Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930451I11Rik |
A |
T |
7: 126,429,894 (GRCm39) |
F101Y |
possibly damaging |
Het |
Adamts14 |
T |
A |
10: 61,054,214 (GRCm39) |
Q606L |
probably damaging |
Het |
Adgrf5 |
C |
A |
17: 43,733,531 (GRCm39) |
N118K |
possibly damaging |
Het |
Baz2b |
A |
T |
2: 59,755,010 (GRCm39) |
Y1073N |
possibly damaging |
Het |
Celf2 |
T |
C |
2: 6,608,936 (GRCm39) |
R282G |
probably damaging |
Het |
Cntnap5c |
A |
T |
17: 58,183,387 (GRCm39) |
D31V |
probably damaging |
Het |
Cobl |
A |
G |
11: 12,328,342 (GRCm39) |
L81P |
probably damaging |
Het |
Cpsf1 |
A |
T |
15: 76,487,051 (GRCm39) |
L209Q |
probably damaging |
Het |
Crocc |
G |
A |
4: 140,746,067 (GRCm39) |
A1684V |
probably damaging |
Het |
Cyp4f37 |
T |
A |
17: 32,848,099 (GRCm39) |
C206S |
probably damaging |
Het |
Dnah3 |
A |
G |
7: 119,567,161 (GRCm39) |
V2355A |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,106,314 (GRCm39) |
K1756E |
probably benign |
Het |
Fis1 |
T |
C |
5: 136,991,971 (GRCm39) |
I55T |
possibly damaging |
Het |
Gm2381 |
G |
A |
7: 42,469,831 (GRCm39) |
P98S |
probably damaging |
Het |
Gpr37 |
C |
T |
6: 25,666,945 (GRCm39) |
|
probably benign |
Het |
Grin2a |
A |
G |
16: 9,579,829 (GRCm39) |
F145L |
possibly damaging |
Het |
Htr4 |
T |
C |
18: 62,561,197 (GRCm39) |
S153P |
probably damaging |
Het |
Igkv9-120 |
T |
A |
6: 68,027,128 (GRCm39) |
|
probably benign |
Het |
Il12rb1 |
G |
A |
8: 71,268,446 (GRCm39) |
W396* |
probably null |
Het |
Itga8 |
A |
T |
2: 12,165,215 (GRCm39) |
V798D |
probably damaging |
Het |
Lfng |
T |
A |
5: 140,597,622 (GRCm39) |
D149E |
probably damaging |
Het |
Magi2 |
A |
AG |
5: 20,807,459 (GRCm39) |
|
probably null |
Het |
Mgam |
C |
A |
6: 40,629,649 (GRCm39) |
A86E |
possibly damaging |
Het |
Myh4 |
A |
G |
11: 67,139,459 (GRCm39) |
N592S |
probably benign |
Het |
Naa16 |
A |
G |
14: 79,573,323 (GRCm39) |
C816R |
probably damaging |
Het |
Nek8 |
A |
G |
11: 78,058,967 (GRCm39) |
S513P |
probably damaging |
Het |
Ociad1 |
A |
G |
5: 73,451,694 (GRCm39) |
|
probably null |
Het |
Or1j4 |
A |
G |
2: 36,740,811 (GRCm39) |
Y251C |
probably damaging |
Het |
Or2t35 |
C |
T |
14: 14,407,398 (GRCm38) |
P57S |
probably damaging |
Het |
Or4g7 |
T |
C |
2: 111,309,699 (GRCm39) |
M190T |
probably benign |
Het |
Osbpl8 |
T |
A |
10: 111,105,297 (GRCm39) |
S251T |
probably benign |
Het |
Pcdh7 |
G |
A |
5: 57,877,618 (GRCm39) |
G391E |
probably damaging |
Het |
Pcdhga10 |
T |
A |
18: 37,881,253 (GRCm39) |
V338E |
possibly damaging |
Het |
Pde4b |
C |
T |
4: 102,458,742 (GRCm39) |
A466V |
probably damaging |
Het |
Peg10 |
C |
T |
6: 4,756,912 (GRCm39) |
|
probably benign |
Het |
Poteg |
A |
T |
8: 27,971,704 (GRCm39) |
N406I |
probably benign |
Het |
Ppargc1a |
A |
G |
5: 51,631,151 (GRCm39) |
F493L |
probably benign |
Het |
Ptpra |
C |
A |
2: 130,386,919 (GRCm39) |
H603Q |
probably benign |
Het |
Rnf10 |
T |
C |
5: 115,387,171 (GRCm39) |
D439G |
probably benign |
Het |
Shfl |
A |
T |
9: 20,784,868 (GRCm39) |
H225L |
probably damaging |
Het |
Syt3 |
G |
A |
7: 44,042,866 (GRCm39) |
V383I |
probably benign |
Het |
Tectb |
C |
G |
19: 55,169,431 (GRCm39) |
|
probably benign |
Het |
Try5 |
C |
T |
6: 41,290,410 (GRCm39) |
V25I |
probably benign |
Het |
Ttn |
G |
T |
2: 76,749,551 (GRCm39) |
Q3833K |
probably benign |
Het |
Usp53 |
G |
A |
3: 122,728,140 (GRCm39) |
P814L |
probably benign |
Het |
Utp25 |
A |
T |
1: 192,810,759 (GRCm39) |
N81K |
probably benign |
Het |
Vmn1r181 |
G |
T |
7: 23,683,943 (GRCm39) |
S136I |
possibly damaging |
Het |
Vmn2r114 |
A |
T |
17: 23,509,948 (GRCm39) |
M844K |
probably benign |
Het |
Vwa8 |
G |
T |
14: 79,184,582 (GRCm39) |
R360L |
probably benign |
Het |
Xlr4b |
A |
T |
X: 72,258,938 (GRCm39) |
Q25L |
probably null |
Het |
Zfp532 |
T |
A |
18: 65,789,697 (GRCm39) |
H1045Q |
possibly damaging |
Het |
Zfp985 |
G |
A |
4: 147,667,468 (GRCm39) |
W112* |
probably null |
Het |
|
Other mutations in Abca17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Abca17
|
APN |
17 |
24,514,165 (GRCm39) |
missense |
probably benign |
0.14 |
IGL00585:Abca17
|
APN |
17 |
24,519,294 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00941:Abca17
|
APN |
17 |
24,536,104 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01987:Abca17
|
APN |
17 |
24,565,202 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01988:Abca17
|
APN |
17 |
24,553,229 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02223:Abca17
|
APN |
17 |
24,506,909 (GRCm39) |
nonsense |
probably null |
|
IGL02368:Abca17
|
APN |
17 |
24,506,767 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02405:Abca17
|
APN |
17 |
24,498,036 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02431:Abca17
|
APN |
17 |
24,517,958 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02607:Abca17
|
APN |
17 |
24,546,679 (GRCm39) |
nonsense |
probably null |
|
IGL02706:Abca17
|
APN |
17 |
24,517,966 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02729:Abca17
|
APN |
17 |
24,499,455 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02818:Abca17
|
APN |
17 |
24,519,326 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02891:Abca17
|
APN |
17 |
24,500,340 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03236:Abca17
|
APN |
17 |
24,545,450 (GRCm39) |
splice site |
probably benign |
|
IGL03299:Abca17
|
APN |
17 |
24,484,565 (GRCm39) |
missense |
probably damaging |
1.00 |
basin
|
UTSW |
17 |
24,537,159 (GRCm39) |
missense |
probably benign |
0.01 |
Bowl
|
UTSW |
17 |
24,536,212 (GRCm39) |
missense |
probably benign |
0.09 |
R0018:Abca17
|
UTSW |
17 |
24,532,162 (GRCm39) |
splice site |
probably null |
|
R0467:Abca17
|
UTSW |
17 |
24,532,151 (GRCm39) |
splice site |
probably benign |
|
R0671:Abca17
|
UTSW |
17 |
24,500,223 (GRCm39) |
missense |
probably benign |
0.00 |
R1175:Abca17
|
UTSW |
17 |
24,508,325 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1397:Abca17
|
UTSW |
17 |
24,504,733 (GRCm39) |
missense |
probably benign |
0.18 |
R1398:Abca17
|
UTSW |
17 |
24,547,511 (GRCm39) |
missense |
probably damaging |
0.96 |
R1678:Abca17
|
UTSW |
17 |
24,554,594 (GRCm39) |
missense |
probably benign |
0.05 |
R1696:Abca17
|
UTSW |
17 |
24,486,632 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1781:Abca17
|
UTSW |
17 |
24,486,531 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1845:Abca17
|
UTSW |
17 |
24,486,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Abca17
|
UTSW |
17 |
24,526,549 (GRCm39) |
missense |
probably benign |
0.00 |
R1997:Abca17
|
UTSW |
17 |
24,504,700 (GRCm39) |
missense |
probably benign |
0.02 |
R2141:Abca17
|
UTSW |
17 |
24,553,240 (GRCm39) |
missense |
probably benign |
0.00 |
R2199:Abca17
|
UTSW |
17 |
24,554,598 (GRCm39) |
missense |
probably benign |
0.19 |
R2394:Abca17
|
UTSW |
17 |
24,500,190 (GRCm39) |
splice site |
probably null |
|
R2442:Abca17
|
UTSW |
17 |
24,547,606 (GRCm39) |
missense |
probably benign |
0.02 |
R2509:Abca17
|
UTSW |
17 |
24,508,587 (GRCm39) |
splice site |
probably benign |
|
R2849:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
R2859:Abca17
|
UTSW |
17 |
24,500,288 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2879:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
R2935:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
R3153:Abca17
|
UTSW |
17 |
24,547,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R3154:Abca17
|
UTSW |
17 |
24,547,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R3434:Abca17
|
UTSW |
17 |
24,508,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R3695:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
R3905:Abca17
|
UTSW |
17 |
24,515,257 (GRCm39) |
missense |
probably benign |
0.13 |
R4282:Abca17
|
UTSW |
17 |
24,518,034 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4334:Abca17
|
UTSW |
17 |
24,537,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R4350:Abca17
|
UTSW |
17 |
24,498,020 (GRCm39) |
critical splice donor site |
probably null |
|
R4548:Abca17
|
UTSW |
17 |
24,553,245 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4626:Abca17
|
UTSW |
17 |
24,540,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R4722:Abca17
|
UTSW |
17 |
24,484,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R4745:Abca17
|
UTSW |
17 |
24,526,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R4818:Abca17
|
UTSW |
17 |
24,536,135 (GRCm39) |
missense |
probably damaging |
0.98 |
R5279:Abca17
|
UTSW |
17 |
24,508,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R5310:Abca17
|
UTSW |
17 |
24,500,204 (GRCm39) |
missense |
probably benign |
0.00 |
R5320:Abca17
|
UTSW |
17 |
24,526,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R5435:Abca17
|
UTSW |
17 |
24,486,588 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5622:Abca17
|
UTSW |
17 |
24,546,642 (GRCm39) |
missense |
probably benign |
0.14 |
R5776:Abca17
|
UTSW |
17 |
24,514,132 (GRCm39) |
missense |
probably benign |
0.09 |
R5928:Abca17
|
UTSW |
17 |
24,537,159 (GRCm39) |
missense |
probably benign |
0.01 |
R6013:Abca17
|
UTSW |
17 |
24,506,820 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6035:Abca17
|
UTSW |
17 |
24,500,219 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6035:Abca17
|
UTSW |
17 |
24,500,219 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6052:Abca17
|
UTSW |
17 |
24,537,165 (GRCm39) |
missense |
probably benign |
0.00 |
R6063:Abca17
|
UTSW |
17 |
24,483,318 (GRCm39) |
missense |
unknown |
|
R6404:Abca17
|
UTSW |
17 |
24,484,892 (GRCm39) |
missense |
probably benign |
0.13 |
R6746:Abca17
|
UTSW |
17 |
24,565,195 (GRCm39) |
nonsense |
probably null |
|
R6819:Abca17
|
UTSW |
17 |
24,506,767 (GRCm39) |
missense |
probably benign |
0.01 |
R6828:Abca17
|
UTSW |
17 |
24,545,389 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7043:Abca17
|
UTSW |
17 |
24,484,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R7065:Abca17
|
UTSW |
17 |
24,546,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7123:Abca17
|
UTSW |
17 |
24,484,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R7157:Abca17
|
UTSW |
17 |
24,554,564 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7188:Abca17
|
UTSW |
17 |
24,554,600 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7294:Abca17
|
UTSW |
17 |
24,539,983 (GRCm39) |
missense |
not run |
|
R7352:Abca17
|
UTSW |
17 |
24,508,028 (GRCm39) |
nonsense |
probably null |
|
R7355:Abca17
|
UTSW |
17 |
24,486,621 (GRCm39) |
missense |
probably benign |
0.00 |
R7358:Abca17
|
UTSW |
17 |
24,510,529 (GRCm39) |
missense |
probably benign |
0.00 |
R7411:Abca17
|
UTSW |
17 |
24,547,543 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7915:Abca17
|
UTSW |
17 |
24,484,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R8039:Abca17
|
UTSW |
17 |
24,547,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R8095:Abca17
|
UTSW |
17 |
24,536,196 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8308:Abca17
|
UTSW |
17 |
24,486,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R8517:Abca17
|
UTSW |
17 |
24,536,207 (GRCm39) |
missense |
probably benign |
0.00 |
R8811:Abca17
|
UTSW |
17 |
24,536,212 (GRCm39) |
missense |
probably benign |
0.09 |
R8819:Abca17
|
UTSW |
17 |
24,547,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R8820:Abca17
|
UTSW |
17 |
24,547,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R8953:Abca17
|
UTSW |
17 |
24,518,015 (GRCm39) |
missense |
probably benign |
|
R9095:Abca17
|
UTSW |
17 |
24,500,370 (GRCm39) |
missense |
probably damaging |
0.97 |
R9313:Abca17
|
UTSW |
17 |
24,565,207 (GRCm39) |
missense |
probably benign |
0.00 |
R9314:Abca17
|
UTSW |
17 |
24,547,593 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9347:Abca17
|
UTSW |
17 |
24,483,479 (GRCm39) |
missense |
probably benign |
|
R9351:Abca17
|
UTSW |
17 |
24,510,751 (GRCm39) |
missense |
probably benign |
0.00 |
R9387:Abca17
|
UTSW |
17 |
24,553,255 (GRCm39) |
missense |
probably benign |
0.02 |
R9388:Abca17
|
UTSW |
17 |
24,483,273 (GRCm39) |
missense |
unknown |
|
R9440:Abca17
|
UTSW |
17 |
24,499,452 (GRCm39) |
missense |
probably benign |
0.02 |
R9498:Abca17
|
UTSW |
17 |
24,484,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R9654:Abca17
|
UTSW |
17 |
24,536,099 (GRCm39) |
missense |
probably benign |
0.09 |
R9709:Abca17
|
UTSW |
17 |
24,517,934 (GRCm39) |
missense |
probably benign |
|
R9770:Abca17
|
UTSW |
17 |
24,514,121 (GRCm39) |
missense |
probably benign |
0.00 |
R9773:Abca17
|
UTSW |
17 |
24,508,565 (GRCm39) |
missense |
probably damaging |
1.00 |
RF024:Abca17
|
UTSW |
17 |
24,506,706 (GRCm39) |
frame shift |
probably null |
|
RF029:Abca17
|
UTSW |
17 |
24,506,701 (GRCm39) |
critical splice donor site |
probably benign |
|
RF032:Abca17
|
UTSW |
17 |
24,506,701 (GRCm39) |
frame shift |
probably null |
|
RF036:Abca17
|
UTSW |
17 |
24,506,701 (GRCm39) |
critical splice donor site |
probably benign |
|
X0017:Abca17
|
UTSW |
17 |
24,536,137 (GRCm39) |
missense |
probably benign |
0.26 |
X0065:Abca17
|
UTSW |
17 |
24,553,258 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Abca17
|
UTSW |
17 |
24,498,081 (GRCm39) |
missense |
probably benign |
0.03 |
Z1088:Abca17
|
UTSW |
17 |
24,498,053 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1088:Abca17
|
UTSW |
17 |
24,565,193 (GRCm39) |
missense |
probably damaging |
0.98 |
|