Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsf3 |
C |
A |
8: 123,512,694 (GRCm39) |
R372S |
probably damaging |
Het |
Bhlhe40 |
T |
C |
6: 108,641,992 (GRCm39) |
L312P |
probably damaging |
Het |
Ccdc180 |
A |
G |
4: 45,902,486 (GRCm39) |
E305G |
possibly damaging |
Het |
Ccdc83 |
T |
A |
7: 89,885,615 (GRCm39) |
R257* |
probably null |
Het |
Cd209e |
G |
A |
8: 3,899,212 (GRCm39) |
Q167* |
probably null |
Het |
Cd300e |
G |
A |
11: 114,945,380 (GRCm39) |
T138I |
probably benign |
Het |
Ces2c |
A |
T |
8: 105,576,331 (GRCm39) |
M115L |
probably benign |
Het |
Cfap61 |
T |
A |
2: 145,971,022 (GRCm39) |
|
probably null |
Het |
Chd1l |
G |
A |
3: 97,494,483 (GRCm39) |
A399V |
probably damaging |
Het |
Cic |
C |
T |
7: 24,985,459 (GRCm39) |
S301L |
probably damaging |
Het |
Cks2 |
A |
G |
13: 51,799,495 (GRCm39) |
H16R |
probably benign |
Het |
Copa |
A |
T |
1: 171,946,415 (GRCm39) |
H953L |
possibly damaging |
Het |
Ctdsp2 |
T |
C |
10: 126,831,749 (GRCm39) |
V145A |
possibly damaging |
Het |
Cyp2j13 |
A |
G |
4: 95,945,074 (GRCm39) |
V377A |
possibly damaging |
Het |
Dhx57 |
A |
G |
17: 80,582,234 (GRCm39) |
V404A |
probably benign |
Het |
Dock2 |
T |
C |
11: 34,598,152 (GRCm39) |
S340G |
probably damaging |
Het |
Ggps1 |
A |
G |
13: 14,232,379 (GRCm39) |
|
probably null |
Het |
Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
Gm11444 |
T |
C |
11: 85,737,617 (GRCm39) |
|
probably null |
Het |
Grina |
A |
G |
15: 76,132,751 (GRCm39) |
T173A |
possibly damaging |
Het |
Hcrtr1 |
G |
A |
4: 130,029,133 (GRCm39) |
T223I |
probably benign |
Het |
Igsf10 |
T |
A |
3: 59,226,870 (GRCm39) |
T2268S |
probably damaging |
Het |
Inhca |
G |
A |
9: 103,159,834 (GRCm39) |
R14* |
probably null |
Het |
Ino80d |
C |
T |
1: 63,101,285 (GRCm39) |
R447Q |
probably damaging |
Het |
Inpp4b |
C |
T |
8: 82,497,462 (GRCm39) |
T94M |
probably damaging |
Het |
Itga2 |
A |
G |
13: 115,005,786 (GRCm39) |
Y465H |
probably damaging |
Het |
Knl1 |
A |
G |
2: 118,900,767 (GRCm39) |
T823A |
probably damaging |
Het |
Krtap4-16 |
A |
G |
11: 99,741,861 (GRCm39) |
S180P |
unknown |
Het |
Ldc1 |
A |
G |
4: 130,115,534 (GRCm39) |
S5P |
probably benign |
Het |
Lpar6 |
A |
T |
14: 73,476,297 (GRCm39) |
D86V |
probably damaging |
Het |
Muc5ac |
C |
A |
7: 141,370,601 (GRCm39) |
C2500* |
probably null |
Het |
Mzf1 |
T |
C |
7: 12,787,296 (GRCm39) |
|
probably benign |
Het |
Or4f58 |
A |
C |
2: 111,851,605 (GRCm39) |
M198R |
possibly damaging |
Het |
Or5d46 |
T |
A |
2: 88,170,002 (GRCm39) |
I31N |
probably benign |
Het |
Or5m3 |
G |
T |
2: 85,838,443 (GRCm39) |
V108L |
possibly damaging |
Het |
Or7a36 |
T |
C |
10: 78,820,113 (GRCm39) |
V163A |
probably benign |
Het |
Otogl |
T |
G |
10: 107,626,361 (GRCm39) |
E1501A |
probably damaging |
Het |
Pcdh10 |
T |
A |
3: 45,335,989 (GRCm39) |
S768T |
possibly damaging |
Het |
Pcnx2 |
G |
T |
8: 126,604,325 (GRCm39) |
Q644K |
probably damaging |
Het |
Pdzd9 |
T |
A |
7: 120,259,449 (GRCm39) |
I180F |
possibly damaging |
Het |
Pinx1 |
A |
C |
14: 64,115,621 (GRCm39) |
N152T |
probably benign |
Het |
Prr14l |
T |
C |
5: 32,987,608 (GRCm39) |
E629G |
probably benign |
Het |
Qpctl |
T |
A |
7: 18,882,345 (GRCm39) |
I104F |
probably benign |
Het |
Rabep1 |
C |
T |
11: 70,808,505 (GRCm39) |
A444V |
probably damaging |
Het |
Rnf150 |
A |
G |
8: 83,717,183 (GRCm39) |
Y230C |
probably damaging |
Het |
Slc25a27 |
A |
C |
17: 43,968,621 (GRCm39) |
V152G |
probably damaging |
Het |
Swt1 |
A |
G |
1: 151,260,084 (GRCm39) |
S772P |
possibly damaging |
Het |
Tenm4 |
A |
G |
7: 96,523,701 (GRCm39) |
T1711A |
probably benign |
Het |
Tfap2d |
G |
C |
1: 19,174,702 (GRCm39) |
G52R |
probably benign |
Het |
Tmem265 |
T |
G |
7: 127,164,044 (GRCm39) |
V86G |
possibly damaging |
Het |
Trpm8 |
C |
T |
1: 88,276,054 (GRCm39) |
H551Y |
probably benign |
Het |
Ttc6 |
T |
G |
12: 57,749,048 (GRCm39) |
Y1327D |
possibly damaging |
Het |
Uevld |
G |
T |
7: 46,587,729 (GRCm39) |
Q324K |
possibly damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r73 |
C |
T |
7: 85,521,049 (GRCm39) |
M306I |
probably benign |
Het |
Vmn2r93 |
T |
A |
17: 18,524,366 (GRCm39) |
M120K |
probably benign |
Het |
Zfp804b |
T |
A |
5: 6,819,908 (GRCm39) |
I1016F |
probably benign |
Het |
Zfp90 |
T |
C |
8: 107,152,026 (GRCm39) |
C580R |
probably damaging |
Het |
|
Other mutations in Adamts20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00433:Adamts20
|
APN |
15 |
94,292,522 (GRCm39) |
missense |
probably benign |
|
IGL00491:Adamts20
|
APN |
15 |
94,171,113 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL00502:Adamts20
|
APN |
15 |
94,301,278 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00672:Adamts20
|
APN |
15 |
94,238,986 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00840:Adamts20
|
APN |
15 |
94,180,363 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00909:Adamts20
|
APN |
15 |
94,277,694 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01101:Adamts20
|
APN |
15 |
94,241,923 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01137:Adamts20
|
APN |
15 |
94,292,492 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01457:Adamts20
|
APN |
15 |
94,229,329 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01685:Adamts20
|
APN |
15 |
94,301,327 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01949:Adamts20
|
APN |
15 |
94,223,987 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02525:Adamts20
|
APN |
15 |
94,180,959 (GRCm39) |
splice site |
probably null |
|
IGL03088:Adamts20
|
APN |
15 |
94,227,795 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03175:Adamts20
|
APN |
15 |
94,171,136 (GRCm39) |
nonsense |
probably null |
|
belt
|
UTSW |
15 |
94,243,871 (GRCm39) |
missense |
probably damaging |
1.00 |
buckeye
|
UTSW |
15 |
94,238,968 (GRCm39) |
missense |
probably damaging |
1.00 |
jack_white
|
UTSW |
15 |
0 () |
unclassified |
|
|
meowth
|
UTSW |
15 |
94,229,339 (GRCm39) |
missense |
probably damaging |
1.00 |
nidoking
|
UTSW |
15 |
94,301,326 (GRCm39) |
missense |
probably damaging |
1.00 |
panda
|
UTSW |
15 |
94,224,580 (GRCm39) |
intron |
probably benign |
|
pikachu
|
UTSW |
15 |
94,243,871 (GRCm39) |
missense |
probably damaging |
1.00 |
poliwag
|
UTSW |
15 |
94,292,503 (GRCm39) |
nonsense |
probably null |
|
splotch2
|
UTSW |
15 |
94,233,442 (GRCm39) |
intron |
probably benign |
|
wash
|
UTSW |
15 |
94,245,551 (GRCm39) |
nonsense |
probably null |
|
whitebelly
|
UTSW |
15 |
0 () |
unclassified |
|
|
whopper
|
UTSW |
15 |
94,245,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R0483:Adamts20
|
UTSW |
15 |
94,251,452 (GRCm39) |
missense |
probably benign |
0.00 |
R0514:Adamts20
|
UTSW |
15 |
94,168,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R0568:Adamts20
|
UTSW |
15 |
94,189,594 (GRCm39) |
splice site |
probably benign |
|
R0730:Adamts20
|
UTSW |
15 |
94,245,571 (GRCm39) |
missense |
probably benign |
0.00 |
R0973:Adamts20
|
UTSW |
15 |
94,184,252 (GRCm39) |
missense |
probably benign |
0.00 |
R1339:Adamts20
|
UTSW |
15 |
94,220,777 (GRCm39) |
missense |
probably benign |
0.19 |
R1721:Adamts20
|
UTSW |
15 |
94,236,340 (GRCm39) |
missense |
probably benign |
0.44 |
R1809:Adamts20
|
UTSW |
15 |
94,238,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R1832:Adamts20
|
UTSW |
15 |
94,184,225 (GRCm39) |
missense |
probably benign |
0.00 |
R1846:Adamts20
|
UTSW |
15 |
94,243,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R1867:Adamts20
|
UTSW |
15 |
94,236,340 (GRCm39) |
missense |
probably benign |
0.44 |
R1875:Adamts20
|
UTSW |
15 |
94,229,277 (GRCm39) |
missense |
probably benign |
0.01 |
R1930:Adamts20
|
UTSW |
15 |
94,301,891 (GRCm39) |
missense |
probably benign |
0.03 |
R1931:Adamts20
|
UTSW |
15 |
94,301,891 (GRCm39) |
missense |
probably benign |
0.03 |
R1932:Adamts20
|
UTSW |
15 |
94,301,891 (GRCm39) |
missense |
probably benign |
0.03 |
R2001:Adamts20
|
UTSW |
15 |
94,245,599 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2116:Adamts20
|
UTSW |
15 |
94,253,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R2162:Adamts20
|
UTSW |
15 |
94,229,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R2350:Adamts20
|
UTSW |
15 |
94,181,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R2887:Adamts20
|
UTSW |
15 |
94,228,459 (GRCm39) |
missense |
probably benign |
0.00 |
R2889:Adamts20
|
UTSW |
15 |
94,228,459 (GRCm39) |
missense |
probably benign |
0.00 |
R2890:Adamts20
|
UTSW |
15 |
94,228,459 (GRCm39) |
missense |
probably benign |
0.00 |
R3109:Adamts20
|
UTSW |
15 |
94,243,785 (GRCm39) |
splice site |
probably benign |
|
R3719:Adamts20
|
UTSW |
15 |
94,259,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R3832:Adamts20
|
UTSW |
15 |
94,229,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R3901:Adamts20
|
UTSW |
15 |
94,226,726 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4398:Adamts20
|
UTSW |
15 |
94,231,576 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4402:Adamts20
|
UTSW |
15 |
94,277,827 (GRCm39) |
missense |
probably benign |
|
R4431:Adamts20
|
UTSW |
15 |
94,241,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R4479:Adamts20
|
UTSW |
15 |
94,301,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R4482:Adamts20
|
UTSW |
15 |
94,243,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R4503:Adamts20
|
UTSW |
15 |
94,277,631 (GRCm39) |
missense |
probably damaging |
0.99 |
R4671:Adamts20
|
UTSW |
15 |
94,301,206 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4700:Adamts20
|
UTSW |
15 |
94,292,503 (GRCm39) |
nonsense |
probably null |
|
R4707:Adamts20
|
UTSW |
15 |
94,231,528 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4725:Adamts20
|
UTSW |
15 |
94,249,643 (GRCm39) |
missense |
probably damaging |
0.99 |
R4771:Adamts20
|
UTSW |
15 |
94,249,516 (GRCm39) |
splice site |
probably null |
|
R4829:Adamts20
|
UTSW |
15 |
94,224,277 (GRCm39) |
missense |
probably benign |
0.01 |
R4937:Adamts20
|
UTSW |
15 |
94,277,656 (GRCm39) |
missense |
probably benign |
|
R4960:Adamts20
|
UTSW |
15 |
94,277,655 (GRCm39) |
missense |
probably benign |
|
R5270:Adamts20
|
UTSW |
15 |
94,180,400 (GRCm39) |
missense |
probably benign |
0.00 |
R5388:Adamts20
|
UTSW |
15 |
94,243,659 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5410:Adamts20
|
UTSW |
15 |
94,179,838 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5453:Adamts20
|
UTSW |
15 |
94,223,969 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5611:Adamts20
|
UTSW |
15 |
94,171,161 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5687:Adamts20
|
UTSW |
15 |
94,223,852 (GRCm39) |
missense |
probably benign |
0.36 |
R5758:Adamts20
|
UTSW |
15 |
94,292,531 (GRCm39) |
missense |
probably benign |
0.00 |
R5801:Adamts20
|
UTSW |
15 |
94,245,551 (GRCm39) |
nonsense |
probably null |
|
R5834:Adamts20
|
UTSW |
15 |
94,251,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R5993:Adamts20
|
UTSW |
15 |
94,236,604 (GRCm39) |
missense |
probably damaging |
0.99 |
R5997:Adamts20
|
UTSW |
15 |
94,277,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R6044:Adamts20
|
UTSW |
15 |
94,180,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R6058:Adamts20
|
UTSW |
15 |
94,227,928 (GRCm39) |
nonsense |
probably null |
|
R6217:Adamts20
|
UTSW |
15 |
94,236,596 (GRCm39) |
missense |
probably benign |
0.00 |
R6354:Adamts20
|
UTSW |
15 |
94,245,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R6415:Adamts20
|
UTSW |
15 |
94,222,540 (GRCm39) |
critical splice donor site |
probably null |
|
R6419:Adamts20
|
UTSW |
15 |
94,231,556 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6476:Adamts20
|
UTSW |
15 |
94,259,691 (GRCm39) |
missense |
probably benign |
0.22 |
R6485:Adamts20
|
UTSW |
15 |
94,241,852 (GRCm39) |
missense |
probably benign |
0.17 |
R6517:Adamts20
|
UTSW |
15 |
94,180,985 (GRCm39) |
splice site |
probably null |
|
R6675:Adamts20
|
UTSW |
15 |
94,229,197 (GRCm39) |
critical splice donor site |
probably null |
|
R6863:Adamts20
|
UTSW |
15 |
94,277,627 (GRCm39) |
nonsense |
probably null |
|
R7186:Adamts20
|
UTSW |
15 |
94,220,689 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7263:Adamts20
|
UTSW |
15 |
94,220,772 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7441:Adamts20
|
UTSW |
15 |
94,251,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R7519:Adamts20
|
UTSW |
15 |
94,223,869 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7747:Adamts20
|
UTSW |
15 |
94,189,468 (GRCm39) |
nonsense |
probably null |
|
R7770:Adamts20
|
UTSW |
15 |
94,231,579 (GRCm39) |
missense |
probably benign |
0.02 |
R7816:Adamts20
|
UTSW |
15 |
94,220,725 (GRCm39) |
missense |
probably benign |
0.00 |
R7827:Adamts20
|
UTSW |
15 |
94,223,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R7853:Adamts20
|
UTSW |
15 |
94,243,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R7894:Adamts20
|
UTSW |
15 |
94,249,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R7951:Adamts20
|
UTSW |
15 |
94,238,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R8233:Adamts20
|
UTSW |
15 |
94,189,533 (GRCm39) |
missense |
probably benign |
0.19 |
R8458:Adamts20
|
UTSW |
15 |
94,251,521 (GRCm39) |
missense |
probably benign |
0.02 |
R8709:Adamts20
|
UTSW |
15 |
94,238,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R8719:Adamts20
|
UTSW |
15 |
94,241,903 (GRCm39) |
missense |
probably damaging |
0.99 |
R8728:Adamts20
|
UTSW |
15 |
94,229,281 (GRCm39) |
missense |
probably benign |
0.00 |
R8787:Adamts20
|
UTSW |
15 |
94,184,294 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8801:Adamts20
|
UTSW |
15 |
94,258,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R9055:Adamts20
|
UTSW |
15 |
94,181,867 (GRCm39) |
missense |
probably damaging |
0.98 |
R9069:Adamts20
|
UTSW |
15 |
94,236,349 (GRCm39) |
missense |
probably benign |
0.00 |
R9297:Adamts20
|
UTSW |
15 |
94,301,321 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9318:Adamts20
|
UTSW |
15 |
94,301,321 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9362:Adamts20
|
UTSW |
15 |
94,236,626 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9658:Adamts20
|
UTSW |
15 |
94,249,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R9747:Adamts20
|
UTSW |
15 |
94,180,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R9769:Adamts20
|
UTSW |
15 |
94,251,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R9795:Adamts20
|
UTSW |
15 |
94,301,180 (GRCm39) |
missense |
possibly damaging |
0.78 |
|