Other mutations in this stock |
Total: 20 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
C |
10: 78,903,767 (GRCm39) |
Y155C |
probably benign |
Homo |
Alpi |
G |
A |
1: 87,026,893 (GRCm39) |
|
probably benign |
Homo |
Arhgdib |
A |
T |
6: 136,909,297 (GRCm39) |
|
probably null |
Het |
Ckap5 |
T |
C |
2: 91,425,868 (GRCm39) |
|
probably benign |
Het |
Ddx50 |
A |
T |
10: 62,457,289 (GRCm39) |
M1K |
probably null |
Het |
Ell3 |
T |
C |
2: 121,269,969 (GRCm39) |
H380R |
probably damaging |
Het |
Epx |
A |
G |
11: 87,755,710 (GRCm39) |
V658A |
probably damaging |
Homo |
Ern1 |
A |
T |
11: 106,291,101 (GRCm39) |
I858N |
probably damaging |
Homo |
Mtmr10 |
G |
A |
7: 63,963,958 (GRCm39) |
G231D |
probably benign |
Het |
Nfx1 |
A |
G |
4: 40,976,803 (GRCm39) |
D159G |
probably damaging |
Homo |
Opn5 |
A |
G |
17: 42,891,522 (GRCm39) |
I305T |
probably damaging |
Homo |
Pak2 |
T |
C |
16: 31,852,602 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
T |
A |
15: 44,400,838 (GRCm39) |
I2204K |
possibly damaging |
Het |
Pkhd1l1 |
A |
T |
15: 44,363,463 (GRCm39) |
T628S |
possibly damaging |
Het |
Smgc |
T |
A |
15: 91,744,453 (GRCm39) |
|
probably benign |
Het |
Stab1 |
G |
A |
14: 30,872,206 (GRCm39) |
L1194F |
probably damaging |
Het |
Stab2 |
A |
G |
10: 86,779,153 (GRCm39) |
|
probably null |
Homo |
Tet1 |
T |
C |
10: 62,714,955 (GRCm39) |
D280G |
probably benign |
Het |
Vcam1 |
A |
G |
3: 115,918,298 (GRCm39) |
I227T |
probably benign |
Homo |
Wdr87-ps |
A |
G |
7: 29,230,417 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Ap4e1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Ap4e1
|
APN |
2 |
126,870,201 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00423:Ap4e1
|
APN |
2 |
126,870,209 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00659:Ap4e1
|
APN |
2 |
126,905,221 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01155:Ap4e1
|
APN |
2 |
126,885,365 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01672:Ap4e1
|
APN |
2 |
126,894,109 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01866:Ap4e1
|
APN |
2 |
126,888,830 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01940:Ap4e1
|
APN |
2 |
126,885,431 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02131:Ap4e1
|
APN |
2 |
126,903,849 (GRCm39) |
missense |
probably benign |
|
IGL02207:Ap4e1
|
APN |
2 |
126,853,736 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03394:Ap4e1
|
APN |
2 |
126,905,317 (GRCm39) |
missense |
probably benign |
0.18 |
quickstep
|
UTSW |
2 |
126,850,822 (GRCm39) |
critical splice donor site |
probably null |
|
R0090:Ap4e1
|
UTSW |
2 |
126,906,905 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0420:Ap4e1
|
UTSW |
2 |
126,891,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R0490:Ap4e1
|
UTSW |
2 |
126,888,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R0632:Ap4e1
|
UTSW |
2 |
126,891,200 (GRCm39) |
nonsense |
probably null |
|
R0670:Ap4e1
|
UTSW |
2 |
126,853,784 (GRCm39) |
critical splice donor site |
probably null |
|
R0698:Ap4e1
|
UTSW |
2 |
126,905,283 (GRCm39) |
missense |
probably benign |
0.00 |
R1183:Ap4e1
|
UTSW |
2 |
126,856,121 (GRCm39) |
missense |
probably damaging |
0.98 |
R1338:Ap4e1
|
UTSW |
2 |
126,888,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Ap4e1
|
UTSW |
2 |
126,903,475 (GRCm39) |
missense |
probably null |
1.00 |
R1528:Ap4e1
|
UTSW |
2 |
126,853,743 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1994:Ap4e1
|
UTSW |
2 |
126,903,467 (GRCm39) |
missense |
probably benign |
0.00 |
R2270:Ap4e1
|
UTSW |
2 |
126,889,083 (GRCm39) |
critical splice donor site |
probably null |
|
R2271:Ap4e1
|
UTSW |
2 |
126,889,083 (GRCm39) |
critical splice donor site |
probably null |
|
R3108:Ap4e1
|
UTSW |
2 |
126,898,226 (GRCm39) |
critical splice donor site |
probably null |
|
R4019:Ap4e1
|
UTSW |
2 |
126,903,846 (GRCm39) |
missense |
probably benign |
0.01 |
R4020:Ap4e1
|
UTSW |
2 |
126,903,846 (GRCm39) |
missense |
probably benign |
0.01 |
R4454:Ap4e1
|
UTSW |
2 |
126,889,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4691:Ap4e1
|
UTSW |
2 |
126,903,791 (GRCm39) |
missense |
probably benign |
0.08 |
R4767:Ap4e1
|
UTSW |
2 |
126,902,358 (GRCm39) |
missense |
probably benign |
|
R4803:Ap4e1
|
UTSW |
2 |
126,891,479 (GRCm39) |
missense |
probably benign |
0.20 |
R4804:Ap4e1
|
UTSW |
2 |
126,885,678 (GRCm39) |
critical splice donor site |
probably null |
|
R5155:Ap4e1
|
UTSW |
2 |
126,905,289 (GRCm39) |
missense |
probably benign |
0.02 |
R5157:Ap4e1
|
UTSW |
2 |
126,903,615 (GRCm39) |
missense |
probably benign |
0.00 |
R5248:Ap4e1
|
UTSW |
2 |
126,906,842 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5363:Ap4e1
|
UTSW |
2 |
126,879,784 (GRCm39) |
splice site |
probably null |
|
R5507:Ap4e1
|
UTSW |
2 |
126,850,818 (GRCm39) |
missense |
probably damaging |
0.98 |
R5642:Ap4e1
|
UTSW |
2 |
126,906,899 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6122:Ap4e1
|
UTSW |
2 |
126,870,080 (GRCm39) |
splice site |
probably null |
|
R6180:Ap4e1
|
UTSW |
2 |
126,908,508 (GRCm39) |
nonsense |
probably null |
|
R6298:Ap4e1
|
UTSW |
2 |
126,889,035 (GRCm39) |
missense |
probably benign |
0.00 |
R6329:Ap4e1
|
UTSW |
2 |
126,903,636 (GRCm39) |
missense |
probably benign |
0.10 |
R6543:Ap4e1
|
UTSW |
2 |
126,908,525 (GRCm39) |
missense |
probably benign |
0.03 |
R6954:Ap4e1
|
UTSW |
2 |
126,906,871 (GRCm39) |
missense |
probably benign |
0.01 |
R7144:Ap4e1
|
UTSW |
2 |
126,853,727 (GRCm39) |
missense |
probably damaging |
0.99 |
R7165:Ap4e1
|
UTSW |
2 |
126,905,238 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7348:Ap4e1
|
UTSW |
2 |
126,903,897 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7348:Ap4e1
|
UTSW |
2 |
126,903,896 (GRCm39) |
missense |
probably damaging |
0.96 |
R7382:Ap4e1
|
UTSW |
2 |
126,850,822 (GRCm39) |
critical splice donor site |
probably null |
|
R7571:Ap4e1
|
UTSW |
2 |
126,861,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R7768:Ap4e1
|
UTSW |
2 |
126,888,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R8875:Ap4e1
|
UTSW |
2 |
126,877,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R9135:Ap4e1
|
UTSW |
2 |
126,861,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R9592:Ap4e1
|
UTSW |
2 |
126,903,588 (GRCm39) |
missense |
probably benign |
0.14 |
R9701:Ap4e1
|
UTSW |
2 |
126,875,563 (GRCm39) |
missense |
probably benign |
0.01 |
X0060:Ap4e1
|
UTSW |
2 |
126,905,330 (GRCm39) |
missense |
probably benign |
0.01 |
X0065:Ap4e1
|
UTSW |
2 |
126,903,570 (GRCm39) |
missense |
probably benign |
0.00 |
|