Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003H04Rik |
C |
T |
3: 124,350,380 (GRCm39) |
|
probably benign |
Het |
Afg3l1 |
G |
A |
8: 124,226,778 (GRCm39) |
V563I |
possibly damaging |
Het |
Ak7 |
A |
G |
12: 105,692,471 (GRCm39) |
E175G |
probably damaging |
Het |
Arhgap5 |
C |
T |
12: 52,565,525 (GRCm39) |
T832I |
possibly damaging |
Het |
Arid4a |
A |
T |
12: 71,116,747 (GRCm39) |
T602S |
probably damaging |
Het |
Caps2 |
C |
T |
10: 112,001,591 (GRCm39) |
|
probably benign |
Het |
Ccdc170 |
G |
T |
10: 4,508,551 (GRCm39) |
E592* |
probably null |
Het |
Clasp1 |
C |
A |
1: 118,434,638 (GRCm39) |
|
probably benign |
Het |
Crhbp |
T |
A |
13: 95,568,564 (GRCm39) |
M291L |
probably benign |
Het |
Cyp3a41b |
T |
A |
5: 145,519,349 (GRCm39) |
L47F |
probably benign |
Het |
Dgcr6 |
A |
G |
16: 17,884,598 (GRCm39) |
D82G |
probably damaging |
Het |
Drc7 |
A |
G |
8: 95,800,754 (GRCm39) |
E592G |
probably damaging |
Het |
Dtl |
G |
A |
1: 191,300,519 (GRCm39) |
T115I |
probably damaging |
Het |
Ece2 |
A |
G |
16: 20,457,510 (GRCm39) |
Y338C |
probably damaging |
Het |
Egr3 |
A |
G |
14: 70,316,897 (GRCm39) |
D198G |
probably damaging |
Het |
Ereg |
A |
C |
5: 91,222,552 (GRCm39) |
|
probably benign |
Het |
Esp31 |
G |
C |
17: 38,951,933 (GRCm39) |
|
probably null |
Het |
Faap100 |
T |
C |
11: 120,267,958 (GRCm39) |
I272V |
possibly damaging |
Het |
Fam3c |
T |
C |
6: 22,328,560 (GRCm39) |
D109G |
probably damaging |
Het |
Fam3c |
T |
A |
6: 22,339,299 (GRCm39) |
M51L |
probably benign |
Het |
Fcnb |
A |
T |
2: 27,966,701 (GRCm39) |
N277K |
probably damaging |
Het |
Fgfr1 |
A |
G |
8: 26,009,325 (GRCm39) |
|
probably benign |
Het |
Gpr158 |
T |
C |
2: 21,373,932 (GRCm39) |
F289S |
possibly damaging |
Het |
Grik4 |
C |
A |
9: 42,502,720 (GRCm39) |
V468F |
probably damaging |
Het |
Gtdc1 |
T |
A |
2: 44,642,076 (GRCm39) |
R168S |
probably benign |
Het |
Gucy2c |
C |
T |
6: 136,699,440 (GRCm39) |
G610R |
probably damaging |
Het |
Gulp1 |
A |
T |
1: 44,793,534 (GRCm39) |
Q65L |
possibly damaging |
Het |
Hectd1 |
A |
T |
12: 51,849,035 (GRCm39) |
D356E |
probably damaging |
Het |
Hnrnpu |
T |
C |
1: 178,157,737 (GRCm39) |
|
probably benign |
Het |
Igkv13-57-2 |
T |
C |
6: 69,500,971 (GRCm39) |
|
noncoding transcript |
Het |
Itih4 |
A |
G |
14: 30,612,612 (GRCm39) |
I213V |
possibly damaging |
Het |
Itpr2 |
T |
C |
6: 146,214,441 (GRCm39) |
K1469E |
probably benign |
Het |
Jkampl |
T |
C |
6: 73,445,674 (GRCm39) |
T292A |
probably damaging |
Het |
Jrk |
T |
C |
15: 74,577,617 (GRCm39) |
D556G |
possibly damaging |
Het |
Kctd16 |
A |
T |
18: 40,663,905 (GRCm39) |
I345F |
probably benign |
Het |
Klhdc1 |
A |
G |
12: 69,303,025 (GRCm39) |
E187G |
possibly damaging |
Het |
Lrch3 |
T |
C |
16: 32,779,833 (GRCm39) |
Y111H |
probably damaging |
Het |
Mlh3 |
A |
T |
12: 85,315,229 (GRCm39) |
V319D |
probably damaging |
Het |
Nsd3 |
T |
C |
8: 26,156,092 (GRCm39) |
L553P |
probably damaging |
Het |
Or1e23 |
T |
A |
11: 73,407,351 (GRCm39) |
I225F |
probably damaging |
Het |
Or51q1 |
A |
T |
7: 103,628,915 (GRCm39) |
H172L |
probably benign |
Het |
Or5d38 |
C |
T |
2: 87,955,027 (GRCm39) |
V101I |
probably benign |
Het |
Or5e1 |
T |
A |
7: 108,354,882 (GRCm39) |
I273N |
probably benign |
Het |
Or5p66 |
T |
A |
7: 107,885,605 (GRCm39) |
T243S |
probably damaging |
Het |
Or7g26 |
T |
C |
9: 19,230,445 (GRCm39) |
I205T |
probably benign |
Het |
Pelp1 |
C |
T |
11: 70,287,740 (GRCm39) |
R394H |
probably damaging |
Het |
Ppp1r13l |
G |
T |
7: 19,109,817 (GRCm39) |
|
probably null |
Het |
Prr5 |
C |
A |
15: 84,585,635 (GRCm39) |
S201* |
probably null |
Het |
Rad23b |
T |
A |
4: 55,370,474 (GRCm39) |
|
probably null |
Het |
Rasgef1a |
T |
A |
6: 118,061,335 (GRCm39) |
|
probably null |
Het |
Ryr3 |
A |
T |
2: 112,738,832 (GRCm39) |
I565N |
probably damaging |
Het |
Slc30a5 |
T |
C |
13: 100,945,600 (GRCm39) |
N527S |
probably damaging |
Het |
Slc39a5 |
T |
A |
10: 128,235,812 (GRCm39) |
N49Y |
probably damaging |
Het |
Spast |
T |
A |
17: 74,694,058 (GRCm39) |
S571T |
probably benign |
Het |
Spdye4c |
C |
T |
2: 128,437,994 (GRCm39) |
R245* |
probably null |
Het |
Tbc1d2 |
C |
T |
4: 46,629,912 (GRCm39) |
G252R |
probably benign |
Het |
Tgm7 |
T |
A |
2: 120,926,454 (GRCm39) |
D480V |
probably benign |
Het |
Thpo |
T |
A |
16: 20,547,546 (GRCm39) |
S22C |
probably null |
Het |
Top2a |
T |
A |
11: 98,907,291 (GRCm39) |
T180S |
possibly damaging |
Het |
Trim37 |
T |
A |
11: 87,087,663 (GRCm39) |
Y34* |
probably null |
Het |
Tsc2 |
T |
C |
17: 24,819,361 (GRCm39) |
E1254G |
possibly damaging |
Het |
Ttc39a |
C |
T |
4: 109,280,168 (GRCm39) |
P150L |
possibly damaging |
Het |
Ttc4 |
T |
C |
4: 106,525,240 (GRCm39) |
D298G |
probably damaging |
Het |
Ttll1 |
A |
G |
15: 83,386,482 (GRCm39) |
V41A |
probably benign |
Het |
Vmn1r20 |
C |
A |
6: 57,408,774 (GRCm39) |
H33Q |
probably benign |
Het |
Zan |
A |
T |
5: 137,456,174 (GRCm39) |
Y1329N |
unknown |
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 |
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 |
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 |
|