Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930546C10Rik |
A |
G |
18: 69,083,060 (GRCm39) |
|
probably benign |
Het |
Aldh4a1 |
G |
A |
4: 139,375,511 (GRCm39) |
W540* |
probably null |
Het |
Antxr2 |
G |
A |
5: 98,097,057 (GRCm39) |
P352L |
probably damaging |
Het |
Atic |
C |
T |
1: 71,603,724 (GRCm39) |
|
probably benign |
Het |
Cfhr1 |
A |
G |
1: 139,475,551 (GRCm39) |
|
probably benign |
Het |
Clspn |
T |
C |
4: 126,459,900 (GRCm39) |
S207P |
probably benign |
Het |
Depdc1b |
A |
C |
13: 108,500,113 (GRCm39) |
T209P |
probably benign |
Het |
Exosc3 |
A |
G |
4: 45,319,671 (GRCm39) |
I117T |
probably damaging |
Het |
Eya2 |
T |
A |
2: 165,605,638 (GRCm39) |
D347E |
probably damaging |
Het |
Gm10748 |
G |
T |
3: 5,280,061 (GRCm39) |
|
probably benign |
Het |
Gm17079 |
T |
C |
14: 51,930,524 (GRCm39) |
N107S |
possibly damaging |
Het |
Gpr68 |
A |
G |
12: 100,845,026 (GRCm39) |
F173L |
probably damaging |
Het |
Hgf |
G |
T |
5: 16,769,792 (GRCm39) |
V89F |
possibly damaging |
Het |
Igsf10 |
A |
T |
3: 59,235,652 (GRCm39) |
S1510T |
probably benign |
Het |
Il4 |
A |
T |
11: 53,503,463 (GRCm39) |
N22K |
probably damaging |
Het |
Izumo2 |
T |
G |
7: 44,358,261 (GRCm39) |
L32R |
probably damaging |
Het |
Mark2 |
A |
G |
19: 7,261,855 (GRCm39) |
L359P |
probably damaging |
Het |
Myo15b |
A |
G |
11: 115,767,828 (GRCm39) |
K1376R |
probably benign |
Het |
Ncam1 |
G |
A |
9: 49,454,383 (GRCm39) |
R543* |
probably null |
Het |
Pax2 |
A |
G |
19: 44,823,848 (GRCm39) |
N347S |
possibly damaging |
Het |
Ppargc1a |
A |
G |
5: 51,631,498 (GRCm39) |
L377P |
probably benign |
Het |
Pum3 |
A |
G |
19: 27,403,357 (GRCm39) |
V48A |
probably benign |
Het |
Rad1 |
T |
C |
15: 10,493,337 (GRCm39) |
Y255H |
probably benign |
Het |
Rimbp2 |
C |
T |
5: 128,865,218 (GRCm39) |
|
probably null |
Het |
Rpn2 |
A |
G |
2: 157,144,328 (GRCm39) |
N330S |
probably benign |
Het |
Rptn |
A |
G |
3: 93,304,478 (GRCm39) |
S604G |
probably benign |
Het |
Rragc |
A |
G |
4: 123,814,904 (GRCm39) |
D200G |
probably benign |
Het |
Slco4a1 |
T |
G |
2: 180,114,921 (GRCm39) |
F615V |
probably damaging |
Het |
Snx2 |
T |
C |
18: 53,322,793 (GRCm39) |
S59P |
probably benign |
Het |
Timp4 |
A |
T |
6: 115,223,360 (GRCm39) |
|
probably null |
Het |
Tln2 |
A |
G |
9: 67,148,092 (GRCm39) |
|
probably benign |
Het |
Txnrd1 |
C |
A |
10: 82,731,808 (GRCm39) |
|
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 |
|
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 |
|
R2848:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
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 |
|