Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alppl2 |
T |
A |
1: 87,016,136 (GRCm39) |
Q241L |
probably benign |
Het |
Apob |
T |
A |
12: 8,065,464 (GRCm39) |
N4144K |
probably benign |
Het |
B4gat1 |
A |
G |
19: 5,090,516 (GRCm39) |
H413R |
probably benign |
Het |
Ccdc179 |
T |
C |
7: 51,664,612 (GRCm39) |
T28A |
probably benign |
Het |
Ceacam5 |
A |
C |
7: 17,491,835 (GRCm39) |
D735A |
probably damaging |
Het |
Col18a1 |
C |
T |
10: 76,949,432 (GRCm39) |
D27N |
unknown |
Het |
Colgalt1 |
A |
G |
8: 72,073,456 (GRCm39) |
E359G |
probably benign |
Het |
Crybg2 |
T |
A |
4: 133,793,148 (GRCm39) |
I261N |
probably benign |
Het |
Cyyr1 |
A |
T |
16: 85,219,203 (GRCm39) |
L68Q |
unknown |
Het |
Dgkz |
T |
A |
2: 91,768,911 (GRCm39) |
|
probably null |
Het |
Efcab3 |
A |
T |
11: 104,867,912 (GRCm39) |
E3947V |
unknown |
Het |
Eif2ak2 |
C |
A |
17: 79,162,783 (GRCm39) |
D472Y |
probably damaging |
Het |
Elp2 |
A |
G |
18: 24,755,539 (GRCm39) |
T429A |
possibly damaging |
Het |
Fen1 |
G |
A |
19: 10,178,016 (GRCm39) |
H143Y |
probably benign |
Het |
Gm10518 |
C |
A |
1: 179,631,113 (GRCm39) |
R58S |
unknown |
Het |
Hspa1b |
T |
C |
17: 35,176,467 (GRCm39) |
D506G |
probably damaging |
Het |
Inhca |
G |
T |
9: 103,132,014 (GRCm39) |
P569H |
probably benign |
Het |
Kcna7 |
A |
G |
7: 45,056,390 (GRCm39) |
D202G |
probably benign |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Mal |
C |
T |
2: 127,498,025 (GRCm39) |
S10N |
possibly damaging |
Het |
Mgat2 |
T |
A |
12: 69,232,115 (GRCm39) |
W230R |
probably damaging |
Het |
Myo3a |
A |
T |
2: 22,436,493 (GRCm39) |
T883S |
probably benign |
Het |
Ncaph2 |
T |
C |
15: 89,249,526 (GRCm39) |
S277P |
probably benign |
Het |
Olfm3 |
G |
A |
3: 114,916,091 (GRCm39) |
W341* |
probably null |
Het |
Or13c7e-ps1 |
A |
C |
4: 43,781,454 (GRCm39) |
M292R |
probably damaging |
Het |
Or1p1 |
A |
C |
11: 74,180,146 (GRCm39) |
I225L |
probably damaging |
Het |
Or5b119 |
A |
G |
19: 13,457,368 (GRCm39) |
S65P |
probably damaging |
Het |
Or5d46 |
T |
A |
2: 88,169,928 (GRCm39) |
N6K |
|
Het |
Or5g26 |
T |
A |
2: 85,494,608 (GRCm39) |
I57F |
probably benign |
Het |
Or6z1 |
C |
A |
7: 6,504,999 (GRCm39) |
M75I |
probably benign |
Het |
Pcnx4 |
T |
C |
12: 72,603,039 (GRCm39) |
Y434H |
probably damaging |
Het |
Ptpn14 |
T |
A |
1: 189,583,484 (GRCm39) |
M777K |
probably benign |
Het |
Rasef |
A |
G |
4: 73,688,102 (GRCm39) |
I17T |
possibly damaging |
Het |
Scel |
A |
T |
14: 103,809,442 (GRCm39) |
|
probably null |
Het |
Scfd2 |
A |
T |
5: 74,386,004 (GRCm39) |
L605Q |
probably damaging |
Het |
Son |
A |
G |
16: 91,456,440 (GRCm39) |
E1729G |
probably damaging |
Het |
Spata31e2 |
C |
G |
1: 26,722,820 (GRCm39) |
E787Q |
probably benign |
Het |
Spout1 |
A |
G |
2: 30,065,813 (GRCm39) |
Y243H |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,276,601 (GRCm39) |
F1765S |
possibly damaging |
Het |
Tet2 |
A |
T |
3: 133,191,803 (GRCm39) |
V877E |
possibly damaging |
Het |
Txn2 |
T |
C |
15: 77,812,289 (GRCm39) |
|
probably benign |
Het |
Vmn1r158 |
T |
C |
7: 22,489,331 (GRCm39) |
I293V |
possibly damaging |
Het |
Vmn1r81 |
G |
A |
7: 11,994,449 (GRCm39) |
T53I |
probably damaging |
Het |
Vps18 |
T |
C |
2: 119,127,553 (GRCm39) |
F792S |
probably damaging |
Het |
Vps25 |
A |
G |
11: 101,146,853 (GRCm39) |
D91G |
probably null |
Het |
Wdr26 |
G |
A |
1: 181,015,224 (GRCm39) |
L396F |
possibly damaging |
Het |
Zfp1005 |
T |
A |
2: 150,111,304 (GRCm39) |
C665S |
possibly damaging |
Het |
Zfp26 |
T |
C |
9: 20,347,861 (GRCm39) |
E901G |
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 |
R6741:Rptor
|
UTSW |
11 |
119,786,803 (GRCm39) |
missense |
possibly damaging |
0.92 |
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 |
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 |
|
|