Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013D24Rik |
T |
C |
6: 124,333,907 (GRCm39) |
I24M |
probably benign |
Het |
Ano5 |
G |
A |
7: 51,220,071 (GRCm39) |
D390N |
probably damaging |
Het |
Atp2c2 |
A |
G |
8: 120,471,073 (GRCm39) |
Y407C |
probably damaging |
Het |
B430306N03Rik |
T |
C |
17: 48,631,223 (GRCm39) |
|
probably benign |
Het |
Cd44 |
A |
T |
2: 102,676,858 (GRCm39) |
M269K |
probably benign |
Het |
Cdin1 |
T |
C |
2: 115,469,547 (GRCm39) |
|
probably null |
Het |
Cpped1 |
G |
T |
16: 11,646,392 (GRCm39) |
P144Q |
probably damaging |
Het |
Epas1 |
C |
T |
17: 87,135,275 (GRCm39) |
T636M |
possibly damaging |
Het |
Hsd17b3 |
G |
T |
13: 64,236,865 (GRCm39) |
H26Q |
probably benign |
Het |
Itih1 |
A |
T |
14: 30,651,544 (GRCm39) |
C883S |
probably damaging |
Het |
Krt16 |
A |
T |
11: 100,137,162 (GRCm39) |
|
probably benign |
Het |
Lcn3 |
A |
T |
2: 25,656,172 (GRCm39) |
M76L |
probably benign |
Het |
Lin9 |
A |
T |
1: 180,478,399 (GRCm39) |
M53L |
probably benign |
Het |
Mast1 |
A |
G |
8: 85,645,384 (GRCm39) |
V687A |
possibly damaging |
Het |
Mmd2 |
C |
T |
5: 142,555,212 (GRCm39) |
|
probably benign |
Het |
Mroh2b |
T |
C |
15: 4,953,123 (GRCm39) |
L619S |
probably damaging |
Het |
Ngef |
T |
C |
1: 87,468,418 (GRCm39) |
T114A |
probably benign |
Het |
Nlrp12 |
T |
C |
7: 3,289,597 (GRCm39) |
D305G |
possibly damaging |
Het |
Nlrp1a |
A |
T |
11: 71,013,944 (GRCm39) |
F435L |
possibly damaging |
Het |
Nup188 |
A |
G |
2: 30,220,653 (GRCm39) |
I909V |
possibly damaging |
Het |
Osbpl3 |
A |
C |
6: 50,304,347 (GRCm39) |
|
probably benign |
Het |
P2ry2 |
G |
T |
7: 100,647,321 (GRCm39) |
P328H |
possibly damaging |
Het |
Prex2 |
A |
T |
1: 11,131,569 (GRCm39) |
N46I |
probably benign |
Het |
Prss42 |
T |
C |
9: 110,632,243 (GRCm39) |
F325L |
possibly damaging |
Het |
Reep5 |
A |
G |
18: 34,482,850 (GRCm39) |
F120L |
probably damaging |
Het |
Scg3 |
G |
T |
9: 75,590,939 (GRCm39) |
F23L |
probably damaging |
Het |
Scx |
A |
G |
15: 76,343,295 (GRCm39) |
D200G |
probably benign |
Het |
Setd5 |
C |
T |
6: 113,098,131 (GRCm39) |
|
probably benign |
Het |
Tcf4 |
T |
A |
18: 69,480,438 (GRCm39) |
S23R |
probably damaging |
Het |
Ttc4 |
A |
G |
4: 106,533,793 (GRCm39) |
|
probably null |
Het |
Tyro3 |
T |
A |
2: 119,643,071 (GRCm39) |
C627S |
probably benign |
Het |
Yipf2 |
T |
C |
9: 21,502,764 (GRCm39) |
N106S |
possibly damaging |
Het |
Zfp619 |
T |
C |
7: 39,186,334 (GRCm39) |
L788P |
probably benign |
Het |
Zfp831 |
G |
A |
2: 174,485,519 (GRCm39) |
V65I |
probably benign |
Het |
Zgpat |
T |
C |
2: 181,020,651 (GRCm39) |
S275P |
probably benign |
Het |
|
Other mutations in Ighv8-9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R2865:Ighv8-9
|
UTSW |
12 |
115,432,066 (GRCm39) |
missense |
probably benign |
0.02 |
R4787:Ighv8-9
|
UTSW |
12 |
115,432,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R7570:Ighv8-9
|
UTSW |
12 |
115,432,358 (GRCm39) |
missense |
probably benign |
0.13 |
R8166:Ighv8-9
|
UTSW |
12 |
115,432,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Ighv8-9
|
UTSW |
12 |
115,432,204 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9406:Ighv8-9
|
UTSW |
12 |
115,432,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R9783:Ighv8-9
|
UTSW |
12 |
115,431,994 (GRCm39) |
missense |
probably benign |
0.20 |
R9784:Ighv8-9
|
UTSW |
12 |
115,431,994 (GRCm39) |
missense |
probably benign |
0.20 |
|