Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ak8 |
T |
C |
2: 28,702,910 (GRCm39) |
S425P |
probably damaging |
Het |
Comt |
T |
C |
16: 18,229,881 (GRCm39) |
D153G |
probably benign |
Het |
Cplane1 |
A |
T |
15: 8,247,921 (GRCm39) |
H1490L |
possibly damaging |
Het |
Exoc6 |
T |
C |
19: 37,597,402 (GRCm39) |
I601T |
probably damaging |
Het |
F11 |
A |
T |
8: 45,694,568 (GRCm39) |
C598S |
probably damaging |
Het |
Galnt13 |
G |
T |
2: 55,002,872 (GRCm39) |
D524Y |
probably damaging |
Het |
Glb1l3 |
T |
C |
9: 26,764,940 (GRCm39) |
E157G |
probably damaging |
Het |
Hc |
T |
C |
2: 34,890,847 (GRCm39) |
H1323R |
probably benign |
Het |
Hsd3b5 |
T |
C |
3: 98,537,421 (GRCm39) |
I32V |
probably benign |
Het |
Il6ra |
A |
G |
3: 89,778,560 (GRCm39) |
S430P |
probably benign |
Het |
Lama2 |
G |
T |
10: 27,242,062 (GRCm39) |
T298K |
probably damaging |
Het |
Ntrk3 |
T |
C |
7: 78,103,085 (GRCm39) |
D405G |
probably benign |
Het |
Opn5 |
T |
C |
17: 42,868,382 (GRCm39) |
D371G |
probably benign |
Het |
Pcdh15 |
G |
T |
10: 74,152,918 (GRCm39) |
A408S |
probably damaging |
Het |
Pim3 |
T |
C |
15: 88,747,116 (GRCm39) |
V54A |
probably benign |
Het |
Prdm5 |
T |
C |
6: 65,771,303 (GRCm39) |
F38S |
probably damaging |
Het |
Ptgs2 |
C |
T |
1: 149,981,460 (GRCm39) |
|
probably null |
Het |
Rnf185 |
A |
G |
11: 3,368,015 (GRCm39) |
I221T |
possibly damaging |
Het |
Slc27a2 |
T |
C |
2: 126,420,870 (GRCm39) |
F318L |
possibly damaging |
Het |
Spata1 |
T |
C |
3: 146,193,119 (GRCm39) |
Y124C |
possibly damaging |
Het |
Tmie |
G |
T |
9: 110,699,821 (GRCm39) |
|
probably benign |
Het |
Tph2 |
T |
C |
10: 114,915,886 (GRCm39) |
K429R |
probably benign |
Het |
Usp32 |
A |
G |
11: 84,935,613 (GRCm39) |
Y388H |
probably benign |
Het |
Vmn2r60 |
A |
T |
7: 41,844,578 (GRCm39) |
Q647L |
probably benign |
Het |
|
Other mutations in Nedd4l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00501:Nedd4l
|
APN |
18 |
65,341,163 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00931:Nedd4l
|
APN |
18 |
65,305,470 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02306:Nedd4l
|
APN |
18 |
65,306,025 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02440:Nedd4l
|
APN |
18 |
65,296,244 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02444:Nedd4l
|
APN |
18 |
65,337,028 (GRCm39) |
splice site |
probably benign |
|
IGL02700:Nedd4l
|
APN |
18 |
65,342,751 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02943:Nedd4l
|
APN |
18 |
65,294,723 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02999:Nedd4l
|
APN |
18 |
65,331,778 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03135:Nedd4l
|
APN |
18 |
65,338,741 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03373:Nedd4l
|
APN |
18 |
65,314,391 (GRCm39) |
splice site |
probably benign |
|
R0036:Nedd4l
|
UTSW |
18 |
65,184,194 (GRCm39) |
intron |
probably benign |
|
R0396:Nedd4l
|
UTSW |
18 |
65,294,725 (GRCm39) |
splice site |
probably benign |
|
R0472:Nedd4l
|
UTSW |
18 |
65,341,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Nedd4l
|
UTSW |
18 |
65,306,092 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0513:Nedd4l
|
UTSW |
18 |
65,328,256 (GRCm39) |
splice site |
probably benign |
|
R0609:Nedd4l
|
UTSW |
18 |
65,341,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R0631:Nedd4l
|
UTSW |
18 |
65,341,574 (GRCm39) |
splice site |
probably benign |
|
R1077:Nedd4l
|
UTSW |
18 |
65,300,570 (GRCm39) |
splice site |
probably benign |
|
R1643:Nedd4l
|
UTSW |
18 |
65,331,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R1722:Nedd4l
|
UTSW |
18 |
65,291,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R1806:Nedd4l
|
UTSW |
18 |
65,345,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R1921:Nedd4l
|
UTSW |
18 |
65,300,646 (GRCm39) |
critical splice donor site |
probably null |
|
R1986:Nedd4l
|
UTSW |
18 |
65,276,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R2070:Nedd4l
|
UTSW |
18 |
65,345,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Nedd4l
|
UTSW |
18 |
65,343,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R2152:Nedd4l
|
UTSW |
18 |
65,343,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R2154:Nedd4l
|
UTSW |
18 |
65,343,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R2358:Nedd4l
|
UTSW |
18 |
65,342,790 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2680:Nedd4l
|
UTSW |
18 |
65,296,201 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3082:Nedd4l
|
UTSW |
18 |
65,312,049 (GRCm39) |
missense |
probably benign |
0.00 |
R3500:Nedd4l
|
UTSW |
18 |
65,345,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R3711:Nedd4l
|
UTSW |
18 |
65,342,790 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3712:Nedd4l
|
UTSW |
18 |
65,342,790 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3874:Nedd4l
|
UTSW |
18 |
65,300,606 (GRCm39) |
missense |
probably benign |
|
R4435:Nedd4l
|
UTSW |
18 |
65,345,896 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4698:Nedd4l
|
UTSW |
18 |
65,336,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R4757:Nedd4l
|
UTSW |
18 |
65,298,676 (GRCm39) |
missense |
probably damaging |
0.98 |
R4783:Nedd4l
|
UTSW |
18 |
65,305,998 (GRCm39) |
missense |
probably damaging |
0.99 |
R4790:Nedd4l
|
UTSW |
18 |
65,337,016 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4980:Nedd4l
|
UTSW |
18 |
65,213,131 (GRCm39) |
nonsense |
probably null |
|
R5106:Nedd4l
|
UTSW |
18 |
65,326,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R5122:Nedd4l
|
UTSW |
18 |
65,324,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R5605:Nedd4l
|
UTSW |
18 |
65,307,315 (GRCm39) |
critical splice donor site |
probably null |
|
R6465:Nedd4l
|
UTSW |
18 |
65,288,335 (GRCm39) |
missense |
probably benign |
0.06 |
R6479:Nedd4l
|
UTSW |
18 |
65,342,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R6622:Nedd4l
|
UTSW |
18 |
65,307,305 (GRCm39) |
missense |
probably damaging |
0.99 |
R6773:Nedd4l
|
UTSW |
18 |
65,300,622 (GRCm39) |
missense |
probably benign |
0.36 |
R7065:Nedd4l
|
UTSW |
18 |
65,329,040 (GRCm39) |
missense |
probably benign |
0.04 |
R7068:Nedd4l
|
UTSW |
18 |
65,338,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:Nedd4l
|
UTSW |
18 |
65,130,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R7496:Nedd4l
|
UTSW |
18 |
65,213,089 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7903:Nedd4l
|
UTSW |
18 |
65,319,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R8123:Nedd4l
|
UTSW |
18 |
65,207,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R8185:Nedd4l
|
UTSW |
18 |
65,342,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R8282:Nedd4l
|
UTSW |
18 |
65,324,560 (GRCm39) |
missense |
probably damaging |
0.98 |
R8440:Nedd4l
|
UTSW |
18 |
65,022,126 (GRCm39) |
splice site |
probably null |
|
R8499:Nedd4l
|
UTSW |
18 |
65,342,728 (GRCm39) |
missense |
probably damaging |
0.98 |
R8557:Nedd4l
|
UTSW |
18 |
65,336,986 (GRCm39) |
missense |
probably benign |
0.00 |
R8801:Nedd4l
|
UTSW |
18 |
65,288,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Nedd4l
|
UTSW |
18 |
65,298,688 (GRCm39) |
missense |
probably benign |
|
R9025:Nedd4l
|
UTSW |
18 |
65,311,995 (GRCm39) |
missense |
probably damaging |
0.98 |
R9040:Nedd4l
|
UTSW |
18 |
65,342,734 (GRCm39) |
missense |
probably damaging |
0.99 |
R9482:Nedd4l
|
UTSW |
18 |
65,021,031 (GRCm39) |
unclassified |
probably benign |
|
R9498:Nedd4l
|
UTSW |
18 |
65,294,723 (GRCm39) |
critical splice donor site |
probably null |
|
R9599:Nedd4l
|
UTSW |
18 |
65,343,400 (GRCm39) |
missense |
probably damaging |
1.00 |
RF013:Nedd4l
|
UTSW |
18 |
65,342,751 (GRCm39) |
missense |
probably damaging |
1.00 |
|