Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
G |
T |
5: 64,056,182 (GRCm39) |
|
probably benign |
Het |
Atg4a-ps |
A |
G |
3: 103,553,171 (GRCm39) |
Y57H |
probably damaging |
Het |
Bag4 |
C |
T |
8: 26,259,516 (GRCm39) |
A228T |
probably benign |
Het |
Bms1 |
G |
A |
6: 118,360,808 (GRCm39) |
T1220I |
probably damaging |
Het |
Brat1 |
T |
C |
5: 140,690,826 (GRCm39) |
|
probably benign |
Het |
Cds2 |
T |
A |
2: 132,136,366 (GRCm39) |
Y39* |
probably null |
Het |
Chrnd |
T |
A |
1: 87,125,099 (GRCm39) |
L384Q |
probably damaging |
Het |
Cpa3 |
A |
T |
3: 20,282,981 (GRCm39) |
Y155* |
probably null |
Het |
Crlf1 |
G |
A |
8: 70,953,606 (GRCm39) |
W260* |
probably null |
Het |
Cux1 |
C |
G |
5: 136,341,576 (GRCm39) |
E605D |
probably damaging |
Het |
Cylc2 |
C |
G |
4: 51,229,651 (GRCm39) |
T331R |
unknown |
Het |
Dmtf1 |
T |
C |
5: 9,186,085 (GRCm39) |
N167S |
probably damaging |
Het |
Dnaaf9 |
A |
G |
2: 130,609,567 (GRCm39) |
I372T |
probably damaging |
Het |
Dnai7 |
A |
T |
6: 145,128,944 (GRCm39) |
|
probably null |
Het |
Dtx2 |
T |
A |
5: 136,040,930 (GRCm39) |
W112R |
probably damaging |
Het |
Elf3 |
A |
G |
1: 135,184,582 (GRCm39) |
I138T |
probably damaging |
Het |
F11 |
T |
A |
8: 45,694,511 (GRCm39) |
I617F |
probably damaging |
Het |
Fdps |
A |
T |
3: 89,008,093 (GRCm39) |
D8E |
possibly damaging |
Het |
Fzd10 |
C |
A |
5: 128,678,340 (GRCm39) |
T20K |
probably benign |
Het |
Gm9978 |
T |
A |
10: 78,322,750 (GRCm39) |
|
noncoding transcript |
Het |
Gpr158 |
T |
A |
2: 21,831,810 (GRCm39) |
M970K |
probably damaging |
Het |
Has1 |
C |
T |
17: 18,064,257 (GRCm39) |
V461M |
probably benign |
Het |
Hdac3 |
C |
T |
18: 38,085,566 (GRCm39) |
G80D |
probably benign |
Het |
Klk12 |
A |
T |
7: 43,422,807 (GRCm39) |
R245W |
probably damaging |
Het |
Lamp5 |
A |
G |
2: 135,900,940 (GRCm39) |
I47V |
probably damaging |
Het |
Or6c1b |
T |
C |
10: 129,272,933 (GRCm39) |
I84T |
probably benign |
Het |
Ovgp1 |
A |
G |
3: 105,885,027 (GRCm39) |
D122G |
probably benign |
Het |
Piezo1 |
T |
C |
8: 123,213,135 (GRCm39) |
E1875G |
probably benign |
Het |
Pih1d1 |
A |
G |
7: 44,807,921 (GRCm39) |
M132V |
possibly damaging |
Het |
Pon2 |
C |
T |
6: 5,267,021 (GRCm39) |
A241T |
probably benign |
Het |
Prkce |
A |
G |
17: 86,927,339 (GRCm39) |
I538V |
possibly damaging |
Het |
Rab36 |
C |
T |
10: 74,887,875 (GRCm39) |
R249* |
probably null |
Het |
Rps6kl1 |
C |
T |
12: 85,194,582 (GRCm39) |
A110T |
probably damaging |
Het |
Slc22a7 |
T |
C |
17: 46,743,436 (GRCm39) |
I532V |
probably benign |
Het |
Slc2a7 |
T |
C |
4: 150,247,731 (GRCm39) |
V377A |
possibly damaging |
Het |
Slx4 |
A |
G |
16: 3,806,919 (GRCm39) |
V508A |
possibly damaging |
Het |
Stag2 |
A |
G |
X: 41,322,749 (GRCm39) |
S400G |
probably benign |
Het |
Stat6 |
T |
G |
10: 127,487,097 (GRCm39) |
I201M |
probably damaging |
Het |
Stim2 |
T |
C |
5: 54,273,536 (GRCm39) |
|
probably null |
Het |
Tbc1d9 |
A |
G |
8: 83,937,107 (GRCm39) |
Y63C |
probably damaging |
Het |
Tctn2 |
T |
C |
5: 124,758,252 (GRCm39) |
|
noncoding transcript |
Het |
Tmem181a |
T |
A |
17: 6,346,061 (GRCm39) |
L185H |
probably damaging |
Het |
Ubr5 |
T |
A |
15: 38,004,580 (GRCm39) |
T1282S |
probably damaging |
Het |
Ufl1 |
A |
T |
4: 25,254,806 (GRCm39) |
I550N |
probably damaging |
Het |
Uty |
A |
G |
Y: 1,158,372 (GRCm39) |
V557A |
possibly damaging |
Het |
Vmn1r54 |
T |
C |
6: 90,246,253 (GRCm39) |
S56P |
probably damaging |
Het |
Zfp980 |
G |
A |
4: 145,428,653 (GRCm39) |
G461S |
probably benign |
Het |
|
Other mutations in Rsad1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01104:Rsad1
|
APN |
11 |
94,434,466 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01915:Rsad1
|
APN |
11 |
94,439,803 (GRCm39) |
splice site |
probably null |
|
R0271:Rsad1
|
UTSW |
11 |
94,439,290 (GRCm39) |
splice site |
probably benign |
|
R0619:Rsad1
|
UTSW |
11 |
94,433,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Rsad1
|
UTSW |
11 |
94,434,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Rsad1
|
UTSW |
11 |
94,434,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R2069:Rsad1
|
UTSW |
11 |
94,439,951 (GRCm39) |
start gained |
probably benign |
|
R3831:Rsad1
|
UTSW |
11 |
94,434,130 (GRCm39) |
missense |
probably benign |
0.45 |
R3833:Rsad1
|
UTSW |
11 |
94,434,130 (GRCm39) |
missense |
probably benign |
0.45 |
R4152:Rsad1
|
UTSW |
11 |
94,439,449 (GRCm39) |
intron |
probably benign |
|
R4672:Rsad1
|
UTSW |
11 |
94,434,444 (GRCm39) |
missense |
probably damaging |
0.99 |
R5452:Rsad1
|
UTSW |
11 |
94,434,515 (GRCm39) |
missense |
probably damaging |
0.98 |
R6190:Rsad1
|
UTSW |
11 |
94,439,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R6608:Rsad1
|
UTSW |
11 |
94,433,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R6749:Rsad1
|
UTSW |
11 |
94,434,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R7821:Rsad1
|
UTSW |
11 |
94,435,288 (GRCm39) |
missense |
probably benign |
|
R8818:Rsad1
|
UTSW |
11 |
94,439,100 (GRCm39) |
missense |
probably benign |
0.20 |
R8984:Rsad1
|
UTSW |
11 |
94,439,010 (GRCm39) |
missense |
probably damaging |
0.99 |
R9714:Rsad1
|
UTSW |
11 |
94,435,298 (GRCm39) |
missense |
probably benign |
0.00 |
X0024:Rsad1
|
UTSW |
11 |
94,439,807 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Rsad1
|
UTSW |
11 |
94,433,811 (GRCm39) |
critical splice acceptor site |
probably null |
|
|