Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
T |
A |
5: 8,752,154 (GRCm39) |
I405N |
probably damaging |
Het |
Abhd17b |
T |
C |
19: 21,661,545 (GRCm39) |
L244P |
probably damaging |
Het |
Aebp2 |
T |
A |
6: 140,579,532 (GRCm39) |
C34* |
probably null |
Het |
Arhgap33 |
A |
G |
7: 30,227,726 (GRCm39) |
V491A |
probably damaging |
Het |
Cacul1 |
C |
T |
19: 60,551,619 (GRCm39) |
R201Q |
probably benign |
Het |
Cald1 |
T |
A |
6: 34,730,515 (GRCm39) |
N77K |
probably damaging |
Het |
Clcn6 |
A |
C |
4: 148,122,774 (GRCm39) |
|
probably benign |
Het |
Copb1 |
A |
T |
7: 113,846,035 (GRCm39) |
H178Q |
probably benign |
Het |
Dnah17 |
C |
T |
11: 117,977,771 (GRCm39) |
V1854I |
probably damaging |
Het |
Dnajc16 |
T |
G |
4: 141,491,994 (GRCm39) |
T610P |
possibly damaging |
Het |
Enpp1 |
T |
C |
10: 24,528,750 (GRCm39) |
N624S |
possibly damaging |
Het |
F2 |
CAGAAAG |
CAG |
2: 91,465,302 (GRCm39) |
|
probably benign |
Het |
Foxn1 |
T |
C |
11: 78,252,459 (GRCm39) |
T310A |
probably benign |
Het |
Galnt16 |
T |
A |
12: 80,628,073 (GRCm39) |
D256E |
possibly damaging |
Het |
Gbp11 |
T |
C |
5: 105,478,919 (GRCm39) |
D173G |
probably damaging |
Het |
Glmn |
A |
G |
5: 107,718,066 (GRCm39) |
S284P |
probably damaging |
Het |
Gm3985 |
A |
G |
8: 33,380,693 (GRCm39) |
|
noncoding transcript |
Het |
Hs3st6 |
A |
T |
17: 24,977,521 (GRCm39) |
M334L |
probably benign |
Het |
Idua |
T |
A |
5: 108,828,180 (GRCm39) |
D155E |
probably damaging |
Het |
Kdm6b |
T |
C |
11: 69,290,881 (GRCm39) |
|
probably benign |
Het |
Kiss1r |
T |
C |
10: 79,757,461 (GRCm39) |
F272L |
probably damaging |
Het |
Krt35 |
T |
C |
11: 99,985,343 (GRCm39) |
K233E |
probably damaging |
Het |
Krt36 |
C |
T |
11: 99,994,328 (GRCm39) |
V250M |
probably damaging |
Het |
Lhpp |
T |
C |
7: 132,307,361 (GRCm39) |
Y253H |
probably damaging |
Het |
Npas3 |
T |
A |
12: 53,547,897 (GRCm39) |
L51* |
probably null |
Het |
Or10ac1 |
T |
C |
6: 42,515,449 (GRCm39) |
H169R |
probably benign |
Het |
Or1j18 |
T |
A |
2: 36,624,510 (GRCm39) |
M59K |
possibly damaging |
Het |
Or4a74 |
T |
C |
2: 89,439,627 (GRCm39) |
Y273C |
probably damaging |
Het |
Or4c119 |
T |
C |
2: 88,987,451 (GRCm39) |
K23E |
probably benign |
Het |
Or56b2 |
T |
C |
7: 104,338,107 (GRCm39) |
M295T |
probably benign |
Het |
Pcdhb9 |
T |
G |
18: 37,534,186 (GRCm39) |
V60G |
probably benign |
Het |
Prkce |
T |
C |
17: 86,789,570 (GRCm39) |
V239A |
probably benign |
Het |
Ralgapa1 |
C |
T |
12: 55,822,937 (GRCm39) |
C293Y |
probably damaging |
Het |
Ralgapa1 |
C |
T |
12: 55,712,459 (GRCm39) |
R1804Q |
probably damaging |
Het |
Rnf26 |
C |
A |
9: 44,024,071 (GRCm39) |
|
probably null |
Het |
Safb2 |
T |
C |
17: 56,884,901 (GRCm39) |
D178G |
probably benign |
Het |
Scn9a |
C |
T |
2: 66,395,511 (GRCm39) |
V178M |
possibly damaging |
Het |
Serpinb9 |
G |
A |
13: 33,190,544 (GRCm39) |
G7R |
probably benign |
Het |
Setd2 |
C |
A |
9: 110,380,197 (GRCm39) |
D1337E |
probably benign |
Het |
Shprh |
T |
A |
10: 11,030,449 (GRCm39) |
M222K |
probably benign |
Het |
Slc25a40 |
T |
C |
5: 8,480,486 (GRCm39) |
Y79H |
probably damaging |
Het |
Slc41a2 |
A |
G |
10: 83,133,155 (GRCm39) |
M297T |
probably damaging |
Het |
Sparcl1 |
C |
T |
5: 104,233,629 (GRCm39) |
M573I |
probably damaging |
Het |
Spcs1 |
A |
G |
14: 30,722,570 (GRCm39) |
L83S |
probably benign |
Het |
Sult1c2 |
T |
C |
17: 54,276,743 (GRCm39) |
N106S |
probably benign |
Het |
Szt2 |
C |
T |
4: 118,244,178 (GRCm39) |
R1309Q |
possibly damaging |
Het |
Ube3c |
T |
A |
5: 29,840,709 (GRCm39) |
F695I |
probably damaging |
Het |
Uimc1 |
A |
G |
13: 55,223,330 (GRCm39) |
L314P |
probably damaging |
Het |
Usp17le |
C |
T |
7: 104,418,645 (GRCm39) |
E166K |
probably damaging |
Het |
Vmn2r92 |
G |
A |
17: 18,372,312 (GRCm39) |
D41N |
probably benign |
Het |
|
Other mutations in Sergef |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00331:Sergef
|
APN |
7 |
46,284,844 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00864:Sergef
|
APN |
7 |
46,165,087 (GRCm39) |
splice site |
probably null |
|
IGL01529:Sergef
|
APN |
7 |
46,092,942 (GRCm39) |
missense |
probably damaging |
1.00 |
G1patch:Sergef
|
UTSW |
7 |
46,282,091 (GRCm39) |
splice site |
probably null |
|
IGL03014:Sergef
|
UTSW |
7 |
46,240,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R0472:Sergef
|
UTSW |
7 |
46,283,170 (GRCm39) |
splice site |
probably benign |
|
R1604:Sergef
|
UTSW |
7 |
46,092,783 (GRCm39) |
missense |
probably benign |
0.00 |
R1892:Sergef
|
UTSW |
7 |
46,264,040 (GRCm39) |
critical splice donor site |
probably null |
|
R3955:Sergef
|
UTSW |
7 |
46,268,176 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4032:Sergef
|
UTSW |
7 |
46,092,726 (GRCm39) |
nonsense |
probably null |
|
R4953:Sergef
|
UTSW |
7 |
46,283,259 (GRCm39) |
missense |
probably benign |
0.01 |
R5533:Sergef
|
UTSW |
7 |
46,264,200 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5697:Sergef
|
UTSW |
7 |
46,288,683 (GRCm39) |
intron |
probably benign |
|
R5930:Sergef
|
UTSW |
7 |
46,092,888 (GRCm39) |
missense |
probably benign |
0.03 |
R6477:Sergef
|
UTSW |
7 |
46,283,250 (GRCm39) |
missense |
probably benign |
0.19 |
R6725:Sergef
|
UTSW |
7 |
46,282,091 (GRCm39) |
splice site |
probably null |
|
R7511:Sergef
|
UTSW |
7 |
46,264,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R8052:Sergef
|
UTSW |
7 |
46,264,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R9729:Sergef
|
UTSW |
7 |
46,284,913 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Sergef
|
UTSW |
7 |
46,289,041 (GRCm39) |
intron |
probably benign |
|
|