Other mutations in this stock |
Total: 17 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aff3 |
T |
C |
1: 38,247,008 (GRCm39) |
H859R |
probably damaging |
Het |
Akip1 |
C |
T |
7: 109,306,716 (GRCm39) |
Q138* |
probably null |
Het |
Cep70 |
T |
C |
9: 99,128,366 (GRCm39) |
|
probably benign |
Het |
Ddx23 |
G |
A |
15: 98,556,132 (GRCm39) |
S62F |
unknown |
Het |
Gabrp |
A |
G |
11: 33,518,092 (GRCm39) |
I72T |
probably damaging |
Het |
Gpsm2 |
C |
T |
3: 108,609,825 (GRCm39) |
A102T |
probably damaging |
Het |
Metap2 |
A |
G |
10: 93,715,427 (GRCm39) |
C112R |
possibly damaging |
Het |
Or4c58 |
T |
G |
2: 89,675,122 (GRCm39) |
D65A |
probably damaging |
Het |
Or8b42 |
T |
A |
9: 38,342,316 (GRCm39) |
I246K |
probably damaging |
Het |
Pde12 |
A |
T |
14: 26,390,144 (GRCm39) |
D188E |
probably benign |
Het |
Pirb |
A |
T |
7: 3,719,031 (GRCm39) |
|
probably null |
Het |
Rreb1 |
T |
A |
13: 38,114,126 (GRCm39) |
L495Q |
possibly damaging |
Het |
Slc12a5 |
T |
C |
2: 164,821,410 (GRCm39) |
I275T |
probably damaging |
Het |
Tas2r122 |
A |
G |
6: 132,688,839 (GRCm39) |
I18T |
probably damaging |
Het |
Tdrkh |
A |
G |
3: 94,335,540 (GRCm39) |
T378A |
possibly damaging |
Het |
Ubr1 |
C |
T |
2: 120,777,103 (GRCm39) |
|
probably null |
Het |
Zglp1 |
A |
G |
9: 20,977,366 (GRCm39) |
F150L |
possibly damaging |
Het |
|
Other mutations in Agap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01385:Agap2
|
APN |
10 |
126,923,865 (GRCm39) |
missense |
unknown |
|
IGL01690:Agap2
|
APN |
10 |
126,918,827 (GRCm39) |
splice site |
probably benign |
|
IGL01765:Agap2
|
APN |
10 |
126,919,104 (GRCm39) |
missense |
unknown |
|
IGL02029:Agap2
|
APN |
10 |
126,916,152 (GRCm39) |
missense |
unknown |
|
IGL02525:Agap2
|
APN |
10 |
126,919,070 (GRCm39) |
splice site |
probably null |
|
IGL03019:Agap2
|
APN |
10 |
126,927,431 (GRCm39) |
splice site |
probably benign |
|
R0086:Agap2
|
UTSW |
10 |
126,923,751 (GRCm39) |
splice site |
probably null |
|
R0197:Agap2
|
UTSW |
10 |
126,927,571 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0345:Agap2
|
UTSW |
10 |
126,923,764 (GRCm39) |
missense |
unknown |
|
R0363:Agap2
|
UTSW |
10 |
126,926,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R0682:Agap2
|
UTSW |
10 |
126,919,351 (GRCm39) |
missense |
unknown |
|
R0787:Agap2
|
UTSW |
10 |
126,921,019 (GRCm39) |
missense |
unknown |
|
R0882:Agap2
|
UTSW |
10 |
126,923,319 (GRCm39) |
missense |
unknown |
|
R0883:Agap2
|
UTSW |
10 |
126,927,571 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1445:Agap2
|
UTSW |
10 |
126,926,981 (GRCm39) |
splice site |
probably benign |
|
R1800:Agap2
|
UTSW |
10 |
126,927,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R1854:Agap2
|
UTSW |
10 |
126,916,385 (GRCm39) |
missense |
unknown |
|
R1925:Agap2
|
UTSW |
10 |
126,926,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R1986:Agap2
|
UTSW |
10 |
126,918,913 (GRCm39) |
nonsense |
probably null |
|
R2050:Agap2
|
UTSW |
10 |
126,916,130 (GRCm39) |
nonsense |
probably null |
|
R2267:Agap2
|
UTSW |
10 |
126,918,297 (GRCm39) |
splice site |
probably benign |
|
R2269:Agap2
|
UTSW |
10 |
126,918,297 (GRCm39) |
splice site |
probably benign |
|
R4397:Agap2
|
UTSW |
10 |
126,926,352 (GRCm39) |
missense |
unknown |
|
R4418:Agap2
|
UTSW |
10 |
126,927,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R4472:Agap2
|
UTSW |
10 |
126,927,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Agap2
|
UTSW |
10 |
126,915,965 (GRCm39) |
missense |
unknown |
|
R4690:Agap2
|
UTSW |
10 |
126,927,244 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4744:Agap2
|
UTSW |
10 |
126,926,072 (GRCm39) |
critical splice donor site |
probably null |
|
R5316:Agap2
|
UTSW |
10 |
126,918,296 (GRCm39) |
splice site |
probably null |
|
R5533:Agap2
|
UTSW |
10 |
126,918,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R5680:Agap2
|
UTSW |
10 |
126,923,880 (GRCm39) |
missense |
unknown |
|
R6010:Agap2
|
UTSW |
10 |
126,926,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R6276:Agap2
|
UTSW |
10 |
126,925,229 (GRCm39) |
critical splice donor site |
probably null |
|
R6356:Agap2
|
UTSW |
10 |
126,918,865 (GRCm39) |
missense |
unknown |
|
R7138:Agap2
|
UTSW |
10 |
126,923,154 (GRCm39) |
missense |
unknown |
|
R7154:Agap2
|
UTSW |
10 |
126,927,524 (GRCm39) |
missense |
probably benign |
0.34 |
R7497:Agap2
|
UTSW |
10 |
126,926,834 (GRCm39) |
missense |
probably damaging |
0.99 |
R7718:Agap2
|
UTSW |
10 |
126,915,734 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7720:Agap2
|
UTSW |
10 |
126,926,957 (GRCm39) |
missense |
probably damaging |
0.96 |
R7893:Agap2
|
UTSW |
10 |
126,916,064 (GRCm39) |
missense |
unknown |
|
R7933:Agap2
|
UTSW |
10 |
126,922,789 (GRCm39) |
splice site |
probably benign |
|
R8337:Agap2
|
UTSW |
10 |
126,924,194 (GRCm39) |
missense |
unknown |
|
R8372:Agap2
|
UTSW |
10 |
126,925,185 (GRCm39) |
missense |
unknown |
|
R8428:Agap2
|
UTSW |
10 |
126,923,175 (GRCm39) |
missense |
unknown |
|
R8861:Agap2
|
UTSW |
10 |
126,926,383 (GRCm39) |
missense |
unknown |
|
R9082:Agap2
|
UTSW |
10 |
126,918,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R9341:Agap2
|
UTSW |
10 |
126,927,559 (GRCm39) |
missense |
unknown |
|
R9354:Agap2
|
UTSW |
10 |
126,923,104 (GRCm39) |
missense |
unknown |
|
R9650:Agap2
|
UTSW |
10 |
126,927,653 (GRCm39) |
missense |
unknown |
|
R9745:Agap2
|
UTSW |
10 |
126,919,380 (GRCm39) |
missense |
unknown |
|
Z1088:Agap2
|
UTSW |
10 |
126,924,111 (GRCm39) |
missense |
unknown |
|
Z1176:Agap2
|
UTSW |
10 |
126,916,094 (GRCm39) |
missense |
unknown |
|
|