Other mutations in this stock |
Total: 16 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bicdl2 |
A |
G |
17: 23,886,155 (GRCm39) |
E361G |
probably damaging |
Het |
Cd163 |
A |
G |
6: 124,286,158 (GRCm39) |
D236G |
possibly damaging |
Het |
Cep76 |
A |
T |
18: 67,773,139 (GRCm39) |
I53N |
possibly damaging |
Het |
Cfap43 |
A |
G |
19: 47,779,851 (GRCm39) |
|
probably benign |
Het |
Champ1 |
T |
C |
8: 13,928,786 (GRCm39) |
S315P |
probably benign |
Het |
Ctdsp2 |
A |
G |
10: 126,832,266 (GRCm39) |
T91A |
probably benign |
Het |
Cyp4a32 |
G |
T |
4: 115,468,280 (GRCm39) |
K283N |
possibly damaging |
Het |
Dgki |
A |
G |
6: 36,914,246 (GRCm39) |
|
probably benign |
Het |
Fads2b |
A |
C |
2: 85,320,751 (GRCm39) |
F351V |
probably damaging |
Het |
Gabrr2 |
A |
G |
4: 33,082,364 (GRCm39) |
|
probably benign |
Het |
Garin4 |
C |
T |
1: 190,895,029 (GRCm39) |
R538H |
probably benign |
Het |
Grik2 |
A |
T |
10: 49,454,365 (GRCm39) |
M50K |
probably benign |
Het |
Muc5ac |
A |
G |
7: 141,367,518 (GRCm39) |
M2980V |
probably benign |
Het |
Pafah2 |
C |
T |
4: 134,145,408 (GRCm39) |
T264M |
probably damaging |
Het |
Tacc2 |
A |
G |
7: 130,343,996 (GRCm39) |
M2552V |
possibly damaging |
Het |
Usp3 |
C |
T |
9: 66,469,831 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Gm5414 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01011:Gm5414
|
APN |
15 |
101,536,569 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01774:Gm5414
|
APN |
15 |
101,535,410 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01939:Gm5414
|
APN |
15 |
101,534,105 (GRCm39) |
splice site |
probably benign |
|
IGL02205:Gm5414
|
APN |
15 |
101,534,304 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02411:Gm5414
|
APN |
15 |
101,536,269 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02720:Gm5414
|
APN |
15 |
101,533,990 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02900:Gm5414
|
APN |
15 |
101,536,242 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4480001:Gm5414
|
UTSW |
15 |
101,536,181 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4504001:Gm5414
|
UTSW |
15 |
101,534,258 (GRCm39) |
missense |
probably damaging |
0.98 |
R1905:Gm5414
|
UTSW |
15 |
101,533,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R2070:Gm5414
|
UTSW |
15 |
101,536,495 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3011:Gm5414
|
UTSW |
15 |
101,534,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R3033:Gm5414
|
UTSW |
15 |
101,533,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R4074:Gm5414
|
UTSW |
15 |
101,533,988 (GRCm39) |
missense |
probably benign |
|
R4257:Gm5414
|
UTSW |
15 |
101,533,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R4396:Gm5414
|
UTSW |
15 |
101,534,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R4648:Gm5414
|
UTSW |
15 |
101,536,543 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4912:Gm5414
|
UTSW |
15 |
101,533,445 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5095:Gm5414
|
UTSW |
15 |
101,532,473 (GRCm39) |
missense |
probably benign |
0.01 |
R5135:Gm5414
|
UTSW |
15 |
101,536,203 (GRCm39) |
missense |
probably damaging |
0.97 |
R5177:Gm5414
|
UTSW |
15 |
101,534,252 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5330:Gm5414
|
UTSW |
15 |
101,533,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R5331:Gm5414
|
UTSW |
15 |
101,533,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R5432:Gm5414
|
UTSW |
15 |
101,533,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R5521:Gm5414
|
UTSW |
15 |
101,536,422 (GRCm39) |
missense |
probably benign |
0.33 |
R5623:Gm5414
|
UTSW |
15 |
101,534,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R6781:Gm5414
|
UTSW |
15 |
101,534,096 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8298:Gm5414
|
UTSW |
15 |
101,532,605 (GRCm39) |
missense |
unknown |
|
R8912:Gm5414
|
UTSW |
15 |
101,536,620 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9092:Gm5414
|
UTSW |
15 |
101,536,345 (GRCm39) |
missense |
probably benign |
0.01 |
R9721:Gm5414
|
UTSW |
15 |
101,536,582 (GRCm39) |
nonsense |
probably null |
|
RF001:Gm5414
|
UTSW |
15 |
101,536,388 (GRCm39) |
missense |
probably benign |
|
|