Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921504E06Rik |
T |
A |
2: 19,538,635 (GRCm39) |
M129L |
probably benign |
Het |
Aadacl2fm1 |
A |
G |
3: 59,843,558 (GRCm39) |
D84G |
probably damaging |
Het |
Abca2 |
T |
C |
2: 25,337,393 (GRCm39) |
I2416T |
probably damaging |
Het |
Akap9 |
C |
T |
5: 4,011,982 (GRCm39) |
T895I |
probably damaging |
Het |
Aldh8a1 |
A |
G |
10: 21,271,444 (GRCm39) |
E390G |
probably damaging |
Het |
Ank2 |
T |
A |
3: 126,741,162 (GRCm39) |
D1574V |
|
Het |
Blmh |
T |
C |
11: 76,859,455 (GRCm39) |
V352A |
probably benign |
Het |
Cacna1i |
T |
C |
15: 80,259,540 (GRCm39) |
L1270P |
probably damaging |
Het |
Ccdc80 |
T |
A |
16: 44,947,792 (GRCm39) |
H923Q |
probably damaging |
Het |
Cdc27 |
G |
A |
11: 104,406,286 (GRCm39) |
H610Y |
probably damaging |
Het |
Cep126 |
T |
C |
9: 8,101,791 (GRCm39) |
I248V |
probably benign |
Het |
Ces5a |
T |
C |
8: 94,257,430 (GRCm39) |
N125S |
probably damaging |
Het |
Chd3 |
G |
A |
11: 69,254,510 (GRCm39) |
H201Y |
probably benign |
Het |
Cpeb1 |
T |
C |
7: 81,007,152 (GRCm39) |
T292A |
probably damaging |
Het |
Gli2 |
G |
A |
1: 118,763,558 (GRCm39) |
T1531I |
probably damaging |
Het |
Gm6871 |
T |
C |
7: 41,197,185 (GRCm39) |
T7A |
|
Het |
Kank1 |
A |
G |
19: 25,388,163 (GRCm39) |
D612G |
possibly damaging |
Het |
Lhcgr |
AT |
ATT |
17: 89,049,677 (GRCm39) |
615 |
probably null |
Het |
Mfsd6 |
T |
A |
1: 52,747,800 (GRCm39) |
D355V |
probably benign |
Het |
Myo7a |
T |
C |
7: 97,712,846 (GRCm39) |
K1710E |
probably benign |
Het |
Or13d1 |
C |
G |
4: 52,970,788 (GRCm39) |
H56D |
probably damaging |
Het |
Or52ae7 |
A |
G |
7: 103,119,459 (GRCm39) |
D71G |
probably damaging |
Het |
Pcdha8 |
G |
A |
18: 37,126,264 (GRCm39) |
V249M |
probably damaging |
Het |
Pglyrp3 |
A |
G |
3: 91,933,790 (GRCm39) |
D145G |
probably benign |
Het |
Pkhd1l1 |
A |
G |
15: 44,410,055 (GRCm39) |
K2521E |
possibly damaging |
Het |
Pld3 |
A |
G |
7: 27,232,086 (GRCm39) |
V398A |
probably damaging |
Het |
Plxnb1 |
A |
T |
9: 108,941,146 (GRCm39) |
T1642S |
probably damaging |
Het |
Ppp2r1a |
T |
G |
17: 21,179,700 (GRCm39) |
V348G |
possibly damaging |
Het |
Prdm2 |
C |
A |
4: 142,859,303 (GRCm39) |
C1329F |
possibly damaging |
Het |
Ric8a |
G |
T |
7: 140,441,269 (GRCm39) |
G423V |
probably damaging |
Het |
Rnf17 |
A |
G |
14: 56,658,593 (GRCm39) |
D94G |
probably benign |
Het |
Serpina3f |
T |
C |
12: 104,185,769 (GRCm39) |
F325L |
probably damaging |
Het |
Sin3a |
T |
A |
9: 57,034,568 (GRCm39) |
V1247E |
possibly damaging |
Het |
Skint5 |
C |
A |
4: 113,798,087 (GRCm39) |
M165I |
probably benign |
Het |
Slc19a3 |
T |
G |
1: 83,000,216 (GRCm39) |
Y267S |
probably damaging |
Het |
Slc22a27 |
A |
T |
19: 7,887,390 (GRCm39) |
F196Y |
possibly damaging |
Het |
Slc5a4b |
A |
T |
10: 75,939,680 (GRCm39) |
I152N |
possibly damaging |
Het |
Tbc1d9 |
T |
A |
8: 83,982,519 (GRCm39) |
V768E |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,063,534 (GRCm39) |
M988K |
probably benign |
Het |
Top2b |
T |
A |
14: 16,393,291 (GRCm38) |
F317I |
probably damaging |
Het |
Wfdc8 |
A |
T |
2: 164,439,455 (GRCm39) |
L309* |
probably null |
Het |
Wipf1 |
G |
A |
2: 73,267,879 (GRCm39) |
P173L |
possibly damaging |
Het |
Zfp217 |
G |
A |
2: 169,961,571 (GRCm39) |
S252F |
possibly damaging |
Het |
Zfp949 |
C |
T |
9: 88,452,053 (GRCm39) |
T541I |
probably benign |
Het |
Zkscan16 |
T |
A |
4: 58,952,407 (GRCm39) |
I235N |
probably benign |
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 |
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 |
R9714:Abca3
|
UTSW |
17 |
24,595,702 (GRCm39) |
missense |
probably benign |
0.44 |
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 |
|
|