Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
A |
G |
11: 30,376,177 (GRCm39) |
L230S |
probably damaging |
Het |
4930505A04Rik |
A |
G |
11: 30,396,389 (GRCm39) |
|
probably benign |
Het |
Atg2b |
A |
G |
12: 105,602,032 (GRCm39) |
I1648T |
probably damaging |
Het |
Ccdc110 |
T |
C |
8: 46,394,817 (GRCm39) |
F236S |
probably damaging |
Het |
Ccdc178 |
T |
C |
18: 22,230,782 (GRCm39) |
D363G |
possibly damaging |
Het |
Cntn5 |
T |
A |
9: 9,831,577 (GRCm39) |
D601V |
probably damaging |
Het |
Cog7 |
C |
T |
7: 121,529,752 (GRCm39) |
|
probably null |
Het |
Dnah7c |
A |
G |
1: 46,651,881 (GRCm39) |
K1365E |
probably damaging |
Het |
Dock9 |
T |
C |
14: 121,837,096 (GRCm39) |
|
probably null |
Het |
Ehd3 |
T |
A |
17: 74,123,321 (GRCm39) |
I108N |
probably benign |
Het |
Erbb4 |
A |
G |
1: 68,348,773 (GRCm39) |
S535P |
probably damaging |
Het |
Gfra3 |
T |
C |
18: 34,823,892 (GRCm39) |
T361A |
probably benign |
Het |
Gm10295 |
A |
T |
7: 71,000,448 (GRCm39) |
I44K |
unknown |
Het |
Gm10553 |
T |
C |
1: 85,078,170 (GRCm39) |
S96P |
probably benign |
Het |
Gm21738 |
T |
A |
14: 19,415,957 (GRCm38) |
Y194F |
probably benign |
Het |
Hspa13 |
A |
T |
16: 75,562,125 (GRCm39) |
Y25N |
probably damaging |
Het |
Lrfn3 |
G |
A |
7: 30,055,347 (GRCm39) |
P533S |
probably damaging |
Het |
Lrp4 |
A |
G |
2: 91,317,372 (GRCm39) |
|
probably benign |
Het |
Mical3 |
T |
C |
6: 120,911,639 (GRCm39) |
D1991G |
probably benign |
Het |
Myoz1 |
A |
G |
14: 20,700,600 (GRCm39) |
Y206H |
probably damaging |
Het |
Or2at1 |
A |
T |
7: 99,416,431 (GRCm39) |
I21F |
probably benign |
Het |
Otog |
A |
G |
7: 45,924,019 (GRCm39) |
E1126G |
probably damaging |
Het |
Pak3 |
TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
X: 142,526,889 (GRCm39) |
|
probably benign |
Het |
Prkdc |
A |
G |
16: 15,472,613 (GRCm39) |
|
probably benign |
Het |
Pttg1ip2 |
C |
T |
5: 5,505,919 (GRCm39) |
A121T |
probably benign |
Het |
Rab7 |
A |
G |
6: 87,990,624 (GRCm39) |
S17P |
probably damaging |
Het |
Slc35e1 |
T |
C |
8: 73,246,415 (GRCm39) |
|
probably benign |
Het |
Sppl2a |
A |
G |
2: 126,765,514 (GRCm39) |
S203P |
probably benign |
Het |
Taar7a |
A |
G |
10: 23,868,439 (GRCm39) |
I314T |
possibly damaging |
Het |
Tgs1 |
T |
C |
4: 3,593,471 (GRCm39) |
I453T |
probably damaging |
Het |
Tmem117 |
C |
A |
15: 94,909,217 (GRCm39) |
T210N |
probably benign |
Het |
Trim55 |
A |
G |
3: 19,698,906 (GRCm39) |
N45S |
probably damaging |
Het |
Ugt2b34 |
G |
C |
5: 87,052,246 (GRCm39) |
S250* |
probably null |
Het |
Vmn2r67 |
G |
A |
7: 84,785,974 (GRCm39) |
T677I |
probably damaging |
Het |
Zfp335 |
C |
G |
2: 164,734,598 (GRCm39) |
|
probably benign |
Het |
Znrf1 |
T |
A |
8: 112,263,986 (GRCm39) |
Y72N |
probably damaging |
Het |
|
Other mutations in Fam170a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01351:Fam170a
|
APN |
18 |
50,414,845 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01637:Fam170a
|
APN |
18 |
50,414,734 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01681:Fam170a
|
APN |
18 |
50,415,302 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL03151:Fam170a
|
APN |
18 |
50,414,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03263:Fam170a
|
APN |
18 |
50,413,588 (GRCm39) |
splice site |
probably benign |
|
R0446:Fam170a
|
UTSW |
18 |
50,413,699 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1242:Fam170a
|
UTSW |
18 |
50,415,206 (GRCm39) |
missense |
probably damaging |
0.96 |
R1958:Fam170a
|
UTSW |
18 |
50,415,181 (GRCm39) |
missense |
probably benign |
0.04 |
R2325:Fam170a
|
UTSW |
18 |
50,414,917 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3722:Fam170a
|
UTSW |
18 |
50,415,271 (GRCm39) |
missense |
probably benign |
0.16 |
R4012:Fam170a
|
UTSW |
18 |
50,415,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R4240:Fam170a
|
UTSW |
18 |
50,414,734 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4835:Fam170a
|
UTSW |
18 |
50,415,050 (GRCm39) |
missense |
probably damaging |
0.98 |
R5030:Fam170a
|
UTSW |
18 |
50,415,021 (GRCm39) |
missense |
probably benign |
0.00 |
R5201:Fam170a
|
UTSW |
18 |
50,415,193 (GRCm39) |
missense |
probably benign |
0.00 |
R5401:Fam170a
|
UTSW |
18 |
50,413,618 (GRCm39) |
missense |
probably benign |
0.20 |
R5907:Fam170a
|
UTSW |
18 |
50,415,321 (GRCm39) |
critical splice donor site |
probably null |
|
R6207:Fam170a
|
UTSW |
18 |
50,415,017 (GRCm39) |
missense |
probably damaging |
0.99 |
R7080:Fam170a
|
UTSW |
18 |
50,413,740 (GRCm39) |
critical splice donor site |
probably null |
|
R7232:Fam170a
|
UTSW |
18 |
50,414,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R7622:Fam170a
|
UTSW |
18 |
50,415,969 (GRCm39) |
missense |
probably benign |
0.20 |
R8359:Fam170a
|
UTSW |
18 |
50,414,677 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fam170a
|
UTSW |
18 |
50,414,651 (GRCm39) |
missense |
possibly damaging |
0.60 |
|