Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgb |
G |
A |
10: 10,267,473 (GRCm39) |
A923V |
probably benign |
Het |
Aldh1a3 |
A |
G |
7: 66,049,970 (GRCm39) |
V416A |
probably damaging |
Het |
Alox5 |
C |
T |
6: 116,397,345 (GRCm39) |
G280R |
probably damaging |
Het |
Anapc5 |
A |
T |
5: 122,938,695 (GRCm39) |
Y360N |
probably damaging |
Het |
Apbb1 |
C |
T |
7: 105,208,170 (GRCm39) |
V685I |
probably damaging |
Het |
Apc2 |
C |
A |
10: 80,143,289 (GRCm39) |
A463E |
probably damaging |
Het |
Arhgap21 |
C |
T |
2: 20,860,198 (GRCm39) |
W1170* |
probably null |
Het |
Atat1 |
G |
A |
17: 36,212,315 (GRCm39) |
R305C |
probably damaging |
Het |
Brd8dc |
A |
G |
18: 34,719,319 (GRCm39) |
V167A |
possibly damaging |
Het |
Cars2 |
T |
C |
8: 11,600,511 (GRCm39) |
D56G |
probably benign |
Het |
Ccdc202 |
T |
G |
14: 96,119,379 (GRCm39) |
N45K |
probably damaging |
Het |
Cdc42bpb |
T |
C |
12: 111,311,989 (GRCm39) |
I108V |
probably damaging |
Het |
Cftr |
T |
A |
6: 18,305,979 (GRCm39) |
I1255K |
probably damaging |
Het |
Ckap5 |
T |
C |
2: 91,381,088 (GRCm39) |
L148P |
probably damaging |
Het |
Cntn4 |
A |
G |
6: 106,656,209 (GRCm39) |
|
probably null |
Het |
Cpe |
G |
A |
8: 65,062,237 (GRCm39) |
P273L |
probably damaging |
Het |
Cpsf7 |
A |
G |
19: 10,509,146 (GRCm39) |
D19G |
probably benign |
Het |
Ddx25 |
C |
A |
9: 35,457,268 (GRCm39) |
R349L |
probably damaging |
Het |
Depdc7 |
T |
C |
2: 104,553,226 (GRCm39) |
D446G |
probably benign |
Het |
Det1 |
T |
A |
7: 78,493,683 (GRCm39) |
N107I |
probably benign |
Het |
Dock6 |
A |
T |
9: 21,755,713 (GRCm39) |
D170E |
probably benign |
Het |
Dvl1 |
C |
T |
4: 155,942,752 (GRCm39) |
L673F |
probably damaging |
Het |
Gucy1b1 |
A |
T |
3: 81,952,767 (GRCm39) |
I222K |
probably benign |
Het |
Hfm1 |
T |
C |
5: 107,065,467 (GRCm39) |
T71A |
possibly damaging |
Het |
Ikzf1 |
A |
G |
11: 11,719,223 (GRCm39) |
E310G |
probably damaging |
Het |
Impg1 |
T |
C |
9: 80,301,437 (GRCm39) |
E163G |
possibly damaging |
Het |
Itpr2 |
G |
T |
6: 146,275,954 (GRCm39) |
H426Q |
probably damaging |
Het |
Itpripl2 |
C |
T |
7: 118,089,479 (GRCm39) |
G360D |
probably benign |
Het |
Kif14 |
C |
T |
1: 136,455,043 (GRCm39) |
R1572C |
probably damaging |
Het |
L3mbtl3 |
A |
T |
10: 26,178,583 (GRCm39) |
H568Q |
unknown |
Het |
Lgi2 |
A |
G |
5: 52,711,802 (GRCm39) |
Y173H |
probably damaging |
Het |
Lpar5 |
A |
C |
6: 125,058,954 (GRCm39) |
Y225S |
probably benign |
Het |
Lpin3 |
A |
G |
2: 160,745,894 (GRCm39) |
H675R |
probably damaging |
Het |
Lrp2 |
C |
A |
2: 69,278,464 (GRCm39) |
G3963V |
probably damaging |
Het |
Man1a2 |
G |
T |
3: 100,591,891 (GRCm39) |
D13E |
possibly damaging |
Het |
Map1a |
T |
C |
2: 121,138,495 (GRCm39) |
V2753A |
probably damaging |
Het |
Mitf |
C |
A |
6: 97,980,865 (GRCm39) |
N97K |
probably damaging |
Het |
Msh2 |
A |
G |
17: 87,980,238 (GRCm39) |
|
probably null |
Het |
Msr1 |
T |
C |
8: 40,073,041 (GRCm39) |
E170G |
probably damaging |
Het |
Myrip |
C |
A |
9: 120,217,302 (GRCm39) |
R79S |
probably damaging |
Het |
Nek10 |
G |
A |
14: 14,857,782 (GRCm38) |
|
probably null |
Het |
Neto1 |
C |
T |
18: 86,422,854 (GRCm39) |
R104* |
probably null |
Het |
Nom1 |
A |
C |
5: 29,656,098 (GRCm39) |
K821T |
probably damaging |
Het |
Nrxn1 |
A |
G |
17: 91,011,609 (GRCm39) |
V340A |
probably damaging |
Het |
Nxpe4 |
A |
T |
9: 48,307,897 (GRCm39) |
I334F |
probably benign |
Het |
Or1e23 |
A |
G |
11: 73,407,753 (GRCm39) |
S91P |
probably benign |
Het |
Or2ag1 |
T |
C |
7: 106,313,184 (GRCm39) |
K235E |
probably benign |
Het |
Or4a74 |
T |
C |
2: 89,439,718 (GRCm39) |
M243V |
probably benign |
Het |
Or5al7 |
T |
A |
2: 85,992,435 (GRCm39) |
N286I |
probably damaging |
Het |
Or5b124 |
T |
C |
19: 13,610,700 (GRCm39) |
V75A |
probably damaging |
Het |
Or8k27 |
C |
T |
2: 86,275,473 (GRCm39) |
M284I |
probably benign |
Het |
Padi4 |
A |
G |
4: 140,484,896 (GRCm39) |
S322P |
probably damaging |
Het |
Peli3 |
A |
G |
19: 4,991,810 (GRCm39) |
Y44H |
probably damaging |
Het |
Prdm4 |
A |
G |
10: 85,743,767 (GRCm39) |
S163P |
probably damaging |
Het |
Prom2 |
T |
C |
2: 127,381,445 (GRCm39) |
D227G |
probably benign |
Het |
Ptgfr |
C |
T |
3: 151,507,400 (GRCm39) |
R321H |
probably benign |
Het |
Resf1 |
A |
T |
6: 149,227,199 (GRCm39) |
I82L |
probably benign |
Het |
Rgs3 |
G |
A |
4: 62,544,143 (GRCm39) |
R136H |
probably damaging |
Het |
Rgsl1 |
T |
G |
1: 153,719,853 (GRCm39) |
N3T |
possibly damaging |
Het |
Rif1 |
T |
C |
2: 52,002,575 (GRCm39) |
S2010P |
probably benign |
Het |
Rngtt |
T |
C |
4: 33,368,690 (GRCm39) |
F408L |
probably damaging |
Het |
Rtn3 |
T |
G |
19: 7,434,958 (GRCm39) |
T326P |
probably benign |
Het |
Slc18b1 |
A |
C |
10: 23,681,936 (GRCm39) |
M167L |
probably benign |
Het |
Slc22a26 |
A |
G |
19: 7,765,575 (GRCm39) |
|
probably null |
Het |
Slitrk6 |
T |
C |
14: 110,989,317 (GRCm39) |
D130G |
probably damaging |
Het |
Snap47 |
A |
G |
11: 59,319,439 (GRCm39) |
V233A |
probably benign |
Het |
Sumf1 |
A |
C |
6: 108,121,632 (GRCm39) |
Y158D |
probably damaging |
Het |
Tbc1d15 |
A |
T |
10: 115,056,215 (GRCm39) |
H252Q |
probably benign |
Het |
Thsd7b |
T |
C |
1: 130,116,263 (GRCm39) |
S1339P |
possibly damaging |
Het |
Tmem45a2 |
T |
C |
16: 56,869,777 (GRCm39) |
I56V |
probably benign |
Het |
Ttc21b |
A |
G |
2: 66,066,577 (GRCm39) |
S359P |
probably benign |
Het |
Ttc27 |
T |
C |
17: 75,036,972 (GRCm39) |
I215T |
probably benign |
Het |
Ttn |
C |
T |
2: 76,554,539 (GRCm39) |
V30759I |
possibly damaging |
Het |
Vdac3 |
T |
C |
8: 23,070,404 (GRCm39) |
N168S |
probably damaging |
Het |
Wdr7 |
T |
C |
18: 63,998,371 (GRCm39) |
V1106A |
probably benign |
Het |
Wrap73 |
T |
A |
4: 154,226,948 (GRCm39) |
F16Y |
probably damaging |
Het |
Zfat |
C |
A |
15: 68,052,652 (GRCm39) |
D381Y |
probably damaging |
Het |
|
Other mutations in Adamts8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Adamts8
|
APN |
9 |
30,864,796 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02049:Adamts8
|
APN |
9 |
30,862,650 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02304:Adamts8
|
APN |
9 |
30,867,952 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02385:Adamts8
|
APN |
9 |
30,873,026 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02536:Adamts8
|
APN |
9 |
30,873,368 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03347:Adamts8
|
APN |
9 |
30,870,534 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1066:Adamts8
|
UTSW |
9 |
30,867,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Adamts8
|
UTSW |
9 |
30,862,673 (GRCm39) |
missense |
probably benign |
|
R1464:Adamts8
|
UTSW |
9 |
30,862,673 (GRCm39) |
missense |
probably benign |
|
R1560:Adamts8
|
UTSW |
9 |
30,867,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R1592:Adamts8
|
UTSW |
9 |
30,854,472 (GRCm39) |
missense |
probably damaging |
0.99 |
R1753:Adamts8
|
UTSW |
9 |
30,865,910 (GRCm39) |
missense |
probably benign |
0.04 |
R1932:Adamts8
|
UTSW |
9 |
30,867,808 (GRCm39) |
missense |
probably benign |
|
R2087:Adamts8
|
UTSW |
9 |
30,873,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R2118:Adamts8
|
UTSW |
9 |
30,854,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R3789:Adamts8
|
UTSW |
9 |
30,870,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R4165:Adamts8
|
UTSW |
9 |
30,862,684 (GRCm39) |
missense |
probably benign |
0.01 |
R4166:Adamts8
|
UTSW |
9 |
30,862,684 (GRCm39) |
missense |
probably benign |
0.01 |
R4193:Adamts8
|
UTSW |
9 |
30,870,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R4425:Adamts8
|
UTSW |
9 |
30,867,952 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5155:Adamts8
|
UTSW |
9 |
30,865,844 (GRCm39) |
missense |
probably benign |
0.33 |
R5433:Adamts8
|
UTSW |
9 |
30,873,012 (GRCm39) |
missense |
probably benign |
0.01 |
R5544:Adamts8
|
UTSW |
9 |
30,863,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R5590:Adamts8
|
UTSW |
9 |
30,862,632 (GRCm39) |
missense |
probably damaging |
0.97 |
R5640:Adamts8
|
UTSW |
9 |
30,867,796 (GRCm39) |
missense |
probably benign |
0.00 |
R5800:Adamts8
|
UTSW |
9 |
30,865,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R5909:Adamts8
|
UTSW |
9 |
30,873,224 (GRCm39) |
missense |
probably benign |
0.00 |
R6821:Adamts8
|
UTSW |
9 |
30,867,922 (GRCm39) |
missense |
probably benign |
0.08 |
R6967:Adamts8
|
UTSW |
9 |
30,865,787 (GRCm39) |
missense |
probably benign |
0.04 |
R7336:Adamts8
|
UTSW |
9 |
30,873,363 (GRCm39) |
missense |
probably benign |
0.00 |
R7538:Adamts8
|
UTSW |
9 |
30,864,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R7540:Adamts8
|
UTSW |
9 |
30,870,360 (GRCm39) |
missense |
probably damaging |
0.96 |
R7942:Adamts8
|
UTSW |
9 |
30,870,209 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7942:Adamts8
|
UTSW |
9 |
30,864,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Adamts8
|
UTSW |
9 |
30,854,611 (GRCm39) |
missense |
probably benign |
0.01 |
R8795:Adamts8
|
UTSW |
9 |
30,854,484 (GRCm39) |
missense |
probably benign |
0.00 |
R8877:Adamts8
|
UTSW |
9 |
30,862,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R8900:Adamts8
|
UTSW |
9 |
30,865,930 (GRCm39) |
missense |
probably benign |
0.01 |
R9141:Adamts8
|
UTSW |
9 |
30,864,721 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9224:Adamts8
|
UTSW |
9 |
30,854,188 (GRCm39) |
missense |
probably benign |
0.18 |
R9326:Adamts8
|
UTSW |
9 |
30,854,886 (GRCm39) |
missense |
probably benign |
|
R9331:Adamts8
|
UTSW |
9 |
30,862,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R9426:Adamts8
|
UTSW |
9 |
30,864,721 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9796:Adamts8
|
UTSW |
9 |
30,862,569 (GRCm39) |
missense |
probably damaging |
0.99 |
|