Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
C |
14: 32,381,762 (GRCm39) |
D1401G |
possibly damaging |
Het |
Cacna2d2 |
A |
C |
9: 107,394,621 (GRCm39) |
S598R |
probably benign |
Het |
Cdkl3 |
A |
G |
11: 51,902,064 (GRCm39) |
Q91R |
probably damaging |
Het |
Celf2 |
T |
C |
2: 6,608,842 (GRCm39) |
Y313C |
probably damaging |
Het |
Clint1 |
C |
A |
11: 45,799,862 (GRCm39) |
N558K |
probably benign |
Het |
Dcbld1 |
A |
G |
10: 52,180,777 (GRCm39) |
H147R |
probably benign |
Het |
Ednrb |
A |
C |
14: 104,058,254 (GRCm39) |
Y350D |
probably damaging |
Het |
Elp2 |
C |
T |
18: 24,759,260 (GRCm39) |
P539L |
probably damaging |
Het |
Fam217b |
G |
A |
2: 178,063,020 (GRCm39) |
R328Q |
probably damaging |
Het |
Gm9991 |
G |
T |
1: 90,603,197 (GRCm39) |
|
noncoding transcript |
Het |
Herc4 |
T |
G |
10: 63,135,020 (GRCm39) |
|
probably null |
Het |
Hus1 |
T |
C |
11: 8,950,088 (GRCm39) |
N211S |
possibly damaging |
Het |
Immt |
A |
G |
6: 71,849,842 (GRCm39) |
D454G |
probably damaging |
Het |
Itga4 |
G |
A |
2: 79,103,471 (GRCm39) |
|
probably benign |
Het |
Kank1 |
A |
T |
19: 25,387,596 (GRCm39) |
N423I |
possibly damaging |
Het |
Kynu |
T |
A |
2: 43,571,352 (GRCm39) |
|
probably benign |
Het |
Mycbp2 |
A |
C |
14: 103,380,647 (GRCm39) |
S3670A |
possibly damaging |
Het |
Ndufv3 |
T |
C |
17: 31,740,583 (GRCm39) |
V30A |
probably benign |
Het |
Or8k17 |
G |
T |
2: 86,066,304 (GRCm39) |
L292I |
probably benign |
Het |
Per2 |
C |
T |
1: 91,351,440 (GRCm39) |
R1022Q |
probably benign |
Het |
Rad23a |
T |
C |
8: 85,565,568 (GRCm39) |
E30G |
probably damaging |
Het |
Ropn1l |
T |
A |
15: 31,449,255 (GRCm39) |
Y91F |
probably benign |
Het |
Sertad4 |
C |
A |
1: 192,529,274 (GRCm39) |
E181* |
probably null |
Het |
Styxl2 |
A |
T |
1: 165,928,105 (GRCm39) |
C502* |
probably null |
Het |
Tnfrsf1b |
G |
A |
4: 144,942,421 (GRCm39) |
P454L |
probably damaging |
Het |
Ttbk2 |
G |
A |
2: 120,616,564 (GRCm39) |
R110W |
probably damaging |
Het |
Usp17le |
G |
T |
7: 104,417,642 (GRCm39) |
S500Y |
probably benign |
Het |
|
Other mutations in Adamts2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01309:Adamts2
|
APN |
11 |
50,694,528 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01366:Adamts2
|
APN |
11 |
50,687,295 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01412:Adamts2
|
APN |
11 |
50,686,230 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01443:Adamts2
|
APN |
11 |
50,694,690 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02267:Adamts2
|
APN |
11 |
50,683,505 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02498:Adamts2
|
APN |
11 |
50,668,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02498:Adamts2
|
APN |
11 |
50,664,135 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02626:Adamts2
|
APN |
11 |
50,667,082 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02634:Adamts2
|
APN |
11 |
50,683,548 (GRCm39) |
nonsense |
probably null |
|
IGL02643:Adamts2
|
APN |
11 |
50,679,527 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02836:Adamts2
|
APN |
11 |
50,678,106 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03012:Adamts2
|
APN |
11 |
50,667,096 (GRCm39) |
splice site |
probably benign |
|
ANU22:Adamts2
|
UTSW |
11 |
50,628,190 (GRCm39) |
missense |
probably benign |
0.06 |
H8441:Adamts2
|
UTSW |
11 |
50,675,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R0050:Adamts2
|
UTSW |
11 |
50,666,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R0050:Adamts2
|
UTSW |
11 |
50,666,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Adamts2
|
UTSW |
11 |
50,666,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Adamts2
|
UTSW |
11 |
50,666,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R0491:Adamts2
|
UTSW |
11 |
50,667,457 (GRCm39) |
missense |
probably damaging |
0.98 |
R0501:Adamts2
|
UTSW |
11 |
50,558,972 (GRCm39) |
missense |
probably benign |
0.16 |
R0570:Adamts2
|
UTSW |
11 |
50,666,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R0588:Adamts2
|
UTSW |
11 |
50,667,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R0647:Adamts2
|
UTSW |
11 |
50,494,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0760:Adamts2
|
UTSW |
11 |
50,666,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R0784:Adamts2
|
UTSW |
11 |
50,558,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R1163:Adamts2
|
UTSW |
11 |
50,670,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R1623:Adamts2
|
UTSW |
11 |
50,558,942 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1641:Adamts2
|
UTSW |
11 |
50,683,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Adamts2
|
UTSW |
11 |
50,647,524 (GRCm39) |
missense |
probably damaging |
0.99 |
R2163:Adamts2
|
UTSW |
11 |
50,679,632 (GRCm39) |
missense |
probably benign |
0.36 |
R2177:Adamts2
|
UTSW |
11 |
50,668,055 (GRCm39) |
missense |
probably damaging |
0.98 |
R2508:Adamts2
|
UTSW |
11 |
50,679,516 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3721:Adamts2
|
UTSW |
11 |
50,664,038 (GRCm39) |
splice site |
probably benign |
|
R4092:Adamts2
|
UTSW |
11 |
50,678,103 (GRCm39) |
missense |
probably damaging |
0.99 |
R4691:Adamts2
|
UTSW |
11 |
50,647,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Adamts2
|
UTSW |
11 |
50,683,549 (GRCm39) |
missense |
probably benign |
0.00 |
R4809:Adamts2
|
UTSW |
11 |
50,694,517 (GRCm39) |
missense |
probably benign |
0.17 |
R4823:Adamts2
|
UTSW |
11 |
50,628,014 (GRCm39) |
missense |
probably benign |
0.26 |
R4927:Adamts2
|
UTSW |
11 |
50,694,639 (GRCm39) |
nonsense |
probably null |
|
R4976:Adamts2
|
UTSW |
11 |
50,628,193 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5118:Adamts2
|
UTSW |
11 |
50,672,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R5478:Adamts2
|
UTSW |
11 |
50,683,478 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5660:Adamts2
|
UTSW |
11 |
50,667,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R5734:Adamts2
|
UTSW |
11 |
50,679,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R5865:Adamts2
|
UTSW |
11 |
50,694,781 (GRCm39) |
nonsense |
probably null |
|
R6079:Adamts2
|
UTSW |
11 |
50,647,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R6138:Adamts2
|
UTSW |
11 |
50,647,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Adamts2
|
UTSW |
11 |
50,666,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R6540:Adamts2
|
UTSW |
11 |
50,679,567 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6897:Adamts2
|
UTSW |
11 |
50,627,991 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7103:Adamts2
|
UTSW |
11 |
50,628,181 (GRCm39) |
missense |
probably damaging |
0.98 |
R7229:Adamts2
|
UTSW |
11 |
50,682,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7261:Adamts2
|
UTSW |
11 |
50,677,424 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7335:Adamts2
|
UTSW |
11 |
50,493,093 (GRCm39) |
missense |
probably benign |
0.18 |
R7373:Adamts2
|
UTSW |
11 |
50,686,262 (GRCm39) |
missense |
probably benign |
0.00 |
R7505:Adamts2
|
UTSW |
11 |
50,687,347 (GRCm39) |
missense |
probably benign |
0.00 |
R7971:Adamts2
|
UTSW |
11 |
50,647,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R8081:Adamts2
|
UTSW |
11 |
50,668,004 (GRCm39) |
missense |
probably damaging |
0.99 |
R8167:Adamts2
|
UTSW |
11 |
50,670,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R8256:Adamts2
|
UTSW |
11 |
50,683,583 (GRCm39) |
missense |
probably benign |
0.41 |
R8298:Adamts2
|
UTSW |
11 |
50,667,958 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8343:Adamts2
|
UTSW |
11 |
50,494,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R8518:Adamts2
|
UTSW |
11 |
50,666,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Adamts2
|
UTSW |
11 |
50,664,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R8865:Adamts2
|
UTSW |
11 |
50,672,571 (GRCm39) |
nonsense |
probably null |
|
R8968:Adamts2
|
UTSW |
11 |
50,683,550 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9436:Adamts2
|
UTSW |
11 |
50,694,507 (GRCm39) |
missense |
probably benign |
0.00 |
R9694:Adamts2
|
UTSW |
11 |
50,558,972 (GRCm39) |
missense |
probably benign |
0.16 |
R9720:Adamts2
|
UTSW |
11 |
50,666,954 (GRCm39) |
missense |
probably damaging |
0.97 |
R9750:Adamts2
|
UTSW |
11 |
50,494,333 (GRCm39) |
missense |
probably benign |
0.00 |
U15987:Adamts2
|
UTSW |
11 |
50,647,533 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Adamts2
|
UTSW |
11 |
50,694,476 (GRCm39) |
nonsense |
probably null |
|
Z1176:Adamts2
|
UTSW |
11 |
50,683,535 (GRCm39) |
missense |
probably damaging |
1.00 |
|