Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre1 |
C |
A |
17: 57,713,859 (GRCm39) |
D181E |
probably benign |
Het |
Arhgap24 |
T |
C |
5: 103,028,652 (GRCm39) |
S183P |
probably damaging |
Het |
Asb1 |
T |
C |
1: 91,474,748 (GRCm39) |
L90P |
probably damaging |
Het |
Bmp3 |
T |
C |
5: 99,020,209 (GRCm39) |
F211L |
probably benign |
Het |
C8a |
A |
G |
4: 104,703,139 (GRCm39) |
I306T |
probably benign |
Het |
Cdkn3 |
G |
A |
14: 47,007,373 (GRCm39) |
G177R |
probably damaging |
Het |
Chat |
A |
G |
14: 32,170,984 (GRCm39) |
S172P |
probably damaging |
Het |
Chd5 |
CAAGAAGAAGAAGAAGAA |
CAAGAAGAAGAAGAA |
4: 152,438,078 (GRCm39) |
|
probably benign |
Het |
Cyp4a12a |
T |
C |
4: 115,184,420 (GRCm39) |
I265T |
probably damaging |
Het |
Dlst |
T |
A |
12: 85,165,664 (GRCm39) |
|
probably null |
Het |
Dnmt1 |
A |
T |
9: 20,837,716 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
C |
T |
2: 125,205,800 (GRCm39) |
E1066K |
probably damaging |
Het |
Fetub |
C |
T |
16: 22,751,081 (GRCm39) |
R143C |
probably damaging |
Het |
Fstl1 |
T |
A |
16: 37,641,538 (GRCm39) |
S105T |
probably benign |
Het |
Gm19410 |
C |
G |
8: 36,276,518 (GRCm39) |
A1725G |
probably benign |
Het |
Hspb7 |
A |
G |
4: 141,151,215 (GRCm39) |
N119S |
probably damaging |
Het |
Il20 |
T |
A |
1: 130,838,478 (GRCm39) |
D73V |
possibly damaging |
Het |
Insrr |
T |
C |
3: 87,716,608 (GRCm39) |
I612T |
possibly damaging |
Het |
Kcnma1 |
T |
C |
14: 23,359,105 (GRCm39) |
Y1107C |
probably benign |
Het |
Klhl32 |
A |
G |
4: 24,792,615 (GRCm39) |
|
probably null |
Het |
Krt77 |
C |
A |
15: 101,769,351 (GRCm39) |
R470L |
possibly damaging |
Het |
Muc1 |
T |
C |
3: 89,139,336 (GRCm39) |
Y579H |
probably damaging |
Het |
Myof |
T |
C |
19: 37,966,132 (GRCm39) |
D396G |
probably damaging |
Het |
Myom1 |
T |
G |
17: 71,417,746 (GRCm39) |
D1316E |
probably damaging |
Het |
Nbea |
T |
C |
3: 55,912,538 (GRCm39) |
E1083G |
probably benign |
Het |
Nek9 |
G |
A |
12: 85,359,859 (GRCm39) |
A531V |
probably benign |
Het |
Nlrp12 |
A |
T |
7: 3,290,002 (GRCm39) |
I170N |
possibly damaging |
Het |
Nup98 |
A |
G |
7: 101,784,002 (GRCm39) |
I1093T |
probably benign |
Het |
Ovch2 |
G |
A |
7: 107,388,318 (GRCm39) |
L421F |
probably damaging |
Het |
Paqr4 |
T |
C |
17: 23,958,968 (GRCm39) |
D11G |
probably damaging |
Het |
Parp8 |
A |
G |
13: 117,014,134 (GRCm39) |
S561P |
probably damaging |
Het |
Pcgf5 |
T |
A |
19: 36,420,306 (GRCm39) |
F179L |
probably damaging |
Het |
Pde4d |
A |
T |
13: 110,084,876 (GRCm39) |
Q422L |
probably damaging |
Het |
Pigs |
T |
A |
11: 78,232,651 (GRCm39) |
V495E |
probably damaging |
Het |
Polh |
C |
T |
17: 46,498,959 (GRCm39) |
R252H |
probably benign |
Het |
Psg28 |
T |
C |
7: 18,160,107 (GRCm39) |
D363G |
possibly damaging |
Het |
Ptgir |
A |
T |
7: 16,640,815 (GRCm39) |
I36F |
possibly damaging |
Het |
Ptprr |
G |
A |
10: 116,072,668 (GRCm39) |
|
probably null |
Het |
Rax |
C |
T |
18: 66,068,418 (GRCm39) |
G229D |
unknown |
Het |
Secisbp2l |
T |
A |
2: 125,615,136 (GRCm39) |
H163L |
probably benign |
Het |
Sf3a2 |
A |
G |
10: 80,637,297 (GRCm39) |
Y45C |
probably damaging |
Het |
Sgo2a |
C |
T |
1: 58,055,775 (GRCm39) |
T653I |
possibly damaging |
Het |
Slc38a9 |
A |
T |
13: 112,806,231 (GRCm39) |
I26F |
probably damaging |
Het |
Slc5a8 |
A |
G |
10: 88,722,436 (GRCm39) |
I90V |
probably benign |
Het |
Slx4 |
G |
A |
16: 3,803,911 (GRCm39) |
H968Y |
possibly damaging |
Het |
Stam2 |
T |
C |
2: 52,599,611 (GRCm39) |
T233A |
probably benign |
Het |
Tln1 |
G |
C |
4: 43,555,052 (GRCm39) |
F259L |
probably damaging |
Het |
Trav4-2 |
G |
A |
14: 53,655,866 (GRCm39) |
V8M |
possibly damaging |
Het |
Ttll5 |
T |
A |
12: 85,878,729 (GRCm39) |
H45Q |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,714,762 (GRCm39) |
|
probably benign |
Het |
Ush2a |
T |
A |
1: 188,051,217 (GRCm39) |
F234L |
possibly damaging |
Het |
Vmn2r74 |
T |
A |
7: 85,607,526 (GRCm39) |
|
probably null |
Het |
Wdr6 |
CTG |
C |
9: 108,450,994 (GRCm39) |
|
probably null |
Het |
Zfp644 |
A |
G |
5: 106,783,291 (GRCm39) |
S997P |
possibly damaging |
Het |
Zfp853 |
G |
A |
5: 143,274,529 (GRCm39) |
Q364* |
probably null |
Het |
|
Other mutations in Adamts9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00565:Adamts9
|
APN |
6 |
92,836,883 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01352:Adamts9
|
APN |
6 |
92,837,155 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01462:Adamts9
|
APN |
6 |
92,871,247 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01551:Adamts9
|
APN |
6 |
92,784,001 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01577:Adamts9
|
APN |
6 |
92,835,128 (GRCm39) |
splice site |
probably benign |
|
IGL01638:Adamts9
|
APN |
6 |
92,849,409 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01757:Adamts9
|
APN |
6 |
92,773,140 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02102:Adamts9
|
APN |
6 |
92,754,420 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02379:Adamts9
|
APN |
6 |
92,774,014 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02419:Adamts9
|
APN |
6 |
92,773,978 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02554:Adamts9
|
APN |
6 |
92,857,828 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02832:Adamts9
|
APN |
6 |
92,784,156 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03164:Adamts9
|
APN |
6 |
92,866,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03347:Adamts9
|
APN |
6 |
92,864,413 (GRCm39) |
nonsense |
probably null |
|
IGL03401:Adamts9
|
APN |
6 |
92,763,849 (GRCm39) |
missense |
probably damaging |
0.97 |
basilisk
|
UTSW |
6 |
92,837,170 (GRCm39) |
missense |
probably benign |
0.35 |
bluebeard
|
UTSW |
6 |
92,856,940 (GRCm39) |
nonsense |
probably null |
|
Serpent
|
UTSW |
6 |
92,885,687 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4402001:Adamts9
|
UTSW |
6 |
92,849,328 (GRCm39) |
missense |
probably benign |
|
PIT4458001:Adamts9
|
UTSW |
6 |
92,866,886 (GRCm39) |
missense |
probably damaging |
0.99 |
R0047:Adamts9
|
UTSW |
6 |
92,882,287 (GRCm39) |
unclassified |
probably benign |
|
R0047:Adamts9
|
UTSW |
6 |
92,882,287 (GRCm39) |
unclassified |
probably benign |
|
R0067:Adamts9
|
UTSW |
6 |
92,867,148 (GRCm39) |
missense |
probably damaging |
0.98 |
R0141:Adamts9
|
UTSW |
6 |
92,920,066 (GRCm39) |
missense |
probably benign |
|
R0326:Adamts9
|
UTSW |
6 |
92,835,038 (GRCm39) |
nonsense |
probably null |
|
R0396:Adamts9
|
UTSW |
6 |
92,774,986 (GRCm39) |
missense |
probably benign |
0.00 |
R0490:Adamts9
|
UTSW |
6 |
92,849,847 (GRCm39) |
missense |
probably benign |
|
R0504:Adamts9
|
UTSW |
6 |
92,889,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R0620:Adamts9
|
UTSW |
6 |
92,835,094 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0669:Adamts9
|
UTSW |
6 |
92,857,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R0682:Adamts9
|
UTSW |
6 |
92,880,783 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1412:Adamts9
|
UTSW |
6 |
92,773,414 (GRCm39) |
missense |
probably benign |
|
R1433:Adamts9
|
UTSW |
6 |
92,826,271 (GRCm39) |
critical splice donor site |
probably null |
|
R1558:Adamts9
|
UTSW |
6 |
92,885,692 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1661:Adamts9
|
UTSW |
6 |
92,857,604 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1801:Adamts9
|
UTSW |
6 |
92,840,357 (GRCm39) |
missense |
probably benign |
0.27 |
R1855:Adamts9
|
UTSW |
6 |
92,878,350 (GRCm39) |
splice site |
probably benign |
|
R1887:Adamts9
|
UTSW |
6 |
92,849,769 (GRCm39) |
critical splice donor site |
probably null |
|
R1934:Adamts9
|
UTSW |
6 |
92,920,102 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1956:Adamts9
|
UTSW |
6 |
92,836,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R1986:Adamts9
|
UTSW |
6 |
92,773,375 (GRCm39) |
missense |
probably benign |
|
R2370:Adamts9
|
UTSW |
6 |
92,837,184 (GRCm39) |
missense |
probably damaging |
0.99 |
R2376:Adamts9
|
UTSW |
6 |
92,889,812 (GRCm39) |
missense |
probably benign |
|
R2432:Adamts9
|
UTSW |
6 |
92,834,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R2876:Adamts9
|
UTSW |
6 |
92,772,891 (GRCm39) |
splice site |
probably benign |
|
R3015:Adamts9
|
UTSW |
6 |
92,849,913 (GRCm39) |
missense |
probably benign |
0.05 |
R3611:Adamts9
|
UTSW |
6 |
92,846,965 (GRCm39) |
missense |
probably benign |
0.05 |
R4024:Adamts9
|
UTSW |
6 |
92,849,765 (GRCm39) |
splice site |
probably benign |
|
R4292:Adamts9
|
UTSW |
6 |
92,772,977 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4403:Adamts9
|
UTSW |
6 |
92,836,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R4574:Adamts9
|
UTSW |
6 |
92,856,940 (GRCm39) |
nonsense |
probably null |
|
R4677:Adamts9
|
UTSW |
6 |
92,793,587 (GRCm39) |
start codon destroyed |
probably null |
|
R5114:Adamts9
|
UTSW |
6 |
92,867,254 (GRCm39) |
missense |
probably benign |
0.03 |
R5260:Adamts9
|
UTSW |
6 |
92,784,118 (GRCm39) |
missense |
probably benign |
0.00 |
R5384:Adamts9
|
UTSW |
6 |
92,774,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Adamts9
|
UTSW |
6 |
92,857,678 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5497:Adamts9
|
UTSW |
6 |
92,831,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R5629:Adamts9
|
UTSW |
6 |
92,775,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R5943:Adamts9
|
UTSW |
6 |
92,880,767 (GRCm39) |
missense |
probably benign |
0.02 |
R6039:Adamts9
|
UTSW |
6 |
92,885,527 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6051:Adamts9
|
UTSW |
6 |
92,867,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R6051:Adamts9
|
UTSW |
6 |
92,836,907 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6082:Adamts9
|
UTSW |
6 |
92,866,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Adamts9
|
UTSW |
6 |
92,774,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R6291:Adamts9
|
UTSW |
6 |
92,867,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R6502:Adamts9
|
UTSW |
6 |
92,849,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R6818:Adamts9
|
UTSW |
6 |
92,882,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R6848:Adamts9
|
UTSW |
6 |
92,840,335 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7028:Adamts9
|
UTSW |
6 |
92,886,774 (GRCm39) |
nonsense |
probably null |
|
R7095:Adamts9
|
UTSW |
6 |
92,864,672 (GRCm39) |
missense |
probably benign |
0.39 |
R7287:Adamts9
|
UTSW |
6 |
92,866,984 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7294:Adamts9
|
UTSW |
6 |
92,871,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Adamts9
|
UTSW |
6 |
92,835,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R7581:Adamts9
|
UTSW |
6 |
92,914,319 (GRCm39) |
missense |
probably benign |
0.00 |
R7682:Adamts9
|
UTSW |
6 |
92,857,679 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7691:Adamts9
|
UTSW |
6 |
92,773,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R7791:Adamts9
|
UTSW |
6 |
92,849,366 (GRCm39) |
missense |
probably benign |
0.00 |
R7851:Adamts9
|
UTSW |
6 |
92,885,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Adamts9
|
UTSW |
6 |
92,886,668 (GRCm39) |
critical splice donor site |
probably null |
|
R8224:Adamts9
|
UTSW |
6 |
92,773,351 (GRCm39) |
missense |
probably damaging |
0.96 |
R8328:Adamts9
|
UTSW |
6 |
92,866,993 (GRCm39) |
missense |
probably benign |
0.17 |
R8334:Adamts9
|
UTSW |
6 |
92,914,225 (GRCm39) |
splice site |
probably null |
|
R8559:Adamts9
|
UTSW |
6 |
92,784,117 (GRCm39) |
missense |
probably benign |
0.01 |
R8709:Adamts9
|
UTSW |
6 |
92,784,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R8735:Adamts9
|
UTSW |
6 |
92,837,048 (GRCm39) |
intron |
probably benign |
|
R8739:Adamts9
|
UTSW |
6 |
92,831,261 (GRCm39) |
missense |
probably benign |
0.04 |
R9108:Adamts9
|
UTSW |
6 |
92,857,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R9171:Adamts9
|
UTSW |
6 |
92,849,381 (GRCm39) |
missense |
probably benign |
0.03 |
R9198:Adamts9
|
UTSW |
6 |
92,837,170 (GRCm39) |
missense |
probably benign |
0.35 |
R9299:Adamts9
|
UTSW |
6 |
92,773,976 (GRCm39) |
missense |
probably benign |
0.00 |
R9300:Adamts9
|
UTSW |
6 |
92,864,371 (GRCm39) |
missense |
probably benign |
0.10 |
R9308:Adamts9
|
UTSW |
6 |
92,857,875 (GRCm39) |
missense |
probably benign |
0.03 |
R9325:Adamts9
|
UTSW |
6 |
92,849,279 (GRCm39) |
missense |
probably benign |
0.00 |
R9397:Adamts9
|
UTSW |
6 |
92,878,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R9550:Adamts9
|
UTSW |
6 |
92,878,429 (GRCm39) |
missense |
probably benign |
0.00 |
R9623:Adamts9
|
UTSW |
6 |
92,857,661 (GRCm39) |
missense |
probably benign |
0.02 |
R9698:Adamts9
|
UTSW |
6 |
92,784,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R9755:Adamts9
|
UTSW |
6 |
92,856,922 (GRCm39) |
missense |
probably benign |
0.15 |
RF013:Adamts9
|
UTSW |
6 |
92,920,126 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1177:Adamts9
|
UTSW |
6 |
92,831,327 (GRCm39) |
missense |
probably damaging |
0.99 |
|