Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ak9 |
G |
A |
10: 41,259,496 (GRCm39) |
V843I |
|
Het |
Bbs12 |
T |
C |
3: 37,373,680 (GRCm39) |
C43R |
possibly damaging |
Het |
Brwd1 |
T |
C |
16: 95,825,028 (GRCm39) |
E1145G |
probably damaging |
Het |
Carmil2 |
A |
G |
8: 106,417,539 (GRCm39) |
N599S |
probably damaging |
Het |
Cd79b |
A |
G |
11: 106,203,457 (GRCm39) |
|
probably null |
Het |
Ces2c |
A |
G |
8: 105,580,249 (GRCm39) |
M489V |
probably benign |
Het |
Clip4 |
A |
G |
17: 72,106,068 (GRCm39) |
N84D |
probably benign |
Het |
Cramp1 |
T |
C |
17: 25,191,320 (GRCm39) |
D1047G |
possibly damaging |
Het |
Cyp2c69 |
C |
T |
19: 39,865,991 (GRCm39) |
V201M |
probably benign |
Het |
Dock2 |
A |
G |
11: 34,223,673 (GRCm39) |
S1154P |
possibly damaging |
Het |
Elk4 |
T |
G |
1: 131,945,881 (GRCm39) |
V253G |
probably benign |
Het |
Erbb4 |
T |
A |
1: 68,238,062 (GRCm39) |
H809L |
probably benign |
Het |
Ext1 |
A |
T |
15: 53,208,067 (GRCm39) |
D231E |
probably damaging |
Het |
Fam221b |
T |
C |
4: 43,665,574 (GRCm39) |
K295E |
probably benign |
Het |
Fbrsl1 |
A |
G |
5: 110,526,835 (GRCm39) |
F2L |
unknown |
Het |
Fnip2 |
C |
T |
3: 79,415,411 (GRCm39) |
R209H |
probably benign |
Het |
Gart |
C |
T |
16: 91,430,949 (GRCm39) |
G371D |
probably damaging |
Het |
Gata6 |
T |
A |
18: 11,064,706 (GRCm39) |
V506D |
possibly damaging |
Het |
Gba2 |
T |
C |
4: 43,568,716 (GRCm39) |
Y620C |
probably damaging |
Het |
Gprc6a |
T |
C |
10: 51,504,364 (GRCm39) |
N160S |
probably benign |
Het |
Gstm3 |
A |
G |
3: 107,875,493 (GRCm39) |
W46R |
probably damaging |
Het |
Hcn4 |
G |
A |
9: 58,751,319 (GRCm39) |
R315H |
unknown |
Het |
Hydin |
T |
C |
8: 111,217,398 (GRCm39) |
F1429L |
possibly damaging |
Het |
Iqgap3 |
C |
A |
3: 88,016,176 (GRCm39) |
F986L |
probably damaging |
Het |
Itgb1bp1 |
A |
G |
12: 21,326,890 (GRCm39) |
S28P |
unknown |
Het |
Krt10 |
A |
G |
11: 99,279,792 (GRCm39) |
F123L |
unknown |
Het |
Krt79 |
T |
G |
15: 101,839,196 (GRCm39) |
E424D |
probably benign |
Het |
Lingo4 |
C |
T |
3: 94,309,493 (GRCm39) |
R144* |
probably null |
Het |
Ltbr |
G |
A |
6: 125,284,348 (GRCm39) |
R365W |
probably damaging |
Het |
Nrsn1 |
C |
A |
13: 25,437,563 (GRCm39) |
V122L |
probably benign |
Het |
Or10h5 |
C |
A |
17: 33,434,688 (GRCm39) |
G210V |
possibly damaging |
Het |
Or2r2 |
T |
C |
6: 42,463,507 (GRCm39) |
M207V |
probably benign |
Het |
Or4d6 |
T |
A |
19: 12,086,056 (GRCm39) |
M59L |
probably benign |
Het |
Pcgf6 |
T |
C |
19: 47,023,073 (GRCm39) |
T353A |
probably damaging |
Het |
Pcsk2 |
T |
C |
2: 143,635,150 (GRCm39) |
Y342H |
probably damaging |
Het |
Pou2af1 |
A |
T |
9: 51,149,636 (GRCm39) |
N243Y |
possibly damaging |
Het |
Prkcz |
T |
C |
4: 155,377,659 (GRCm39) |
D197G |
probably benign |
Het |
Sec14l4 |
G |
A |
11: 3,989,982 (GRCm39) |
E94K |
probably benign |
Het |
Sik2 |
T |
C |
9: 50,807,139 (GRCm39) |
E757G |
probably damaging |
Het |
Sipa1l1 |
T |
A |
12: 82,463,763 (GRCm39) |
S1154T |
possibly damaging |
Het |
Speer1k |
A |
T |
5: 10,999,020 (GRCm39) |
T53S |
|
Het |
Ssb |
T |
C |
2: 69,697,865 (GRCm39) |
Y175H |
probably damaging |
Het |
St6galnac6 |
T |
C |
2: 32,502,261 (GRCm39) |
I50T |
probably benign |
Het |
Styk1 |
CTCTTCATGATTTTCTT |
CTCTT |
6: 131,278,612 (GRCm39) |
|
probably benign |
Het |
Tmcc1 |
G |
C |
6: 115,999,071 (GRCm39) |
R323G |
possibly damaging |
Het |
Unc13b |
C |
T |
4: 43,182,842 (GRCm39) |
R396* |
probably null |
Het |
Vezt |
A |
G |
10: 93,806,183 (GRCm39) |
S743P |
probably benign |
Het |
Vmn1r77 |
A |
C |
7: 11,775,659 (GRCm39) |
N145T |
probably damaging |
Het |
Vmn2r98 |
A |
C |
17: 19,285,665 (GRCm39) |
T162P |
probably benign |
Het |
|
Other mutations in C2cd4c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02660:C2cd4c
|
APN |
10 |
79,449,136 (GRCm39) |
missense |
probably benign |
|
IGL02950:C2cd4c
|
APN |
10 |
79,448,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R0400:C2cd4c
|
UTSW |
10 |
79,449,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R0925:C2cd4c
|
UTSW |
10 |
79,448,584 (GRCm39) |
missense |
probably benign |
|
R1428:C2cd4c
|
UTSW |
10 |
79,448,064 (GRCm39) |
missense |
probably damaging |
0.97 |
R2017:C2cd4c
|
UTSW |
10 |
79,448,823 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2111:C2cd4c
|
UTSW |
10 |
79,448,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R4951:C2cd4c
|
UTSW |
10 |
79,448,839 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4982:C2cd4c
|
UTSW |
10 |
79,449,075 (GRCm39) |
missense |
probably benign |
0.01 |
R5006:C2cd4c
|
UTSW |
10 |
79,448,341 (GRCm39) |
missense |
probably benign |
0.12 |
R5281:C2cd4c
|
UTSW |
10 |
79,448,878 (GRCm39) |
missense |
probably benign |
0.00 |
R5699:C2cd4c
|
UTSW |
10 |
79,448,385 (GRCm39) |
missense |
probably benign |
0.00 |
R5870:C2cd4c
|
UTSW |
10 |
79,448,043 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8221:C2cd4c
|
UTSW |
10 |
79,448,482 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:C2cd4c
|
UTSW |
10 |
79,448,299 (GRCm39) |
missense |
possibly damaging |
0.73 |
|