Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
T |
C |
17: 24,553,255 (GRCm39) |
D152G |
probably benign |
Het |
Abcb1b |
G |
A |
5: 8,875,614 (GRCm39) |
V596I |
probably benign |
Het |
Acss3 |
A |
G |
10: 106,959,255 (GRCm39) |
S64P |
probably damaging |
Het |
Aggf1 |
T |
C |
13: 95,507,461 (GRCm39) |
Y108C |
probably damaging |
Het |
Arpc5l |
T |
C |
2: 38,903,195 (GRCm39) |
V73A |
probably benign |
Het |
Atp5f1d |
A |
G |
10: 79,981,134 (GRCm39) |
D126G |
probably damaging |
Het |
Carmil3 |
T |
A |
14: 55,731,869 (GRCm39) |
L199* |
probably null |
Het |
Cblb |
A |
G |
16: 51,853,515 (GRCm39) |
R44G |
probably benign |
Het |
Cdcp3 |
A |
G |
7: 130,863,620 (GRCm39) |
I1208V |
unknown |
Het |
Chaf1b |
T |
G |
16: 93,689,629 (GRCm39) |
F225V |
probably benign |
Het |
Creb3l2 |
A |
T |
6: 37,356,751 (GRCm39) |
N105K |
probably damaging |
Het |
Dagla |
A |
T |
19: 10,248,465 (GRCm39) |
I65N |
probably damaging |
Het |
Dclre1c |
T |
G |
2: 3,425,342 (GRCm39) |
F30V |
probably damaging |
Het |
Dicer1 |
A |
G |
12: 104,695,499 (GRCm39) |
V144A |
possibly damaging |
Het |
Dlg5 |
C |
T |
14: 24,197,168 (GRCm39) |
G1593D |
probably damaging |
Het |
Enpp3 |
A |
T |
10: 24,711,990 (GRCm39) |
M1K |
probably null |
Het |
Fmod |
C |
A |
1: 133,968,514 (GRCm39) |
H185N |
probably benign |
Het |
Gon4l |
A |
G |
3: 88,802,260 (GRCm39) |
E957G |
probably benign |
Het |
Hat1 |
A |
G |
2: 71,264,512 (GRCm39) |
M310V |
possibly damaging |
Het |
Klhl31 |
A |
T |
9: 77,557,826 (GRCm39) |
T181S |
probably benign |
Het |
Krt36 |
T |
A |
11: 99,994,906 (GRCm39) |
E222V |
probably damaging |
Het |
Lrrc27 |
A |
T |
7: 138,807,837 (GRCm39) |
K315* |
probably null |
Het |
Mak16 |
T |
G |
8: 31,650,794 (GRCm39) |
D232A |
probably damaging |
Het |
Mepce |
A |
G |
5: 137,783,322 (GRCm39) |
S335P |
possibly damaging |
Het |
Mki67 |
T |
A |
7: 135,302,378 (GRCm39) |
R885S |
probably damaging |
Het |
Mmrn1 |
G |
A |
6: 60,935,176 (GRCm39) |
W224* |
probably null |
Het |
Mroh8 |
T |
A |
2: 157,098,386 (GRCm39) |
Q254L |
possibly damaging |
Het |
Mup18 |
A |
T |
4: 61,590,854 (GRCm39) |
V101E |
probably damaging |
Het |
Nbea |
T |
C |
3: 55,898,460 (GRCm39) |
K1508R |
probably benign |
Het |
Or5aq6 |
A |
T |
2: 86,923,390 (GRCm39) |
M117K |
possibly damaging |
Het |
Or5g9 |
A |
G |
2: 85,551,806 (GRCm39) |
Y19C |
probably benign |
Het |
Pcdh15 |
A |
T |
10: 74,066,192 (GRCm39) |
I286F |
probably damaging |
Het |
Pcdhb8 |
A |
T |
18: 37,488,751 (GRCm39) |
Q143L |
probably benign |
Het |
Pibf1 |
T |
C |
14: 99,448,436 (GRCm39) |
S632P |
probably damaging |
Het |
Senp6 |
A |
G |
9: 79,999,646 (GRCm39) |
K100R |
probably damaging |
Het |
Slc5a9 |
A |
G |
4: 111,750,864 (GRCm39) |
S81P |
probably damaging |
Het |
Sox8 |
T |
C |
17: 25,786,338 (GRCm39) |
Q455R |
probably damaging |
Het |
Stard13 |
A |
T |
5: 151,113,483 (GRCm39) |
M26K |
probably benign |
Het |
Sulf1 |
T |
A |
1: 12,908,778 (GRCm39) |
M597K |
probably benign |
Het |
Ugt2a3 |
T |
A |
5: 87,484,832 (GRCm39) |
D64V |
probably benign |
Het |
Unc80 |
T |
C |
1: 66,589,097 (GRCm39) |
|
probably null |
Het |
Vav3 |
A |
T |
3: 109,565,291 (GRCm39) |
H729L |
probably benign |
Het |
Wdtc1 |
A |
G |
4: 133,036,058 (GRCm39) |
|
probably null |
Het |
Zfp984 |
A |
G |
4: 147,840,002 (GRCm39) |
M283T |
probably benign |
Het |
Zik1 |
A |
G |
7: 10,224,623 (GRCm39) |
L158P |
probably damaging |
Het |
|
Other mutations in Vmn1r226 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01081:Vmn1r226
|
APN |
17 |
20,908,166 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02103:Vmn1r226
|
APN |
17 |
20,907,926 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03394:Vmn1r226
|
APN |
17 |
20,908,446 (GRCm39) |
missense |
probably benign |
0.00 |
R0243:Vmn1r226
|
UTSW |
17 |
20,907,839 (GRCm39) |
missense |
probably benign |
0.00 |
R0605:Vmn1r226
|
UTSW |
17 |
20,908,133 (GRCm39) |
missense |
probably benign |
0.12 |
R1463:Vmn1r226
|
UTSW |
17 |
20,907,994 (GRCm39) |
missense |
probably benign |
0.00 |
R1571:Vmn1r226
|
UTSW |
17 |
20,908,538 (GRCm39) |
missense |
probably damaging |
0.97 |
R1677:Vmn1r226
|
UTSW |
17 |
20,908,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Vmn1r226
|
UTSW |
17 |
20,907,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R1918:Vmn1r226
|
UTSW |
17 |
20,907,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R1919:Vmn1r226
|
UTSW |
17 |
20,907,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R1980:Vmn1r226
|
UTSW |
17 |
20,908,308 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2291:Vmn1r226
|
UTSW |
17 |
20,908,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R2377:Vmn1r226
|
UTSW |
17 |
20,907,992 (GRCm39) |
missense |
probably benign |
0.05 |
R3878:Vmn1r226
|
UTSW |
17 |
20,908,260 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5166:Vmn1r226
|
UTSW |
17 |
20,908,125 (GRCm39) |
missense |
probably benign |
0.43 |
R6510:Vmn1r226
|
UTSW |
17 |
20,908,115 (GRCm39) |
missense |
probably benign |
0.37 |
R6599:Vmn1r226
|
UTSW |
17 |
20,908,551 (GRCm39) |
missense |
probably benign |
0.01 |
R7304:Vmn1r226
|
UTSW |
17 |
20,908,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8836:Vmn1r226
|
UTSW |
17 |
20,908,133 (GRCm39) |
missense |
probably benign |
0.00 |
R8955:Vmn1r226
|
UTSW |
17 |
20,908,287 (GRCm39) |
missense |
possibly damaging |
0.79 |
X0066:Vmn1r226
|
UTSW |
17 |
20,908,512 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Vmn1r226
|
UTSW |
17 |
20,908,479 (GRCm39) |
nonsense |
probably null |
|
|