Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank1 |
T |
C |
8: 23,589,636 (GRCm39) |
V608A |
probably damaging |
Het |
Arl14epl |
T |
C |
18: 47,065,661 (GRCm39) |
V142A |
possibly damaging |
Het |
Atp8a1 |
T |
C |
5: 67,932,159 (GRCm39) |
D210G |
|
Het |
Baz1b |
T |
C |
5: 135,260,538 (GRCm39) |
F1112L |
probably damaging |
Het |
Cage1 |
T |
A |
13: 38,206,898 (GRCm39) |
I316F |
probably damaging |
Het |
Car2 |
A |
C |
3: 14,952,968 (GRCm39) |
T37P |
probably benign |
Het |
Catsper2 |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
2: 121,228,053 (GRCm39) |
|
probably benign |
Het |
Cntnap3 |
T |
A |
13: 64,929,573 (GRCm39) |
D542V |
probably damaging |
Het |
Coro1b |
T |
C |
19: 4,202,525 (GRCm39) |
Y338H |
probably damaging |
Het |
Ctdspl2 |
G |
A |
2: 121,838,298 (GRCm39) |
|
probably null |
Het |
Cyp2a12 |
T |
C |
7: 26,735,944 (GRCm39) |
F451S |
probably damaging |
Het |
Dpm2 |
T |
C |
2: 32,462,391 (GRCm39) |
L59P |
probably damaging |
Het |
Duoxa2 |
A |
G |
2: 122,131,821 (GRCm39) |
Y170C |
probably damaging |
Het |
Dus2 |
T |
A |
8: 106,742,573 (GRCm39) |
Y34* |
probably null |
Het |
Dzip3 |
A |
G |
16: 48,781,493 (GRCm39) |
I266T |
possibly damaging |
Het |
Ebf3 |
T |
C |
7: 136,800,994 (GRCm39) |
T455A |
possibly damaging |
Het |
Echdc2 |
C |
T |
4: 108,027,076 (GRCm39) |
Q74* |
probably null |
Het |
Efhc1 |
T |
C |
1: 21,025,592 (GRCm39) |
Y33H |
probably damaging |
Het |
Fam20a |
A |
T |
11: 109,566,754 (GRCm39) |
C378* |
probably null |
Het |
Fbxo25 |
C |
A |
8: 13,989,621 (GRCm39) |
P356Q |
probably damaging |
Het |
Fig4 |
G |
T |
10: 41,161,399 (GRCm39) |
T59K |
possibly damaging |
Het |
Gbp10 |
T |
A |
5: 105,366,369 (GRCm39) |
M512L |
probably benign |
Het |
Gdf10 |
T |
A |
14: 33,654,221 (GRCm39) |
Y243N |
probably damaging |
Het |
Golga5 |
T |
A |
12: 102,458,476 (GRCm39) |
S640T |
probably benign |
Het |
H1f9 |
A |
T |
11: 94,859,083 (GRCm39) |
K126M |
possibly damaging |
Het |
Ints1 |
A |
T |
5: 139,743,947 (GRCm39) |
H1540Q |
probably benign |
Het |
Lipo3 |
A |
T |
19: 33,534,529 (GRCm39) |
L310Q |
probably benign |
Het |
Lrrk2 |
A |
G |
15: 91,640,051 (GRCm39) |
K1532R |
probably benign |
Het |
Ltc4s |
T |
C |
11: 50,128,074 (GRCm39) |
Y59C |
probably damaging |
Het |
Macf1 |
T |
A |
4: 123,377,944 (GRCm39) |
H1427L |
probably damaging |
Het |
Mroh2b |
A |
G |
15: 4,982,754 (GRCm39) |
|
probably null |
Het |
Mthfd1l |
A |
T |
10: 3,923,412 (GRCm39) |
D53V |
probably benign |
Het |
Muc4 |
C |
A |
16: 32,577,842 (GRCm39) |
P303Q |
|
Het |
Nrxn1 |
A |
G |
17: 90,469,792 (GRCm39) |
F1293S |
probably damaging |
Het |
Nrxn2 |
G |
A |
19: 6,540,108 (GRCm39) |
E803K |
probably damaging |
Het |
Nup155 |
A |
G |
15: 8,177,830 (GRCm39) |
D1071G |
possibly damaging |
Het |
Or1l4b |
T |
A |
2: 37,036,426 (GRCm39) |
D67E |
probably damaging |
Het |
Or2ag18 |
A |
T |
7: 106,405,126 (GRCm39) |
I181N |
probably benign |
Het |
Or2ak6 |
T |
A |
11: 58,592,955 (GRCm39) |
S143T |
possibly damaging |
Het |
Papln |
A |
G |
12: 83,821,633 (GRCm39) |
E287G |
probably damaging |
Het |
Pex13 |
C |
A |
11: 23,615,760 (GRCm39) |
G29C |
probably damaging |
Het |
Phrf1 |
C |
A |
7: 140,839,412 (GRCm39) |
T869K |
unknown |
Het |
Pitrm1 |
A |
G |
13: 6,627,517 (GRCm39) |
T912A |
probably benign |
Het |
Pla2g4c |
A |
G |
7: 13,071,692 (GRCm39) |
K171E |
probably benign |
Het |
Pnpla7 |
A |
T |
2: 24,929,709 (GRCm39) |
T833S |
probably damaging |
Het |
Por |
G |
T |
5: 135,744,918 (GRCm39) |
|
probably null |
Het |
Rab3ip |
G |
A |
10: 116,775,310 (GRCm39) |
S16L |
probably damaging |
Het |
Rabgef1 |
A |
T |
5: 130,240,792 (GRCm39) |
I304F |
probably benign |
Het |
Rbbp8 |
T |
C |
18: 11,875,736 (GRCm39) |
V883A |
possibly damaging |
Het |
Rnase4 |
A |
G |
14: 51,342,429 (GRCm39) |
D51G |
possibly damaging |
Het |
Rnf13 |
A |
C |
3: 57,740,997 (GRCm39) |
D291A |
probably benign |
Het |
Rps6kb2 |
A |
T |
19: 4,209,270 (GRCm39) |
I191N |
probably damaging |
Het |
Scn1a |
A |
G |
2: 66,181,358 (GRCm39) |
L55S |
probably benign |
Het |
Son |
T |
A |
16: 91,467,418 (GRCm39) |
F2260I |
unknown |
Het |
Spata31h1 |
C |
T |
10: 82,124,577 (GRCm39) |
S2811N |
probably benign |
Het |
Ssr1 |
A |
G |
13: 38,167,449 (GRCm39) |
I238T |
probably benign |
Het |
Stk11ip |
A |
G |
1: 75,506,818 (GRCm39) |
E633G |
possibly damaging |
Het |
Svs3a |
A |
G |
2: 164,132,062 (GRCm39) |
Y211C |
probably benign |
Het |
Sytl1 |
T |
A |
4: 132,988,175 (GRCm39) |
E60D |
possibly damaging |
Het |
Tlcd5 |
C |
T |
9: 43,022,664 (GRCm39) |
R230Q |
probably benign |
Het |
Tlr1 |
T |
C |
5: 65,083,198 (GRCm39) |
I460V |
probably damaging |
Het |
Tmem64 |
T |
C |
4: 15,266,718 (GRCm39) |
I256T |
probably damaging |
Het |
Ttll5 |
G |
A |
12: 85,964,516 (GRCm39) |
A553T |
possibly damaging |
Het |
Ttll5 |
A |
T |
12: 86,071,107 (GRCm39) |
T1327S |
probably benign |
Het |
Upp2 |
T |
A |
2: 58,680,177 (GRCm39) |
C334* |
probably null |
Het |
Wdr74 |
C |
A |
19: 8,713,358 (GRCm39) |
N24K |
possibly damaging |
Het |
Zbtb42 |
G |
A |
12: 112,645,848 (GRCm39) |
V8I |
probably benign |
Het |
Zfp541 |
T |
A |
7: 15,824,329 (GRCm39) |
L1078Q |
probably damaging |
Het |
Zfr2 |
T |
C |
10: 81,076,029 (GRCm39) |
V212A |
probably damaging |
Het |
|
Other mutations in Abca9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00309:Abca9
|
APN |
11 |
110,051,342 (GRCm39) |
missense |
probably benign |
|
IGL00467:Abca9
|
APN |
11 |
110,036,496 (GRCm39) |
splice site |
probably benign |
|
IGL00886:Abca9
|
APN |
11 |
110,054,101 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01340:Abca9
|
APN |
11 |
110,021,453 (GRCm39) |
missense |
probably benign |
|
IGL01351:Abca9
|
APN |
11 |
110,039,729 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01383:Abca9
|
APN |
11 |
110,004,119 (GRCm39) |
splice site |
probably benign |
|
IGL01384:Abca9
|
APN |
11 |
110,036,463 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01482:Abca9
|
APN |
11 |
110,011,599 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01586:Abca9
|
APN |
11 |
110,045,243 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01589:Abca9
|
APN |
11 |
110,046,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01926:Abca9
|
APN |
11 |
110,026,155 (GRCm39) |
splice site |
probably benign |
|
IGL02059:Abca9
|
APN |
11 |
110,051,220 (GRCm39) |
splice site |
probably benign |
|
IGL02084:Abca9
|
APN |
11 |
110,021,423 (GRCm39) |
missense |
probably benign |
|
IGL02096:Abca9
|
APN |
11 |
110,056,806 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02096:Abca9
|
APN |
11 |
109,993,359 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02290:Abca9
|
APN |
11 |
110,026,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02303:Abca9
|
APN |
11 |
110,045,376 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02549:Abca9
|
APN |
11 |
109,992,879 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02687:Abca9
|
APN |
11 |
110,005,058 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02752:Abca9
|
APN |
11 |
110,018,194 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02814:Abca9
|
APN |
11 |
110,045,293 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02878:Abca9
|
APN |
11 |
110,029,155 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03088:Abca9
|
APN |
11 |
110,035,087 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03231:Abca9
|
APN |
11 |
110,046,094 (GRCm39) |
missense |
probably damaging |
0.96 |
R0050:Abca9
|
UTSW |
11 |
110,036,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0050:Abca9
|
UTSW |
11 |
110,036,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Abca9
|
UTSW |
11 |
110,035,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Abca9
|
UTSW |
11 |
110,035,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Abca9
|
UTSW |
11 |
110,036,405 (GRCm39) |
missense |
probably damaging |
0.99 |
R0189:Abca9
|
UTSW |
11 |
110,032,488 (GRCm39) |
splice site |
probably benign |
|
R0189:Abca9
|
UTSW |
11 |
109,999,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R0375:Abca9
|
UTSW |
11 |
110,006,273 (GRCm39) |
missense |
probably benign |
0.00 |
R0601:Abca9
|
UTSW |
11 |
110,007,884 (GRCm39) |
critical splice donor site |
probably null |
|
R0624:Abca9
|
UTSW |
11 |
110,030,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Abca9
|
UTSW |
11 |
110,042,889 (GRCm39) |
missense |
probably benign |
0.02 |
R1004:Abca9
|
UTSW |
11 |
110,042,780 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1222:Abca9
|
UTSW |
11 |
110,035,890 (GRCm39) |
splice site |
probably benign |
|
R1451:Abca9
|
UTSW |
11 |
110,018,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Abca9
|
UTSW |
11 |
110,051,342 (GRCm39) |
missense |
probably benign |
|
R1462:Abca9
|
UTSW |
11 |
110,051,342 (GRCm39) |
missense |
probably benign |
|
R1474:Abca9
|
UTSW |
11 |
110,036,405 (GRCm39) |
missense |
probably damaging |
0.99 |
R1499:Abca9
|
UTSW |
11 |
110,030,458 (GRCm39) |
missense |
probably benign |
0.00 |
R1778:Abca9
|
UTSW |
11 |
110,021,542 (GRCm39) |
nonsense |
probably null |
|
R2015:Abca9
|
UTSW |
11 |
110,022,672 (GRCm39) |
missense |
probably benign |
0.01 |
R2295:Abca9
|
UTSW |
11 |
110,039,729 (GRCm39) |
missense |
probably damaging |
0.99 |
R2303:Abca9
|
UTSW |
11 |
110,049,052 (GRCm39) |
missense |
probably benign |
0.01 |
R2403:Abca9
|
UTSW |
11 |
110,006,280 (GRCm39) |
missense |
probably benign |
0.16 |
R2886:Abca9
|
UTSW |
11 |
110,035,712 (GRCm39) |
splice site |
probably benign |
|
R3435:Abca9
|
UTSW |
11 |
110,045,256 (GRCm39) |
missense |
probably benign |
0.24 |
R3976:Abca9
|
UTSW |
11 |
110,039,615 (GRCm39) |
missense |
probably benign |
0.25 |
R4335:Abca9
|
UTSW |
11 |
110,042,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4411:Abca9
|
UTSW |
11 |
110,042,781 (GRCm39) |
missense |
probably benign |
0.00 |
R4613:Abca9
|
UTSW |
11 |
110,035,610 (GRCm39) |
missense |
probably benign |
0.26 |
R4690:Abca9
|
UTSW |
11 |
110,039,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R4720:Abca9
|
UTSW |
11 |
110,018,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4751:Abca9
|
UTSW |
11 |
110,021,396 (GRCm39) |
missense |
probably benign |
0.00 |
R4797:Abca9
|
UTSW |
11 |
110,008,945 (GRCm39) |
missense |
probably benign |
|
R4818:Abca9
|
UTSW |
11 |
110,045,980 (GRCm39) |
critical splice donor site |
probably null |
|
R4903:Abca9
|
UTSW |
11 |
110,037,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:Abca9
|
UTSW |
11 |
110,042,874 (GRCm39) |
missense |
probably benign |
0.43 |
R4977:Abca9
|
UTSW |
11 |
110,026,899 (GRCm39) |
missense |
probably benign |
0.00 |
R5019:Abca9
|
UTSW |
11 |
110,056,760 (GRCm39) |
missense |
probably benign |
|
R5079:Abca9
|
UTSW |
11 |
110,036,395 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5082:Abca9
|
UTSW |
11 |
110,022,694 (GRCm39) |
missense |
probably benign |
|
R5093:Abca9
|
UTSW |
11 |
110,032,358 (GRCm39) |
missense |
probably damaging |
0.98 |
R5212:Abca9
|
UTSW |
11 |
109,998,052 (GRCm39) |
missense |
probably benign |
0.02 |
R5350:Abca9
|
UTSW |
11 |
110,006,364 (GRCm39) |
missense |
probably benign |
|
R5368:Abca9
|
UTSW |
11 |
110,036,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R5432:Abca9
|
UTSW |
11 |
110,032,380 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5436:Abca9
|
UTSW |
11 |
110,025,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R5497:Abca9
|
UTSW |
11 |
110,021,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R5503:Abca9
|
UTSW |
11 |
110,032,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R5594:Abca9
|
UTSW |
11 |
110,035,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R5742:Abca9
|
UTSW |
11 |
110,051,243 (GRCm39) |
missense |
probably damaging |
0.98 |
R5776:Abca9
|
UTSW |
11 |
109,998,286 (GRCm39) |
splice site |
probably null |
|
R5781:Abca9
|
UTSW |
11 |
109,992,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Abca9
|
UTSW |
11 |
110,007,902 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5923:Abca9
|
UTSW |
11 |
110,051,378 (GRCm39) |
missense |
probably benign |
0.09 |
R6020:Abca9
|
UTSW |
11 |
110,036,439 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6179:Abca9
|
UTSW |
11 |
110,025,080 (GRCm39) |
missense |
probably benign |
0.05 |
R6245:Abca9
|
UTSW |
11 |
110,026,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R6249:Abca9
|
UTSW |
11 |
110,036,453 (GRCm39) |
missense |
probably benign |
|
R6365:Abca9
|
UTSW |
11 |
110,036,481 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6385:Abca9
|
UTSW |
11 |
110,025,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R6481:Abca9
|
UTSW |
11 |
110,056,788 (GRCm39) |
nonsense |
probably null |
|
R6675:Abca9
|
UTSW |
11 |
110,006,302 (GRCm39) |
missense |
probably benign |
|
R6909:Abca9
|
UTSW |
11 |
110,006,323 (GRCm39) |
missense |
probably benign |
0.01 |
R7390:Abca9
|
UTSW |
11 |
110,036,487 (GRCm39) |
missense |
probably benign |
0.01 |
R7429:Abca9
|
UTSW |
11 |
110,018,252 (GRCm39) |
frame shift |
probably null |
|
R7431:Abca9
|
UTSW |
11 |
110,018,252 (GRCm39) |
frame shift |
probably null |
|
R7621:Abca9
|
UTSW |
11 |
110,051,359 (GRCm39) |
missense |
probably benign |
0.00 |
R7623:Abca9
|
UTSW |
11 |
109,998,384 (GRCm39) |
missense |
probably benign |
0.27 |
R7660:Abca9
|
UTSW |
11 |
110,006,278 (GRCm39) |
missense |
probably benign |
|
R7784:Abca9
|
UTSW |
11 |
110,045,243 (GRCm39) |
nonsense |
probably null |
|
R7798:Abca9
|
UTSW |
11 |
110,029,005 (GRCm39) |
missense |
probably benign |
0.45 |
R7839:Abca9
|
UTSW |
11 |
110,025,085 (GRCm39) |
missense |
probably benign |
0.43 |
R7891:Abca9
|
UTSW |
11 |
110,054,098 (GRCm39) |
missense |
probably benign |
0.03 |
R7894:Abca9
|
UTSW |
11 |
109,997,415 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8030:Abca9
|
UTSW |
11 |
110,011,534 (GRCm39) |
missense |
probably benign |
|
R8133:Abca9
|
UTSW |
11 |
110,018,289 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8195:Abca9
|
UTSW |
11 |
110,029,155 (GRCm39) |
missense |
probably benign |
0.01 |
R8304:Abca9
|
UTSW |
11 |
109,997,954 (GRCm39) |
critical splice donor site |
probably null |
|
R8386:Abca9
|
UTSW |
11 |
110,021,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R8390:Abca9
|
UTSW |
11 |
110,036,456 (GRCm39) |
missense |
probably benign |
0.01 |
R8692:Abca9
|
UTSW |
11 |
110,032,409 (GRCm39) |
missense |
probably benign |
0.11 |
R8721:Abca9
|
UTSW |
11 |
110,035,115 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8738:Abca9
|
UTSW |
11 |
110,056,817 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R8900:Abca9
|
UTSW |
11 |
110,045,218 (GRCm39) |
missense |
probably benign |
|
R8948:Abca9
|
UTSW |
11 |
110,054,206 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8950:Abca9
|
UTSW |
11 |
110,054,206 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8964:Abca9
|
UTSW |
11 |
110,038,075 (GRCm39) |
nonsense |
probably null |
|
R9019:Abca9
|
UTSW |
11 |
110,011,522 (GRCm39) |
missense |
|
|
R9034:Abca9
|
UTSW |
11 |
110,039,615 (GRCm39) |
missense |
probably benign |
0.25 |
R9035:Abca9
|
UTSW |
11 |
110,021,461 (GRCm39) |
missense |
probably damaging |
0.97 |
R9199:Abca9
|
UTSW |
11 |
110,056,770 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9402:Abca9
|
UTSW |
11 |
110,049,154 (GRCm39) |
missense |
probably benign |
0.14 |
R9414:Abca9
|
UTSW |
11 |
110,035,100 (GRCm39) |
missense |
probably damaging |
0.97 |
R9554:Abca9
|
UTSW |
11 |
110,029,107 (GRCm39) |
missense |
probably benign |
|
R9626:Abca9
|
UTSW |
11 |
110,011,606 (GRCm39) |
missense |
probably benign |
0.01 |
R9651:Abca9
|
UTSW |
11 |
110,006,319 (GRCm39) |
missense |
probably benign |
0.09 |
R9665:Abca9
|
UTSW |
11 |
110,006,281 (GRCm39) |
missense |
probably benign |
0.00 |
R9665:Abca9
|
UTSW |
11 |
110,006,280 (GRCm39) |
missense |
probably benign |
|
R9731:Abca9
|
UTSW |
11 |
110,025,024 (GRCm39) |
missense |
probably benign |
|
Z1176:Abca9
|
UTSW |
11 |
110,026,201 (GRCm39) |
missense |
probably benign |
0.02 |
|