Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
T |
1: 71,334,220 (GRCm39) |
|
probably benign |
Het |
Agbl4 |
G |
C |
4: 110,335,791 (GRCm39) |
|
probably benign |
Het |
Ano6 |
T |
C |
15: 95,847,843 (GRCm39) |
|
probably null |
Het |
B3gnt8 |
C |
G |
7: 25,327,736 (GRCm39) |
N55K |
probably damaging |
Het |
Brox |
A |
G |
1: 183,064,052 (GRCm39) |
Y252H |
probably damaging |
Het |
Cfap100 |
T |
A |
6: 90,380,890 (GRCm39) |
K605* |
probably null |
Het |
Chd7 |
A |
G |
4: 8,866,458 (GRCm39) |
T877A |
probably benign |
Het |
Csmd3 |
T |
A |
15: 47,559,151 (GRCm39) |
I2371F |
probably damaging |
Het |
Cwc22 |
T |
A |
2: 77,754,824 (GRCm39) |
|
probably benign |
Het |
Cyp2s1 |
A |
T |
7: 25,505,422 (GRCm39) |
D347E |
probably damaging |
Het |
Dab1 |
C |
A |
4: 104,185,769 (GRCm39) |
|
probably benign |
Het |
Dis3l2 |
G |
A |
1: 86,917,871 (GRCm39) |
D493N |
probably benign |
Het |
Got1l1 |
A |
G |
8: 27,688,007 (GRCm39) |
W341R |
probably damaging |
Het |
Gps2 |
A |
G |
11: 69,806,050 (GRCm39) |
|
probably benign |
Het |
Haus1 |
A |
C |
18: 77,854,553 (GRCm39) |
|
probably benign |
Het |
Itgam |
T |
C |
7: 127,679,436 (GRCm39) |
S193P |
probably damaging |
Het |
Itpr2 |
C |
A |
6: 146,251,543 (GRCm39) |
A1034S |
probably damaging |
Het |
Lrp5 |
T |
C |
19: 3,699,476 (GRCm39) |
R270G |
probably benign |
Het |
Ltbr |
G |
A |
6: 125,289,703 (GRCm39) |
|
probably benign |
Het |
Mdga2 |
T |
C |
12: 66,552,876 (GRCm39) |
|
probably benign |
Het |
Mug1 |
T |
A |
6: 121,862,813 (GRCm39) |
M1387K |
probably damaging |
Het |
Nwd2 |
C |
T |
5: 63,963,917 (GRCm39) |
S1167L |
probably damaging |
Het |
Or5h19 |
T |
A |
16: 58,856,626 (GRCm39) |
H158L |
probably damaging |
Het |
Pfkm |
T |
C |
15: 98,029,546 (GRCm39) |
V719A |
probably benign |
Het |
Ppfia3 |
C |
G |
7: 45,011,182 (GRCm39) |
G16A |
probably damaging |
Het |
Ppp2r3d |
G |
A |
9: 101,031,021 (GRCm39) |
T245I |
possibly damaging |
Het |
Ptprd |
T |
C |
4: 76,051,495 (GRCm39) |
T256A |
probably damaging |
Het |
Ptprg |
C |
T |
14: 11,952,706 (GRCm38) |
|
probably benign |
Het |
Rabgap1 |
T |
C |
2: 37,359,458 (GRCm39) |
V7A |
probably damaging |
Het |
Rnh1 |
T |
G |
7: 140,743,282 (GRCm39) |
Q231P |
probably benign |
Het |
Saal1 |
T |
C |
7: 46,338,883 (GRCm39) |
|
probably benign |
Het |
Sap130 |
G |
A |
18: 31,783,673 (GRCm39) |
|
probably benign |
Het |
Serpina1d |
T |
G |
12: 103,730,046 (GRCm39) |
M379L |
probably benign |
Het |
Skor2 |
A |
C |
18: 76,946,994 (GRCm39) |
S239R |
unknown |
Het |
Slc16a13 |
A |
G |
11: 70,109,850 (GRCm39) |
L217P |
probably damaging |
Het |
Slc18b1 |
T |
C |
10: 23,679,693 (GRCm39) |
M74T |
probably benign |
Het |
Speer4e2 |
T |
C |
5: 15,028,804 (GRCm39) |
D29G |
probably benign |
Het |
Tacc2 |
A |
T |
7: 130,228,227 (GRCm39) |
E1637D |
possibly damaging |
Het |
Tedc2 |
T |
A |
17: 24,435,291 (GRCm39) |
E366V |
probably damaging |
Het |
Tedc2 |
C |
A |
17: 24,435,292 (GRCm39) |
E366* |
probably null |
Het |
Tg |
A |
C |
15: 66,555,911 (GRCm39) |
I868L |
probably benign |
Het |
Ttll5 |
G |
A |
12: 85,937,853 (GRCm39) |
V395I |
possibly damaging |
Het |
Uba6 |
C |
A |
5: 86,275,578 (GRCm39) |
C739F |
probably benign |
Het |
Unc5d |
A |
C |
8: 29,365,658 (GRCm39) |
V109G |
possibly damaging |
Het |
Zfp407 |
C |
T |
18: 84,577,898 (GRCm39) |
A1072T |
probably benign |
Het |
Zfp462 |
G |
T |
4: 55,013,000 (GRCm39) |
K507N |
probably damaging |
Het |
|
Other mutations in Rwdd2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02000:Rwdd2b
|
APN |
16 |
87,233,828 (GRCm39) |
unclassified |
probably benign |
|
IGL02351:Rwdd2b
|
APN |
16 |
87,234,336 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02358:Rwdd2b
|
APN |
16 |
87,234,336 (GRCm39) |
missense |
probably benign |
0.06 |
R1022:Rwdd2b
|
UTSW |
16 |
87,233,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R1024:Rwdd2b
|
UTSW |
16 |
87,233,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R1886:Rwdd2b
|
UTSW |
16 |
87,234,013 (GRCm39) |
missense |
probably benign |
0.08 |
R2359:Rwdd2b
|
UTSW |
16 |
87,233,809 (GRCm39) |
missense |
probably benign |
0.06 |
R4308:Rwdd2b
|
UTSW |
16 |
87,233,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R4495:Rwdd2b
|
UTSW |
16 |
87,231,450 (GRCm39) |
missense |
probably benign |
0.00 |
R4680:Rwdd2b
|
UTSW |
16 |
87,233,950 (GRCm39) |
critical splice donor site |
probably null |
|
R4943:Rwdd2b
|
UTSW |
16 |
87,231,422 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6260:Rwdd2b
|
UTSW |
16 |
87,231,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R7622:Rwdd2b
|
UTSW |
16 |
87,231,500 (GRCm39) |
missense |
probably benign |
0.03 |
R7768:Rwdd2b
|
UTSW |
16 |
87,233,633 (GRCm39) |
missense |
probably benign |
0.01 |
R8100:Rwdd2b
|
UTSW |
16 |
87,233,509 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9746:Rwdd2b
|
UTSW |
16 |
87,233,641 (GRCm39) |
missense |
probably benign |
0.05 |
RF022:Rwdd2b
|
UTSW |
16 |
87,233,558 (GRCm39) |
missense |
probably benign |
0.01 |
|