Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm2 |
G |
A |
4: 144,291,590 (GRCm39) |
R39* |
probably null |
Het |
Brca2 |
A |
T |
5: 150,460,058 (GRCm39) |
E444D |
possibly damaging |
Het |
Camkk2 |
G |
T |
5: 122,884,382 (GRCm39) |
N346K |
probably damaging |
Het |
Car4 |
C |
A |
11: 84,856,469 (GRCm39) |
D252E |
possibly damaging |
Het |
Chd1 |
A |
G |
17: 15,958,895 (GRCm39) |
K649R |
probably benign |
Het |
Col12a1 |
A |
G |
9: 79,557,231 (GRCm39) |
Y1966H |
probably damaging |
Het |
Crppa |
C |
T |
12: 36,476,298 (GRCm39) |
A180V |
possibly damaging |
Het |
Cts6 |
T |
A |
13: 61,344,221 (GRCm39) |
H277L |
probably damaging |
Het |
Dcc |
G |
T |
18: 71,439,144 (GRCm39) |
P1246Q |
probably damaging |
Het |
Dlg5 |
G |
A |
14: 24,188,774 (GRCm39) |
T1739I |
probably benign |
Het |
Eci1 |
T |
A |
17: 24,656,283 (GRCm39) |
N164K |
probably damaging |
Het |
Entpd7 |
G |
A |
19: 43,679,525 (GRCm39) |
R26H |
probably damaging |
Het |
Fanci |
A |
G |
7: 79,093,516 (GRCm39) |
K1008E |
probably damaging |
Het |
Htr2b |
T |
C |
1: 86,030,186 (GRCm39) |
T170A |
possibly damaging |
Het |
Irgm2 |
A |
G |
11: 58,110,327 (GRCm39) |
E18G |
probably benign |
Het |
Kdm1a |
A |
T |
4: 136,281,621 (GRCm39) |
V630E |
probably damaging |
Het |
Keap1 |
G |
A |
9: 21,143,010 (GRCm39) |
T501I |
possibly damaging |
Het |
L3mbtl3 |
T |
A |
10: 26,194,325 (GRCm39) |
H424L |
unknown |
Het |
Lrrc14b |
C |
T |
13: 74,511,337 (GRCm39) |
D248N |
possibly damaging |
Het |
Macf1 |
T |
A |
4: 123,363,535 (GRCm39) |
D3364V |
probably damaging |
Het |
Map3k20 |
G |
A |
2: 72,272,253 (GRCm39) |
G794S |
probably benign |
Het |
Mcat |
T |
C |
15: 83,433,452 (GRCm39) |
Q34R |
probably benign |
Het |
Mettl4 |
T |
C |
17: 95,051,373 (GRCm39) |
E148G |
probably damaging |
Het |
Mllt1 |
A |
T |
17: 57,234,054 (GRCm39) |
I44N |
probably damaging |
Het |
Mlxipl |
G |
T |
5: 135,157,474 (GRCm39) |
A337S |
probably benign |
Het |
Naip1 |
A |
G |
13: 100,572,973 (GRCm39) |
F254L |
probably damaging |
Het |
Obscn |
A |
T |
11: 58,944,973 (GRCm39) |
|
probably null |
Het |
Or10q1 |
C |
T |
19: 13,726,718 (GRCm39) |
P83S |
probably damaging |
Het |
Pcdh12 |
G |
A |
18: 38,414,390 (GRCm39) |
R912* |
probably null |
Het |
Pcdh17 |
A |
G |
14: 84,685,419 (GRCm39) |
N629D |
probably damaging |
Het |
Pcnx1 |
T |
C |
12: 81,959,479 (GRCm39) |
I170T |
probably damaging |
Het |
Pgr |
A |
G |
9: 8,956,290 (GRCm39) |
Y746C |
probably damaging |
Het |
Pramel29 |
A |
T |
4: 143,934,171 (GRCm39) |
L312* |
probably null |
Het |
Pum2 |
T |
C |
12: 8,798,861 (GRCm39) |
Y991H |
probably benign |
Het |
Rcc1l |
A |
T |
5: 134,198,077 (GRCm39) |
V185D |
probably damaging |
Het |
Scarb1 |
A |
T |
5: 125,381,389 (GRCm39) |
S52T |
possibly damaging |
Het |
Smc1b |
C |
T |
15: 84,976,232 (GRCm39) |
R825Q |
probably benign |
Het |
Spata4 |
T |
C |
8: 55,053,887 (GRCm39) |
S18P |
probably benign |
Het |
Stard13 |
G |
A |
5: 150,986,754 (GRCm39) |
T134I |
probably benign |
Het |
Tbc1d32 |
C |
T |
10: 56,100,786 (GRCm39) |
C64Y |
probably damaging |
Het |
Tll1 |
T |
G |
8: 64,551,494 (GRCm39) |
I296L |
probably damaging |
Het |
Tmem229b |
T |
G |
12: 79,011,680 (GRCm39) |
T84P |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,544,757 (GRCm39) |
T32782A |
possibly damaging |
Het |
Vmn1r73 |
G |
A |
7: 11,490,631 (GRCm39) |
V150I |
possibly damaging |
Het |
Vmn2r80 |
T |
A |
10: 79,030,290 (GRCm39) |
F705L |
probably benign |
Het |
|
Other mutations in Mgat3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00965:Mgat3
|
APN |
15 |
80,096,634 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01134:Mgat3
|
APN |
15 |
80,096,377 (GRCm39) |
missense |
probably benign |
0.17 |
R0077:Mgat3
|
UTSW |
15 |
80,096,778 (GRCm39) |
missense |
probably benign |
0.00 |
R1171:Mgat3
|
UTSW |
15 |
80,095,838 (GRCm39) |
missense |
probably benign |
0.26 |
R1885:Mgat3
|
UTSW |
15 |
80,095,820 (GRCm39) |
missense |
probably benign |
0.25 |
R1886:Mgat3
|
UTSW |
15 |
80,095,820 (GRCm39) |
missense |
probably benign |
0.25 |
R1986:Mgat3
|
UTSW |
15 |
80,096,390 (GRCm39) |
missense |
probably benign |
0.04 |
R2125:Mgat3
|
UTSW |
15 |
80,096,087 (GRCm39) |
missense |
probably benign |
0.00 |
R3081:Mgat3
|
UTSW |
15 |
80,096,055 (GRCm39) |
missense |
probably benign |
0.33 |
R4819:Mgat3
|
UTSW |
15 |
80,096,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Mgat3
|
UTSW |
15 |
80,096,743 (GRCm39) |
missense |
probably benign |
|
R5083:Mgat3
|
UTSW |
15 |
80,095,499 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5356:Mgat3
|
UTSW |
15 |
80,096,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R5356:Mgat3
|
UTSW |
15 |
80,095,811 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6784:Mgat3
|
UTSW |
15 |
80,096,401 (GRCm39) |
missense |
probably damaging |
0.98 |
R7021:Mgat3
|
UTSW |
15 |
80,096,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R7056:Mgat3
|
UTSW |
15 |
80,096,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R7592:Mgat3
|
UTSW |
15 |
80,095,193 (GRCm39) |
missense |
probably damaging |
0.96 |
R7774:Mgat3
|
UTSW |
15 |
80,095,743 (GRCm39) |
missense |
probably damaging |
0.96 |
R7819:Mgat3
|
UTSW |
15 |
80,095,973 (GRCm39) |
nonsense |
probably null |
|
R8559:Mgat3
|
UTSW |
15 |
80,096,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R8678:Mgat3
|
UTSW |
15 |
80,096,472 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9285:Mgat3
|
UTSW |
15 |
80,096,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R9483:Mgat3
|
UTSW |
15 |
80,095,641 (GRCm39) |
missense |
probably benign |
|
|