Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd13a |
A |
T |
5: 114,924,063 (GRCm39) |
H53L |
possibly damaging |
Het |
Becn1 |
T |
C |
11: 101,185,811 (GRCm39) |
D145G |
possibly damaging |
Het |
Bod1l |
A |
G |
5: 41,974,942 (GRCm39) |
V2124A |
probably benign |
Het |
Cdcp3 |
A |
G |
7: 130,796,060 (GRCm39) |
T72A |
possibly damaging |
Het |
Celsr1 |
C |
T |
15: 85,914,692 (GRCm39) |
A1094T |
probably damaging |
Het |
Clstn2 |
A |
T |
9: 97,365,128 (GRCm39) |
Y459* |
probably null |
Het |
Cnksr3 |
A |
G |
10: 7,104,281 (GRCm39) |
|
probably null |
Het |
Cux2 |
A |
T |
5: 122,003,991 (GRCm39) |
F1048L |
probably benign |
Het |
Cybrd1 |
A |
G |
2: 70,960,050 (GRCm39) |
K83E |
probably damaging |
Het |
Dpp8 |
A |
T |
9: 64,962,294 (GRCm39) |
|
probably benign |
Het |
Eef2 |
T |
A |
10: 81,017,777 (GRCm39) |
V813E |
possibly damaging |
Het |
Eef2 |
A |
T |
10: 81,017,816 (GRCm39) |
|
probably null |
Het |
Etnk1 |
T |
G |
6: 143,126,392 (GRCm39) |
I79S |
probably damaging |
Het |
Fam151a |
A |
G |
4: 106,604,790 (GRCm39) |
N384S |
possibly damaging |
Het |
Fam83c |
A |
G |
2: 155,676,362 (GRCm39) |
L136P |
probably damaging |
Het |
Gfra2 |
G |
A |
14: 71,133,292 (GRCm39) |
V41I |
probably benign |
Het |
Mroh9 |
A |
G |
1: 162,908,144 (GRCm39) |
I2T |
probably benign |
Het |
Muc2 |
A |
G |
7: 141,306,132 (GRCm39) |
I274V |
probably benign |
Het |
Nacad |
T |
G |
11: 6,548,279 (GRCm39) |
E1456A |
possibly damaging |
Het |
Npy4r |
T |
A |
14: 33,868,614 (GRCm39) |
I225F |
possibly damaging |
Het |
Or3a1b |
T |
G |
11: 74,012,160 (GRCm39) |
F15C |
probably damaging |
Het |
Pik3c2a |
T |
C |
7: 115,973,038 (GRCm39) |
D719G |
possibly damaging |
Het |
Pparg |
G |
T |
6: 115,449,915 (GRCm39) |
V305L |
possibly damaging |
Het |
Rictor |
A |
G |
15: 6,738,119 (GRCm39) |
N19D |
probably benign |
Het |
Slc4a1 |
T |
C |
11: 102,248,790 (GRCm39) |
T292A |
probably benign |
Het |
Slc6a11 |
C |
T |
6: 114,111,626 (GRCm39) |
T103M |
probably damaging |
Het |
Sorl1 |
A |
G |
9: 41,935,774 (GRCm39) |
|
probably benign |
Het |
Tal1 |
T |
C |
4: 114,925,489 (GRCm39) |
V186A |
probably benign |
Het |
Top6bl |
T |
C |
19: 4,709,510 (GRCm39) |
T318A |
possibly damaging |
Het |
Trpm1 |
T |
A |
7: 63,860,578 (GRCm39) |
|
probably benign |
Het |
Tyw5 |
A |
T |
1: 57,427,712 (GRCm39) |
Y297* |
probably null |
Het |
Unc79 |
C |
A |
12: 103,128,126 (GRCm39) |
Q2131K |
possibly damaging |
Het |
|
Other mutations in Adamts7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00547:Adamts7
|
APN |
9 |
90,076,302 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL00673:Adamts7
|
APN |
9 |
90,075,714 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL00902:Adamts7
|
APN |
9 |
90,070,847 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01333:Adamts7
|
APN |
9 |
90,069,032 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01431:Adamts7
|
APN |
9 |
90,089,838 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01595:Adamts7
|
APN |
9 |
90,075,359 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02728:Adamts7
|
APN |
9 |
90,073,880 (GRCm39) |
splice site |
probably benign |
|
IGL02860:Adamts7
|
APN |
9 |
90,073,915 (GRCm39) |
missense |
probably benign |
|
IGL03237:Adamts7
|
APN |
9 |
90,070,717 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4495001:Adamts7
|
UTSW |
9 |
90,056,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Adamts7
|
UTSW |
9 |
90,053,641 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0078:Adamts7
|
UTSW |
9 |
90,061,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R0107:Adamts7
|
UTSW |
9 |
90,062,773 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0122:Adamts7
|
UTSW |
9 |
90,061,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R0166:Adamts7
|
UTSW |
9 |
90,075,745 (GRCm39) |
missense |
probably benign |
0.00 |
R0517:Adamts7
|
UTSW |
9 |
90,081,911 (GRCm39) |
missense |
probably benign |
0.01 |
R1442:Adamts7
|
UTSW |
9 |
90,070,823 (GRCm39) |
missense |
probably damaging |
0.99 |
R1468:Adamts7
|
UTSW |
9 |
90,070,851 (GRCm39) |
splice site |
probably benign |
|
R1554:Adamts7
|
UTSW |
9 |
90,055,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R1612:Adamts7
|
UTSW |
9 |
90,070,750 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1652:Adamts7
|
UTSW |
9 |
90,071,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R2007:Adamts7
|
UTSW |
9 |
90,059,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R2091:Adamts7
|
UTSW |
9 |
90,070,493 (GRCm39) |
critical splice donor site |
probably null |
|
R2202:Adamts7
|
UTSW |
9 |
90,062,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R2204:Adamts7
|
UTSW |
9 |
90,062,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R2205:Adamts7
|
UTSW |
9 |
90,062,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R2305:Adamts7
|
UTSW |
9 |
90,062,764 (GRCm39) |
missense |
probably benign |
0.39 |
R2409:Adamts7
|
UTSW |
9 |
90,062,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R4157:Adamts7
|
UTSW |
9 |
90,070,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R4210:Adamts7
|
UTSW |
9 |
90,076,063 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4368:Adamts7
|
UTSW |
9 |
90,077,904 (GRCm39) |
critical splice donor site |
probably null |
|
R4533:Adamts7
|
UTSW |
9 |
90,062,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R4608:Adamts7
|
UTSW |
9 |
90,056,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Adamts7
|
UTSW |
9 |
90,068,515 (GRCm39) |
missense |
probably benign |
0.17 |
R4661:Adamts7
|
UTSW |
9 |
90,075,383 (GRCm39) |
missense |
probably benign |
0.02 |
R4820:Adamts7
|
UTSW |
9 |
90,071,739 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4942:Adamts7
|
UTSW |
9 |
90,045,364 (GRCm39) |
missense |
probably benign |
|
R4961:Adamts7
|
UTSW |
9 |
90,067,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R5064:Adamts7
|
UTSW |
9 |
90,077,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R5763:Adamts7
|
UTSW |
9 |
90,070,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R5921:Adamts7
|
UTSW |
9 |
90,070,747 (GRCm39) |
missense |
probably benign |
0.20 |
R6027:Adamts7
|
UTSW |
9 |
90,073,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R6182:Adamts7
|
UTSW |
9 |
90,074,489 (GRCm39) |
missense |
probably benign |
0.01 |
R6306:Adamts7
|
UTSW |
9 |
90,060,331 (GRCm39) |
critical splice donor site |
probably null |
|
R6404:Adamts7
|
UTSW |
9 |
90,062,509 (GRCm39) |
splice site |
probably null |
|
R6488:Adamts7
|
UTSW |
9 |
90,053,535 (GRCm39) |
missense |
probably benign |
0.00 |
R6649:Adamts7
|
UTSW |
9 |
90,073,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R6658:Adamts7
|
UTSW |
9 |
90,077,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R6874:Adamts7
|
UTSW |
9 |
90,070,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R6947:Adamts7
|
UTSW |
9 |
90,073,857 (GRCm39) |
splice site |
probably null |
|
R7110:Adamts7
|
UTSW |
9 |
90,076,017 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7224:Adamts7
|
UTSW |
9 |
90,067,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R7239:Adamts7
|
UTSW |
9 |
90,068,610 (GRCm39) |
splice site |
probably null |
|
R7519:Adamts7
|
UTSW |
9 |
90,079,132 (GRCm39) |
missense |
probably benign |
0.22 |
R7608:Adamts7
|
UTSW |
9 |
90,055,826 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7635:Adamts7
|
UTSW |
9 |
90,077,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Adamts7
|
UTSW |
9 |
90,070,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R8519:Adamts7
|
UTSW |
9 |
90,075,610 (GRCm39) |
nonsense |
probably null |
|
R8680:Adamts7
|
UTSW |
9 |
90,077,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R8743:Adamts7
|
UTSW |
9 |
90,077,296 (GRCm39) |
missense |
probably damaging |
0.99 |
R8784:Adamts7
|
UTSW |
9 |
90,075,918 (GRCm39) |
missense |
probably null |
0.00 |
R8794:Adamts7
|
UTSW |
9 |
90,076,239 (GRCm39) |
nonsense |
probably null |
|
R8851:Adamts7
|
UTSW |
9 |
90,075,163 (GRCm39) |
missense |
probably benign |
0.00 |
R9025:Adamts7
|
UTSW |
9 |
90,067,848 (GRCm39) |
nonsense |
probably null |
|
R9038:Adamts7
|
UTSW |
9 |
90,056,692 (GRCm39) |
missense |
|
|
R9101:Adamts7
|
UTSW |
9 |
90,071,794 (GRCm39) |
critical splice donor site |
probably null |
|
R9256:Adamts7
|
UTSW |
9 |
90,060,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R9261:Adamts7
|
UTSW |
9 |
90,075,397 (GRCm39) |
missense |
probably benign |
0.01 |
R9385:Adamts7
|
UTSW |
9 |
90,077,258 (GRCm39) |
nonsense |
probably null |
|
R9614:Adamts7
|
UTSW |
9 |
90,077,251 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Adamts7
|
UTSW |
9 |
90,060,270 (GRCm39) |
missense |
probably benign |
0.30 |
|