Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510009E07Rik |
G |
T |
16: 21,513,092 (GRCm39) |
L22M |
probably damaging |
Het |
Abcc5 |
C |
T |
16: 20,163,446 (GRCm39) |
D1264N |
possibly damaging |
Het |
Abhd10 |
A |
G |
16: 45,553,099 (GRCm39) |
|
probably benign |
Het |
Acadvl |
G |
T |
11: 69,901,569 (GRCm39) |
A570E |
probably damaging |
Het |
Adgrb3 |
T |
A |
1: 25,586,629 (GRCm39) |
S355C |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,570,344 (GRCm39) |
V4953A |
possibly damaging |
Het |
Ano2 |
T |
A |
6: 125,992,536 (GRCm39) |
Y836* |
probably null |
Het |
Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
Ccdc8 |
T |
A |
7: 16,730,537 (GRCm39) |
D675E |
possibly damaging |
Het |
Ccnb2 |
A |
G |
9: 70,326,170 (GRCm39) |
V58A |
probably benign |
Het |
Cdcp3 |
T |
A |
7: 130,879,295 (GRCm39) |
|
probably null |
Het |
Cdh24 |
A |
T |
14: 54,875,547 (GRCm39) |
Y296N |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,198,266 (GRCm39) |
E2054G |
unknown |
Het |
Cnot1 |
A |
T |
8: 96,454,276 (GRCm39) |
F2067I |
probably damaging |
Het |
Csmd3 |
A |
G |
15: 47,813,334 (GRCm39) |
F329S |
|
Het |
Dact3 |
C |
A |
7: 16,619,840 (GRCm39) |
T445K |
unknown |
Het |
Dph6 |
C |
A |
2: 114,485,379 (GRCm39) |
|
probably benign |
Het |
Dst |
T |
A |
1: 34,209,517 (GRCm39) |
C1195S |
probably damaging |
Het |
Eeig1 |
A |
G |
2: 32,456,346 (GRCm39) |
D336G |
possibly damaging |
Het |
Fat3 |
T |
A |
9: 15,899,620 (GRCm39) |
N3138Y |
probably damaging |
Het |
Fbxw25 |
T |
C |
9: 109,483,651 (GRCm39) |
N187S |
|
Het |
Fuca1 |
A |
G |
4: 135,660,405 (GRCm39) |
I308V |
probably benign |
Het |
Galnt5 |
A |
G |
2: 57,907,222 (GRCm39) |
R562G |
probably damaging |
Het |
Gas8 |
G |
T |
8: 124,249,718 (GRCm39) |
R44S |
probably damaging |
Het |
Gja5 |
T |
C |
3: 96,958,071 (GRCm39) |
S43P |
possibly damaging |
Het |
Gm14403 |
A |
G |
2: 177,200,405 (GRCm39) |
D117G |
probably benign |
Het |
Gmpr2 |
G |
A |
14: 55,910,491 (GRCm39) |
V58M |
probably damaging |
Het |
Gtpbp6 |
T |
A |
5: 110,252,950 (GRCm39) |
I301F |
probably damaging |
Het |
H2bc22 |
T |
A |
13: 21,971,762 (GRCm39) |
D26E |
probably benign |
Het |
Hdhd5 |
T |
C |
6: 120,498,212 (GRCm39) |
Y129C |
probably damaging |
Het |
Hemgn |
A |
G |
4: 46,396,504 (GRCm39) |
M244T |
probably benign |
Het |
Hoxa1 |
T |
G |
6: 52,135,238 (GRCm39) |
|
probably null |
Het |
Iglc1 |
T |
A |
16: 18,880,551 (GRCm39) |
H90L |
|
Het |
Lamb2 |
C |
T |
9: 108,366,423 (GRCm39) |
S1545F |
possibly damaging |
Het |
Mc4r |
T |
C |
18: 66,992,580 (GRCm39) |
T178A |
probably benign |
Het |
Mcam |
T |
A |
9: 44,050,955 (GRCm39) |
S346T |
probably benign |
Het |
Mis18bp1 |
A |
G |
12: 65,195,626 (GRCm39) |
S713P |
probably benign |
Het |
Mybl2 |
A |
G |
2: 162,914,752 (GRCm39) |
Y290C |
probably damaging |
Het |
Or4k44 |
T |
C |
2: 111,368,281 (GRCm39) |
M118V |
probably damaging |
Het |
Or7e168 |
A |
T |
9: 19,720,225 (GRCm39) |
I204F |
possibly damaging |
Het |
Pak6 |
A |
G |
2: 118,525,068 (GRCm39) |
T565A |
probably damaging |
Het |
Pde5a |
A |
G |
3: 122,568,250 (GRCm39) |
T284A |
probably benign |
Het |
Pkd1l2 |
A |
T |
8: 117,756,384 (GRCm39) |
F1616Y |
probably damaging |
Het |
Pp2d1 |
T |
C |
17: 53,822,907 (GRCm39) |
E53G |
probably benign |
Het |
Ppp3cc |
A |
C |
14: 70,478,394 (GRCm39) |
S269R |
probably benign |
Het |
Ptprb |
A |
C |
10: 116,205,214 (GRCm39) |
D1856A |
possibly damaging |
Het |
Rgs22 |
A |
T |
15: 36,040,856 (GRCm39) |
V1001E |
probably benign |
Het |
Rnf8 |
T |
A |
17: 29,847,980 (GRCm39) |
V344E |
probably benign |
Het |
Rpn1 |
T |
C |
6: 88,061,550 (GRCm39) |
L13P |
possibly damaging |
Het |
Rsbn1 |
A |
T |
3: 103,822,326 (GRCm39) |
H187L |
probably benign |
Het |
Sdr16c6 |
T |
A |
4: 4,058,801 (GRCm39) |
I262F |
not run |
Het |
Sec22a |
A |
G |
16: 35,149,894 (GRCm39) |
F211L |
probably benign |
Het |
Slc16a4 |
G |
A |
3: 107,205,297 (GRCm39) |
A42T |
possibly damaging |
Het |
Smap1 |
T |
A |
1: 23,887,376 (GRCm39) |
Q386L |
probably benign |
Het |
Sos1 |
A |
T |
17: 80,787,323 (GRCm39) |
F10L |
probably benign |
Het |
Sptbn2 |
A |
G |
19: 4,776,196 (GRCm39) |
T202A |
probably damaging |
Het |
Stab1 |
C |
A |
14: 30,862,578 (GRCm39) |
V2282L |
probably benign |
Het |
Tex55 |
C |
T |
16: 38,648,453 (GRCm39) |
D219N |
possibly damaging |
Het |
Tmprss11f |
C |
T |
5: 86,672,019 (GRCm39) |
G391D |
probably damaging |
Het |
Tnfaip2 |
A |
G |
12: 111,412,072 (GRCm39) |
S158G |
probably damaging |
Het |
Trav6d-5 |
A |
G |
14: 53,032,843 (GRCm39) |
T31A |
probably benign |
Het |
Tst |
G |
A |
15: 78,289,903 (GRCm39) |
A44V |
probably damaging |
Het |
Vmn1r210 |
A |
T |
13: 23,011,405 (GRCm39) |
F294I |
probably benign |
Het |
Vwc2 |
T |
C |
11: 11,066,415 (GRCm39) |
F168L |
probably damaging |
Het |
Wdr25 |
G |
A |
12: 108,958,819 (GRCm39) |
G344S |
possibly damaging |
Het |
Zfp605 |
A |
G |
5: 110,275,386 (GRCm39) |
Y168C |
probably benign |
Het |
Zfp790 |
T |
A |
7: 29,525,130 (GRCm39) |
Y49* |
probably null |
Het |
Zfp93 |
T |
C |
7: 23,975,794 (GRCm39) |
F593S |
probably damaging |
Het |
Zfr |
C |
T |
15: 12,160,614 (GRCm39) |
T729I |
possibly 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 |
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 |
R9086:Abca9
|
UTSW |
11 |
109,992,879 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|