Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
C |
7: 120,030,383 (GRCm39) |
D165A |
probably benign |
Het |
AC157566.4 |
T |
C |
15: 76,418,354 (GRCm39) |
T52A |
probably benign |
Het |
Cd19 |
T |
C |
7: 126,010,230 (GRCm39) |
I381V |
probably benign |
Het |
Col17a1 |
C |
T |
19: 47,636,634 (GRCm39) |
V1374I |
unknown |
Het |
Crb2 |
G |
A |
2: 37,681,215 (GRCm39) |
G686D |
probably damaging |
Het |
Dok1 |
A |
G |
6: 83,008,275 (GRCm39) |
V469A |
probably benign |
Het |
Glg1 |
A |
G |
8: 111,924,301 (GRCm39) |
L229S |
probably damaging |
Het |
Hsd3b6 |
A |
G |
3: 98,713,645 (GRCm39) |
F218S |
probably benign |
Het |
Kif1c |
T |
C |
11: 70,615,660 (GRCm39) |
V588A |
probably benign |
Het |
Krt79 |
T |
G |
15: 101,839,196 (GRCm39) |
E424D |
probably benign |
Het |
Med13l |
T |
A |
5: 118,866,438 (GRCm39) |
D497E |
probably benign |
Het |
Mms19 |
A |
G |
19: 41,935,410 (GRCm39) |
F869L |
possibly damaging |
Het |
Myo19 |
A |
G |
11: 84,773,542 (GRCm39) |
M1V |
probably null |
Het |
Notum |
T |
C |
11: 120,551,019 (GRCm39) |
E49G |
probably benign |
Het |
Nup153 |
G |
A |
13: 46,866,435 (GRCm39) |
T203I |
possibly damaging |
Het |
Parvb |
G |
T |
15: 84,167,041 (GRCm39) |
G119C |
probably damaging |
Het |
Pcdh10 |
G |
A |
3: 45,336,010 (GRCm39) |
A775T |
probably damaging |
Het |
Pla2g4f |
C |
T |
2: 120,142,900 (GRCm39) |
R70Q |
probably benign |
Het |
Plxna1 |
A |
T |
6: 89,296,440 (GRCm39) |
L1868Q |
probably damaging |
Het |
Pmm2 |
T |
C |
16: 8,473,506 (GRCm39) |
L240P |
probably damaging |
Het |
Ptprc |
T |
A |
1: 138,008,687 (GRCm39) |
T667S |
probably damaging |
Het |
Rsad1 |
A |
G |
11: 94,435,298 (GRCm39) |
V263A |
probably benign |
Het |
Sardh |
C |
T |
2: 27,079,641 (GRCm39) |
V884M |
possibly damaging |
Het |
Slc35a5 |
T |
C |
16: 44,964,426 (GRCm39) |
E269G |
probably damaging |
Het |
Slc35f3 |
CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
8: 127,115,781 (GRCm39) |
|
probably benign |
Het |
Styk1 |
CTCTTCATGATTTTCTT |
CTCTT |
6: 131,278,612 (GRCm39) |
|
probably benign |
Het |
Taf11 |
T |
C |
17: 28,122,136 (GRCm39) |
E116G |
probably damaging |
Het |
Tbc1d10a |
G |
T |
11: 4,163,683 (GRCm39) |
A312S |
probably damaging |
Het |
Tiam1 |
T |
A |
16: 89,694,647 (GRCm39) |
H270L |
probably benign |
Het |
Vmn2r31 |
T |
A |
7: 7,387,367 (GRCm39) |
I735F |
probably damaging |
Het |
Vwf |
G |
A |
6: 125,601,536 (GRCm39) |
R826Q |
|
Het |
|
Other mutations in Abca3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00915:Abca3
|
APN |
17 |
24,593,220 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01538:Abca3
|
APN |
17 |
24,595,447 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01633:Abca3
|
APN |
17 |
24,616,327 (GRCm39) |
nonsense |
probably null |
|
IGL01837:Abca3
|
APN |
17 |
24,627,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01986:Abca3
|
APN |
17 |
24,627,088 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02049:Abca3
|
APN |
17 |
24,595,704 (GRCm39) |
nonsense |
probably null |
|
IGL02186:Abca3
|
APN |
17 |
24,596,714 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02794:Abca3
|
APN |
17 |
24,621,385 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02962:Abca3
|
APN |
17 |
24,619,383 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02963:Abca3
|
APN |
17 |
24,603,503 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03118:Abca3
|
APN |
17 |
24,619,424 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03144:Abca3
|
APN |
17 |
24,600,938 (GRCm39) |
missense |
probably benign |
0.37 |
R0028:Abca3
|
UTSW |
17 |
24,596,698 (GRCm39) |
missense |
probably benign |
0.39 |
R0278:Abca3
|
UTSW |
17 |
24,600,894 (GRCm39) |
missense |
probably benign |
0.09 |
R0570:Abca3
|
UTSW |
17 |
24,593,373 (GRCm39) |
missense |
probably benign |
|
R0825:Abca3
|
UTSW |
17 |
24,619,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R1164:Abca3
|
UTSW |
17 |
24,621,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R1348:Abca3
|
UTSW |
17 |
24,593,212 (GRCm39) |
splice site |
probably null |
|
R1557:Abca3
|
UTSW |
17 |
24,618,954 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1661:Abca3
|
UTSW |
17 |
24,596,816 (GRCm39) |
missense |
probably damaging |
0.99 |
R1665:Abca3
|
UTSW |
17 |
24,596,816 (GRCm39) |
missense |
probably damaging |
0.99 |
R1754:Abca3
|
UTSW |
17 |
24,596,753 (GRCm39) |
missense |
probably benign |
0.00 |
R1828:Abca3
|
UTSW |
17 |
24,585,171 (GRCm39) |
missense |
probably benign |
0.34 |
R1834:Abca3
|
UTSW |
17 |
24,595,666 (GRCm39) |
missense |
probably benign |
0.00 |
R1996:Abca3
|
UTSW |
17 |
24,606,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R2032:Abca3
|
UTSW |
17 |
24,585,056 (GRCm39) |
splice site |
probably benign |
|
R2100:Abca3
|
UTSW |
17 |
24,627,183 (GRCm39) |
missense |
probably damaging |
0.99 |
R2154:Abca3
|
UTSW |
17 |
24,596,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:Abca3
|
UTSW |
17 |
24,595,417 (GRCm39) |
missense |
probably damaging |
0.98 |
R2281:Abca3
|
UTSW |
17 |
24,595,700 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2994:Abca3
|
UTSW |
17 |
24,603,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R4091:Abca3
|
UTSW |
17 |
24,616,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R4294:Abca3
|
UTSW |
17 |
24,619,543 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4496:Abca3
|
UTSW |
17 |
24,602,947 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4633:Abca3
|
UTSW |
17 |
24,606,503 (GRCm39) |
missense |
probably null |
1.00 |
R4866:Abca3
|
UTSW |
17 |
24,593,274 (GRCm39) |
missense |
probably damaging |
0.97 |
R5022:Abca3
|
UTSW |
17 |
24,593,274 (GRCm39) |
missense |
probably damaging |
0.97 |
R5023:Abca3
|
UTSW |
17 |
24,593,274 (GRCm39) |
missense |
probably damaging |
0.97 |
R5072:Abca3
|
UTSW |
17 |
24,593,274 (GRCm39) |
missense |
probably damaging |
0.97 |
R5073:Abca3
|
UTSW |
17 |
24,593,274 (GRCm39) |
missense |
probably damaging |
0.97 |
R5074:Abca3
|
UTSW |
17 |
24,593,274 (GRCm39) |
missense |
probably damaging |
0.97 |
R5123:Abca3
|
UTSW |
17 |
24,603,434 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5157:Abca3
|
UTSW |
17 |
24,627,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R5183:Abca3
|
UTSW |
17 |
24,593,427 (GRCm39) |
missense |
probably benign |
0.39 |
R5269:Abca3
|
UTSW |
17 |
24,595,717 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5566:Abca3
|
UTSW |
17 |
24,602,901 (GRCm39) |
missense |
probably benign |
|
R5579:Abca3
|
UTSW |
17 |
24,595,703 (GRCm39) |
missense |
probably damaging |
0.97 |
R5620:Abca3
|
UTSW |
17 |
24,615,444 (GRCm39) |
missense |
probably benign |
0.05 |
R5755:Abca3
|
UTSW |
17 |
24,617,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R5954:Abca3
|
UTSW |
17 |
24,616,390 (GRCm39) |
missense |
probably benign |
0.00 |
R6041:Abca3
|
UTSW |
17 |
24,595,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R6187:Abca3
|
UTSW |
17 |
24,627,141 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6253:Abca3
|
UTSW |
17 |
24,616,526 (GRCm39) |
missense |
probably benign |
0.01 |
R6375:Abca3
|
UTSW |
17 |
24,606,536 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6487:Abca3
|
UTSW |
17 |
24,616,446 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6616:Abca3
|
UTSW |
17 |
24,603,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R6632:Abca3
|
UTSW |
17 |
24,603,444 (GRCm39) |
missense |
probably benign |
|
R6781:Abca3
|
UTSW |
17 |
24,593,380 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6918:Abca3
|
UTSW |
17 |
24,627,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R6962:Abca3
|
UTSW |
17 |
24,583,700 (GRCm39) |
missense |
probably benign |
0.39 |
R7163:Abca3
|
UTSW |
17 |
24,583,916 (GRCm39) |
missense |
probably benign |
|
R7199:Abca3
|
UTSW |
17 |
24,596,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R7287:Abca3
|
UTSW |
17 |
24,604,861 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7303:Abca3
|
UTSW |
17 |
24,617,495 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7338:Abca3
|
UTSW |
17 |
24,595,717 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7430:Abca3
|
UTSW |
17 |
24,583,932 (GRCm39) |
critical splice donor site |
probably null |
|
R7437:Abca3
|
UTSW |
17 |
24,619,472 (GRCm39) |
missense |
probably damaging |
0.99 |
R7776:Abca3
|
UTSW |
17 |
24,605,250 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7805:Abca3
|
UTSW |
17 |
24,624,128 (GRCm39) |
critical splice donor site |
probably null |
|
R7811:Abca3
|
UTSW |
17 |
24,616,362 (GRCm39) |
missense |
probably benign |
0.00 |
R7848:Abca3
|
UTSW |
17 |
24,603,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R7859:Abca3
|
UTSW |
17 |
24,603,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R7877:Abca3
|
UTSW |
17 |
24,602,997 (GRCm39) |
nonsense |
probably null |
|
R7893:Abca3
|
UTSW |
17 |
24,604,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R7910:Abca3
|
UTSW |
17 |
24,604,827 (GRCm39) |
missense |
probably benign |
0.09 |
R7911:Abca3
|
UTSW |
17 |
24,617,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R7964:Abca3
|
UTSW |
17 |
24,621,410 (GRCm39) |
missense |
probably benign |
0.26 |
R8016:Abca3
|
UTSW |
17 |
24,583,926 (GRCm39) |
missense |
probably benign |
0.06 |
R8028:Abca3
|
UTSW |
17 |
24,626,671 (GRCm39) |
missense |
probably benign |
0.02 |
R8150:Abca3
|
UTSW |
17 |
24,615,522 (GRCm39) |
missense |
probably benign |
0.08 |
R8298:Abca3
|
UTSW |
17 |
24,604,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R8444:Abca3
|
UTSW |
17 |
24,602,959 (GRCm39) |
missense |
probably damaging |
0.98 |
R8505:Abca3
|
UTSW |
17 |
24,593,471 (GRCm39) |
missense |
probably damaging |
0.97 |
R8547:Abca3
|
UTSW |
17 |
24,616,474 (GRCm39) |
missense |
probably benign |
0.00 |
R8699:Abca3
|
UTSW |
17 |
24,627,199 (GRCm39) |
missense |
probably benign |
0.01 |
R8903:Abca3
|
UTSW |
17 |
24,602,959 (GRCm39) |
missense |
probably damaging |
0.98 |
R9046:Abca3
|
UTSW |
17 |
24,617,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R9136:Abca3
|
UTSW |
17 |
24,596,807 (GRCm39) |
missense |
probably benign |
0.01 |
R9236:Abca3
|
UTSW |
17 |
24,626,712 (GRCm39) |
missense |
probably benign |
0.16 |
R9331:Abca3
|
UTSW |
17 |
24,616,324 (GRCm39) |
missense |
probably benign |
0.00 |
R9585:Abca3
|
UTSW |
17 |
24,619,486 (GRCm39) |
missense |
probably benign |
0.12 |
R9602:Abca3
|
UTSW |
17 |
24,617,378 (GRCm39) |
missense |
probably benign |
0.35 |
X0018:Abca3
|
UTSW |
17 |
24,615,454 (GRCm39) |
missense |
possibly damaging |
0.63 |
Z1177:Abca3
|
UTSW |
17 |
24,627,210 (GRCm39) |
frame shift |
probably null |
|
|