Other mutations in this stock |
Total: 16 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cep162 |
T |
C |
9: 87,103,143 (GRCm39) |
|
probably benign |
Het |
Dusp19 |
G |
A |
2: 80,461,126 (GRCm39) |
|
probably null |
Het |
Eif4g1 |
C |
A |
16: 20,505,504 (GRCm39) |
|
probably benign |
Het |
Farp1 |
T |
G |
14: 121,474,561 (GRCm39) |
I258S |
probably damaging |
Het |
Galnt18 |
T |
A |
7: 111,071,202 (GRCm39) |
Q589L |
probably damaging |
Het |
Gimap7 |
T |
A |
6: 48,700,667 (GRCm39) |
C84* |
probably null |
Het |
Il12rb2 |
T |
C |
6: 67,334,676 (GRCm39) |
T168A |
probably damaging |
Het |
Krba1 |
T |
C |
6: 48,383,252 (GRCm39) |
L216S |
possibly damaging |
Het |
Mki67 |
T |
C |
7: 135,297,424 (GRCm39) |
K2537E |
probably damaging |
Het |
Myo6 |
G |
T |
9: 80,149,555 (GRCm39) |
|
probably benign |
Het |
Nbea |
T |
A |
3: 55,989,869 (GRCm39) |
N329I |
probably damaging |
Het |
Ndufb11 |
T |
A |
X: 20,483,339 (GRCm39) |
Q54L |
possibly damaging |
Het |
Nudt1 |
T |
C |
5: 140,323,465 (GRCm39) |
F139S |
probably damaging |
Het |
Rgn |
A |
T |
X: 20,423,756 (GRCm39) |
M118L |
probably benign |
Het |
Syt12 |
C |
T |
19: 4,497,873 (GRCm39) |
V370M |
probably damaging |
Het |
Syt14 |
A |
T |
1: 192,612,792 (GRCm39) |
N669K |
possibly damaging |
Het |
|
Other mutations in Ces4a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01574:Ces4a
|
APN |
8 |
105,871,859 (GRCm39) |
splice site |
probably benign |
|
IGL01655:Ces4a
|
APN |
8 |
105,873,806 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03092:Ces4a
|
APN |
8 |
105,874,836 (GRCm39) |
splice site |
probably benign |
|
IGL03151:Ces4a
|
APN |
8 |
105,874,829 (GRCm39) |
critical splice donor site |
probably null |
|
F6893:Ces4a
|
UTSW |
8 |
105,873,859 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0266:Ces4a
|
UTSW |
8 |
105,868,598 (GRCm39) |
missense |
probably benign |
|
R0659:Ces4a
|
UTSW |
8 |
105,871,554 (GRCm39) |
splice site |
probably benign |
|
R1239:Ces4a
|
UTSW |
8 |
105,876,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Ces4a
|
UTSW |
8 |
105,864,667 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1467:Ces4a
|
UTSW |
8 |
105,864,667 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1505:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1509:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1598:Ces4a
|
UTSW |
8 |
105,869,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R1734:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1736:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1737:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1738:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1744:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1789:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1951:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1953:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R2126:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R2202:Ces4a
|
UTSW |
8 |
105,872,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R4512:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R4865:Ces4a
|
UTSW |
8 |
105,873,790 (GRCm39) |
missense |
probably benign |
0.05 |
R4934:Ces4a
|
UTSW |
8 |
105,864,613 (GRCm39) |
missense |
probably benign |
0.30 |
R4936:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R5255:Ces4a
|
UTSW |
8 |
105,869,121 (GRCm39) |
missense |
probably benign |
0.00 |
R5342:Ces4a
|
UTSW |
8 |
105,872,775 (GRCm39) |
missense |
probably benign |
0.07 |
R5647:Ces4a
|
UTSW |
8 |
105,872,712 (GRCm39) |
missense |
probably benign |
0.10 |
R6062:Ces4a
|
UTSW |
8 |
105,864,806 (GRCm39) |
critical splice donor site |
probably null |
|
R6490:Ces4a
|
UTSW |
8 |
105,876,090 (GRCm39) |
missense |
probably benign |
0.09 |
R6606:Ces4a
|
UTSW |
8 |
105,876,010 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6876:Ces4a
|
UTSW |
8 |
105,871,624 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6901:Ces4a
|
UTSW |
8 |
105,873,330 (GRCm39) |
missense |
probably benign |
|
R7519:Ces4a
|
UTSW |
8 |
105,871,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R7682:Ces4a
|
UTSW |
8 |
105,873,297 (GRCm39) |
missense |
probably benign |
0.00 |
R8171:Ces4a
|
UTSW |
8 |
105,873,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R8329:Ces4a
|
UTSW |
8 |
105,874,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R8833:Ces4a
|
UTSW |
8 |
105,858,614 (GRCm39) |
missense |
probably benign |
0.00 |
R9168:Ces4a
|
UTSW |
8 |
105,876,050 (GRCm39) |
missense |
probably benign |
0.00 |
R9557:Ces4a
|
UTSW |
8 |
105,869,527 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9758:Ces4a
|
UTSW |
8 |
105,869,054 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1176:Ces4a
|
UTSW |
8 |
105,858,609 (GRCm39) |
missense |
probably benign |
0.00 |
|