Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acr |
T |
A |
15: 89,458,146 (GRCm39) |
Y276N |
probably damaging |
Het |
AI987944 |
A |
T |
7: 41,023,814 (GRCm39) |
Y388* |
probably null |
Het |
Ankrd29 |
G |
A |
18: 12,412,835 (GRCm39) |
T114I |
probably damaging |
Het |
Ap5z1 |
T |
C |
5: 142,453,536 (GRCm39) |
M168T |
probably benign |
Het |
Bard1 |
A |
C |
1: 71,085,880 (GRCm39) |
C608W |
probably damaging |
Het |
Brd10 |
A |
G |
19: 29,731,072 (GRCm39) |
S647P |
possibly damaging |
Het |
Clspn |
A |
G |
4: 126,471,566 (GRCm39) |
R907G |
probably benign |
Het |
Cubn |
C |
T |
2: 13,355,743 (GRCm39) |
V1830I |
probably benign |
Het |
Cwc22 |
T |
C |
2: 77,754,913 (GRCm39) |
N221S |
probably damaging |
Het |
Dact3 |
A |
G |
7: 16,609,540 (GRCm39) |
E64G |
possibly damaging |
Het |
Dhx40 |
T |
C |
11: 86,680,330 (GRCm39) |
E381G |
possibly damaging |
Het |
Dnah7a |
A |
G |
1: 53,458,907 (GRCm39) |
S3744P |
possibly damaging |
Het |
Epha4 |
A |
G |
1: 77,351,513 (GRCm39) |
V914A |
probably benign |
Het |
Fbxw10 |
G |
A |
11: 62,753,482 (GRCm39) |
C492Y |
probably damaging |
Het |
G930045G22Rik |
C |
A |
6: 50,824,756 (GRCm39) |
|
noncoding transcript |
Het |
Gm21103 |
A |
T |
14: 17,484,855 (GRCm39) |
I63K |
probably damaging |
Het |
Gpr156 |
T |
C |
16: 37,825,619 (GRCm39) |
V612A |
probably benign |
Het |
Gucy2g |
A |
G |
19: 55,229,572 (GRCm39) |
S33P |
probably benign |
Het |
Hibch |
A |
G |
1: 52,884,228 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,619,539 (GRCm39) |
C1192S |
probably damaging |
Het |
Hsd11b1 |
CGG |
CG |
1: 192,922,557 (GRCm39) |
|
probably null |
Het |
Ifi214 |
A |
G |
1: 173,352,686 (GRCm39) |
Y248H |
probably damaging |
Het |
Igf2bp2 |
T |
G |
16: 21,907,835 (GRCm39) |
I89L |
probably damaging |
Het |
Il2ra |
A |
T |
2: 11,681,703 (GRCm39) |
T103S |
possibly damaging |
Het |
Ino80 |
T |
A |
2: 119,276,056 (GRCm39) |
M407L |
probably benign |
Het |
Jade1 |
A |
C |
3: 41,567,946 (GRCm39) |
K671N |
probably benign |
Het |
Lca5 |
C |
T |
9: 83,280,648 (GRCm39) |
S384N |
probably benign |
Het |
Lce1l |
G |
T |
3: 92,757,804 (GRCm39) |
P18H |
unknown |
Het |
Lrrc8d |
T |
C |
5: 105,945,536 (GRCm39) |
|
probably benign |
Het |
Ly75 |
T |
C |
2: 60,195,489 (GRCm39) |
N223S |
probably damaging |
Het |
Mcm3 |
A |
T |
1: 20,873,768 (GRCm39) |
F784Y |
possibly damaging |
Het |
Ncf4 |
T |
G |
15: 78,144,988 (GRCm39) |
|
probably benign |
Het |
Ncoa1 |
T |
A |
12: 4,303,746 (GRCm39) |
M1362L |
probably benign |
Het |
Or1e16 |
T |
C |
11: 73,286,003 (GRCm39) |
T282A |
probably benign |
Het |
Or5p5 |
A |
G |
7: 107,414,451 (GRCm39) |
Y220C |
probably benign |
Het |
Or6c8b |
G |
C |
10: 128,882,433 (GRCm39) |
F166L |
probably damaging |
Het |
Prkg2 |
T |
C |
5: 99,115,593 (GRCm39) |
R543G |
probably damaging |
Het |
Ptprd |
A |
C |
4: 75,977,904 (GRCm39) |
|
probably null |
Het |
Scap |
A |
G |
9: 110,210,497 (GRCm39) |
S969G |
possibly damaging |
Het |
Sgk2 |
T |
C |
2: 162,836,624 (GRCm39) |
F60S |
probably benign |
Het |
Sgpp1 |
G |
T |
12: 75,781,981 (GRCm39) |
Y119* |
probably null |
Het |
Siglech |
A |
T |
7: 55,418,413 (GRCm39) |
K31* |
probably null |
Het |
Slc40a1 |
A |
G |
1: 45,951,498 (GRCm39) |
Y220H |
probably damaging |
Het |
Smurf2 |
G |
A |
11: 106,743,389 (GRCm39) |
T219M |
possibly damaging |
Het |
Speer4f2 |
A |
G |
5: 17,581,526 (GRCm39) |
K156R |
possibly damaging |
Het |
Spp1 |
T |
G |
5: 104,588,424 (GRCm39) |
D276E |
probably benign |
Het |
Stk32b |
T |
C |
5: 37,617,078 (GRCm39) |
|
probably null |
Het |
Stxbp5 |
G |
A |
10: 9,638,668 (GRCm39) |
Q1044* |
probably null |
Het |
Sv2c |
T |
A |
13: 96,097,886 (GRCm39) |
T696S |
probably damaging |
Het |
Tubgcp2 |
A |
C |
7: 139,584,937 (GRCm39) |
|
probably null |
Het |
Ubap1l |
C |
T |
9: 65,278,973 (GRCm39) |
P91S |
probably damaging |
Het |
Vmn2r76 |
A |
T |
7: 85,874,657 (GRCm39) |
D773E |
probably damaging |
Het |
Xirp2 |
C |
G |
2: 67,345,646 (GRCm39) |
S2629C |
probably benign |
Het |
Zbtb20 |
C |
A |
16: 43,431,230 (GRCm39) |
C580* |
probably null |
Het |
Zfp957 |
T |
A |
14: 79,450,622 (GRCm39) |
Q392H |
unknown |
Het |
Zfyve19 |
C |
T |
2: 119,042,427 (GRCm39) |
T178M |
probably damaging |
Het |
Zswim6 |
T |
C |
13: 107,906,128 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Acacb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00482:Acacb
|
APN |
5 |
114,338,350 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01291:Acacb
|
APN |
5 |
114,363,931 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01301:Acacb
|
APN |
5 |
114,384,559 (GRCm39) |
missense |
probably benign |
|
IGL01633:Acacb
|
APN |
5 |
114,356,919 (GRCm39) |
splice site |
probably benign |
|
IGL01736:Acacb
|
APN |
5 |
114,326,503 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01782:Acacb
|
APN |
5 |
114,338,581 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01924:Acacb
|
APN |
5 |
114,362,047 (GRCm39) |
splice site |
probably benign |
|
IGL01933:Acacb
|
APN |
5 |
114,322,251 (GRCm39) |
splice site |
probably benign |
|
IGL02028:Acacb
|
APN |
5 |
114,304,076 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02045:Acacb
|
APN |
5 |
114,378,721 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02346:Acacb
|
APN |
5 |
114,376,760 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02421:Acacb
|
APN |
5 |
114,361,939 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02445:Acacb
|
APN |
5 |
114,383,198 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02491:Acacb
|
APN |
5 |
114,330,166 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02598:Acacb
|
APN |
5 |
114,384,098 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02700:Acacb
|
APN |
5 |
114,356,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02730:Acacb
|
APN |
5 |
114,304,210 (GRCm39) |
splice site |
probably benign |
|
IGL03110:Acacb
|
APN |
5 |
114,333,295 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03125:Acacb
|
APN |
5 |
114,342,866 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03263:Acacb
|
APN |
5 |
114,351,754 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03324:Acacb
|
APN |
5 |
114,363,915 (GRCm39) |
nonsense |
probably null |
|
acetone
|
UTSW |
5 |
114,364,918 (GRCm39) |
nonsense |
probably null |
|
anabolism
|
UTSW |
5 |
114,383,281 (GRCm39) |
missense |
possibly damaging |
0.63 |
ANU05:Acacb
|
UTSW |
5 |
114,363,931 (GRCm39) |
missense |
probably benign |
0.03 |
ANU18:Acacb
|
UTSW |
5 |
114,384,559 (GRCm39) |
missense |
probably benign |
|
BB001:Acacb
|
UTSW |
5 |
114,383,281 (GRCm39) |
missense |
possibly damaging |
0.63 |
BB011:Acacb
|
UTSW |
5 |
114,383,281 (GRCm39) |
missense |
possibly damaging |
0.63 |
I0000:Acacb
|
UTSW |
5 |
114,376,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R0001:Acacb
|
UTSW |
5 |
114,342,894 (GRCm39) |
splice site |
probably benign |
|
R0219:Acacb
|
UTSW |
5 |
114,371,005 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0234:Acacb
|
UTSW |
5 |
114,347,878 (GRCm39) |
missense |
probably damaging |
0.99 |
R0234:Acacb
|
UTSW |
5 |
114,347,878 (GRCm39) |
missense |
probably damaging |
0.99 |
R0278:Acacb
|
UTSW |
5 |
114,371,320 (GRCm39) |
nonsense |
probably null |
|
R0607:Acacb
|
UTSW |
5 |
114,338,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R0964:Acacb
|
UTSW |
5 |
114,367,813 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1116:Acacb
|
UTSW |
5 |
114,349,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R1196:Acacb
|
UTSW |
5 |
114,383,153 (GRCm39) |
missense |
probably benign |
0.00 |
R1204:Acacb
|
UTSW |
5 |
114,328,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R1387:Acacb
|
UTSW |
5 |
114,338,573 (GRCm39) |
missense |
probably benign |
|
R1415:Acacb
|
UTSW |
5 |
114,303,982 (GRCm39) |
missense |
probably benign |
|
R1475:Acacb
|
UTSW |
5 |
114,333,313 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1497:Acacb
|
UTSW |
5 |
114,334,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R1520:Acacb
|
UTSW |
5 |
114,340,001 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1591:Acacb
|
UTSW |
5 |
114,341,484 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1644:Acacb
|
UTSW |
5 |
114,333,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Acacb
|
UTSW |
5 |
114,328,148 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1783:Acacb
|
UTSW |
5 |
114,347,828 (GRCm39) |
frame shift |
probably null |
|
R1784:Acacb
|
UTSW |
5 |
114,347,828 (GRCm39) |
frame shift |
probably null |
|
R1834:Acacb
|
UTSW |
5 |
114,373,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Acacb
|
UTSW |
5 |
114,334,770 (GRCm39) |
missense |
probably benign |
0.13 |
R1886:Acacb
|
UTSW |
5 |
114,357,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R1901:Acacb
|
UTSW |
5 |
114,303,795 (GRCm39) |
nonsense |
probably null |
|
R1902:Acacb
|
UTSW |
5 |
114,303,795 (GRCm39) |
nonsense |
probably null |
|
R1903:Acacb
|
UTSW |
5 |
114,303,795 (GRCm39) |
nonsense |
probably null |
|
R1924:Acacb
|
UTSW |
5 |
114,368,781 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1934:Acacb
|
UTSW |
5 |
114,336,343 (GRCm39) |
missense |
probably benign |
0.27 |
R2051:Acacb
|
UTSW |
5 |
114,383,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Acacb
|
UTSW |
5 |
114,347,828 (GRCm39) |
frame shift |
probably null |
|
R2133:Acacb
|
UTSW |
5 |
114,347,828 (GRCm39) |
frame shift |
probably null |
|
R2260:Acacb
|
UTSW |
5 |
114,354,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R2967:Acacb
|
UTSW |
5 |
114,304,131 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3421:Acacb
|
UTSW |
5 |
114,350,697 (GRCm39) |
splice site |
probably null |
|
R3729:Acacb
|
UTSW |
5 |
114,345,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R4206:Acacb
|
UTSW |
5 |
114,351,712 (GRCm39) |
missense |
probably benign |
|
R4245:Acacb
|
UTSW |
5 |
114,368,845 (GRCm39) |
missense |
probably damaging |
0.97 |
R4386:Acacb
|
UTSW |
5 |
114,379,982 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4439:Acacb
|
UTSW |
5 |
114,384,557 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4577:Acacb
|
UTSW |
5 |
114,364,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R4658:Acacb
|
UTSW |
5 |
114,338,625 (GRCm39) |
missense |
probably damaging |
0.96 |
R4688:Acacb
|
UTSW |
5 |
114,342,824 (GRCm39) |
missense |
probably benign |
0.01 |
R4720:Acacb
|
UTSW |
5 |
114,367,975 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4898:Acacb
|
UTSW |
5 |
114,370,999 (GRCm39) |
missense |
probably benign |
0.04 |
R5044:Acacb
|
UTSW |
5 |
114,304,088 (GRCm39) |
missense |
probably benign |
0.03 |
R5070:Acacb
|
UTSW |
5 |
114,384,089 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5294:Acacb
|
UTSW |
5 |
114,380,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R5350:Acacb
|
UTSW |
5 |
114,382,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R5401:Acacb
|
UTSW |
5 |
114,347,914 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5542:Acacb
|
UTSW |
5 |
114,333,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R5751:Acacb
|
UTSW |
5 |
114,368,893 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5821:Acacb
|
UTSW |
5 |
114,322,167 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5893:Acacb
|
UTSW |
5 |
114,367,912 (GRCm39) |
missense |
probably benign |
0.01 |
R5911:Acacb
|
UTSW |
5 |
114,370,951 (GRCm39) |
missense |
probably damaging |
0.97 |
R5944:Acacb
|
UTSW |
5 |
114,384,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R5973:Acacb
|
UTSW |
5 |
114,364,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R6027:Acacb
|
UTSW |
5 |
114,303,661 (GRCm39) |
missense |
probably benign |
0.43 |
R6103:Acacb
|
UTSW |
5 |
114,383,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R6139:Acacb
|
UTSW |
5 |
114,350,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R6292:Acacb
|
UTSW |
5 |
114,338,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R6368:Acacb
|
UTSW |
5 |
114,354,884 (GRCm39) |
missense |
probably damaging |
0.98 |
R6429:Acacb
|
UTSW |
5 |
114,366,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R6942:Acacb
|
UTSW |
5 |
114,330,024 (GRCm39) |
critical splice donor site |
probably null |
|
R7138:Acacb
|
UTSW |
5 |
114,345,387 (GRCm39) |
missense |
probably benign |
0.12 |
R7241:Acacb
|
UTSW |
5 |
114,383,161 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7254:Acacb
|
UTSW |
5 |
114,347,812 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7396:Acacb
|
UTSW |
5 |
114,351,722 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7439:Acacb
|
UTSW |
5 |
114,333,703 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7484:Acacb
|
UTSW |
5 |
114,356,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R7585:Acacb
|
UTSW |
5 |
114,384,073 (GRCm39) |
missense |
probably damaging |
0.99 |
R7712:Acacb
|
UTSW |
5 |
114,303,799 (GRCm39) |
missense |
probably benign |
0.13 |
R7868:Acacb
|
UTSW |
5 |
114,386,288 (GRCm39) |
missense |
probably benign |
0.22 |
R7873:Acacb
|
UTSW |
5 |
114,361,339 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7924:Acacb
|
UTSW |
5 |
114,383,281 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7940:Acacb
|
UTSW |
5 |
114,304,108 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7951:Acacb
|
UTSW |
5 |
114,326,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R7960:Acacb
|
UTSW |
5 |
114,368,922 (GRCm39) |
missense |
probably benign |
0.00 |
R7972:Acacb
|
UTSW |
5 |
114,364,918 (GRCm39) |
nonsense |
probably null |
|
R8007:Acacb
|
UTSW |
5 |
114,356,935 (GRCm39) |
missense |
probably damaging |
0.97 |
R8022:Acacb
|
UTSW |
5 |
114,361,915 (GRCm39) |
missense |
probably benign |
|
R8030:Acacb
|
UTSW |
5 |
114,371,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R8241:Acacb
|
UTSW |
5 |
114,333,297 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8264:Acacb
|
UTSW |
5 |
114,345,427 (GRCm39) |
missense |
probably benign |
0.00 |
R8292:Acacb
|
UTSW |
5 |
114,338,555 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8678:Acacb
|
UTSW |
5 |
114,340,032 (GRCm39) |
nonsense |
probably null |
|
R8693:Acacb
|
UTSW |
5 |
114,364,844 (GRCm39) |
missense |
probably damaging |
0.99 |
R8697:Acacb
|
UTSW |
5 |
114,351,441 (GRCm39) |
missense |
probably damaging |
0.96 |
R8772:Acacb
|
UTSW |
5 |
114,322,179 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8918:Acacb
|
UTSW |
5 |
114,333,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R9008:Acacb
|
UTSW |
5 |
114,386,815 (GRCm39) |
splice site |
silent |
|
R9044:Acacb
|
UTSW |
5 |
114,373,578 (GRCm39) |
missense |
probably benign |
0.00 |
R9165:Acacb
|
UTSW |
5 |
114,354,744 (GRCm39) |
missense |
probably benign |
0.01 |
R9231:Acacb
|
UTSW |
5 |
114,349,153 (GRCm39) |
missense |
probably benign |
0.01 |
R9440:Acacb
|
UTSW |
5 |
114,384,085 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9444:Acacb
|
UTSW |
5 |
114,384,020 (GRCm39) |
missense |
probably damaging |
0.99 |
R9562:Acacb
|
UTSW |
5 |
114,371,397 (GRCm39) |
missense |
probably damaging |
0.99 |
R9794:Acacb
|
UTSW |
5 |
114,387,578 (GRCm39) |
missense |
probably benign |
0.00 |
V1662:Acacb
|
UTSW |
5 |
114,376,769 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Acacb
|
UTSW |
5 |
114,387,009 (GRCm39) |
missense |
probably benign |
0.02 |
|