Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6820408C15Rik |
T |
C |
2: 152,282,790 (GRCm39) |
V215A |
probably damaging |
Het |
Abcc8 |
T |
C |
7: 45,755,268 (GRCm39) |
M1511V |
probably benign |
Het |
Abcc9 |
A |
G |
6: 142,585,301 (GRCm39) |
F801S |
probably damaging |
Het |
Abhd14a |
A |
T |
9: 106,321,065 (GRCm39) |
S97T |
possibly damaging |
Het |
Adam39 |
C |
T |
8: 41,277,630 (GRCm39) |
A7V |
probably benign |
Het |
Akap9 |
T |
C |
5: 4,117,924 (GRCm39) |
|
probably null |
Het |
Cbfa2t3 |
T |
C |
8: 123,370,236 (GRCm39) |
H53R |
probably benign |
Het |
Cdc20b |
T |
C |
13: 113,220,576 (GRCm39) |
F485S |
probably damaging |
Het |
Ctnna1 |
T |
C |
18: 35,287,567 (GRCm39) |
V92A |
probably benign |
Het |
Dlat |
A |
T |
9: 50,556,417 (GRCm39) |
|
probably null |
Het |
Edc4 |
C |
T |
8: 106,614,180 (GRCm39) |
R19C |
probably benign |
Het |
Fam90a1b |
T |
C |
X: 93,400,191 (GRCm39) |
N213S |
probably benign |
Het |
Gcg |
A |
G |
2: 62,306,148 (GRCm39) |
S150P |
probably damaging |
Het |
Gk5 |
C |
T |
9: 96,058,290 (GRCm39) |
Q424* |
probably null |
Het |
Insm2 |
T |
C |
12: 55,646,799 (GRCm39) |
I181T |
probably damaging |
Het |
Itgae |
A |
G |
11: 73,006,400 (GRCm39) |
E356G |
possibly damaging |
Het |
Kitl |
G |
A |
10: 99,912,768 (GRCm39) |
|
probably null |
Het |
Msl1 |
G |
T |
11: 98,689,519 (GRCm39) |
G9C |
probably benign |
Het |
Muc4 |
T |
A |
16: 32,575,621 (GRCm39) |
|
probably benign |
Het |
Muc4 |
C |
A |
16: 32,754,529 (GRCm38) |
H1468N |
probably benign |
Het |
Myo3b |
T |
C |
2: 70,069,243 (GRCm39) |
V494A |
possibly damaging |
Het |
Myo7a |
C |
T |
7: 97,714,997 (GRCm39) |
W1558* |
probably null |
Het |
Nop14 |
T |
C |
5: 34,815,295 (GRCm39) |
D85G |
probably damaging |
Het |
Or1ak2 |
G |
A |
2: 36,827,241 (GRCm39) |
V37I |
probably benign |
Het |
Or5p81 |
T |
A |
7: 108,267,412 (GRCm39) |
V263E |
probably damaging |
Het |
Pgk1 |
C |
A |
X: 105,238,098 (GRCm39) |
L85I |
possibly damaging |
Het |
Pik3c2b |
G |
A |
1: 133,002,365 (GRCm39) |
|
probably null |
Het |
Plagl1 |
G |
A |
10: 13,003,490 (GRCm39) |
G253R |
probably damaging |
Het |
Ppp4r1 |
G |
A |
17: 66,121,343 (GRCm39) |
V268I |
possibly damaging |
Het |
Pramel27 |
T |
G |
4: 143,578,155 (GRCm39) |
H87Q |
possibly damaging |
Het |
Rad23b |
C |
T |
4: 55,370,400 (GRCm39) |
A142V |
probably damaging |
Het |
Satl1 |
T |
C |
X: 111,315,613 (GRCm39) |
T281A |
probably benign |
Het |
Slc13a1 |
T |
C |
6: 24,133,656 (GRCm39) |
T199A |
probably benign |
Het |
Spmap2 |
A |
G |
10: 79,420,589 (GRCm39) |
S159P |
probably damaging |
Het |
Synrg |
A |
G |
11: 83,915,126 (GRCm39) |
E1044G |
probably damaging |
Het |
Syt12 |
T |
C |
19: 4,506,896 (GRCm39) |
D83G |
probably benign |
Het |
Tbx5 |
T |
C |
5: 120,021,211 (GRCm39) |
S406P |
probably benign |
Het |
Tfe3 |
T |
C |
X: 7,637,288 (GRCm39) |
L231P |
probably damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Vmn1r29 |
T |
C |
6: 58,285,080 (GRCm39) |
F267L |
probably benign |
Het |
Vmn2r79 |
T |
A |
7: 86,653,319 (GRCm39) |
V528D |
possibly damaging |
Het |
Zfp1 |
T |
C |
8: 112,396,975 (GRCm39) |
F299S |
probably damaging |
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 |
IGL01974:Adamts2
|
APN |
11 |
50,667,001 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
X0065:Adamts2
|
UTSW |
11 |
50,694,476 (GRCm39) |
nonsense |
probably null |
|
Z1176:Adamts2
|
UTSW |
11 |
50,683,535 (GRCm39) |
missense |
probably damaging |
1.00 |
|