Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
A |
10: 100,446,455 (GRCm39) |
|
probably null |
Het |
9530068E07Rik |
T |
C |
11: 52,294,362 (GRCm39) |
V209A |
possibly damaging |
Het |
Acvrl1 |
T |
C |
15: 101,033,382 (GRCm39) |
Y90H |
probably benign |
Het |
Aff3 |
T |
C |
1: 38,574,737 (GRCm39) |
D81G |
probably damaging |
Het |
Amn |
G |
T |
12: 111,240,951 (GRCm39) |
V152L |
probably damaging |
Het |
Arhgap44 |
A |
G |
11: 64,957,987 (GRCm39) |
|
probably benign |
Het |
Atad5 |
T |
A |
11: 79,999,405 (GRCm39) |
V895D |
possibly damaging |
Het |
Card9 |
T |
G |
2: 26,248,029 (GRCm39) |
|
probably null |
Het |
Ccer1 |
T |
C |
10: 97,529,702 (GRCm39) |
S122P |
unknown |
Het |
Ccr2 |
A |
G |
9: 123,905,712 (GRCm39) |
|
probably benign |
Het |
Dsg1a |
T |
A |
18: 20,473,381 (GRCm39) |
I818N |
possibly damaging |
Het |
Ear10 |
G |
T |
14: 44,160,774 (GRCm39) |
L18I |
probably damaging |
Het |
Mertk |
A |
G |
2: 128,619,374 (GRCm39) |
Y544C |
probably damaging |
Het |
Miga1 |
A |
T |
3: 151,990,978 (GRCm39) |
|
probably benign |
Het |
Myo18a |
T |
C |
11: 77,669,061 (GRCm39) |
V307A |
probably damaging |
Het |
Or5p64 |
A |
T |
7: 107,854,910 (GRCm39) |
I145N |
possibly damaging |
Het |
Or7a38 |
T |
A |
10: 78,752,773 (GRCm39) |
L33H |
probably damaging |
Het |
Pou2f3 |
T |
C |
9: 43,036,384 (GRCm39) |
|
probably benign |
Het |
Pramel23 |
T |
A |
4: 143,423,910 (GRCm39) |
E293V |
probably benign |
Het |
Prickle2 |
A |
C |
6: 92,353,403 (GRCm39) |
S744A |
probably benign |
Het |
Prkcb |
T |
A |
7: 122,024,270 (GRCm39) |
|
probably null |
Het |
Prkd2 |
A |
G |
7: 16,603,757 (GRCm39) |
T813A |
probably benign |
Het |
Prkra |
G |
A |
2: 76,463,891 (GRCm39) |
T257M |
probably damaging |
Het |
Rbm18 |
C |
T |
2: 36,012,886 (GRCm39) |
R102Q |
probably damaging |
Het |
Rbsn |
A |
G |
6: 92,167,307 (GRCm39) |
S446P |
probably benign |
Het |
Rpgrip1l |
A |
T |
8: 91,996,990 (GRCm39) |
V28D |
possibly damaging |
Het |
Sdccag8 |
A |
T |
1: 176,775,928 (GRCm39) |
K613I |
probably damaging |
Het |
Serbp1 |
G |
A |
6: 67,244,103 (GRCm39) |
G8D |
probably damaging |
Het |
Slc6a2 |
T |
A |
8: 93,699,390 (GRCm39) |
Y139* |
probably null |
Het |
Slc7a2 |
T |
A |
8: 41,358,621 (GRCm39) |
F321L |
probably damaging |
Het |
Slco1b2 |
G |
A |
6: 141,594,279 (GRCm39) |
S48N |
probably damaging |
Het |
Ssbp2 |
G |
T |
13: 91,790,490 (GRCm39) |
V118L |
possibly damaging |
Het |
Sugp1 |
T |
A |
8: 70,512,512 (GRCm39) |
|
probably benign |
Het |
Taar5 |
C |
A |
10: 23,846,883 (GRCm39) |
R94S |
possibly damaging |
Het |
Tgs1 |
G |
T |
4: 3,586,181 (GRCm39) |
A353S |
probably benign |
Het |
Trav1 |
A |
G |
14: 52,666,099 (GRCm39) |
E32G |
probably damaging |
Het |
Trp53bp2 |
T |
C |
1: 182,259,160 (GRCm39) |
V71A |
probably benign |
Het |
Vmn2r50 |
T |
C |
7: 9,784,252 (GRCm39) |
Y74C |
probably damaging |
Het |
Wars1 |
A |
T |
12: 108,841,706 (GRCm39) |
M147K |
probably damaging |
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 |
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 |
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 |
|
|