Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Add3 |
T |
A |
19: 53,220,589 (GRCm39) |
I174K |
probably damaging |
Het |
Ano2 |
A |
T |
6: 125,940,667 (GRCm39) |
I597F |
probably damaging |
Het |
Ap1g1 |
T |
C |
8: 110,586,796 (GRCm39) |
V813A |
probably damaging |
Het |
Bpnt1 |
A |
T |
1: 185,084,523 (GRCm39) |
I207F |
possibly damaging |
Het |
Brinp3 |
T |
A |
1: 146,777,139 (GRCm39) |
W529R |
probably damaging |
Het |
C2cd2l |
C |
T |
9: 44,226,681 (GRCm39) |
R355Q |
probably benign |
Het |
Ccser1 |
T |
A |
6: 62,356,915 (GRCm39) |
C784* |
probably null |
Het |
Cdh20 |
A |
T |
1: 110,065,889 (GRCm39) |
D721V |
probably damaging |
Het |
Chd9 |
A |
G |
8: 91,721,193 (GRCm39) |
I994V |
unknown |
Het |
Cst13 |
T |
G |
2: 148,665,127 (GRCm39) |
Y41D |
probably benign |
Het |
Cyth2 |
C |
T |
7: 45,457,448 (GRCm39) |
A342T |
probably benign |
Het |
Dapk1 |
T |
C |
13: 60,878,700 (GRCm39) |
L563P |
probably damaging |
Het |
Dclk3 |
T |
G |
9: 111,296,596 (GRCm39) |
S47A |
probably benign |
Het |
Dync1h1 |
C |
A |
12: 110,618,011 (GRCm39) |
N3183K |
probably benign |
Het |
Enpp1 |
C |
T |
10: 24,551,885 (GRCm39) |
V165M |
probably benign |
Het |
Ephx3 |
T |
C |
17: 32,407,763 (GRCm39) |
N173S |
possibly damaging |
Het |
Erc1 |
T |
A |
6: 119,756,592 (GRCm39) |
D388V |
probably benign |
Het |
Esp34 |
T |
G |
17: 38,870,511 (GRCm39) |
V135G |
possibly damaging |
Het |
Gfy |
G |
A |
7: 44,827,461 (GRCm39) |
P212S |
probably damaging |
Het |
Gm5239 |
C |
T |
18: 35,669,795 (GRCm39) |
R54C |
probably benign |
Het |
Gtpbp3 |
T |
C |
8: 71,942,107 (GRCm39) |
F113L |
probably benign |
Het |
Hectd1 |
T |
A |
12: 51,837,233 (GRCm39) |
D775V |
probably damaging |
Het |
Ifrd2 |
T |
G |
9: 107,469,721 (GRCm39) |
S431R |
probably damaging |
Het |
Impg2 |
G |
A |
16: 56,087,543 (GRCm39) |
A1121T |
probably damaging |
Het |
Irx1 |
A |
G |
13: 72,108,314 (GRCm39) |
F123L |
possibly damaging |
Het |
Itgb6 |
C |
T |
2: 60,499,557 (GRCm39) |
V79I |
probably benign |
Het |
Kcnd3 |
G |
A |
3: 105,575,526 (GRCm39) |
R550H |
probably damaging |
Het |
Klhl9 |
A |
T |
4: 88,639,090 (GRCm39) |
S384T |
possibly damaging |
Het |
Kng2 |
T |
C |
16: 22,845,794 (GRCm39) |
|
probably null |
Het |
Lipo3 |
T |
C |
19: 33,560,464 (GRCm39) |
N67S |
possibly damaging |
Het |
Mgst1 |
T |
C |
6: 138,130,504 (GRCm39) |
S78P |
probably benign |
Het |
Ms4a14 |
A |
G |
19: 11,281,323 (GRCm39) |
Y412H |
possibly damaging |
Het |
Mucl2 |
A |
C |
15: 103,926,318 (GRCm39) |
I124S |
unknown |
Het |
Myh3 |
A |
G |
11: 66,981,921 (GRCm39) |
M806V |
probably benign |
Het |
Nelfcd |
T |
C |
2: 174,268,189 (GRCm39) |
L501P |
probably damaging |
Het |
Nlrp6 |
C |
A |
7: 140,505,097 (GRCm39) |
P748Q |
probably benign |
Het |
Or1j13 |
C |
T |
2: 36,370,138 (GRCm39) |
M1I |
probably null |
Het |
Or6n2 |
T |
C |
1: 173,897,664 (GRCm39) |
S267P |
probably benign |
Het |
Plxna2 |
G |
A |
1: 194,327,127 (GRCm39) |
A354T |
probably benign |
Het |
Prpf39 |
G |
T |
12: 65,100,145 (GRCm39) |
V273L |
probably benign |
Het |
Rad9a |
T |
C |
19: 4,251,522 (GRCm39) |
|
probably benign |
Het |
Rnf135 |
A |
G |
11: 80,089,732 (GRCm39) |
D356G |
probably benign |
Het |
Selenot |
G |
T |
3: 58,492,653 (GRCm39) |
V47L |
probably benign |
Het |
Smc2 |
T |
C |
4: 52,451,013 (GRCm39) |
L277P |
probably damaging |
Het |
Sp7 |
A |
G |
15: 102,267,584 (GRCm39) |
F92S |
possibly damaging |
Het |
Spata1 |
A |
T |
3: 146,173,946 (GRCm39) |
I380N |
possibly damaging |
Het |
Spdye4b |
G |
T |
5: 143,180,652 (GRCm39) |
R39S |
possibly damaging |
Het |
Spmip9 |
T |
C |
6: 70,890,621 (GRCm39) |
K57R |
probably benign |
Het |
Stom |
C |
A |
2: 35,211,589 (GRCm39) |
R144L |
possibly damaging |
Het |
Tsc22d1 |
T |
C |
14: 76,653,486 (GRCm39) |
|
probably benign |
Het |
Unc13b |
A |
G |
4: 43,249,565 (GRCm39) |
T998A |
probably benign |
Het |
Vcl |
C |
A |
14: 21,079,392 (GRCm39) |
A965D |
probably damaging |
Het |
Vmn1r69 |
A |
T |
7: 10,314,281 (GRCm39) |
V150D |
probably damaging |
Het |
Vmn1r90 |
T |
G |
7: 14,295,189 (GRCm39) |
N303T |
possibly damaging |
Het |
Vmn2r69 |
A |
T |
7: 85,059,622 (GRCm39) |
M429K |
probably benign |
Het |
Vmn2r8 |
T |
A |
5: 108,950,106 (GRCm39) |
Y247F |
probably benign |
Het |
Washc5 |
A |
T |
15: 59,239,260 (GRCm39) |
S168T |
possibly damaging |
Het |
|
Other mutations in Rragd |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00434:Rragd
|
APN |
4 |
33,007,219 (GRCm39) |
splice site |
probably benign |
|
R0432:Rragd
|
UTSW |
4 |
33,004,332 (GRCm39) |
missense |
probably damaging |
0.98 |
R0542:Rragd
|
UTSW |
4 |
33,007,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R1521:Rragd
|
UTSW |
4 |
32,996,005 (GRCm39) |
missense |
probably damaging |
0.96 |
R4090:Rragd
|
UTSW |
4 |
33,007,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R4272:Rragd
|
UTSW |
4 |
32,996,099 (GRCm39) |
critical splice donor site |
probably null |
|
R4812:Rragd
|
UTSW |
4 |
33,018,766 (GRCm39) |
missense |
probably benign |
0.11 |
R4817:Rragd
|
UTSW |
4 |
32,995,072 (GRCm39) |
missense |
probably benign |
|
R6235:Rragd
|
UTSW |
4 |
32,995,985 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7124:Rragd
|
UTSW |
4 |
32,996,027 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7640:Rragd
|
UTSW |
4 |
32,983,527 (GRCm39) |
missense |
probably benign |
0.09 |
R8280:Rragd
|
UTSW |
4 |
32,995,112 (GRCm39) |
missense |
probably benign |
|
R8479:Rragd
|
UTSW |
4 |
33,018,734 (GRCm39) |
missense |
probably benign |
|
R8813:Rragd
|
UTSW |
4 |
33,012,953 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9027:Rragd
|
UTSW |
4 |
32,996,083 (GRCm39) |
missense |
probably damaging |
0.96 |
R9220:Rragd
|
UTSW |
4 |
32,995,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R9643:Rragd
|
UTSW |
4 |
33,012,998 (GRCm39) |
missense |
probably benign |
0.00 |
RF040:Rragd
|
UTSW |
4 |
32,995,150 (GRCm39) |
intron |
probably benign |
|
RF061:Rragd
|
UTSW |
4 |
32,995,150 (GRCm39) |
intron |
probably benign |
|
Z1177:Rragd
|
UTSW |
4 |
33,005,141 (GRCm39) |
missense |
probably damaging |
1.00 |
|