Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam4 |
A |
G |
12: 81,468,261 (GRCm39) |
L120P |
probably damaging |
Het |
Asb6 |
A |
G |
2: 30,714,334 (GRCm39) |
S259P |
probably damaging |
Het |
Atp6v0a2 |
C |
A |
5: 124,767,259 (GRCm39) |
S7R |
possibly damaging |
Het |
Btbd16 |
C |
T |
7: 130,417,516 (GRCm39) |
R344C |
probably damaging |
Het |
Cacna1h |
G |
A |
17: 25,594,336 (GRCm39) |
A2274V |
probably benign |
Het |
Caml |
A |
C |
13: 55,771,030 (GRCm39) |
N43H |
probably damaging |
Het |
Ccar2 |
A |
G |
14: 70,379,445 (GRCm39) |
S518P |
probably damaging |
Het |
Cdkl3 |
A |
G |
11: 51,924,349 (GRCm39) |
I546V |
probably null |
Het |
Chac1 |
C |
T |
2: 119,182,854 (GRCm39) |
T84I |
probably damaging |
Het |
Col6a6 |
T |
C |
9: 105,644,686 (GRCm39) |
T1201A |
probably benign |
Het |
Csf1 |
T |
C |
3: 107,661,158 (GRCm39) |
T120A |
possibly damaging |
Het |
Ctsj |
T |
A |
13: 61,151,634 (GRCm39) |
I95F |
probably benign |
Het |
Cyp4f17 |
C |
T |
17: 32,743,880 (GRCm39) |
R353C |
probably benign |
Het |
Depdc1a |
A |
G |
3: 159,232,168 (GRCm39) |
M640V |
possibly damaging |
Het |
Dgkq |
A |
G |
5: 108,798,469 (GRCm39) |
V633A |
probably damaging |
Het |
Fdft1 |
A |
T |
14: 63,415,189 (GRCm39) |
Y14* |
probably null |
Het |
Fktn |
G |
A |
4: 53,734,854 (GRCm39) |
G125D |
probably benign |
Het |
Ftdc1 |
T |
C |
16: 58,434,234 (GRCm39) |
D161G |
probably benign |
Het |
Gfm2 |
T |
A |
13: 97,289,752 (GRCm39) |
V179E |
probably damaging |
Het |
Gpr12 |
A |
G |
5: 146,520,299 (GRCm39) |
F208L |
probably benign |
Het |
Greb1 |
A |
G |
12: 16,790,037 (GRCm39) |
S4P |
probably damaging |
Het |
Hlcs |
A |
T |
16: 93,932,672 (GRCm39) |
I717N |
probably damaging |
Het |
Hormad1 |
G |
A |
3: 95,483,622 (GRCm39) |
A145T |
probably benign |
Het |
Kcmf1 |
A |
T |
6: 72,838,826 (GRCm39) |
C33* |
probably null |
Het |
Kif13a |
A |
T |
13: 46,962,472 (GRCm39) |
S561T |
probably benign |
Het |
Klhl20 |
G |
T |
1: 160,921,269 (GRCm39) |
P571Q |
probably benign |
Het |
Kpna6 |
A |
T |
4: 129,547,635 (GRCm39) |
M304K |
probably benign |
Het |
Krt75 |
T |
C |
15: 101,476,729 (GRCm39) |
K387E |
probably damaging |
Het |
Lum |
A |
T |
10: 97,404,752 (GRCm39) |
K216* |
probably null |
Het |
Meioc |
A |
G |
11: 102,565,779 (GRCm39) |
N409S |
probably benign |
Het |
Mrpl20 |
T |
C |
4: 155,888,402 (GRCm39) |
|
probably null |
Het |
Naa16 |
A |
T |
14: 79,593,943 (GRCm39) |
I374N |
probably benign |
Het |
Nbea |
A |
G |
3: 55,943,319 (GRCm39) |
I652T |
possibly damaging |
Het |
Nhsl1 |
G |
A |
10: 18,194,898 (GRCm39) |
G56R |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,973,650 (GRCm39) |
I1894V |
probably benign |
Het |
Olig2 |
A |
C |
16: 91,023,774 (GRCm39) |
T163P |
probably damaging |
Het |
Or13c7c |
A |
G |
4: 43,835,765 (GRCm39) |
S242P |
probably benign |
Het |
Or4g7 |
T |
C |
2: 111,309,684 (GRCm39) |
I185T |
probably benign |
Het |
Or5p81 |
T |
A |
7: 108,266,977 (GRCm39) |
L118Q |
probably damaging |
Het |
Or7e168 |
T |
A |
9: 19,720,529 (GRCm39) |
V305D |
possibly damaging |
Het |
Parp4 |
G |
A |
14: 56,878,775 (GRCm39) |
|
probably null |
Het |
Pcdhb2 |
T |
C |
18: 37,429,551 (GRCm39) |
I508T |
probably damaging |
Het |
Pcdhga8 |
T |
C |
18: 37,859,787 (GRCm39) |
F281S |
probably damaging |
Het |
Pom121l12 |
T |
A |
11: 14,549,516 (GRCm39) |
M74K |
possibly damaging |
Het |
Pramel39-ps |
G |
T |
5: 94,451,001 (GRCm39) |
P375H |
probably damaging |
Het |
Prpf8 |
T |
C |
11: 75,381,156 (GRCm39) |
Y219H |
possibly damaging |
Het |
Rhag |
T |
C |
17: 41,142,548 (GRCm39) |
V251A |
possibly damaging |
Het |
Rrs1 |
A |
G |
1: 9,616,845 (GRCm39) |
*366W |
probably null |
Het |
Sgpp2 |
A |
G |
1: 78,367,143 (GRCm39) |
D92G |
probably damaging |
Het |
Slc44a3 |
C |
A |
3: 121,325,908 (GRCm39) |
|
probably benign |
Het |
Taar7e |
T |
A |
10: 23,913,949 (GRCm39) |
Y146* |
probably null |
Het |
Tet2 |
G |
T |
3: 133,192,903 (GRCm39) |
N510K |
possibly damaging |
Het |
Tgfbr3 |
T |
C |
5: 107,257,550 (GRCm39) |
I836M |
unknown |
Het |
Thada |
A |
G |
17: 84,499,410 (GRCm39) |
V1929A |
probably benign |
Het |
Tram1l1 |
A |
T |
3: 124,115,899 (GRCm39) |
D353V |
probably damaging |
Het |
Trf |
T |
A |
9: 103,094,734 (GRCm39) |
|
probably null |
Het |
Trim15 |
A |
T |
17: 37,177,942 (GRCm39) |
C18S |
probably damaging |
Het |
Vmn1r62 |
T |
C |
7: 5,678,952 (GRCm39) |
I211T |
probably damaging |
Het |
Zdhhc17 |
A |
G |
10: 110,783,165 (GRCm39) |
V501A |
probably benign |
Het |
Zfp563 |
A |
G |
17: 33,324,428 (GRCm39) |
E341G |
probably benign |
Het |
|
Other mutations in Smg8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00765:Smg8
|
APN |
11 |
86,968,867 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01591:Smg8
|
APN |
11 |
86,975,979 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01844:Smg8
|
APN |
11 |
86,971,102 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02634:Smg8
|
APN |
11 |
86,977,498 (GRCm39) |
missense |
probably benign |
|
IGL03170:Smg8
|
APN |
11 |
86,977,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03206:Smg8
|
APN |
11 |
86,976,814 (GRCm39) |
splice site |
probably null |
|
R0218:Smg8
|
UTSW |
11 |
86,976,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R0378:Smg8
|
UTSW |
11 |
86,971,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R0497:Smg8
|
UTSW |
11 |
86,976,910 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0522:Smg8
|
UTSW |
11 |
86,977,288 (GRCm39) |
missense |
probably benign |
|
R0546:Smg8
|
UTSW |
11 |
86,974,439 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0634:Smg8
|
UTSW |
11 |
86,976,934 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1245:Smg8
|
UTSW |
11 |
86,974,436 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1710:Smg8
|
UTSW |
11 |
86,977,113 (GRCm39) |
missense |
probably damaging |
0.98 |
R1726:Smg8
|
UTSW |
11 |
86,971,439 (GRCm39) |
nonsense |
probably null |
|
R1747:Smg8
|
UTSW |
11 |
86,976,129 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1748:Smg8
|
UTSW |
11 |
86,976,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R1909:Smg8
|
UTSW |
11 |
86,971,439 (GRCm39) |
nonsense |
probably null |
|
R1981:Smg8
|
UTSW |
11 |
86,976,157 (GRCm39) |
missense |
probably benign |
0.00 |
R2356:Smg8
|
UTSW |
11 |
86,976,554 (GRCm39) |
missense |
probably benign |
0.00 |
R4459:Smg8
|
UTSW |
11 |
86,976,396 (GRCm39) |
missense |
probably benign |
0.09 |
R4724:Smg8
|
UTSW |
11 |
86,977,047 (GRCm39) |
missense |
probably benign |
0.39 |
R4914:Smg8
|
UTSW |
11 |
86,971,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R5023:Smg8
|
UTSW |
11 |
86,976,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R5284:Smg8
|
UTSW |
11 |
86,971,137 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5368:Smg8
|
UTSW |
11 |
86,971,086 (GRCm39) |
missense |
probably benign |
0.21 |
R5534:Smg8
|
UTSW |
11 |
86,976,296 (GRCm39) |
missense |
probably benign |
0.06 |
R5689:Smg8
|
UTSW |
11 |
86,975,949 (GRCm39) |
missense |
probably damaging |
0.98 |
R6651:Smg8
|
UTSW |
11 |
86,977,372 (GRCm39) |
missense |
probably benign |
0.30 |
R6896:Smg8
|
UTSW |
11 |
86,968,787 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7030:Smg8
|
UTSW |
11 |
86,975,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R7317:Smg8
|
UTSW |
11 |
86,976,391 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8154:Smg8
|
UTSW |
11 |
86,976,063 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8362:Smg8
|
UTSW |
11 |
86,968,881 (GRCm39) |
nonsense |
probably null |
|
R8781:Smg8
|
UTSW |
11 |
86,971,147 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9295:Smg8
|
UTSW |
11 |
86,968,789 (GRCm39) |
missense |
probably benign |
0.00 |
X0028:Smg8
|
UTSW |
11 |
86,976,948 (GRCm39) |
missense |
probably damaging |
1.00 |
|