Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Baz1b |
T |
C |
5: 135,246,138 (GRCm39) |
L529P |
probably damaging |
Het |
Bdp1 |
A |
T |
13: 100,197,399 (GRCm39) |
D995E |
probably benign |
Het |
Cd22 |
T |
C |
7: 30,566,893 (GRCm39) |
N607S |
possibly damaging |
Het |
Ddx10 |
T |
A |
9: 53,146,682 (GRCm39) |
D180V |
probably damaging |
Het |
Dennd4c |
T |
C |
4: 86,725,672 (GRCm39) |
Y709H |
possibly damaging |
Het |
Dhrs3 |
A |
C |
4: 144,620,133 (GRCm39) |
I17L |
probably benign |
Het |
Dnah8 |
A |
T |
17: 30,868,747 (GRCm39) |
K394* |
probably null |
Het |
Flnc |
T |
A |
6: 29,454,375 (GRCm39) |
I1896N |
probably damaging |
Het |
Glipr1l2 |
A |
G |
10: 111,928,534 (GRCm39) |
Y143C |
probably damaging |
Het |
Lmo7 |
T |
C |
14: 102,163,524 (GRCm39) |
|
probably benign |
Het |
Lpp |
C |
T |
16: 24,580,895 (GRCm39) |
R204W |
probably damaging |
Het |
Mast3 |
A |
G |
8: 71,241,888 (GRCm39) |
S98P |
probably benign |
Het |
Myf5 |
A |
G |
10: 107,320,051 (GRCm39) |
S200P |
possibly damaging |
Het |
Or52r1b |
T |
G |
7: 102,690,928 (GRCm39) |
S76A |
possibly damaging |
Het |
Pramel12 |
G |
A |
4: 143,143,512 (GRCm39) |
V93I |
probably benign |
Het |
Recql5 |
A |
C |
11: 115,784,856 (GRCm39) |
S824A |
probably benign |
Het |
Reg2 |
A |
G |
6: 78,383,188 (GRCm39) |
E45G |
probably damaging |
Het |
Rnf224 |
T |
C |
2: 25,126,260 (GRCm39) |
D31G |
probably damaging |
Het |
Sema4c |
C |
T |
1: 36,592,166 (GRCm39) |
S227N |
probably damaging |
Het |
Sgsm2 |
C |
T |
11: 74,750,698 (GRCm39) |
G439D |
probably damaging |
Het |
Smap2 |
T |
A |
4: 120,832,587 (GRCm39) |
M185L |
probably benign |
Het |
Spty2d1 |
A |
G |
7: 46,647,360 (GRCm39) |
V523A |
probably benign |
Het |
Stk17b |
C |
A |
1: 53,803,247 (GRCm39) |
R184L |
probably damaging |
Het |
Syt13 |
A |
G |
2: 92,771,210 (GRCm39) |
D99G |
probably damaging |
Het |
Trav14-1 |
T |
A |
14: 53,791,763 (GRCm39) |
S38T |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,700,812 (GRCm39) |
|
probably benign |
Het |
Usp17la |
G |
A |
7: 104,510,353 (GRCm39) |
W319* |
probably null |
Het |
Vmn2r73 |
T |
C |
7: 85,521,902 (GRCm39) |
T146A |
probably benign |
Het |
Vwa3b |
C |
T |
1: 37,193,132 (GRCm39) |
|
probably benign |
Het |
Zfp13 |
A |
T |
17: 23,799,739 (GRCm39) |
|
probably benign |
Het |
Zscan18 |
A |
C |
7: 12,503,251 (GRCm39) |
D769E |
probably benign |
Het |
|
Other mutations in Rergl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01309:Rergl
|
APN |
6 |
139,470,256 (GRCm39) |
nonsense |
probably null |
|
IGL01542:Rergl
|
APN |
6 |
139,470,496 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01761:Rergl
|
APN |
6 |
139,478,863 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02507:Rergl
|
APN |
6 |
139,470,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02523:Rergl
|
APN |
6 |
139,473,458 (GRCm39) |
splice site |
probably benign |
|
R0518:Rergl
|
UTSW |
6 |
139,473,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Rergl
|
UTSW |
6 |
139,473,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R2086:Rergl
|
UTSW |
6 |
139,471,832 (GRCm39) |
missense |
probably benign |
|
R4629:Rergl
|
UTSW |
6 |
139,478,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R5275:Rergl
|
UTSW |
6 |
139,478,819 (GRCm39) |
critical splice donor site |
probably null |
|
R6364:Rergl
|
UTSW |
6 |
139,477,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7175:Rergl
|
UTSW |
6 |
139,473,533 (GRCm39) |
missense |
probably benign |
0.01 |
R8808:Rergl
|
UTSW |
6 |
139,478,865 (GRCm39) |
missense |
probably benign |
0.18 |
R9033:Rergl
|
UTSW |
6 |
139,471,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R9403:Rergl
|
UTSW |
6 |
139,471,852 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9803:Rergl
|
UTSW |
6 |
139,477,761 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Rergl
|
UTSW |
6 |
139,470,424 (GRCm39) |
nonsense |
probably null |
|
|