Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankub1 |
T |
C |
3: 57,597,778 (GRCm39) |
D64G |
probably damaging |
Het |
Apobec2 |
C |
T |
17: 48,730,303 (GRCm39) |
W121* |
probably null |
Het |
Arid2 |
A |
G |
15: 96,269,199 (GRCm39) |
N1104S |
probably benign |
Het |
Bltp1 |
T |
A |
3: 37,088,751 (GRCm39) |
M569K |
probably damaging |
Het |
Brap |
T |
C |
5: 121,803,156 (GRCm39) |
|
probably benign |
Het |
Cilp |
A |
C |
9: 65,185,450 (GRCm39) |
N515T |
probably benign |
Het |
Cpeb2 |
T |
A |
5: 43,419,067 (GRCm39) |
|
probably benign |
Het |
Creb1 |
C |
T |
1: 64,615,374 (GRCm39) |
T242I |
possibly damaging |
Het |
Ddx60 |
T |
C |
8: 62,441,117 (GRCm39) |
V1062A |
possibly damaging |
Het |
Dock8 |
A |
G |
19: 25,133,312 (GRCm39) |
E1153G |
probably benign |
Het |
Gk5 |
A |
G |
9: 96,058,345 (GRCm39) |
|
probably benign |
Het |
Hmcn2 |
T |
A |
2: 31,252,242 (GRCm39) |
V904D |
probably damaging |
Het |
Hnmt |
T |
A |
2: 23,938,751 (GRCm39) |
H29L |
probably damaging |
Het |
Hsf1 |
A |
G |
15: 76,380,649 (GRCm39) |
|
probably benign |
Het |
Igkv1-122 |
C |
A |
6: 67,994,400 (GRCm39) |
T96K |
probably damaging |
Het |
Iyd |
T |
C |
10: 3,501,987 (GRCm39) |
I211T |
probably damaging |
Het |
Kcnn1 |
G |
T |
8: 71,303,381 (GRCm39) |
H34N |
probably damaging |
Het |
Krtap5-3 |
G |
T |
7: 141,755,946 (GRCm39) |
|
probably benign |
Het |
Map3k19 |
C |
T |
1: 127,752,052 (GRCm39) |
R433K |
probably benign |
Het |
Mss51 |
A |
C |
14: 20,537,200 (GRCm39) |
C89W |
probably damaging |
Het |
Myh9 |
A |
T |
15: 77,675,289 (GRCm39) |
I276N |
probably damaging |
Het |
Myof |
T |
C |
19: 37,963,337 (GRCm39) |
E420G |
probably damaging |
Het |
Nfatc2ip |
C |
A |
7: 125,989,740 (GRCm39) |
V215L |
possibly damaging |
Het |
Or10ag52 |
A |
T |
2: 87,043,500 (GRCm39) |
Y88F |
probably benign |
Het |
Or51m1 |
T |
C |
7: 103,578,801 (GRCm39) |
M257T |
probably benign |
Het |
Or5d18 |
G |
A |
2: 87,864,754 (GRCm39) |
A243V |
probably benign |
Het |
Pcdhb4 |
T |
C |
18: 37,441,569 (GRCm39) |
I293T |
probably damaging |
Het |
Pdcd6ip |
A |
G |
9: 113,486,213 (GRCm39) |
S729P |
possibly damaging |
Het |
Pick1 |
C |
A |
15: 79,129,501 (GRCm39) |
H169N |
possibly damaging |
Het |
Ppp4r4 |
A |
C |
12: 103,547,643 (GRCm39) |
K212T |
probably damaging |
Het |
Racgap1 |
A |
G |
15: 99,526,622 (GRCm39) |
S314P |
probably damaging |
Het |
Rasef |
C |
A |
4: 73,652,720 (GRCm39) |
E594* |
probably null |
Het |
Ryr3 |
T |
G |
2: 112,740,742 (GRCm39) |
K522Q |
probably benign |
Het |
Shoc1 |
G |
T |
4: 59,094,162 (GRCm39) |
F187L |
probably benign |
Het |
Six5 |
T |
C |
7: 18,831,072 (GRCm39) |
|
probably benign |
Het |
Slc26a9 |
G |
T |
1: 131,691,615 (GRCm39) |
E619D |
probably benign |
Het |
Sqor |
A |
G |
2: 122,649,991 (GRCm39) |
I412V |
probably benign |
Het |
Srrt |
T |
A |
5: 137,294,379 (GRCm39) |
|
probably benign |
Het |
Sult1e1 |
C |
T |
5: 87,726,475 (GRCm39) |
R213K |
probably benign |
Het |
Tmc2 |
T |
A |
2: 130,082,050 (GRCm39) |
L411H |
probably damaging |
Het |
Tmem63b |
T |
A |
17: 45,975,921 (GRCm39) |
N511Y |
probably damaging |
Het |
Ucp3 |
T |
A |
7: 100,131,969 (GRCm39) |
|
probably benign |
Het |
Vmn1r201 |
A |
T |
13: 22,658,974 (GRCm39) |
I63F |
probably benign |
Het |
Vps13c |
G |
T |
9: 67,797,662 (GRCm39) |
L522F |
probably damaging |
Het |
Wwp1 |
T |
A |
4: 19,678,408 (GRCm39) |
T3S |
probably damaging |
Het |
Zc3hav1 |
A |
G |
6: 38,309,329 (GRCm39) |
S498P |
probably benign |
Het |
|
Other mutations in Gm5478 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0325:Gm5478
|
UTSW |
15 |
101,552,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Gm5478
|
UTSW |
15 |
101,553,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R1476:Gm5478
|
UTSW |
15 |
101,553,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Gm5478
|
UTSW |
15 |
101,552,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R2924:Gm5478
|
UTSW |
15 |
101,552,229 (GRCm39) |
critical splice donor site |
probably null |
|
R3236:Gm5478
|
UTSW |
15 |
101,552,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R4133:Gm5478
|
UTSW |
15 |
101,553,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Gm5478
|
UTSW |
15 |
101,552,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R5480:Gm5478
|
UTSW |
15 |
101,552,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R5524:Gm5478
|
UTSW |
15 |
101,553,102 (GRCm39) |
missense |
probably benign |
0.31 |
R6959:Gm5478
|
UTSW |
15 |
101,553,883 (GRCm39) |
missense |
probably damaging |
0.99 |
R7035:Gm5478
|
UTSW |
15 |
101,553,632 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8458:Gm5478
|
UTSW |
15 |
101,553,862 (GRCm39) |
missense |
probably benign |
0.00 |
R8461:Gm5478
|
UTSW |
15 |
101,554,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Gm5478
|
UTSW |
15 |
101,553,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R8727:Gm5478
|
UTSW |
15 |
101,553,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R9448:Gm5478
|
UTSW |
15 |
101,553,662 (GRCm39) |
missense |
probably damaging |
1.00 |
|