Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl2 |
T |
C |
1: 156,457,652 (GRCm39) |
V306A |
possibly damaging |
Het |
Adcy4 |
T |
C |
14: 56,006,900 (GRCm39) |
Y1006C |
probably damaging |
Het |
Adprhl1 |
T |
C |
8: 13,296,114 (GRCm39) |
K144E |
probably benign |
Het |
Arid5b |
T |
C |
10: 67,932,519 (GRCm39) |
R885G |
probably damaging |
Het |
Atp9a |
A |
T |
2: 168,503,853 (GRCm39) |
V613E |
probably damaging |
Het |
Atxn7l1 |
G |
T |
12: 33,244,886 (GRCm39) |
|
probably benign |
Het |
Brd8 |
C |
A |
18: 34,756,497 (GRCm39) |
|
probably benign |
Het |
Bsnd |
C |
T |
4: 106,343,868 (GRCm39) |
R146H |
probably benign |
Het |
C4b |
C |
T |
17: 34,947,838 (GRCm39) |
R1659H |
probably damaging |
Het |
Duox1 |
G |
A |
2: 122,168,115 (GRCm39) |
R1080H |
probably benign |
Het |
Eml2 |
T |
C |
7: 18,916,326 (GRCm39) |
|
probably null |
Het |
Fbxo44 |
G |
A |
4: 148,238,065 (GRCm39) |
R221C |
probably damaging |
Het |
Frem1 |
T |
C |
4: 82,881,481 (GRCm39) |
D166G |
probably damaging |
Het |
Galnt5 |
T |
C |
2: 57,889,207 (GRCm39) |
L269P |
probably benign |
Het |
Gigyf2 |
A |
G |
1: 87,364,582 (GRCm39) |
E954G |
probably damaging |
Het |
Gpc6 |
T |
C |
14: 118,188,590 (GRCm39) |
V408A |
probably benign |
Het |
Hspg2 |
A |
G |
4: 137,289,535 (GRCm39) |
T3832A |
probably benign |
Het |
Ift88 |
A |
G |
14: 57,715,436 (GRCm39) |
N493S |
probably damaging |
Het |
Ighv1-76 |
A |
T |
12: 115,811,731 (GRCm39) |
C41S |
probably damaging |
Het |
Igkv12-46 |
G |
A |
6: 69,741,930 (GRCm39) |
T16I |
probably benign |
Het |
Igkv3-9 |
G |
T |
6: 70,565,547 (GRCm39) |
V49F |
probably damaging |
Het |
Isoc2b |
A |
T |
7: 4,852,433 (GRCm39) |
|
probably benign |
Het |
Lcp2 |
T |
A |
11: 34,037,173 (GRCm39) |
|
probably benign |
Het |
Lmntd1 |
A |
G |
6: 145,373,003 (GRCm39) |
|
probably null |
Het |
Mdm2 |
A |
T |
10: 117,545,694 (GRCm39) |
|
probably null |
Het |
Mrgprx3-ps |
T |
C |
7: 46,959,746 (GRCm39) |
|
noncoding transcript |
Het |
Msh2 |
T |
C |
17: 88,025,032 (GRCm39) |
S637P |
probably damaging |
Het |
Myo5b |
T |
C |
18: 74,831,345 (GRCm39) |
F765S |
possibly damaging |
Het |
Nav2 |
T |
A |
7: 49,047,857 (GRCm39) |
N91K |
probably benign |
Het |
Ndor1 |
G |
A |
2: 25,138,492 (GRCm39) |
P363S |
probably benign |
Het |
Npr3 |
G |
C |
15: 11,905,235 (GRCm39) |
T164R |
probably benign |
Het |
Pcdhb5 |
T |
C |
18: 37,455,050 (GRCm39) |
S477P |
possibly damaging |
Het |
Pde3b |
GTGATGATGATGATGATGATGATGATG |
GTGATGATGATGATGATGATGATG |
7: 114,133,984 (GRCm39) |
|
probably benign |
Het |
Pnpla7 |
G |
A |
2: 24,941,716 (GRCm39) |
W13* |
probably null |
Het |
Pnpla8 |
T |
C |
12: 44,330,225 (GRCm39) |
V41A |
probably benign |
Het |
Prdm2 |
A |
T |
4: 142,860,240 (GRCm39) |
S1017T |
probably benign |
Het |
Prdm5 |
T |
A |
6: 65,878,771 (GRCm39) |
Y108* |
probably null |
Het |
Rab34 |
T |
A |
11: 78,079,592 (GRCm39) |
|
probably null |
Het |
Skic3 |
A |
G |
13: 76,275,623 (GRCm39) |
E410G |
possibly damaging |
Het |
Smpd5 |
G |
T |
15: 76,179,112 (GRCm39) |
R160L |
possibly damaging |
Het |
Spmip10 |
A |
G |
18: 56,727,720 (GRCm39) |
T65A |
probably benign |
Het |
Srrm2 |
A |
G |
17: 24,029,442 (GRCm39) |
|
probably benign |
Het |
Taf5 |
T |
A |
19: 47,059,453 (GRCm39) |
V199D |
probably damaging |
Het |
Tas2r114 |
C |
T |
6: 131,666,585 (GRCm39) |
V148I |
probably benign |
Het |
Tas2r136 |
C |
A |
6: 132,754,972 (GRCm39) |
V52L |
probably damaging |
Het |
Tnfrsf25 |
G |
A |
4: 152,202,843 (GRCm39) |
|
probably benign |
Het |
Tpd52l1 |
T |
C |
10: 31,255,315 (GRCm39) |
T11A |
possibly damaging |
Het |
Trmt1l |
G |
A |
1: 151,327,905 (GRCm39) |
E472K |
probably benign |
Het |
Ttc17 |
T |
C |
2: 94,173,098 (GRCm39) |
K766E |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,560,633 (GRCm39) |
R29256Q |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,572,414 (GRCm39) |
I26160V |
probably damaging |
Het |
Ubxn6 |
A |
T |
17: 56,376,303 (GRCm39) |
V311E |
probably damaging |
Het |
Usp2 |
T |
C |
9: 44,002,360 (GRCm39) |
S351P |
probably damaging |
Het |
Usp7 |
C |
A |
16: 8,526,778 (GRCm39) |
D187Y |
probably damaging |
Het |
Vmn1r115 |
C |
T |
7: 20,578,207 (GRCm39) |
R235K |
probably benign |
Het |
Vmn2r50 |
A |
C |
7: 9,784,235 (GRCm39) |
F80V |
probably damaging |
Het |
Vmn2r58 |
T |
A |
7: 41,511,360 (GRCm39) |
K481M |
possibly damaging |
Het |
Vmn2r86 |
A |
G |
10: 130,288,469 (GRCm39) |
I344T |
possibly damaging |
Het |
Zfp455 |
A |
T |
13: 67,355,389 (GRCm39) |
N219I |
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 |
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 |
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 |
|