Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700093K21Rik |
T |
C |
11: 23,467,213 (GRCm39) |
E140G |
probably null |
Het |
Adgrl3 |
A |
G |
5: 81,874,570 (GRCm39) |
T956A |
probably damaging |
Het |
Aff4 |
G |
A |
11: 53,293,327 (GRCm39) |
S772N |
probably benign |
Het |
Ark2n |
A |
G |
18: 77,761,613 (GRCm39) |
I233T |
possibly damaging |
Het |
Atad5 |
A |
G |
11: 79,986,390 (GRCm39) |
I492M |
probably benign |
Het |
Atf4 |
T |
C |
15: 80,140,728 (GRCm39) |
|
probably benign |
Het |
Atrip |
A |
G |
9: 108,898,363 (GRCm39) |
S219P |
probably damaging |
Het |
Axl |
G |
A |
7: 25,462,734 (GRCm39) |
R656W |
probably damaging |
Het |
B3gnt3 |
T |
A |
8: 72,145,648 (GRCm39) |
Q240L |
possibly damaging |
Het |
Baz2b |
A |
G |
2: 59,764,031 (GRCm39) |
V915A |
possibly damaging |
Het |
Cacna1s |
T |
C |
1: 136,002,890 (GRCm39) |
V329A |
possibly damaging |
Het |
Celf3 |
C |
A |
3: 94,395,535 (GRCm39) |
Q388K |
possibly damaging |
Het |
Ciita |
T |
C |
16: 10,328,591 (GRCm39) |
S292P |
probably damaging |
Het |
Cip2a |
A |
G |
16: 48,833,551 (GRCm39) |
I551V |
probably damaging |
Het |
Clec18a |
G |
A |
8: 111,798,245 (GRCm39) |
A423V |
probably damaging |
Het |
Clnk |
T |
C |
5: 38,870,550 (GRCm39) |
D336G |
probably damaging |
Het |
Csmd1 |
T |
G |
8: 15,960,596 (GRCm39) |
H3273P |
probably damaging |
Het |
Cyp3a11 |
A |
T |
5: 145,805,817 (GRCm39) |
V157E |
possibly damaging |
Het |
Dcp1b |
T |
C |
6: 119,160,679 (GRCm39) |
I87T |
probably damaging |
Het |
Ell3 |
A |
G |
2: 121,272,277 (GRCm39) |
S66P |
probably damaging |
Het |
Ercc4 |
T |
C |
16: 12,950,798 (GRCm39) |
F631L |
probably damaging |
Het |
Etl4 |
T |
A |
2: 20,811,784 (GRCm39) |
V1289D |
probably damaging |
Het |
Gm16372 |
T |
C |
12: 24,543,606 (GRCm39) |
|
probably benign |
Het |
Gm4553 |
C |
T |
7: 141,718,909 (GRCm39) |
C173Y |
unknown |
Het |
Gvin-ps5 |
T |
A |
7: 105,929,042 (GRCm39) |
H285L |
unknown |
Het |
Gykl1 |
A |
T |
18: 52,827,808 (GRCm39) |
I339F |
possibly damaging |
Het |
H60b |
A |
C |
10: 22,162,078 (GRCm39) |
N101T |
possibly damaging |
Het |
Inpp4a |
C |
T |
1: 37,427,986 (GRCm39) |
T407I |
probably damaging |
Het |
Itga11 |
A |
G |
9: 62,651,861 (GRCm39) |
N331S |
possibly damaging |
Het |
Kbtbd6 |
T |
A |
14: 79,690,783 (GRCm39) |
C430S |
probably damaging |
Het |
Mfsd4a |
T |
C |
1: 131,995,564 (GRCm39) |
S1G |
probably null |
Het |
Mybpc2 |
C |
A |
7: 44,165,352 (GRCm39) |
M372I |
probably benign |
Het |
Myh10 |
A |
T |
11: 68,702,629 (GRCm39) |
T1768S |
probably benign |
Het |
Myh8 |
A |
G |
11: 67,188,606 (GRCm39) |
K1063E |
probably damaging |
Het |
Nat8f5 |
A |
T |
6: 85,794,862 (GRCm39) |
F33I |
probably damaging |
Het |
Nbeal2 |
T |
G |
9: 110,458,214 (GRCm39) |
N2119T |
probably damaging |
Het |
Nek11 |
C |
T |
9: 105,270,112 (GRCm39) |
G37S |
probably damaging |
Het |
Npc1l1 |
T |
C |
11: 6,177,974 (GRCm39) |
N479D |
probably damaging |
Het |
Nup160 |
A |
G |
2: 90,530,772 (GRCm39) |
T477A |
probably benign |
Het |
Or10al5 |
A |
T |
17: 38,063,177 (GRCm39) |
H144L |
probably benign |
Het |
Or5h18 |
T |
A |
16: 58,848,157 (GRCm39) |
T38S |
probably damaging |
Het |
Pcgf2 |
A |
G |
11: 97,581,066 (GRCm39) |
V259A |
probably benign |
Het |
Pmm1 |
A |
G |
15: 81,836,219 (GRCm39) |
V131A |
probably damaging |
Het |
Polr3a |
A |
T |
14: 24,511,831 (GRCm39) |
D908E |
probably damaging |
Het |
Psg29 |
A |
C |
7: 16,944,598 (GRCm39) |
R369S |
probably benign |
Het |
Ptprq |
T |
A |
10: 107,547,765 (GRCm39) |
D211V |
probably damaging |
Het |
Rdh9 |
A |
G |
10: 127,612,661 (GRCm39) |
N103S |
probably benign |
Het |
Serpinb1b |
A |
T |
13: 33,275,398 (GRCm39) |
Q174H |
probably benign |
Het |
Sgip1 |
G |
T |
4: 102,772,353 (GRCm39) |
|
probably null |
Het |
Sgpp1 |
A |
T |
12: 75,781,767 (GRCm39) |
Y191N |
probably damaging |
Het |
Slc12a1 |
A |
G |
2: 125,036,051 (GRCm39) |
N641S |
probably damaging |
Het |
Slc5a4b |
T |
C |
10: 75,906,422 (GRCm39) |
N399S |
probably damaging |
Het |
Snx16 |
C |
T |
3: 10,484,219 (GRCm39) |
A335T |
probably damaging |
Het |
Sos2 |
C |
T |
12: 69,664,866 (GRCm39) |
R355H |
probably damaging |
Het |
Szt2 |
A |
G |
4: 118,250,821 (GRCm39) |
|
probably benign |
Het |
Tbcd |
T |
A |
11: 121,387,902 (GRCm39) |
D344E |
probably benign |
Het |
Tek |
C |
A |
4: 94,747,895 (GRCm39) |
Q988K |
probably damaging |
Het |
Tgm6 |
A |
G |
2: 129,979,299 (GRCm39) |
D143G |
probably damaging |
Het |
Tpx2 |
A |
G |
2: 152,735,511 (GRCm39) |
K713R |
probably damaging |
Het |
Trappc9 |
T |
A |
15: 72,808,858 (GRCm39) |
E556V |
possibly damaging |
Het |
Trpm6 |
A |
T |
19: 18,855,015 (GRCm39) |
K1891N |
probably damaging |
Het |
Trpv1 |
G |
A |
11: 73,129,078 (GRCm39) |
|
probably null |
Het |
Usp37 |
T |
C |
1: 74,500,861 (GRCm39) |
S567G |
probably damaging |
Het |
Zfp773 |
A |
T |
7: 7,138,314 (GRCm39) |
V107D |
possibly damaging |
Het |
|
Other mutations in Riok3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Riok3
|
APN |
18 |
12,281,948 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00229:Riok3
|
APN |
18 |
12,270,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00434:Riok3
|
APN |
18 |
12,281,904 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01886:Riok3
|
APN |
18 |
12,272,442 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02553:Riok3
|
APN |
18 |
12,276,073 (GRCm39) |
nonsense |
probably null |
|
IGL02622:Riok3
|
APN |
18 |
12,276,017 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02718:Riok3
|
APN |
18 |
12,286,053 (GRCm39) |
nonsense |
probably null |
|
LCD18:Riok3
|
UTSW |
18 |
12,263,039 (GRCm39) |
intron |
probably benign |
|
R0240:Riok3
|
UTSW |
18 |
12,288,284 (GRCm39) |
missense |
probably benign |
0.37 |
R0359:Riok3
|
UTSW |
18 |
12,282,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R1505:Riok3
|
UTSW |
18 |
12,285,935 (GRCm39) |
missense |
probably benign |
0.06 |
R1519:Riok3
|
UTSW |
18 |
12,270,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R1698:Riok3
|
UTSW |
18 |
12,261,986 (GRCm39) |
missense |
probably benign |
0.02 |
R1710:Riok3
|
UTSW |
18 |
12,276,018 (GRCm39) |
missense |
probably benign |
0.24 |
R1965:Riok3
|
UTSW |
18 |
12,270,019 (GRCm39) |
missense |
probably damaging |
0.99 |
R2351:Riok3
|
UTSW |
18 |
12,282,724 (GRCm39) |
nonsense |
probably null |
|
R3705:Riok3
|
UTSW |
18 |
12,282,011 (GRCm39) |
missense |
probably benign |
0.07 |
R3914:Riok3
|
UTSW |
18 |
12,281,879 (GRCm39) |
missense |
probably benign |
|
R3956:Riok3
|
UTSW |
18 |
12,276,031 (GRCm39) |
nonsense |
probably null |
|
R4272:Riok3
|
UTSW |
18 |
12,268,998 (GRCm39) |
small deletion |
probably benign |
|
R4273:Riok3
|
UTSW |
18 |
12,268,998 (GRCm39) |
small deletion |
probably benign |
|
R4564:Riok3
|
UTSW |
18 |
12,281,936 (GRCm39) |
missense |
probably damaging |
0.99 |
R4589:Riok3
|
UTSW |
18 |
12,269,844 (GRCm39) |
missense |
probably benign |
0.06 |
R4729:Riok3
|
UTSW |
18 |
12,261,984 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4751:Riok3
|
UTSW |
18 |
12,287,040 (GRCm39) |
missense |
probably benign |
0.00 |
R4938:Riok3
|
UTSW |
18 |
12,288,300 (GRCm39) |
missense |
probably benign |
0.06 |
R4945:Riok3
|
UTSW |
18 |
12,261,972 (GRCm39) |
missense |
probably damaging |
0.96 |
R5449:Riok3
|
UTSW |
18 |
12,288,303 (GRCm39) |
missense |
probably damaging |
0.97 |
R5928:Riok3
|
UTSW |
18 |
12,286,075 (GRCm39) |
missense |
probably benign |
0.16 |
R6220:Riok3
|
UTSW |
18 |
12,282,608 (GRCm39) |
missense |
probably damaging |
0.97 |
R7962:Riok3
|
UTSW |
18 |
12,269,776 (GRCm39) |
missense |
probably benign |
|
R8422:Riok3
|
UTSW |
18 |
12,269,869 (GRCm39) |
missense |
probably null |
1.00 |
R9194:Riok3
|
UTSW |
18 |
12,282,642 (GRCm39) |
frame shift |
probably null |
|
R9195:Riok3
|
UTSW |
18 |
12,282,642 (GRCm39) |
frame shift |
probably null |
|
|