Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
T |
A |
8: 111,773,587 (GRCm39) |
V506E |
probably damaging |
Het |
Acaa2 |
G |
T |
18: 74,937,213 (GRCm39) |
V366F |
possibly damaging |
Het |
Ago1 |
G |
A |
4: 126,337,022 (GRCm39) |
R532C |
probably benign |
Het |
Ank2 |
T |
G |
3: 126,846,449 (GRCm39) |
D182A |
probably damaging |
Het |
Anxa4 |
T |
C |
6: 86,714,801 (GRCm39) |
D302G |
probably damaging |
Het |
Atf1 |
A |
G |
15: 100,152,158 (GRCm39) |
|
probably null |
Het |
Atp8b3 |
A |
C |
10: 80,355,980 (GRCm39) |
V1244G |
probably benign |
Het |
Cactin |
CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG |
CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG |
10: 81,157,152 (GRCm39) |
|
probably benign |
Het |
Camk2a |
G |
A |
18: 61,085,412 (GRCm39) |
V132M |
probably damaging |
Het |
Cdc40 |
A |
T |
10: 40,724,048 (GRCm39) |
Y247N |
probably benign |
Het |
Chd8 |
G |
A |
14: 52,474,534 (GRCm39) |
P166S |
probably benign |
Het |
Chl1 |
T |
A |
6: 103,706,086 (GRCm39) |
S1140R |
probably damaging |
Het |
Clstn3 |
G |
T |
6: 124,414,377 (GRCm39) |
S783* |
probably null |
Het |
Col6a1 |
A |
G |
10: 76,549,760 (GRCm39) |
S562P |
unknown |
Het |
Cpb2 |
G |
A |
14: 75,509,989 (GRCm39) |
V250M |
possibly damaging |
Het |
Cyp2c38 |
T |
A |
19: 39,451,368 (GRCm39) |
Q44L |
possibly damaging |
Het |
Dgat1 |
T |
C |
15: 76,387,395 (GRCm39) |
M325V |
possibly damaging |
Het |
Dnah11 |
T |
A |
12: 118,160,377 (GRCm39) |
M118L |
probably benign |
Het |
Dpy19l3 |
T |
A |
7: 35,452,106 (GRCm39) |
I13L |
probably benign |
Het |
Enkd1 |
A |
G |
8: 106,431,265 (GRCm39) |
|
probably null |
Het |
Fam241b |
A |
G |
10: 61,970,479 (GRCm39) |
|
probably benign |
Het |
Fhit |
T |
A |
14: 9,870,177 (GRCm38) |
|
probably null |
Het |
Gp6 |
T |
C |
7: 4,373,173 (GRCm39) |
E250G |
probably benign |
Het |
Hmgb1 |
T |
C |
5: 148,987,150 (GRCm39) |
E84G |
probably benign |
Het |
Hscb |
T |
A |
5: 110,977,012 (GRCm39) |
I227F |
probably damaging |
Het |
Hspg2 |
T |
A |
4: 137,292,249 (GRCm39) |
L4047Q |
probably damaging |
Het |
Hsph1 |
A |
G |
5: 149,541,901 (GRCm39) |
L775P |
probably benign |
Het |
Hydin |
A |
T |
8: 111,268,476 (GRCm39) |
S2947C |
probably benign |
Het |
Intu |
T |
C |
3: 40,652,029 (GRCm39) |
S829P |
probably benign |
Het |
Kcnn3 |
C |
A |
3: 89,516,977 (GRCm39) |
T462K |
probably damaging |
Het |
Kndc1 |
G |
A |
7: 139,517,930 (GRCm39) |
C1622Y |
possibly damaging |
Het |
Lifr |
T |
C |
15: 7,198,723 (GRCm39) |
Y318H |
probably damaging |
Het |
Mier2 |
A |
G |
10: 79,378,543 (GRCm39) |
S332P |
probably damaging |
Het |
Mindy4 |
T |
C |
6: 55,253,598 (GRCm39) |
I489T |
possibly damaging |
Het |
Mmp8 |
A |
T |
9: 7,566,218 (GRCm39) |
Q358L |
probably benign |
Het |
Ms4a4a |
T |
A |
19: 11,367,728 (GRCm39) |
|
probably null |
Het |
Nav1 |
G |
C |
1: 135,395,483 (GRCm39) |
S962C |
probably damaging |
Het |
Nfe2l1 |
G |
A |
11: 96,710,271 (GRCm39) |
R653C |
probably damaging |
Het |
Nherf4 |
A |
T |
9: 44,161,594 (GRCm39) |
I95N |
probably damaging |
Het |
Nod2 |
A |
T |
8: 89,391,906 (GRCm39) |
I738F |
probably damaging |
Het |
Nrf1 |
G |
A |
6: 30,116,230 (GRCm39) |
V301I |
probably benign |
Het |
Oog1 |
T |
C |
12: 87,655,082 (GRCm39) |
F410S |
probably benign |
Het |
Or52a33 |
A |
G |
7: 103,289,165 (GRCm39) |
Y61H |
probably damaging |
Het |
Or6k4 |
G |
A |
1: 173,964,733 (GRCm39) |
C141Y |
probably benign |
Het |
Pcdhga8 |
G |
A |
18: 37,859,954 (GRCm39) |
V337I |
probably benign |
Het |
Pelp1 |
G |
T |
11: 70,286,260 (GRCm39) |
N572K |
probably benign |
Het |
Pikfyve |
T |
C |
1: 65,307,036 (GRCm39) |
V1808A |
possibly damaging |
Het |
Pirt |
A |
C |
11: 66,816,769 (GRCm39) |
S27R |
probably damaging |
Het |
Pramel20 |
A |
T |
4: 143,298,821 (GRCm39) |
I255L |
probably benign |
Het |
Rgs17 |
A |
T |
10: 5,791,488 (GRCm39) |
D96E |
probably benign |
Het |
Senp1 |
A |
G |
15: 97,964,679 (GRCm39) |
F206L |
probably benign |
Het |
Sh3rf1 |
T |
A |
8: 61,825,756 (GRCm39) |
S584T |
probably benign |
Het |
Tex44 |
A |
T |
1: 86,354,459 (GRCm39) |
K123* |
probably null |
Het |
Tpst2 |
C |
A |
5: 112,455,887 (GRCm39) |
T142K |
probably damaging |
Het |
Ttc28 |
G |
A |
5: 111,433,085 (GRCm39) |
G2040R |
possibly damaging |
Het |
Uggt2 |
T |
A |
14: 119,263,905 (GRCm39) |
I1042F |
probably damaging |
Het |
Vmn2r91 |
T |
C |
17: 18,325,693 (GRCm39) |
S104P |
probably damaging |
Het |
Wdfy3 |
T |
C |
5: 102,003,252 (GRCm39) |
|
probably null |
Het |
Zeb2 |
G |
A |
2: 44,892,584 (GRCm39) |
A223V |
probably damaging |
Het |
Zfp1002 |
T |
C |
2: 150,096,520 (GRCm39) |
D303G |
probably benign |
Het |
Zfp566 |
A |
G |
7: 29,777,930 (GRCm39) |
S84P |
probably benign |
Het |
Zfp994 |
T |
A |
17: 22,420,736 (GRCm39) |
H71L |
possibly damaging |
Het |
|
Other mutations in Apoa4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01574:Apoa4
|
APN |
9 |
46,154,283 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02321:Apoa4
|
APN |
9 |
46,154,218 (GRCm39) |
missense |
probably damaging |
0.98 |
R0001:Apoa4
|
UTSW |
9 |
46,154,190 (GRCm39) |
missense |
probably benign |
0.03 |
R0054:Apoa4
|
UTSW |
9 |
46,153,822 (GRCm39) |
missense |
probably benign |
0.00 |
R0054:Apoa4
|
UTSW |
9 |
46,153,822 (GRCm39) |
missense |
probably benign |
0.00 |
R0401:Apoa4
|
UTSW |
9 |
46,154,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R1446:Apoa4
|
UTSW |
9 |
46,153,591 (GRCm39) |
missense |
probably benign |
0.03 |
R2027:Apoa4
|
UTSW |
9 |
46,154,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R2332:Apoa4
|
UTSW |
9 |
46,153,653 (GRCm39) |
missense |
probably benign |
0.00 |
R4979:Apoa4
|
UTSW |
9 |
46,152,803 (GRCm39) |
missense |
probably benign |
0.01 |
R5120:Apoa4
|
UTSW |
9 |
46,154,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R5780:Apoa4
|
UTSW |
9 |
46,153,890 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6769:Apoa4
|
UTSW |
9 |
46,154,465 (GRCm39) |
missense |
probably benign |
0.01 |
R6771:Apoa4
|
UTSW |
9 |
46,154,465 (GRCm39) |
missense |
probably benign |
0.01 |
R7009:Apoa4
|
UTSW |
9 |
46,154,178 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7384:Apoa4
|
UTSW |
9 |
46,152,772 (GRCm39) |
missense |
not run |
|
R8039:Apoa4
|
UTSW |
9 |
46,153,591 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8305:Apoa4
|
UTSW |
9 |
46,152,453 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R8851:Apoa4
|
UTSW |
9 |
46,153,906 (GRCm39) |
missense |
probably benign |
0.00 |
R9032:Apoa4
|
UTSW |
9 |
46,154,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R9485:Apoa4
|
UTSW |
9 |
46,152,453 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
Z1176:Apoa4
|
UTSW |
9 |
46,153,887 (GRCm39) |
missense |
possibly damaging |
0.82 |
|