Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actrt3 |
A |
C |
3: 30,652,663 (GRCm39) |
F144V |
possibly damaging |
Het |
Arhgef12 |
A |
G |
9: 42,883,503 (GRCm39) |
I1342T |
probably benign |
Het |
Dbn1 |
A |
G |
13: 55,629,350 (GRCm39) |
|
probably null |
Het |
Defb12 |
T |
C |
8: 19,164,757 (GRCm39) |
E27G |
probably benign |
Het |
Dennd2b |
A |
G |
7: 109,144,304 (GRCm39) |
Y534H |
possibly damaging |
Het |
Dthd1 |
A |
T |
5: 63,000,289 (GRCm39) |
H537L |
probably damaging |
Het |
Ep400 |
A |
T |
5: 110,824,761 (GRCm39) |
S2359T |
unknown |
Het |
Epha5 |
T |
C |
5: 84,254,557 (GRCm39) |
I572V |
possibly damaging |
Het |
Grb10 |
C |
A |
11: 11,886,717 (GRCm39) |
|
probably null |
Het |
Hectd2 |
T |
C |
19: 36,589,759 (GRCm39) |
I628T |
probably damaging |
Het |
Il17rb |
T |
A |
14: 29,722,293 (GRCm39) |
Q246L |
possibly damaging |
Het |
Knop1 |
C |
T |
7: 118,445,061 (GRCm39) |
R301Q |
possibly damaging |
Het |
Lrp1b |
T |
C |
2: 41,136,001 (GRCm39) |
I1770M |
possibly damaging |
Het |
Mgst1 |
A |
C |
6: 138,127,836 (GRCm39) |
D66A |
probably damaging |
Het |
Nags |
A |
G |
11: 102,037,718 (GRCm39) |
D237G |
possibly damaging |
Het |
Nfatc2ip |
T |
A |
7: 125,995,182 (GRCm39) |
Q122L |
possibly damaging |
Het |
Nod2 |
T |
C |
8: 89,379,694 (GRCm39) |
V72A |
probably damaging |
Het |
Notch3 |
G |
T |
17: 32,362,458 (GRCm39) |
P1389Q |
probably benign |
Het |
Or5ac25 |
A |
G |
16: 59,181,918 (GRCm39) |
L221P |
probably damaging |
Het |
Plekhn1 |
A |
T |
4: 156,306,249 (GRCm39) |
I607N |
probably damaging |
Het |
Plekho2 |
C |
A |
9: 65,471,197 (GRCm39) |
R84L |
probably damaging |
Het |
Prag1 |
A |
T |
8: 36,614,434 (GRCm39) |
M1329L |
probably benign |
Het |
Prpsap2 |
C |
T |
11: 61,631,771 (GRCm39) |
|
probably null |
Het |
Ptprf |
A |
G |
4: 118,080,565 (GRCm39) |
S1230P |
probably benign |
Het |
Rigi |
A |
G |
4: 40,211,624 (GRCm39) |
I648T |
probably damaging |
Het |
Sesn3 |
T |
C |
9: 14,231,636 (GRCm39) |
I189T |
possibly damaging |
Het |
Skic2 |
G |
A |
17: 35,064,166 (GRCm39) |
R507* |
probably null |
Het |
Slc39a4 |
C |
T |
15: 76,498,283 (GRCm39) |
D385N |
probably damaging |
Het |
Tnfsf13b |
T |
C |
8: 10,057,314 (GRCm39) |
F128S |
possibly damaging |
Het |
Vmn1r49 |
A |
G |
6: 90,049,195 (GRCm39) |
V269A |
probably benign |
Het |
Vmn2r69 |
T |
A |
7: 85,061,724 (GRCm39) |
E83D |
probably benign |
Het |
Vmn2r76 |
T |
C |
7: 85,879,560 (GRCm39) |
N247D |
probably benign |
Het |
Zmym4 |
A |
G |
4: 126,808,878 (GRCm39) |
S390P |
possibly damaging |
Het |
|
Other mutations in Rptor |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00537:Rptor
|
APN |
11 |
119,690,271 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01319:Rptor
|
APN |
11 |
119,781,996 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01375:Rptor
|
APN |
11 |
119,787,262 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01899:Rptor
|
APN |
11 |
119,748,279 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01927:Rptor
|
APN |
11 |
119,548,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02312:Rptor
|
APN |
11 |
119,737,741 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02620:Rptor
|
APN |
11 |
119,671,413 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02651:Rptor
|
APN |
11 |
119,783,438 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03182:Rptor
|
APN |
11 |
119,615,971 (GRCm39) |
missense |
probably damaging |
1.00 |
Velocipede
|
UTSW |
11 |
119,786,803 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0103:Rptor
|
UTSW |
11 |
119,775,793 (GRCm39) |
missense |
probably benign |
0.01 |
R0179:Rptor
|
UTSW |
11 |
119,763,193 (GRCm39) |
missense |
probably benign |
0.14 |
R0217:Rptor
|
UTSW |
11 |
119,785,738 (GRCm39) |
splice site |
probably benign |
|
R0219:Rptor
|
UTSW |
11 |
119,712,603 (GRCm39) |
intron |
probably benign |
|
R0324:Rptor
|
UTSW |
11 |
119,783,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R0432:Rptor
|
UTSW |
11 |
119,671,379 (GRCm39) |
nonsense |
probably null |
|
R0718:Rptor
|
UTSW |
11 |
119,763,202 (GRCm39) |
missense |
probably benign |
0.15 |
R0730:Rptor
|
UTSW |
11 |
119,775,780 (GRCm39) |
missense |
probably benign |
0.06 |
R1019:Rptor
|
UTSW |
11 |
119,734,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R1073:Rptor
|
UTSW |
11 |
119,634,717 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1424:Rptor
|
UTSW |
11 |
119,671,419 (GRCm39) |
nonsense |
probably null |
|
R1579:Rptor
|
UTSW |
11 |
119,786,827 (GRCm39) |
missense |
probably benign |
0.00 |
R1766:Rptor
|
UTSW |
11 |
119,615,887 (GRCm39) |
missense |
probably damaging |
0.99 |
R1844:Rptor
|
UTSW |
11 |
119,647,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R2180:Rptor
|
UTSW |
11 |
119,615,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R2274:Rptor
|
UTSW |
11 |
119,647,148 (GRCm39) |
nonsense |
probably null |
|
R2275:Rptor
|
UTSW |
11 |
119,647,148 (GRCm39) |
nonsense |
probably null |
|
R2408:Rptor
|
UTSW |
11 |
119,748,277 (GRCm39) |
missense |
probably damaging |
0.99 |
R2981:Rptor
|
UTSW |
11 |
119,756,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2996:Rptor
|
UTSW |
11 |
119,747,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R3001:Rptor
|
UTSW |
11 |
119,763,197 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3002:Rptor
|
UTSW |
11 |
119,763,197 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3003:Rptor
|
UTSW |
11 |
119,763,197 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4358:Rptor
|
UTSW |
11 |
119,562,171 (GRCm39) |
missense |
probably damaging |
0.98 |
R4592:Rptor
|
UTSW |
11 |
119,689,666 (GRCm39) |
missense |
probably null |
1.00 |
R4647:Rptor
|
UTSW |
11 |
119,781,989 (GRCm39) |
missense |
probably benign |
0.33 |
R4666:Rptor
|
UTSW |
11 |
119,634,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R4958:Rptor
|
UTSW |
11 |
119,748,217 (GRCm39) |
missense |
probably benign |
0.29 |
R4974:Rptor
|
UTSW |
11 |
119,712,466 (GRCm39) |
intron |
probably benign |
|
R5073:Rptor
|
UTSW |
11 |
119,787,305 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5199:Rptor
|
UTSW |
11 |
119,494,642 (GRCm39) |
missense |
probably benign |
|
R5216:Rptor
|
UTSW |
11 |
119,734,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R5219:Rptor
|
UTSW |
11 |
119,734,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R5277:Rptor
|
UTSW |
11 |
119,713,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R5365:Rptor
|
UTSW |
11 |
119,734,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R5366:Rptor
|
UTSW |
11 |
119,734,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R5447:Rptor
|
UTSW |
11 |
119,734,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R5630:Rptor
|
UTSW |
11 |
119,647,075 (GRCm39) |
missense |
probably benign |
0.01 |
R6220:Rptor
|
UTSW |
11 |
119,788,268 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6567:Rptor
|
UTSW |
11 |
119,786,838 (GRCm39) |
missense |
probably benign |
0.00 |
R6915:Rptor
|
UTSW |
11 |
119,647,171 (GRCm39) |
missense |
probably damaging |
0.99 |
R7032:Rptor
|
UTSW |
11 |
119,737,762 (GRCm39) |
missense |
probably benign |
0.00 |
R7051:Rptor
|
UTSW |
11 |
119,765,012 (GRCm39) |
utr 3 prime |
probably benign |
|
R7396:Rptor
|
UTSW |
11 |
119,763,181 (GRCm39) |
missense |
probably benign |
0.10 |
R7429:Rptor
|
UTSW |
11 |
119,737,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R7430:Rptor
|
UTSW |
11 |
119,737,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Rptor
|
UTSW |
11 |
119,775,805 (GRCm39) |
missense |
probably benign |
0.00 |
R7595:Rptor
|
UTSW |
11 |
119,634,779 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7776:Rptor
|
UTSW |
11 |
119,783,453 (GRCm39) |
missense |
probably benign |
0.01 |
R7854:Rptor
|
UTSW |
11 |
119,748,779 (GRCm39) |
missense |
probably benign |
0.02 |
R8288:Rptor
|
UTSW |
11 |
119,748,763 (GRCm39) |
missense |
probably benign |
0.02 |
R8305:Rptor
|
UTSW |
11 |
119,702,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R8328:Rptor
|
UTSW |
11 |
119,783,473 (GRCm39) |
missense |
probably benign |
0.00 |
R8351:Rptor
|
UTSW |
11 |
119,783,465 (GRCm39) |
missense |
probably benign |
0.22 |
R8772:Rptor
|
UTSW |
11 |
119,615,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Rptor
|
UTSW |
11 |
119,494,751 (GRCm39) |
missense |
probably benign |
0.01 |
R8925:Rptor
|
UTSW |
11 |
119,782,036 (GRCm39) |
missense |
probably benign |
0.11 |
R8927:Rptor
|
UTSW |
11 |
119,782,036 (GRCm39) |
missense |
probably benign |
0.11 |
R8981:Rptor
|
UTSW |
11 |
119,734,508 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9149:Rptor
|
UTSW |
11 |
119,777,896 (GRCm39) |
missense |
probably benign |
0.05 |
R9213:Rptor
|
UTSW |
11 |
119,494,765 (GRCm39) |
missense |
probably benign |
|
R9224:Rptor
|
UTSW |
11 |
119,785,113 (GRCm39) |
missense |
probably benign |
0.11 |
R9290:Rptor
|
UTSW |
11 |
119,702,823 (GRCm39) |
missense |
probably benign |
0.00 |
R9314:Rptor
|
UTSW |
11 |
119,786,772 (GRCm39) |
missense |
probably benign |
0.43 |
R9371:Rptor
|
UTSW |
11 |
119,562,152 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9719:Rptor
|
UTSW |
11 |
119,781,940 (GRCm39) |
missense |
probably benign |
0.13 |
R9751:Rptor
|
UTSW |
11 |
119,777,964 (GRCm39) |
missense |
probably benign |
0.02 |
X0050:Rptor
|
UTSW |
11 |
119,737,231 (GRCm39) |
missense |
probably benign |
0.14 |
X0066:Rptor
|
UTSW |
11 |
119,748,692 (GRCm39) |
missense |
probably benign |
0.31 |
Z0001:Rptor
|
UTSW |
11 |
119,762,318 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,748,279 (GRCm39) |
critical splice donor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,742,294 (GRCm39) |
critical splice donor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,737,578 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z0001:Rptor
|
UTSW |
11 |
119,690,145 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,647,241 (GRCm39) |
critical splice donor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,647,062 (GRCm39) |
splice site |
probably null |
|
Z0001:Rptor
|
UTSW |
11 |
119,494,798 (GRCm39) |
critical splice donor site |
probably null |
|
Z0001:Rptor
|
UTSW |
11 |
119,787,375 (GRCm39) |
critical splice donor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,764,977 (GRCm39) |
critical splice acceptor site |
probably benign |
|
|