Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim3 |
A |
G |
18: 61,955,092 (GRCm39) |
V299A |
probably benign |
Het |
Actr5 |
T |
C |
2: 158,478,722 (GRCm39) |
|
probably null |
Het |
Arhgap18 |
A |
G |
10: 26,756,744 (GRCm39) |
D448G |
possibly damaging |
Het |
Bcl9 |
T |
C |
3: 97,116,291 (GRCm39) |
E801G |
probably benign |
Het |
Bin1 |
A |
G |
18: 32,552,978 (GRCm39) |
N232S |
probably damaging |
Het |
Brf1 |
A |
C |
12: 112,927,211 (GRCm39) |
Y459D |
probably damaging |
Het |
Clca4a |
T |
A |
3: 144,659,541 (GRCm39) |
I772F |
probably damaging |
Het |
Cyp2a4 |
G |
A |
7: 26,008,088 (GRCm39) |
|
probably null |
Het |
Dync1i2 |
T |
A |
2: 71,077,352 (GRCm39) |
|
probably benign |
Het |
Frem3 |
T |
A |
8: 81,339,333 (GRCm39) |
M542K |
probably benign |
Het |
Gpbp1 |
T |
C |
13: 111,575,736 (GRCm39) |
T256A |
possibly damaging |
Het |
Ighm |
T |
C |
12: 113,384,854 (GRCm39) |
|
probably benign |
Het |
Igkv3-12 |
A |
G |
6: 70,495,232 (GRCm39) |
|
probably benign |
Het |
Kdm4d |
A |
G |
9: 14,375,714 (GRCm39) |
V48A |
probably damaging |
Het |
Lama2 |
T |
C |
10: 27,220,417 (GRCm39) |
S483G |
probably benign |
Het |
Lbp |
A |
C |
2: 158,170,332 (GRCm39) |
Q464P |
probably damaging |
Het |
Lipo4 |
T |
C |
19: 33,476,654 (GRCm39) |
T365A |
probably benign |
Het |
Mark3 |
T |
C |
12: 111,593,956 (GRCm39) |
F274S |
probably damaging |
Het |
Mcm3 |
A |
T |
1: 20,884,904 (GRCm39) |
|
probably benign |
Het |
Mrpl9 |
T |
A |
3: 94,352,001 (GRCm39) |
F137I |
probably damaging |
Het |
Msh4 |
G |
T |
3: 153,603,034 (GRCm39) |
A93E |
probably damaging |
Het |
Mthfd1l |
T |
A |
10: 3,968,567 (GRCm39) |
D407E |
probably benign |
Het |
Or10j7 |
G |
A |
1: 173,011,843 (GRCm39) |
H53Y |
probably benign |
Het |
Or12d12 |
C |
T |
17: 37,610,629 (GRCm39) |
R228H |
probably benign |
Het |
Or1i2 |
A |
C |
10: 78,447,960 (GRCm39) |
S172A |
probably benign |
Het |
Pcsk2 |
G |
T |
2: 143,643,078 (GRCm39) |
V452L |
possibly damaging |
Het |
Pcsk6 |
G |
A |
7: 65,685,021 (GRCm39) |
|
probably null |
Het |
Pmfbp1 |
A |
G |
8: 110,254,348 (GRCm39) |
E461G |
probably benign |
Het |
Pole2 |
A |
G |
12: 69,254,631 (GRCm39) |
|
probably null |
Het |
Postn |
T |
C |
3: 54,276,649 (GRCm39) |
M176T |
probably damaging |
Het |
Prss12 |
T |
A |
3: 123,276,483 (GRCm39) |
C371S |
probably damaging |
Het |
Rnf11 |
T |
A |
4: 109,314,173 (GRCm39) |
Q72L |
possibly damaging |
Het |
Slitrk3 |
T |
A |
3: 72,957,570 (GRCm39) |
I401F |
probably damaging |
Het |
Themis |
A |
G |
10: 28,544,749 (GRCm39) |
|
probably benign |
Het |
Tmem45a |
A |
G |
16: 56,631,928 (GRCm39) |
I230T |
probably benign |
Het |
Tnni1 |
C |
A |
1: 135,733,234 (GRCm39) |
|
probably null |
Het |
Trpa1 |
A |
T |
1: 14,982,607 (GRCm39) |
I83N |
probably damaging |
Het |
Uggt1 |
T |
C |
1: 36,221,555 (GRCm39) |
Y54C |
probably damaging |
Het |
Umodl1 |
C |
T |
17: 31,217,800 (GRCm39) |
T1202I |
possibly damaging |
Het |
Unc93a2 |
A |
G |
17: 7,637,138 (GRCm39) |
V130A |
probably damaging |
Het |
Usp37 |
G |
A |
1: 74,514,199 (GRCm39) |
A324V |
probably benign |
Het |
Zfp808 |
T |
A |
13: 62,321,023 (GRCm39) |
C751S |
probably damaging |
Het |
|
Other mutations in Rrad |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01291:Rrad
|
APN |
8 |
105,357,283 (GRCm39) |
missense |
probably benign |
0.00 |
ANU05:Rrad
|
UTSW |
8 |
105,357,283 (GRCm39) |
missense |
probably benign |
0.00 |
R0003:Rrad
|
UTSW |
8 |
105,355,299 (GRCm39) |
missense |
probably benign |
0.00 |
R0508:Rrad
|
UTSW |
8 |
105,356,500 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0514:Rrad
|
UTSW |
8 |
105,355,259 (GRCm39) |
missense |
probably benign |
0.00 |
R6330:Rrad
|
UTSW |
8 |
105,356,492 (GRCm39) |
missense |
probably benign |
0.07 |
R6988:Rrad
|
UTSW |
8 |
105,357,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R8936:Rrad
|
UTSW |
8 |
105,355,222 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8940:Rrad
|
UTSW |
8 |
105,355,222 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8986:Rrad
|
UTSW |
8 |
105,355,222 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9154:Rrad
|
UTSW |
8 |
105,355,343 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9457:Rrad
|
UTSW |
8 |
105,356,359 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9563:Rrad
|
UTSW |
8 |
105,355,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R9632:Rrad
|
UTSW |
8 |
105,356,320 (GRCm39) |
missense |
probably benign |
0.15 |
|