Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Adam22 |
C |
A |
5: 8,140,182 (GRCm39) |
G202W |
probably damaging |
Het |
Ak4 |
T |
G |
4: 101,317,760 (GRCm39) |
I110S |
probably damaging |
Het |
Arhgap9 |
T |
G |
10: 127,165,418 (GRCm39) |
I609S |
probably damaging |
Het |
Arid4a |
C |
A |
12: 71,116,634 (GRCm39) |
S242* |
probably null |
Het |
Ceacam1 |
T |
G |
7: 25,173,951 (GRCm39) |
I235L |
probably benign |
Het |
Chil3 |
T |
C |
3: 106,055,978 (GRCm39) |
D365G |
probably damaging |
Het |
Ckap2 |
A |
C |
8: 22,667,212 (GRCm39) |
S216R |
probably benign |
Het |
Cyp2e1 |
G |
T |
7: 140,350,031 (GRCm39) |
V239L |
probably benign |
Het |
Dnah7b |
T |
A |
1: 46,397,431 (GRCm39) |
M3954K |
probably benign |
Het |
Ercc6l2 |
A |
T |
13: 64,020,072 (GRCm39) |
|
probably benign |
Het |
Etv5 |
T |
C |
16: 22,202,404 (GRCm39) |
D468G |
probably damaging |
Het |
Fbxo44 |
T |
A |
4: 148,238,686 (GRCm39) |
I213F |
probably benign |
Het |
Gm5084 |
A |
G |
13: 60,360,356 (GRCm39) |
|
noncoding transcript |
Het |
Gpr17 |
G |
A |
18: 32,080,694 (GRCm39) |
T123I |
probably damaging |
Het |
Grin3a |
A |
G |
4: 49,770,376 (GRCm39) |
|
probably benign |
Het |
H2-D1 |
T |
G |
17: 35,484,883 (GRCm39) |
L248R |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,577,723 (GRCm39) |
I2013V |
probably damaging |
Het |
Hp1bp3 |
A |
T |
4: 137,953,208 (GRCm39) |
D84V |
probably damaging |
Het |
Ift140 |
T |
C |
17: 25,252,059 (GRCm39) |
F33S |
probably damaging |
Het |
Inhbc |
C |
G |
10: 127,193,296 (GRCm39) |
C240S |
probably damaging |
Het |
Iqgap1 |
T |
A |
7: 80,449,610 (GRCm39) |
E62V |
probably damaging |
Het |
Kcna4 |
G |
A |
2: 107,126,151 (GRCm39) |
W295* |
probably null |
Het |
Kdm4a |
C |
T |
4: 117,996,105 (GRCm39) |
A975T |
probably damaging |
Het |
Lrrtm3 |
T |
C |
10: 63,923,931 (GRCm39) |
D412G |
possibly damaging |
Het |
Midn |
A |
C |
10: 79,991,027 (GRCm39) |
I346L |
probably benign |
Het |
Ndufa10 |
C |
T |
1: 92,390,042 (GRCm39) |
D259N |
probably benign |
Het |
Nefh |
C |
A |
11: 4,890,985 (GRCm39) |
A545S |
possibly damaging |
Het |
Prpf8 |
A |
G |
11: 75,399,784 (GRCm39) |
Y2281C |
probably damaging |
Het |
Psip1 |
G |
A |
4: 83,378,367 (GRCm39) |
|
probably benign |
Het |
Ptpro |
G |
T |
6: 137,419,705 (GRCm39) |
A184S |
probably damaging |
Het |
Rab37 |
T |
A |
11: 115,047,853 (GRCm39) |
I65K |
possibly damaging |
Het |
Rasgrp4 |
T |
C |
7: 28,844,561 (GRCm39) |
L247P |
probably damaging |
Het |
Rnf20 |
T |
C |
4: 49,644,620 (GRCm39) |
V295A |
probably damaging |
Het |
Serpina3g |
A |
G |
12: 104,204,253 (GRCm39) |
|
probably benign |
Het |
Shox2 |
A |
G |
3: 66,881,087 (GRCm39) |
|
probably benign |
Het |
Skint6 |
T |
G |
4: 112,707,937 (GRCm39) |
D977A |
possibly damaging |
Het |
Slc25a23 |
C |
T |
17: 57,360,597 (GRCm39) |
V248M |
probably damaging |
Het |
Slco1a7 |
T |
A |
6: 141,690,188 (GRCm39) |
K188N |
probably damaging |
Het |
Smg1 |
A |
T |
7: 117,745,294 (GRCm39) |
D3008E |
possibly damaging |
Het |
St18 |
A |
G |
1: 6,872,840 (GRCm39) |
S192G |
possibly damaging |
Het |
Supt20 |
T |
A |
3: 54,616,746 (GRCm39) |
V306E |
probably damaging |
Het |
T |
T |
C |
17: 8,660,597 (GRCm39) |
Y403H |
probably damaging |
Het |
Tars3 |
C |
A |
7: 65,333,567 (GRCm39) |
N588K |
probably benign |
Het |
Tmem132c |
T |
C |
5: 127,640,907 (GRCm39) |
V1026A |
probably benign |
Het |
Trpv4 |
T |
C |
5: 114,774,506 (GRCm39) |
T193A |
probably benign |
Het |
Ubqln4 |
A |
G |
3: 88,470,506 (GRCm39) |
N326S |
probably damaging |
Het |
Uggt2 |
G |
A |
14: 119,256,898 (GRCm39) |
T1112I |
probably damaging |
Het |
Vasn |
C |
T |
16: 4,466,284 (GRCm39) |
P77L |
probably benign |
Het |
Vps9d1 |
A |
C |
8: 123,974,704 (GRCm39) |
|
probably null |
Het |
Washc4 |
C |
A |
10: 83,415,418 (GRCm39) |
Q803K |
possibly damaging |
Het |
Zcchc2 |
C |
T |
1: 105,958,430 (GRCm39) |
T967I |
probably damaging |
Het |
Zfp874a |
G |
A |
13: 67,590,473 (GRCm39) |
L404F |
possibly damaging |
Het |
Zscan30 |
T |
C |
18: 24,104,773 (GRCm39) |
|
noncoding transcript |
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 |
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 |
|