Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arid5a |
T |
C |
1: 36,358,578 (GRCm39) |
F450S |
probably damaging |
Het |
Astn1 |
C |
T |
1: 158,502,184 (GRCm39) |
R1133C |
probably damaging |
Het |
Cd101 |
G |
A |
3: 100,919,398 (GRCm39) |
P568L |
probably benign |
Het |
Cdkl4 |
T |
C |
17: 80,851,192 (GRCm39) |
E170G |
probably damaging |
Het |
Chit1 |
A |
G |
1: 134,074,413 (GRCm39) |
E240G |
probably benign |
Het |
Duox2 |
T |
C |
2: 122,121,190 (GRCm39) |
T741A |
probably benign |
Het |
Eef2 |
T |
C |
10: 81,015,845 (GRCm39) |
V427A |
probably benign |
Het |
Ewsr1 |
T |
C |
11: 5,038,077 (GRCm39) |
D105G |
probably damaging |
Het |
Ftsj3 |
C |
T |
11: 106,141,233 (GRCm39) |
R629Q |
probably benign |
Het |
Gm10406 |
C |
T |
14: 18,341,703 (GRCm39) |
G181E |
probably benign |
Het |
Ilk |
A |
G |
7: 105,390,376 (GRCm39) |
H185R |
probably benign |
Het |
Lamc1 |
A |
T |
1: 153,116,179 (GRCm39) |
C1001S |
probably damaging |
Het |
Mcidas |
T |
C |
13: 113,133,974 (GRCm39) |
S153P |
probably benign |
Het |
Mtcl1 |
T |
C |
17: 66,661,185 (GRCm39) |
E931G |
probably benign |
Het |
Myo10 |
C |
T |
15: 25,808,152 (GRCm39) |
R1925C |
probably damaging |
Het |
Notch3 |
A |
G |
17: 32,341,716 (GRCm39) |
V2012A |
probably damaging |
Het |
Or6c76 |
C |
A |
10: 129,611,938 (GRCm39) |
H67N |
probably benign |
Het |
Parp6 |
A |
G |
9: 59,556,175 (GRCm39) |
M542V |
probably benign |
Het |
Rab27a |
G |
A |
9: 72,992,254 (GRCm39) |
G94D |
probably damaging |
Het |
Ralgapb |
A |
G |
2: 158,296,034 (GRCm39) |
|
probably benign |
Het |
Rassf4 |
T |
C |
6: 116,622,933 (GRCm39) |
E26G |
probably benign |
Het |
Rnf166 |
C |
T |
8: 123,193,961 (GRCm39) |
D221N |
probably damaging |
Het |
Rptn |
G |
T |
3: 93,303,735 (GRCm39) |
G356V |
probably benign |
Het |
Scfd1 |
T |
A |
12: 51,460,900 (GRCm39) |
S337T |
probably benign |
Het |
Sel1l3 |
T |
A |
5: 53,302,835 (GRCm39) |
D678V |
probably damaging |
Het |
Sidt1 |
A |
T |
16: 44,106,732 (GRCm39) |
F233I |
probably damaging |
Het |
Slc12a4 |
T |
C |
8: 106,671,864 (GRCm39) |
D917G |
probably damaging |
Het |
Slc22a2 |
A |
T |
17: 12,803,270 (GRCm39) |
I35F |
possibly damaging |
Het |
Smco1 |
A |
T |
16: 32,092,751 (GRCm39) |
T141S |
possibly damaging |
Het |
Svs6 |
T |
C |
2: 164,159,352 (GRCm39) |
|
probably benign |
Het |
Syne2 |
C |
T |
12: 76,062,419 (GRCm39) |
A4247V |
probably damaging |
Het |
Tacc2 |
T |
A |
7: 130,330,898 (GRCm39) |
|
probably null |
Het |
Tgm4 |
A |
T |
9: 122,885,531 (GRCm39) |
I358F |
probably damaging |
Het |
Thnsl2 |
A |
G |
6: 71,111,203 (GRCm39) |
S222P |
probably damaging |
Het |
Tmem25 |
G |
A |
9: 44,709,568 (GRCm39) |
R78* |
probably null |
Het |
Ube2l6 |
T |
C |
2: 84,639,506 (GRCm39) |
|
probably benign |
Het |
Usp10 |
T |
A |
8: 120,675,480 (GRCm39) |
Y63N |
possibly damaging |
Het |
Vit |
A |
G |
17: 78,912,915 (GRCm39) |
I283V |
possibly damaging |
Het |
Vmn1r214 |
G |
A |
13: 23,219,270 (GRCm39) |
V255I |
possibly damaging |
Het |
Xpo1 |
A |
G |
11: 23,246,003 (GRCm39) |
R1038G |
probably damaging |
Het |
Ybx1 |
T |
A |
4: 119,139,509 (GRCm39) |
N50I |
probably damaging |
Het |
Zhx1 |
T |
C |
15: 57,917,683 (GRCm39) |
K188E |
probably damaging |
Het |
|
Other mutations in Rwdd2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
R1086:Rwdd2b
|
UTSW |
16 |
87,233,446 (GRCm39) |
unclassified |
probably benign |
|
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 |
|