Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr3 |
A |
G |
1: 125,346,025 (GRCm39) |
Y21H |
possibly damaging |
Het |
Brat1 |
A |
G |
5: 140,703,670 (GRCm39) |
D641G |
probably benign |
Het |
Ccdc42 |
G |
A |
11: 68,485,101 (GRCm39) |
R205H |
probably benign |
Het |
Cdadc1 |
T |
C |
14: 59,829,986 (GRCm39) |
|
probably null |
Het |
Cfi |
T |
C |
3: 129,652,034 (GRCm39) |
V235A |
probably damaging |
Het |
Ctps1 |
T |
A |
4: 120,424,476 (GRCm39) |
D46V |
probably damaging |
Het |
Cyb5d1 |
A |
T |
11: 69,284,587 (GRCm39) |
D188E |
probably benign |
Het |
Cyp19a1 |
G |
T |
9: 54,075,813 (GRCm39) |
T414N |
probably benign |
Het |
Cyp2c40 |
A |
T |
19: 39,792,217 (GRCm39) |
C242* |
probably null |
Het |
Eif3b |
A |
T |
5: 140,411,202 (GRCm39) |
T218S |
possibly damaging |
Het |
Fasn |
A |
T |
11: 120,698,765 (GRCm39) |
L2475Q |
probably damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Heyl |
A |
T |
4: 123,140,400 (GRCm39) |
I320F |
probably damaging |
Het |
Itpr3 |
T |
A |
17: 27,330,236 (GRCm39) |
V1618E |
probably damaging |
Het |
Kif7 |
A |
T |
7: 79,350,800 (GRCm39) |
I1007N |
probably damaging |
Het |
Lat2 |
A |
G |
5: 134,635,481 (GRCm39) |
|
probably benign |
Het |
Lipm |
A |
T |
19: 34,098,708 (GRCm39) |
D394V |
probably damaging |
Het |
Lmbrd1 |
T |
A |
1: 24,782,977 (GRCm39) |
I307K |
possibly damaging |
Het |
Mief1 |
T |
C |
15: 80,132,709 (GRCm39) |
|
probably benign |
Het |
Mta2 |
C |
T |
19: 8,925,130 (GRCm39) |
Q333* |
probably null |
Het |
Neb |
T |
A |
2: 52,170,587 (GRCm39) |
E1695V |
possibly damaging |
Het |
Npc1l1 |
A |
T |
11: 6,177,879 (GRCm39) |
N510K |
probably benign |
Het |
Or5af1 |
T |
C |
11: 58,722,465 (GRCm39) |
F162L |
probably damaging |
Het |
P2rx3 |
A |
C |
2: 84,853,825 (GRCm39) |
|
probably benign |
Het |
Pdgfc |
A |
G |
3: 81,111,639 (GRCm39) |
E198G |
possibly damaging |
Het |
Pkdcc |
T |
A |
17: 83,527,548 (GRCm39) |
I242N |
probably damaging |
Het |
Pkn3 |
C |
T |
2: 29,972,824 (GRCm39) |
|
probably benign |
Het |
Rcan2 |
T |
G |
17: 44,147,325 (GRCm39) |
D54E |
probably damaging |
Het |
Tmeff2 |
T |
A |
1: 51,171,369 (GRCm39) |
Y202N |
probably damaging |
Het |
Unc13c |
A |
G |
9: 73,453,309 (GRCm39) |
L1827P |
probably damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Wfdc15a |
G |
T |
2: 164,041,896 (GRCm39) |
Q21K |
probably benign |
Het |
Zfp951 |
C |
A |
5: 104,963,149 (GRCm39) |
S139I |
probably benign |
Het |
|
Other mutations in Adamts15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00930:Adamts15
|
APN |
9 |
30,813,349 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01325:Adamts15
|
APN |
9 |
30,832,984 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01506:Adamts15
|
APN |
9 |
30,833,430 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02137:Adamts15
|
APN |
9 |
30,821,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02876:Adamts15
|
APN |
9 |
30,815,818 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02997:Adamts15
|
APN |
9 |
30,817,353 (GRCm39) |
splice site |
probably benign |
|
IGL03094:Adamts15
|
APN |
9 |
30,815,768 (GRCm39) |
splice site |
probably benign |
|
IGL03146:Adamts15
|
APN |
9 |
30,832,863 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03241:Adamts15
|
APN |
9 |
30,815,781 (GRCm39) |
missense |
probably damaging |
1.00 |
Awareness
|
UTSW |
9 |
30,822,404 (GRCm39) |
critical splice donor site |
probably null |
|
heightened
|
UTSW |
9 |
30,816,066 (GRCm39) |
missense |
probably damaging |
1.00 |
Pugsley
|
UTSW |
9 |
30,817,454 (GRCm39) |
missense |
probably damaging |
1.00 |
sparticus
|
UTSW |
9 |
30,821,898 (GRCm39) |
missense |
probably benign |
0.40 |
R0118:Adamts15
|
UTSW |
9 |
30,823,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R0635:Adamts15
|
UTSW |
9 |
30,816,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R0827:Adamts15
|
UTSW |
9 |
30,832,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R0946:Adamts15
|
UTSW |
9 |
30,813,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R1608:Adamts15
|
UTSW |
9 |
30,813,775 (GRCm39) |
missense |
probably damaging |
0.99 |
R1806:Adamts15
|
UTSW |
9 |
30,816,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Adamts15
|
UTSW |
9 |
30,822,004 (GRCm39) |
missense |
probably benign |
|
R1967:Adamts15
|
UTSW |
9 |
30,832,605 (GRCm39) |
nonsense |
probably null |
|
R2009:Adamts15
|
UTSW |
9 |
30,833,433 (GRCm39) |
missense |
probably benign |
0.17 |
R2129:Adamts15
|
UTSW |
9 |
30,815,799 (GRCm39) |
missense |
probably benign |
0.05 |
R2329:Adamts15
|
UTSW |
9 |
30,813,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R2991:Adamts15
|
UTSW |
9 |
30,832,690 (GRCm39) |
missense |
probably benign |
|
R3970:Adamts15
|
UTSW |
9 |
30,821,898 (GRCm39) |
missense |
probably benign |
0.40 |
R4212:Adamts15
|
UTSW |
9 |
30,817,470 (GRCm39) |
missense |
probably damaging |
0.99 |
R4326:Adamts15
|
UTSW |
9 |
30,815,814 (GRCm39) |
missense |
probably benign |
|
R4329:Adamts15
|
UTSW |
9 |
30,815,814 (GRCm39) |
missense |
probably benign |
|
R4594:Adamts15
|
UTSW |
9 |
30,832,743 (GRCm39) |
missense |
probably damaging |
0.99 |
R5110:Adamts15
|
UTSW |
9 |
30,832,740 (GRCm39) |
missense |
probably benign |
0.01 |
R5120:Adamts15
|
UTSW |
9 |
30,832,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R5697:Adamts15
|
UTSW |
9 |
30,823,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R5901:Adamts15
|
UTSW |
9 |
30,813,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R6011:Adamts15
|
UTSW |
9 |
30,814,082 (GRCm39) |
missense |
probably damaging |
0.98 |
R6020:Adamts15
|
UTSW |
9 |
30,813,358 (GRCm39) |
missense |
probably benign |
0.03 |
R6651:Adamts15
|
UTSW |
9 |
30,833,448 (GRCm39) |
missense |
probably damaging |
0.98 |
R6665:Adamts15
|
UTSW |
9 |
30,815,775 (GRCm39) |
critical splice donor site |
probably null |
|
R7021:Adamts15
|
UTSW |
9 |
30,832,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R7231:Adamts15
|
UTSW |
9 |
30,817,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R7290:Adamts15
|
UTSW |
9 |
30,813,906 (GRCm39) |
missense |
probably benign |
0.05 |
R7390:Adamts15
|
UTSW |
9 |
30,822,404 (GRCm39) |
critical splice donor site |
probably null |
|
R7798:Adamts15
|
UTSW |
9 |
30,815,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7833:Adamts15
|
UTSW |
9 |
30,833,401 (GRCm39) |
missense |
probably benign |
|
R7908:Adamts15
|
UTSW |
9 |
30,813,522 (GRCm39) |
missense |
probably benign |
|
R8175:Adamts15
|
UTSW |
9 |
30,815,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8177:Adamts15
|
UTSW |
9 |
30,833,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R8347:Adamts15
|
UTSW |
9 |
30,813,846 (GRCm39) |
missense |
probably benign |
0.07 |
R8348:Adamts15
|
UTSW |
9 |
30,813,846 (GRCm39) |
missense |
probably benign |
0.07 |
R8374:Adamts15
|
UTSW |
9 |
30,814,002 (GRCm39) |
missense |
probably benign |
0.21 |
R8473:Adamts15
|
UTSW |
9 |
30,816,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Adamts15
|
UTSW |
9 |
30,823,055 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9113:Adamts15
|
UTSW |
9 |
30,822,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R9336:Adamts15
|
UTSW |
9 |
30,816,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R9381:Adamts15
|
UTSW |
9 |
30,813,816 (GRCm39) |
missense |
probably damaging |
0.99 |
X0063:Adamts15
|
UTSW |
9 |
30,833,526 (GRCm39) |
missense |
possibly damaging |
0.96 |
X0067:Adamts15
|
UTSW |
9 |
30,832,878 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Adamts15
|
UTSW |
9 |
30,821,996 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Adamts15
|
UTSW |
9 |
30,813,787 (GRCm39) |
missense |
probably damaging |
1.00 |
|