Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aspg |
A |
G |
12: 112,089,387 (GRCm39) |
T392A |
probably benign |
Het |
Atp8b5 |
C |
A |
4: 43,368,010 (GRCm39) |
Q878K |
possibly damaging |
Het |
Ccdc85a |
G |
T |
11: 28,526,506 (GRCm39) |
H339Q |
probably damaging |
Het |
Clca3a1 |
C |
T |
3: 144,713,539 (GRCm39) |
M697I |
probably benign |
Het |
Cog4 |
C |
T |
8: 111,592,717 (GRCm39) |
T430M |
probably benign |
Het |
Col6a5 |
A |
G |
9: 105,823,274 (GRCm39) |
Y28H |
unknown |
Het |
Cth |
A |
T |
3: 157,610,804 (GRCm39) |
Y343N |
probably damaging |
Het |
Dctn3 |
A |
T |
4: 41,719,854 (GRCm39) |
L84* |
probably null |
Het |
Epha5 |
A |
T |
5: 84,219,092 (GRCm39) |
I868N |
probably damaging |
Het |
Ephb2 |
T |
C |
4: 136,498,681 (GRCm39) |
N133D |
possibly damaging |
Het |
Epor |
G |
A |
9: 21,870,752 (GRCm39) |
P376L |
probably damaging |
Het |
Gsdme |
A |
G |
6: 50,204,354 (GRCm39) |
V201A |
possibly damaging |
Het |
Hdgf |
G |
A |
3: 87,821,831 (GRCm39) |
E149K |
possibly damaging |
Het |
Lrrfip2 |
T |
C |
9: 111,034,917 (GRCm39) |
|
probably null |
Het |
Ly6g6d |
T |
C |
17: 35,293,226 (GRCm39) |
I40V |
probably benign |
Het |
Mlh3 |
G |
A |
12: 85,313,510 (GRCm39) |
T892I |
probably benign |
Het |
Mmp19 |
C |
T |
10: 128,634,011 (GRCm39) |
T304I |
probably damaging |
Het |
Mmp28 |
T |
C |
11: 83,334,602 (GRCm39) |
D384G |
possibly damaging |
Het |
Moxd1 |
T |
C |
10: 24,120,286 (GRCm39) |
|
probably null |
Het |
Mtcl3 |
T |
G |
10: 29,024,254 (GRCm39) |
L390R |
probably damaging |
Het |
Ncapg |
T |
C |
5: 45,828,477 (GRCm39) |
V76A |
probably benign |
Het |
Nos1 |
C |
T |
5: 118,005,774 (GRCm39) |
R165C |
probably benign |
Het |
Or1e1c |
T |
C |
11: 73,265,578 (GRCm39) |
M1T |
probably null |
Het |
Or2a57 |
A |
G |
6: 43,212,559 (GRCm39) |
T6A |
possibly damaging |
Het |
Pik3c2a |
T |
A |
7: 115,975,485 (GRCm39) |
H694L |
possibly damaging |
Het |
Psme2 |
A |
G |
14: 55,827,128 (GRCm39) |
L60P |
probably damaging |
Het |
Ptpn23 |
A |
G |
9: 110,237,175 (GRCm39) |
V4A |
probably benign |
Het |
Rgr |
G |
T |
14: 36,766,566 (GRCm39) |
T160K |
probably damaging |
Het |
Serpind1 |
A |
G |
16: 17,154,787 (GRCm39) |
I205V |
probably benign |
Het |
Skap2 |
T |
C |
6: 51,898,280 (GRCm39) |
Y150C |
probably damaging |
Het |
Srsf9 |
T |
C |
5: 115,470,187 (GRCm39) |
S122P |
probably damaging |
Het |
Stox1 |
T |
G |
10: 62,500,461 (GRCm39) |
I700L |
probably benign |
Het |
Tada1 |
A |
G |
1: 166,216,294 (GRCm39) |
D165G |
probably damaging |
Het |
Traf5 |
A |
G |
1: 191,731,828 (GRCm39) |
S338P |
probably benign |
Het |
Trim39 |
G |
A |
17: 36,574,617 (GRCm39) |
|
probably benign |
Het |
Wbp2 |
G |
A |
11: 115,972,066 (GRCm39) |
A130V |
possibly damaging |
Het |
Zcchc17 |
T |
C |
4: 130,230,902 (GRCm39) |
K96E |
probably benign |
Het |
Zfp800 |
G |
A |
6: 28,242,983 (GRCm39) |
L661F |
possibly damaging |
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 |
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 |
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 |
|