Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
T |
C |
5: 125,561,727 (GRCm39) |
|
probably null |
Het |
Acot9 |
T |
A |
X: 154,078,207 (GRCm39) |
V251E |
possibly damaging |
Het |
Agtpbp1 |
A |
G |
13: 59,648,021 (GRCm39) |
S600P |
possibly damaging |
Het |
Amfr |
A |
T |
8: 94,726,964 (GRCm39) |
M157K |
probably damaging |
Het |
Arvcf |
T |
C |
16: 18,222,875 (GRCm39) |
|
probably benign |
Het |
Ascc3 |
T |
C |
10: 50,699,949 (GRCm39) |
V1924A |
possibly damaging |
Het |
Atp10a |
T |
A |
7: 58,438,196 (GRCm39) |
|
probably null |
Het |
Atp1a2 |
T |
A |
1: 172,116,870 (GRCm39) |
E249V |
probably null |
Het |
C1qc |
A |
G |
4: 136,617,598 (GRCm39) |
L166P |
probably damaging |
Het |
Col4a3 |
C |
A |
1: 82,620,927 (GRCm39) |
|
probably benign |
Het |
Def8 |
A |
G |
8: 124,183,175 (GRCm39) |
D258G |
probably damaging |
Het |
Dll1 |
T |
C |
17: 15,593,830 (GRCm39) |
D179G |
probably benign |
Het |
Dnah14 |
C |
A |
1: 181,582,834 (GRCm39) |
H3124Q |
probably benign |
Het |
Fabp5 |
T |
A |
3: 10,080,023 (GRCm39) |
|
probably benign |
Het |
Fam133b |
C |
T |
5: 3,604,684 (GRCm39) |
Q24* |
probably null |
Het |
Fam13c |
A |
C |
10: 70,284,599 (GRCm39) |
D25A |
possibly damaging |
Het |
Flna |
A |
G |
X: 73,278,208 (GRCm39) |
|
probably null |
Het |
Frem1 |
T |
A |
4: 82,832,883 (GRCm39) |
T1917S |
probably benign |
Het |
Frmd4b |
T |
C |
6: 97,285,075 (GRCm39) |
T337A |
probably benign |
Het |
Fxyd7 |
C |
T |
7: 30,743,995 (GRCm39) |
|
probably null |
Het |
Galnt5 |
T |
G |
2: 57,889,401 (GRCm39) |
S334A |
possibly damaging |
Het |
Gpd2 |
T |
A |
2: 57,197,066 (GRCm39) |
L207H |
probably damaging |
Het |
H2-M10.3 |
T |
A |
17: 36,678,279 (GRCm39) |
Y182F |
probably damaging |
Het |
Itga8 |
T |
C |
2: 12,115,836 (GRCm39) |
I1018V |
possibly damaging |
Het |
Letmd1 |
T |
C |
15: 100,367,709 (GRCm39) |
F89S |
probably damaging |
Het |
Mcm3ap |
A |
G |
10: 76,318,567 (GRCm39) |
Y696C |
probably damaging |
Het |
Mcpt9 |
A |
G |
14: 56,264,908 (GRCm39) |
Y198H |
probably damaging |
Het |
Mmp1b |
A |
G |
9: 7,387,907 (GRCm39) |
V29A |
probably benign |
Het |
Myom1 |
A |
G |
17: 71,391,311 (GRCm39) |
D940G |
possibly damaging |
Het |
Myzap |
A |
G |
9: 71,462,871 (GRCm39) |
M225T |
probably benign |
Het |
Naa25 |
A |
G |
5: 121,564,133 (GRCm39) |
Y516C |
probably damaging |
Het |
Nsdhl |
T |
A |
X: 72,000,052 (GRCm39) |
|
probably benign |
Het |
Olfml1 |
A |
G |
7: 107,170,476 (GRCm39) |
E121G |
possibly damaging |
Het |
Or11j4 |
A |
T |
14: 50,631,115 (GRCm39) |
M301L |
probably damaging |
Het |
Or4a72 |
A |
G |
2: 89,405,935 (GRCm39) |
V45A |
probably benign |
Het |
Or8k38 |
A |
G |
2: 86,488,703 (GRCm39) |
I33T |
probably benign |
Het |
Phex |
C |
T |
X: 155,961,783 (GRCm39) |
G636E |
probably damaging |
Het |
Pkd2l2 |
A |
T |
18: 34,563,373 (GRCm39) |
I475F |
probably damaging |
Het |
Polr2b |
T |
A |
5: 77,463,764 (GRCm39) |
S54T |
probably benign |
Het |
Prkx |
A |
T |
X: 76,829,806 (GRCm39) |
L85Q |
probably damaging |
Het |
Smc1b |
A |
T |
15: 84,973,914 (GRCm39) |
I914N |
probably benign |
Het |
Susd2 |
A |
G |
10: 75,478,459 (GRCm39) |
L39P |
probably benign |
Het |
Teddm2 |
C |
T |
1: 153,726,770 (GRCm39) |
V35I |
probably benign |
Het |
Tspo |
T |
A |
15: 83,455,631 (GRCm39) |
V6E |
possibly damaging |
Het |
Vps41 |
G |
T |
13: 19,013,440 (GRCm39) |
V353F |
possibly damaging |
Het |
Wfdc18 |
T |
A |
11: 83,600,033 (GRCm39) |
|
probably null |
Het |
Wsb1 |
C |
T |
11: 79,139,324 (GRCm39) |
S124N |
probably damaging |
Het |
Zfp445 |
T |
C |
9: 122,686,594 (GRCm39) |
E177G |
probably benign |
Het |
Zfp759 |
G |
T |
13: 67,287,480 (GRCm39) |
V344L |
probably benign |
Het |
|
Other mutations in Gm10220 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00401:Gm10220
|
APN |
5 |
26,323,609 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01782:Gm10220
|
APN |
5 |
26,322,021 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03194:Gm10220
|
APN |
5 |
26,326,231 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03255:Gm10220
|
APN |
5 |
26,321,899 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3014:Gm10220
|
UTSW |
5 |
26,322,826 (GRCm39) |
missense |
probably damaging |
0.99 |
R3883:Gm10220
|
UTSW |
5 |
26,321,908 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4577:Gm10220
|
UTSW |
5 |
26,322,869 (GRCm39) |
missense |
probably benign |
|
R5484:Gm10220
|
UTSW |
5 |
26,322,930 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6358:Gm10220
|
UTSW |
5 |
26,325,303 (GRCm39) |
splice site |
probably null |
|
R8300:Gm10220
|
UTSW |
5 |
26,322,818 (GRCm39) |
missense |
probably damaging |
0.99 |
R8871:Gm10220
|
UTSW |
5 |
26,322,863 (GRCm39) |
missense |
probably benign |
0.01 |
|