |
A |
G |
11: 73,705,143 (GRCm39) |
I255T |
probably damaging |
Het |
Or56a5 |
T |
G |
7: 104,793,498 (GRCm39) |
M7L |
probably benign |
Het |
Or7e171-ps1 |
A |
G |
9: 19,853,200 (GRCm39) |
W179R |
probably benign |
Het |
Pde4dip |
T |
C |
3: 97,660,468 (GRCm39) |
Q670R |
possibly damaging |
Het |
Pex13 |
C |
A |
11: 23,601,034 (GRCm39) |
G272V |
probably damaging |
Het |
Pfkl |
A |
T |
10: 77,824,081 (GRCm39) |
V769D |
probably damaging |
Het |
Pkn3 |
A |
G |
2: 29,968,332 (GRCm39) |
Y10C |
probably benign |
Het |
Pomgnt1 |
A |
G |
4: 116,013,378 (GRCm39) |
H500R |
probably damaging |
Het |
Rasef |
T |
C |
4: 73,645,882 (GRCm39) |
T496A |
probably benign |
Het |
Rgs6 |
A |
G |
12: 83,184,166 (GRCm39) |
S459G |
probably benign |
Het |
Serpinb6b |
A |
T |
13: 33,159,002 (GRCm39) |
M187L |
|
Het |
Shcbp1l |
A |
G |
1: 153,321,627 (GRCm39) |
I408M |
possibly damaging |
Het |
Slc25a45 |
T |
C |
19: 5,934,967 (GRCm39) |
V272A |
probably damaging |
Het |
Tlr4 |
T |
C |
4: 66,746,160 (GRCm39) |
|
probably null |
Het |
Unc80 |
A |
T |
1: 66,550,064 (GRCm39) |
N774I |
|
Het |
Urb2 |
T |
A |
8: 124,756,613 (GRCm39) |
S773R |
possibly damaging |
Het |
Vps13d |
A |
C |
4: 144,796,527 (GRCm39) |
V3691G |
|
Het |
Wdtc1 |
A |
G |
4: 133,022,684 (GRCm39) |
V554A |
possibly damaging |
Het |
Xrn1 |
A |
T |
9: 95,851,527 (GRCm39) |
M182L |
probably damaging |
Het |
Zfp747 |
T |
C |
7: 126,973,198 (GRCm39) |
H324R |
possibly damaging |
Het |
|
Other mutations in Vmn1r35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00962:Vmn1r35
|
APN |
6 |
66,656,361 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01417:Vmn1r35
|
APN |
6 |
66,656,191 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01517:Vmn1r35
|
APN |
6 |
66,656,434 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02142:Vmn1r35
|
APN |
6 |
66,656,334 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02178:Vmn1r35
|
APN |
6 |
66,656,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02383:Vmn1r35
|
APN |
6 |
66,655,876 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02383:Vmn1r35
|
APN |
6 |
66,655,875 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02493:Vmn1r35
|
APN |
6 |
66,656,463 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0360:Vmn1r35
|
UTSW |
6 |
66,655,827 (GRCm39) |
missense |
probably damaging |
0.99 |
R0364:Vmn1r35
|
UTSW |
6 |
66,655,827 (GRCm39) |
missense |
probably damaging |
0.99 |
R0599:Vmn1r35
|
UTSW |
6 |
66,656,497 (GRCm39) |
missense |
probably benign |
0.06 |
R1447:Vmn1r35
|
UTSW |
6 |
66,655,890 (GRCm39) |
missense |
probably benign |
0.13 |
R1781:Vmn1r35
|
UTSW |
6 |
66,656,550 (GRCm39) |
missense |
probably benign |
0.24 |
R2096:Vmn1r35
|
UTSW |
6 |
66,655,929 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2937:Vmn1r35
|
UTSW |
6 |
66,655,950 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2938:Vmn1r35
|
UTSW |
6 |
66,655,950 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3937:Vmn1r35
|
UTSW |
6 |
66,656,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R3938:Vmn1r35
|
UTSW |
6 |
66,656,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R4386:Vmn1r35
|
UTSW |
6 |
66,656,573 (GRCm39) |
nonsense |
probably null |
|
R5329:Vmn1r35
|
UTSW |
6 |
66,656,490 (GRCm39) |
nonsense |
probably null |
|
R6638:Vmn1r35
|
UTSW |
6 |
66,655,848 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7175:Vmn1r35
|
UTSW |
6 |
66,655,906 (GRCm39) |
missense |
probably benign |
0.06 |
R7448:Vmn1r35
|
UTSW |
6 |
66,656,219 (GRCm39) |
start gained |
probably benign |
|
R7825:Vmn1r35
|
UTSW |
6 |
66,656,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Vmn1r35
|
UTSW |
6 |
66,655,933 (GRCm39) |
missense |
probably benign |
0.10 |
|