Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
A |
G |
6: 91,922,441 (GRCm39) |
T35A |
|
Het |
Adamts16 |
A |
C |
13: 70,886,701 (GRCm39) |
S1030A |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,588,344 (GRCm39) |
V4414E |
possibly damaging |
Het |
Aff4 |
C |
T |
11: 53,300,175 (GRCm39) |
T1026I |
probably damaging |
Het |
Arfgef1 |
T |
C |
1: 10,243,145 (GRCm39) |
Y1065C |
probably damaging |
Het |
Arhgef3 |
G |
T |
14: 27,108,070 (GRCm39) |
D192Y |
probably damaging |
Het |
Arhgef3 |
G |
A |
14: 27,116,062 (GRCm39) |
R268Q |
probably damaging |
Het |
Atp6v0e |
T |
A |
17: 26,913,885 (GRCm39) |
|
probably null |
Het |
B3galt9 |
A |
G |
2: 34,728,257 (GRCm39) |
N19D |
probably damaging |
Het |
Cenpc1 |
A |
G |
5: 86,181,551 (GRCm39) |
Y605H |
probably benign |
Het |
Cftr |
T |
C |
6: 18,226,048 (GRCm39) |
V332A |
probably benign |
Het |
Csmd2 |
A |
G |
4: 128,091,118 (GRCm39) |
H219R |
|
Het |
Cyp4f17 |
T |
C |
17: 32,743,116 (GRCm39) |
V263A |
possibly damaging |
Het |
Dao |
AGG |
AG |
5: 114,153,270 (GRCm39) |
|
probably benign |
Het |
Entrep1 |
G |
T |
19: 23,962,091 (GRCm39) |
T304K |
probably damaging |
Het |
Evl |
C |
T |
12: 108,647,783 (GRCm39) |
R295* |
probably null |
Het |
Gstm4 |
A |
T |
3: 107,951,677 (GRCm39) |
M35K |
probably damaging |
Het |
Kcna2 |
A |
G |
3: 107,012,460 (GRCm39) |
Y347C |
possibly damaging |
Het |
Kcnh7 |
G |
A |
2: 62,566,444 (GRCm39) |
T829M |
probably damaging |
Het |
Kcnu1 |
T |
C |
8: 26,400,898 (GRCm39) |
V682A |
probably benign |
Het |
Kctd17 |
CAGCTGGAGGAGC |
CAGC |
15: 78,321,113 (GRCm39) |
|
probably benign |
Het |
Kera |
A |
G |
10: 97,444,821 (GRCm39) |
E60G |
possibly damaging |
Het |
Letm2 |
C |
T |
8: 26,083,766 (GRCm39) |
G155D |
probably damaging |
Het |
Lrfn4 |
G |
A |
19: 4,663,343 (GRCm39) |
A397V |
probably benign |
Het |
Lrp4 |
A |
G |
2: 91,324,424 (GRCm39) |
Q1253R |
possibly damaging |
Het |
Mob1a |
T |
A |
6: 83,315,287 (GRCm39) |
M145K |
probably benign |
Het |
Nab1 |
A |
G |
1: 52,529,295 (GRCm39) |
C201R |
probably damaging |
Het |
Nlrp9b |
A |
G |
7: 19,762,493 (GRCm39) |
E710G |
probably benign |
Het |
Oas2 |
A |
G |
5: 120,876,437 (GRCm39) |
V502A |
probably benign |
Het |
Or1e26 |
T |
C |
11: 73,480,154 (GRCm39) |
S137G |
probably benign |
Het |
Or52d3 |
T |
A |
7: 104,229,595 (GRCm39) |
C247* |
probably null |
Het |
Or52h7 |
A |
T |
7: 104,213,857 (GRCm39) |
H143L |
probably benign |
Het |
Parg |
A |
T |
14: 31,936,327 (GRCm39) |
H494L |
possibly damaging |
Het |
Phf20 |
T |
A |
2: 156,135,464 (GRCm39) |
D600E |
probably benign |
Het |
Ppef2 |
G |
A |
5: 92,397,022 (GRCm39) |
R118C |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 22,959,675 (GRCm39) |
N57K |
probably damaging |
Het |
Rrbp1 |
A |
T |
2: 143,832,081 (GRCm39) |
S29T |
probably damaging |
Het |
Sema3g |
C |
A |
14: 30,942,605 (GRCm39) |
R69S |
probably damaging |
Het |
Slc12a4 |
G |
A |
8: 106,678,237 (GRCm39) |
R319W |
possibly damaging |
Het |
Slc4a3 |
A |
G |
1: 75,528,007 (GRCm39) |
T419A |
probably benign |
Het |
Smc3 |
T |
C |
19: 53,611,649 (GRCm39) |
|
probably null |
Het |
Sntg1 |
C |
T |
1: 8,535,760 (GRCm39) |
W288* |
probably null |
Het |
Synpo2l |
G |
T |
14: 20,716,870 (GRCm39) |
|
probably null |
Het |
Tap1 |
A |
G |
17: 34,413,886 (GRCm39) |
I634V |
probably damaging |
Het |
Tmem25 |
A |
G |
9: 44,706,983 (GRCm39) |
S278P |
probably benign |
Het |
Togaram2 |
T |
C |
17: 72,024,428 (GRCm39) |
S871P |
probably benign |
Het |
Trim37 |
T |
C |
11: 87,040,179 (GRCm39) |
V225A |
possibly damaging |
Het |
Tubg1 |
G |
T |
11: 101,014,854 (GRCm39) |
A199S |
probably benign |
Het |
|
Other mutations in Csnk1g3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Csnk1g3
|
APN |
18 |
54,052,075 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02148:Csnk1g3
|
APN |
18 |
54,086,360 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02379:Csnk1g3
|
APN |
18 |
54,066,564 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02447:Csnk1g3
|
APN |
18 |
54,028,942 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03172:Csnk1g3
|
APN |
18 |
54,086,356 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0153:Csnk1g3
|
UTSW |
18 |
54,051,861 (GRCm39) |
splice site |
probably benign |
|
R0606:Csnk1g3
|
UTSW |
18 |
54,050,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R1399:Csnk1g3
|
UTSW |
18 |
54,028,982 (GRCm39) |
missense |
probably damaging |
0.97 |
R1435:Csnk1g3
|
UTSW |
18 |
54,039,746 (GRCm39) |
splice site |
probably null |
|
R4829:Csnk1g3
|
UTSW |
18 |
54,028,895 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5552:Csnk1g3
|
UTSW |
18 |
54,065,355 (GRCm39) |
missense |
probably benign |
0.04 |
R6305:Csnk1g3
|
UTSW |
18 |
54,065,384 (GRCm39) |
nonsense |
probably null |
|
R6556:Csnk1g3
|
UTSW |
18 |
54,063,354 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7324:Csnk1g3
|
UTSW |
18 |
54,052,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R7401:Csnk1g3
|
UTSW |
18 |
54,063,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R7545:Csnk1g3
|
UTSW |
18 |
54,028,897 (GRCm39) |
missense |
probably damaging |
0.97 |
R7846:Csnk1g3
|
UTSW |
18 |
54,081,177 (GRCm39) |
missense |
probably benign |
0.03 |
R8215:Csnk1g3
|
UTSW |
18 |
54,081,151 (GRCm39) |
missense |
probably benign |
0.04 |
R8390:Csnk1g3
|
UTSW |
18 |
54,081,150 (GRCm39) |
missense |
probably benign |
0.09 |
R8400:Csnk1g3
|
UTSW |
18 |
54,086,360 (GRCm39) |
missense |
probably benign |
0.11 |
|