Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
G |
A |
13: 77,408,116 (GRCm39) |
V148I |
probably benign |
Het |
Ahcyl2 |
T |
C |
6: 29,906,500 (GRCm39) |
|
probably benign |
Het |
Ahnak |
T |
C |
19: 8,983,872 (GRCm39) |
S1719P |
probably benign |
Het |
C2cd5 |
A |
G |
6: 143,025,609 (GRCm39) |
I196T |
possibly damaging |
Het |
Cdhr2 |
A |
G |
13: 54,874,474 (GRCm39) |
I849V |
probably benign |
Het |
Cpsf3 |
A |
G |
12: 21,345,089 (GRCm39) |
K134E |
possibly damaging |
Het |
Dnai1 |
A |
G |
4: 41,602,979 (GRCm39) |
T161A |
probably benign |
Het |
Igf2bp2 |
A |
G |
16: 21,886,891 (GRCm39) |
|
probably null |
Het |
Lcor |
T |
C |
19: 41,547,253 (GRCm39) |
V279A |
possibly damaging |
Het |
Myo9a |
C |
A |
9: 59,716,725 (GRCm39) |
T475K |
possibly damaging |
Het |
Nat8f4 |
A |
G |
6: 85,877,836 (GRCm39) |
|
probably benign |
Het |
Neto1 |
A |
G |
18: 86,516,714 (GRCm39) |
T344A |
probably benign |
Het |
Or6c203 |
A |
T |
10: 129,010,358 (GRCm39) |
D177E |
probably damaging |
Het |
Or7c19 |
A |
G |
8: 85,957,139 (GRCm39) |
N5S |
probably benign |
Het |
Or8k17 |
A |
T |
2: 86,066,804 (GRCm39) |
M118K |
probably damaging |
Het |
Pde8a |
A |
T |
7: 80,958,557 (GRCm39) |
I312F |
probably damaging |
Het |
Ppp3cb |
A |
G |
14: 20,581,793 (GRCm39) |
I74T |
probably damaging |
Het |
Prom1 |
T |
C |
5: 44,216,004 (GRCm39) |
|
probably benign |
Het |
Psg29 |
T |
C |
7: 16,942,719 (GRCm39) |
V240A |
probably benign |
Het |
Reep4 |
T |
C |
14: 70,785,675 (GRCm39) |
S238P |
probably damaging |
Het |
Stxbp2 |
A |
T |
8: 3,691,971 (GRCm39) |
I538F |
probably benign |
Het |
Tmprss5 |
T |
A |
9: 49,020,318 (GRCm39) |
N99K |
possibly damaging |
Het |
Tph1 |
G |
A |
7: 46,302,283 (GRCm39) |
T313M |
probably damaging |
Het |
Tprn |
T |
C |
2: 25,154,530 (GRCm39) |
S611P |
probably damaging |
Het |
Upp2 |
G |
T |
2: 58,645,435 (GRCm39) |
|
probably null |
Het |
Vezt |
C |
A |
10: 93,809,895 (GRCm39) |
A549S |
probably damaging |
Het |
Zfp786 |
A |
G |
6: 47,798,177 (GRCm39) |
Y254H |
probably benign |
Het |
|
Other mutations in Gm17093 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01401:Gm17093
|
APN |
14 |
44,758,984 (GRCm39) |
missense |
unknown |
|
IGL01431:Gm17093
|
APN |
14 |
44,759,122 (GRCm39) |
splice site |
probably benign |
|
IGL01911:Gm17093
|
APN |
14 |
44,758,277 (GRCm39) |
splice site |
probably benign |
|
IGL02324:Gm17093
|
APN |
14 |
44,755,807 (GRCm39) |
missense |
unknown |
|
IGL02418:Gm17093
|
APN |
14 |
44,758,185 (GRCm39) |
missense |
unknown |
|
R3419:Gm17093
|
UTSW |
14 |
44,759,047 (GRCm39) |
missense |
unknown |
|
R4838:Gm17093
|
UTSW |
14 |
44,755,805 (GRCm39) |
missense |
unknown |
|
R4994:Gm17093
|
UTSW |
14 |
44,756,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R5819:Gm17093
|
UTSW |
14 |
44,758,986 (GRCm39) |
missense |
unknown |
|
R8167:Gm17093
|
UTSW |
14 |
44,758,139 (GRCm39) |
missense |
|
|
R8962:Gm17093
|
UTSW |
14 |
44,758,149 (GRCm39) |
missense |
|
|
R9757:Gm17093
|
UTSW |
14 |
44,758,990 (GRCm39) |
missense |
|
|
|