Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Axin1 |
A |
T |
17: 26,361,779 (GRCm39) |
D41V |
possibly damaging |
Het |
BC034090 |
C |
A |
1: 155,101,197 (GRCm39) |
E718* |
probably null |
Het |
Cdc123 |
G |
T |
2: 5,809,746 (GRCm39) |
Q222K |
probably benign |
Het |
Clip1 |
A |
C |
5: 123,741,717 (GRCm39) |
V1053G |
possibly damaging |
Het |
Dock7 |
T |
A |
4: 98,952,222 (GRCm39) |
E416V |
probably damaging |
Het |
Dydc1 |
T |
C |
14: 40,809,370 (GRCm39) |
L143P |
probably damaging |
Het |
Dync2h1 |
A |
G |
9: 7,158,839 (GRCm39) |
V732A |
probably benign |
Het |
Dzip1l |
T |
A |
9: 99,519,830 (GRCm39) |
L119Q |
probably damaging |
Het |
Fbn1 |
A |
G |
2: 125,239,793 (GRCm39) |
V298A |
probably benign |
Het |
Fbxo34 |
A |
G |
14: 47,766,931 (GRCm39) |
H97R |
probably damaging |
Het |
Gm20521 |
C |
T |
14: 55,122,079 (GRCm39) |
Q81* |
probably null |
Het |
Gspt1 |
T |
C |
16: 11,040,476 (GRCm39) |
M610V |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,344,964 (GRCm39) |
Q1919R |
possibly damaging |
Het |
Il19 |
A |
G |
1: 130,862,792 (GRCm39) |
|
probably benign |
Het |
Kif14 |
G |
A |
1: 136,396,756 (GRCm39) |
S354N |
probably benign |
Het |
Lrrk2 |
A |
G |
15: 91,632,002 (GRCm39) |
K1309E |
possibly damaging |
Het |
Lurap1 |
T |
C |
4: 115,994,887 (GRCm39) |
T115A |
probably damaging |
Het |
Myo18b |
G |
T |
5: 113,021,997 (GRCm39) |
T465K |
probably benign |
Het |
Nwd1 |
A |
T |
8: 73,397,705 (GRCm39) |
D648V |
probably damaging |
Het |
Or13c25 |
T |
G |
4: 52,911,618 (GRCm39) |
M59L |
possibly damaging |
Het |
Or2at4 |
G |
A |
7: 99,384,524 (GRCm39) |
R58H |
probably benign |
Het |
Otof |
T |
C |
5: 30,533,248 (GRCm39) |
Y1527C |
probably damaging |
Het |
Otop3 |
G |
A |
11: 115,235,223 (GRCm39) |
C285Y |
probably damaging |
Het |
Parp3 |
A |
G |
9: 106,348,586 (GRCm39) |
I478T |
probably benign |
Het |
Pdzd2 |
C |
T |
15: 12,458,069 (GRCm39) |
E265K |
possibly damaging |
Het |
Pik3c2g |
T |
C |
6: 139,841,851 (GRCm39) |
L634P |
probably damaging |
Het |
Prkg1 |
C |
A |
19: 31,279,740 (GRCm39) |
V165L |
probably benign |
Het |
Riok3 |
A |
G |
18: 12,281,948 (GRCm39) |
I306V |
possibly damaging |
Het |
Ror2 |
T |
C |
13: 53,267,118 (GRCm39) |
D439G |
probably benign |
Het |
Scn2a |
T |
A |
2: 65,573,434 (GRCm39) |
I1428N |
probably damaging |
Het |
Sgcg |
C |
T |
14: 61,469,924 (GRCm39) |
D146N |
probably benign |
Het |
Skic3 |
T |
C |
13: 76,291,397 (GRCm39) |
|
probably null |
Het |
Slc16a9 |
A |
G |
10: 70,118,529 (GRCm39) |
R283G |
probably benign |
Het |
Sptb |
T |
C |
12: 76,668,105 (GRCm39) |
D664G |
probably benign |
Het |
Tmprss3 |
T |
A |
17: 31,413,982 (GRCm39) |
D54V |
probably damaging |
Het |
Tubd1 |
G |
T |
11: 86,456,555 (GRCm39) |
V374F |
probably benign |
Het |
Vmn2r57 |
A |
T |
7: 41,078,209 (GRCm39) |
M83K |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,853,281 (GRCm39) |
E2458G |
probably benign |
Het |
Vps35l |
G |
A |
7: 118,396,270 (GRCm39) |
|
probably null |
Het |
Zhx2 |
A |
T |
15: 57,686,266 (GRCm39) |
E545V |
probably damaging |
Het |
|
Other mutations in Erp27 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01976:Erp27
|
APN |
6 |
136,896,987 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02348:Erp27
|
APN |
6 |
136,888,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R0452:Erp27
|
UTSW |
6 |
136,886,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R0498:Erp27
|
UTSW |
6 |
136,896,862 (GRCm39) |
unclassified |
probably benign |
|
R2055:Erp27
|
UTSW |
6 |
136,885,227 (GRCm39) |
splice site |
probably benign |
|
R3777:Erp27
|
UTSW |
6 |
136,896,901 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3778:Erp27
|
UTSW |
6 |
136,896,901 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4603:Erp27
|
UTSW |
6 |
136,896,947 (GRCm39) |
missense |
probably damaging |
0.98 |
R4667:Erp27
|
UTSW |
6 |
136,885,150 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4668:Erp27
|
UTSW |
6 |
136,885,150 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5753:Erp27
|
UTSW |
6 |
136,896,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R5814:Erp27
|
UTSW |
6 |
136,888,564 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5864:Erp27
|
UTSW |
6 |
136,885,098 (GRCm39) |
missense |
probably benign |
0.09 |
R6029:Erp27
|
UTSW |
6 |
136,888,609 (GRCm39) |
missense |
probably damaging |
0.98 |
R6131:Erp27
|
UTSW |
6 |
136,885,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Erp27
|
UTSW |
6 |
136,885,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R8781:Erp27
|
UTSW |
6 |
136,886,458 (GRCm39) |
nonsense |
probably null |
|
R9339:Erp27
|
UTSW |
6 |
136,896,945 (GRCm39) |
missense |
probably benign |
0.01 |
R9485:Erp27
|
UTSW |
6 |
136,886,548 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9516:Erp27
|
UTSW |
6 |
136,885,066 (GRCm39) |
missense |
probably benign |
0.00 |
R9526:Erp27
|
UTSW |
6 |
136,886,550 (GRCm39) |
missense |
probably benign |
0.43 |
Z1177:Erp27
|
UTSW |
6 |
136,888,644 (GRCm39) |
critical splice acceptor site |
probably null |
|
|