Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apmap |
A |
C |
2: 150,429,035 (GRCm39) |
M196R |
possibly damaging |
Het |
Arhgap27 |
T |
A |
11: 103,229,891 (GRCm39) |
|
probably null |
Het |
Baz1a |
A |
G |
12: 54,976,375 (GRCm39) |
F434L |
probably damaging |
Het |
Birc2 |
A |
G |
9: 7,849,722 (GRCm39) |
|
probably benign |
Het |
Brwd1 |
C |
A |
16: 95,822,458 (GRCm39) |
R1249I |
probably damaging |
Het |
Cab39l |
T |
C |
14: 59,757,100 (GRCm39) |
F161L |
probably benign |
Het |
Ccr8 |
A |
T |
9: 119,923,689 (GRCm39) |
D268V |
possibly damaging |
Het |
Col25a1 |
A |
T |
3: 130,323,332 (GRCm39) |
|
probably benign |
Het |
Cpn1 |
A |
G |
19: 43,974,693 (GRCm39) |
L12P |
possibly damaging |
Het |
Dnah6 |
A |
G |
6: 73,121,987 (GRCm39) |
I1360T |
probably benign |
Het |
Dnajb8 |
A |
G |
6: 88,200,013 (GRCm39) |
E183G |
probably damaging |
Het |
Dpp8 |
T |
A |
9: 64,960,322 (GRCm39) |
|
probably null |
Het |
Fsd1 |
C |
A |
17: 56,297,416 (GRCm39) |
|
probably null |
Het |
Grina |
T |
A |
15: 76,132,162 (GRCm39) |
F28I |
possibly damaging |
Het |
H2-M3 |
G |
A |
17: 37,583,324 (GRCm39) |
D262N |
possibly damaging |
Het |
Hdgfl3 |
G |
A |
7: 81,543,587 (GRCm39) |
T188M |
probably damaging |
Het |
Kif18b |
A |
G |
11: 102,805,086 (GRCm39) |
I353T |
probably damaging |
Het |
Lrrc41 |
C |
A |
4: 115,945,728 (GRCm39) |
R148S |
probably benign |
Het |
Lrrc8e |
T |
A |
8: 4,285,776 (GRCm39) |
L667Q |
probably damaging |
Het |
Lrrk1 |
A |
G |
7: 65,912,638 (GRCm39) |
F1641L |
probably benign |
Het |
Naaladl1 |
A |
T |
19: 6,162,386 (GRCm39) |
T443S |
probably benign |
Het |
Naga |
C |
A |
15: 82,214,942 (GRCm39) |
V339F |
probably damaging |
Het |
Nedd4l |
A |
G |
18: 65,338,741 (GRCm39) |
K702E |
probably damaging |
Het |
Nwd2 |
T |
A |
5: 63,963,338 (GRCm39) |
L974H |
probably damaging |
Het |
Parp14 |
A |
G |
16: 35,678,381 (GRCm39) |
M529T |
probably damaging |
Het |
Parp8 |
A |
G |
13: 117,047,478 (GRCm39) |
V198A |
probably benign |
Het |
Pcdhb19 |
A |
T |
18: 37,631,588 (GRCm39) |
H461L |
probably benign |
Het |
Ppp6r1 |
T |
C |
7: 4,645,159 (GRCm39) |
D236G |
possibly damaging |
Het |
Psg21 |
T |
C |
7: 18,388,843 (GRCm39) |
D83G |
probably benign |
Het |
Ptpru |
A |
G |
4: 131,546,111 (GRCm39) |
C308R |
probably damaging |
Het |
Ralgds |
T |
A |
2: 28,439,100 (GRCm39) |
S696T |
probably damaging |
Het |
Rttn |
T |
A |
18: 89,033,274 (GRCm39) |
L695Q |
probably damaging |
Het |
Scel |
A |
T |
14: 103,823,950 (GRCm39) |
I393F |
probably benign |
Het |
Serpina3j |
T |
A |
12: 104,281,166 (GRCm39) |
I113N |
probably damaging |
Het |
Slc4a3 |
C |
A |
1: 75,524,579 (GRCm39) |
|
probably benign |
Het |
Slc6a11 |
A |
T |
6: 114,171,570 (GRCm39) |
|
probably null |
Het |
Slc8a3 |
C |
T |
12: 81,249,023 (GRCm39) |
V802M |
probably damaging |
Het |
Smarcal1 |
T |
A |
1: 72,655,660 (GRCm39) |
|
probably null |
Het |
Tmprss11c |
A |
G |
5: 86,385,509 (GRCm39) |
V308A |
probably damaging |
Het |
Trim10 |
A |
G |
17: 37,185,113 (GRCm39) |
R279G |
possibly damaging |
Het |
Trim30a |
A |
G |
7: 104,060,348 (GRCm39) |
V476A |
probably damaging |
Het |
Trio |
T |
C |
15: 27,832,097 (GRCm39) |
|
probably benign |
Het |
Urgcp |
G |
A |
11: 5,666,091 (GRCm39) |
T749I |
possibly damaging |
Het |
Vmn2r60 |
A |
G |
7: 41,786,018 (GRCm39) |
I274V |
probably benign |
Het |
Vps11 |
A |
G |
9: 44,267,653 (GRCm39) |
F40L |
probably benign |
Het |
Ywhab |
A |
G |
2: 163,857,195 (GRCm39) |
I157V |
probably benign |
Het |
Zfp638 |
G |
A |
6: 83,919,857 (GRCm39) |
R485H |
probably damaging |
Het |
Zfp944 |
A |
G |
17: 22,558,737 (GRCm39) |
I170T |
probably benign |
Het |
|
Other mutations in Arl8b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01919:Arl8b
|
APN |
6 |
108,798,518 (GRCm39) |
utr 3 prime |
probably benign |
|
R0486:Arl8b
|
UTSW |
6 |
108,792,287 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0544:Arl8b
|
UTSW |
6 |
108,760,189 (GRCm39) |
start gained |
probably benign |
|
R1018:Arl8b
|
UTSW |
6 |
108,795,572 (GRCm39) |
missense |
probably damaging |
0.98 |
R2248:Arl8b
|
UTSW |
6 |
108,760,304 (GRCm39) |
missense |
probably benign |
0.00 |
R2351:Arl8b
|
UTSW |
6 |
108,798,484 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3815:Arl8b
|
UTSW |
6 |
108,790,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R3816:Arl8b
|
UTSW |
6 |
108,790,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R5538:Arl8b
|
UTSW |
6 |
108,760,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R6480:Arl8b
|
UTSW |
6 |
108,792,010 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7147:Arl8b
|
UTSW |
6 |
108,791,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R8394:Arl8b
|
UTSW |
6 |
108,760,244 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8478:Arl8b
|
UTSW |
6 |
108,760,285 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8828:Arl8b
|
UTSW |
6 |
108,792,250 (GRCm39) |
missense |
probably benign |
0.00 |
|