Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AAdacl4fm3 |
A |
C |
4: 144,442,062 (GRCm39) |
L63R |
probably damaging |
Het |
Abcb5 |
C |
T |
12: 118,895,660 (GRCm39) |
V379I |
probably benign |
Het |
Adamts15 |
T |
C |
9: 30,832,776 (GRCm39) |
Y253C |
probably damaging |
Het |
Ahsa1 |
T |
C |
12: 87,318,154 (GRCm39) |
S37P |
possibly damaging |
Het |
Arnt2 |
A |
T |
7: 83,993,150 (GRCm39) |
L130H |
probably damaging |
Het |
Atp8b5 |
T |
A |
4: 43,355,618 (GRCm39) |
F533I |
probably damaging |
Het |
Best1 |
A |
G |
19: 9,964,143 (GRCm39) |
V439A |
probably benign |
Het |
Bicc1 |
A |
G |
10: 70,796,978 (GRCm39) |
V127A |
probably damaging |
Het |
Brd7 |
T |
C |
8: 89,073,632 (GRCm39) |
T253A |
probably benign |
Het |
Btd |
A |
G |
14: 31,389,788 (GRCm39) |
D503G |
probably benign |
Het |
Ccdc80 |
A |
G |
16: 44,924,804 (GRCm39) |
E646G |
probably damaging |
Het |
Ccl25 |
A |
G |
8: 4,399,641 (GRCm39) |
|
probably benign |
Het |
Ccnf |
C |
A |
17: 24,461,205 (GRCm39) |
W150L |
probably damaging |
Het |
Cdk11b |
A |
T |
4: 155,726,024 (GRCm39) |
|
probably benign |
Het |
Cfap73 |
T |
C |
5: 120,768,149 (GRCm39) |
E203G |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,230,063 (GRCm39) |
E1675G |
possibly damaging |
Het |
Copg1 |
T |
A |
6: 87,871,087 (GRCm39) |
Y268N |
possibly damaging |
Het |
Csnk2a1 |
T |
A |
2: 152,102,732 (GRCm39) |
H126Q |
probably damaging |
Het |
Ctbs |
G |
A |
3: 146,160,703 (GRCm39) |
G90D |
probably damaging |
Het |
Ctnna2 |
T |
C |
6: 77,613,888 (GRCm39) |
Y221C |
probably damaging |
Het |
Cypt12 |
C |
T |
3: 18,002,635 (GRCm39) |
R3C |
unknown |
Het |
D630003M21Rik |
A |
T |
2: 158,058,670 (GRCm39) |
M410K |
possibly damaging |
Het |
Dnah9 |
A |
T |
11: 65,872,057 (GRCm39) |
N2724K |
probably benign |
Het |
Dok3 |
T |
C |
13: 55,672,097 (GRCm39) |
T194A |
probably benign |
Het |
Edem3 |
T |
G |
1: 151,631,423 (GRCm39) |
S36A |
probably benign |
Het |
Eed |
C |
T |
7: 89,629,727 (GRCm39) |
E3K |
possibly damaging |
Het |
Efcab2 |
A |
G |
1: 178,308,925 (GRCm39) |
I143V |
probably benign |
Het |
Ensa |
A |
T |
3: 95,534,359 (GRCm39) |
|
probably null |
Het |
Galnt16 |
A |
T |
12: 80,626,826 (GRCm39) |
E219V |
probably damaging |
Het |
Gfra3 |
C |
A |
18: 34,823,933 (GRCm39) |
R347L |
probably benign |
Het |
Gm2042 |
T |
A |
12: 87,927,009 (GRCm39) |
I442K |
probably damaging |
Het |
Gpld1 |
A |
T |
13: 25,168,691 (GRCm39) |
D735V |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,269,580 (GRCm39) |
S2253P |
possibly damaging |
Het |
Kit |
T |
C |
5: 75,781,627 (GRCm39) |
I352T |
probably benign |
Het |
Klra6 |
A |
T |
6: 129,995,821 (GRCm39) |
V179E |
possibly damaging |
Het |
Lctl |
T |
A |
9: 64,040,075 (GRCm39) |
|
probably null |
Het |
Lman1 |
C |
A |
18: 66,124,714 (GRCm39) |
V342L |
probably benign |
Het |
Lrrn2 |
T |
C |
1: 132,866,522 (GRCm39) |
L529P |
probably damaging |
Het |
Mab21l2 |
A |
G |
3: 86,454,793 (GRCm39) |
I69T |
probably benign |
Het |
Mapkapk5 |
G |
T |
5: 121,665,274 (GRCm39) |
A327E |
probably benign |
Het |
Mex3b |
G |
T |
7: 82,519,080 (GRCm39) |
R465L |
possibly damaging |
Het |
Mgat4c |
A |
G |
10: 102,224,289 (GRCm39) |
R168G |
possibly damaging |
Het |
Mkks |
A |
G |
2: 136,718,007 (GRCm39) |
|
probably null |
Het |
Muc16 |
G |
T |
9: 18,466,215 (GRCm39) |
H7368N |
unknown |
Het |
Muc16 |
T |
C |
9: 18,462,127 (GRCm39) |
|
probably null |
Het |
Nbeal1 |
G |
A |
1: 60,300,745 (GRCm39) |
|
probably null |
Het |
Notch2 |
T |
C |
3: 98,042,762 (GRCm39) |
S1376P |
probably benign |
Het |
Obox5 |
A |
G |
7: 15,491,681 (GRCm39) |
|
probably null |
Het |
Or10j5 |
T |
C |
1: 172,784,494 (GRCm39) |
I44T |
probably benign |
Het |
Or6c8b |
A |
T |
10: 128,882,899 (GRCm39) |
I11N |
probably damaging |
Het |
Pbrm1 |
A |
G |
14: 30,789,773 (GRCm39) |
I807V |
probably damaging |
Het |
Pitrm1 |
T |
A |
13: 6,628,593 (GRCm39) |
V962E |
probably damaging |
Het |
Pkd2l1 |
T |
C |
19: 44,142,647 (GRCm39) |
Q465R |
probably damaging |
Het |
Pla1a |
A |
G |
16: 38,221,244 (GRCm39) |
I372T |
probably damaging |
Het |
Prmt5 |
A |
C |
14: 54,752,845 (GRCm39) |
F122C |
probably damaging |
Het |
Prrc2b |
T |
A |
2: 32,111,498 (GRCm39) |
S1905T |
probably damaging |
Het |
Ptprf |
T |
G |
4: 118,081,101 (GRCm39) |
K1163N |
probably benign |
Het |
Rab3ip |
A |
G |
10: 116,775,283 (GRCm39) |
V25A |
probably damaging |
Het |
Raf1 |
T |
C |
6: 115,597,300 (GRCm39) |
|
probably null |
Het |
Rnf180 |
T |
C |
13: 105,407,429 (GRCm39) |
E40G |
probably benign |
Het |
Rpl6 |
T |
A |
5: 121,346,972 (GRCm39) |
M289K |
probably benign |
Het |
Slc25a32 |
A |
G |
15: 38,963,321 (GRCm39) |
F167L |
probably benign |
Het |
Slc30a2 |
G |
A |
4: 134,074,726 (GRCm39) |
R161Q |
probably damaging |
Het |
Slc4a4 |
T |
A |
5: 89,188,205 (GRCm39) |
|
probably null |
Het |
Sppl2a |
A |
G |
2: 126,769,663 (GRCm39) |
|
probably null |
Het |
Tbr1 |
T |
A |
2: 61,637,688 (GRCm39) |
D82E |
probably benign |
Het |
Tbx10 |
A |
T |
19: 4,048,961 (GRCm39) |
T291S |
probably benign |
Het |
Tlr1 |
T |
A |
5: 65,083,056 (GRCm39) |
H507L |
possibly damaging |
Het |
Trim37 |
A |
C |
11: 87,058,335 (GRCm39) |
T338P |
probably benign |
Het |
Trpv5 |
T |
C |
6: 41,630,204 (GRCm39) |
T629A |
probably benign |
Het |
Ttc14 |
T |
A |
3: 33,857,646 (GRCm39) |
I249N |
probably damaging |
Het |
Uhrf1 |
A |
G |
17: 56,627,450 (GRCm39) |
T661A |
probably benign |
Het |
Vmn2r65 |
A |
G |
7: 84,596,587 (GRCm39) |
I156T |
probably benign |
Het |
Vwde |
T |
C |
6: 13,186,905 (GRCm39) |
N861D |
probably damaging |
Het |
Zan |
A |
G |
5: 137,422,213 (GRCm39) |
C2802R |
unknown |
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 |
R6508:Mgat3
|
UTSW |
15 |
80,096,225 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6784:Mgat3
|
UTSW |
15 |
80,096,401 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
|
|