Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930449A18Rik |
T |
A |
3: 59,733,203 (GRCm39) |
|
noncoding transcript |
Het |
Actr1b |
T |
C |
1: 36,740,911 (GRCm39) |
Y171C |
possibly damaging |
Het |
C8a |
A |
G |
4: 104,733,543 (GRCm39) |
V4A |
probably benign |
Het |
Ccdc171 |
A |
G |
4: 83,473,045 (GRCm39) |
D158G |
probably damaging |
Het |
Ccdc184 |
T |
A |
15: 98,066,750 (GRCm39) |
|
probably null |
Het |
Cdc23 |
T |
C |
18: 34,770,100 (GRCm39) |
|
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,219,335 (GRCm39) |
N51S |
probably benign |
Het |
Dock10 |
T |
A |
1: 80,544,472 (GRCm39) |
E905V |
probably benign |
Het |
Eepd1 |
T |
C |
9: 25,505,920 (GRCm39) |
I460T |
probably benign |
Het |
Fen1 |
T |
A |
19: 10,177,731 (GRCm39) |
I238F |
probably damaging |
Het |
Fhdc1 |
C |
A |
3: 84,352,133 (GRCm39) |
V1031F |
probably benign |
Het |
Gm5493 |
A |
G |
17: 22,966,199 (GRCm39) |
E28G |
probably benign |
Het |
Jakmip2 |
A |
G |
18: 43,710,501 (GRCm39) |
V234A |
probably benign |
Het |
Map3k6 |
T |
C |
4: 132,979,258 (GRCm39) |
Y1204H |
possibly damaging |
Het |
Mpeg1 |
C |
A |
19: 12,440,272 (GRCm39) |
Q577K |
probably damaging |
Het |
Mthfd1 |
T |
C |
12: 76,348,047 (GRCm39) |
S564P |
probably damaging |
Het |
Mtmr11 |
T |
A |
3: 96,075,393 (GRCm39) |
C358S |
probably damaging |
Het |
Muc4 |
T |
C |
16: 32,753,802 (GRCm38) |
I1226T |
probably benign |
Het |
Myo18b |
G |
A |
5: 112,840,261 (GRCm39) |
H2511Y |
possibly damaging |
Het |
Ndufs6 |
A |
T |
13: 73,468,512 (GRCm39) |
D62E |
probably damaging |
Het |
Or5af2 |
T |
C |
11: 58,708,604 (GRCm39) |
Y257H |
probably damaging |
Het |
Or7e178 |
T |
C |
9: 20,225,629 (GRCm39) |
I196V |
possibly damaging |
Het |
Pcdhga1 |
T |
A |
18: 37,796,605 (GRCm39) |
D536E |
probably damaging |
Het |
Phactr3 |
G |
A |
2: 177,924,982 (GRCm39) |
|
probably null |
Het |
Ptgir |
A |
G |
7: 16,640,794 (GRCm39) |
M29V |
possibly damaging |
Het |
Ptk2 |
C |
T |
15: 73,103,825 (GRCm39) |
G749D |
probably benign |
Het |
Rab3il1 |
A |
T |
19: 10,007,518 (GRCm39) |
D222V |
probably damaging |
Het |
Radil |
T |
C |
5: 142,529,546 (GRCm39) |
D50G |
probably damaging |
Het |
Rfx7 |
A |
G |
9: 72,499,051 (GRCm39) |
T72A |
possibly damaging |
Het |
Scn7a |
T |
C |
2: 66,572,345 (GRCm39) |
I209V |
probably benign |
Het |
Sf3a1 |
C |
T |
11: 4,117,774 (GRCm39) |
R179C |
probably damaging |
Het |
Spata31e2 |
T |
C |
1: 26,721,161 (GRCm39) |
N1340D |
probably benign |
Het |
Styxl2 |
T |
C |
1: 165,928,685 (GRCm39) |
E309G |
probably damaging |
Het |
Tg |
T |
C |
15: 66,568,318 (GRCm39) |
V1335A |
possibly damaging |
Het |
Thnsl1 |
A |
G |
2: 21,217,059 (GRCm39) |
E271G |
probably benign |
Het |
Vill |
T |
A |
9: 118,900,359 (GRCm39) |
|
probably benign |
Het |
Vmn2r79 |
A |
G |
7: 86,651,624 (GRCm39) |
D341G |
possibly damaging |
Het |
Wdr59 |
T |
C |
8: 112,216,996 (GRCm39) |
N272D |
possibly damaging |
Het |
Zar1 |
T |
C |
5: 72,737,736 (GRCm39) |
E121G |
possibly damaging |
Het |
Zfp985 |
A |
G |
4: 147,667,396 (GRCm39) |
K88R |
probably damaging |
Het |
Zscan29 |
C |
T |
2: 120,995,275 (GRCm39) |
|
probably null |
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 |
|
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 |
R5531:Acacb
|
UTSW |
5 |
114,342,767 (GRCm39) |
missense |
possibly damaging |
0.92 |
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 |
|