Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap6 |
A |
G |
12: 53,188,925 (GRCm39) |
D2113G |
probably damaging |
Het |
Atf6b |
T |
A |
17: 34,868,111 (GRCm39) |
V125E |
probably damaging |
Het |
Cdan1 |
T |
A |
2: 120,556,466 (GRCm39) |
Y653F |
probably damaging |
Het |
Dnah2 |
G |
T |
11: 69,321,913 (GRCm39) |
N3802K |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,236,783 (GRCm39) |
I370V |
probably benign |
Het |
Dpp10 |
T |
C |
1: 123,262,099 (GRCm39) |
E761G |
probably damaging |
Het |
Dusp19 |
A |
G |
2: 80,447,825 (GRCm39) |
E33G |
probably damaging |
Het |
E2f7 |
T |
A |
10: 110,582,267 (GRCm39) |
D25E |
possibly damaging |
Het |
E2f8 |
T |
C |
7: 48,517,605 (GRCm39) |
T733A |
probably damaging |
Het |
Golga1 |
T |
C |
2: 38,953,294 (GRCm39) |
E32G |
probably damaging |
Het |
Grip1 |
T |
A |
10: 119,765,908 (GRCm39) |
V80E |
probably damaging |
Het |
Igsf6 |
T |
C |
7: 120,670,016 (GRCm39) |
Y42C |
probably damaging |
Het |
Katna1 |
T |
G |
10: 7,617,218 (GRCm39) |
M70R |
probably damaging |
Het |
Limk2 |
T |
C |
11: 3,309,052 (GRCm39) |
K102R |
probably benign |
Het |
Lypla1 |
T |
A |
1: 4,898,874 (GRCm39) |
|
probably null |
Het |
Or2z9 |
T |
A |
8: 72,854,356 (GRCm39) |
F251I |
probably damaging |
Het |
Or6c69b |
A |
G |
10: 129,627,188 (GRCm39) |
I90T |
probably damaging |
Het |
Pgap1 |
G |
A |
1: 54,560,470 (GRCm39) |
P444L |
probably damaging |
Het |
Pigr |
G |
A |
1: 130,776,795 (GRCm39) |
V657M |
probably damaging |
Het |
Plscr1 |
T |
A |
9: 92,148,803 (GRCm39) |
Y214* |
probably null |
Het |
Polq |
A |
C |
16: 36,855,212 (GRCm39) |
I436L |
probably benign |
Het |
Ppfia2 |
T |
A |
10: 106,671,909 (GRCm39) |
|
probably benign |
Het |
Serpina12 |
A |
G |
12: 104,004,381 (GRCm39) |
S84P |
probably damaging |
Het |
Slc30a6 |
T |
A |
17: 74,726,523 (GRCm39) |
|
probably benign |
Het |
Trim38 |
A |
G |
13: 23,975,410 (GRCm39) |
T450A |
possibly damaging |
Het |
Ubqlnl |
A |
T |
7: 103,799,496 (GRCm39) |
|
probably benign |
Het |
Vmn2r24 |
A |
G |
6: 123,764,445 (GRCm39) |
K441E |
probably benign |
Het |
Wnt8a |
A |
G |
18: 34,677,846 (GRCm39) |
T85A |
probably damaging |
Het |
|
Other mutations in Ces1d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01707:Ces1d
|
APN |
8 |
93,916,178 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL01753:Ces1d
|
APN |
8 |
93,919,438 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01918:Ces1d
|
APN |
8 |
93,904,703 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02730:Ces1d
|
APN |
8 |
93,912,644 (GRCm39) |
missense |
probably benign |
|
IGL02819:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL02824:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL02825:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL02858:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL02877:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL02946:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL02990:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL03024:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL03080:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL03081:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL03082:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL03096:Ces1d
|
APN |
8 |
93,904,670 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03165:Ces1d
|
APN |
8 |
93,916,147 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03233:Ces1d
|
APN |
8 |
93,921,707 (GRCm39) |
missense |
probably benign |
|
IGL03263:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL03310:Ces1d
|
APN |
8 |
93,901,816 (GRCm39) |
splice site |
probably benign |
|
IGL03338:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
IGL03357:Ces1d
|
APN |
8 |
93,896,346 (GRCm39) |
splice site |
probably null |
|
R0125:Ces1d
|
UTSW |
8 |
93,901,810 (GRCm39) |
splice site |
probably benign |
|
R0393:Ces1d
|
UTSW |
8 |
93,919,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R0483:Ces1d
|
UTSW |
8 |
93,924,307 (GRCm39) |
missense |
probably benign |
|
R0746:Ces1d
|
UTSW |
8 |
93,916,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Ces1d
|
UTSW |
8 |
93,921,649 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1470:Ces1d
|
UTSW |
8 |
93,921,649 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1607:Ces1d
|
UTSW |
8 |
93,912,746 (GRCm39) |
missense |
probably benign |
0.08 |
R1879:Ces1d
|
UTSW |
8 |
93,916,126 (GRCm39) |
missense |
probably benign |
0.35 |
R2881:Ces1d
|
UTSW |
8 |
93,921,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R3870:Ces1d
|
UTSW |
8 |
93,901,714 (GRCm39) |
missense |
probably benign |
0.15 |
R4004:Ces1d
|
UTSW |
8 |
93,904,720 (GRCm39) |
missense |
probably benign |
0.03 |
R4573:Ces1d
|
UTSW |
8 |
93,908,162 (GRCm39) |
missense |
probably benign |
0.00 |
R4647:Ces1d
|
UTSW |
8 |
93,893,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R4985:Ces1d
|
UTSW |
8 |
93,901,772 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5080:Ces1d
|
UTSW |
8 |
93,908,175 (GRCm39) |
missense |
probably benign |
0.02 |
R5209:Ces1d
|
UTSW |
8 |
93,901,816 (GRCm39) |
splice site |
probably benign |
|
R5351:Ces1d
|
UTSW |
8 |
93,904,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R5433:Ces1d
|
UTSW |
8 |
93,912,664 (GRCm39) |
missense |
probably benign |
0.02 |
R5614:Ces1d
|
UTSW |
8 |
93,902,832 (GRCm39) |
missense |
probably benign |
0.00 |
R5722:Ces1d
|
UTSW |
8 |
93,904,756 (GRCm39) |
missense |
probably benign |
0.01 |
R6257:Ces1d
|
UTSW |
8 |
93,893,025 (GRCm39) |
missense |
probably benign |
0.03 |
R7238:Ces1d
|
UTSW |
8 |
93,904,763 (GRCm39) |
missense |
probably benign |
0.01 |
R7410:Ces1d
|
UTSW |
8 |
93,919,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R7489:Ces1d
|
UTSW |
8 |
93,904,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R7563:Ces1d
|
UTSW |
8 |
93,904,667 (GRCm39) |
missense |
probably benign |
0.25 |
R7827:Ces1d
|
UTSW |
8 |
93,924,294 (GRCm39) |
critical splice donor site |
probably null |
|
R7853:Ces1d
|
UTSW |
8 |
93,901,695 (GRCm39) |
missense |
probably benign |
0.29 |
R7860:Ces1d
|
UTSW |
8 |
93,897,765 (GRCm39) |
missense |
probably benign |
0.08 |
R8202:Ces1d
|
UTSW |
8 |
93,919,495 (GRCm39) |
missense |
probably benign |
0.08 |
R8282:Ces1d
|
UTSW |
8 |
93,912,740 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8968:Ces1d
|
UTSW |
8 |
93,914,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R8981:Ces1d
|
UTSW |
8 |
93,919,457 (GRCm39) |
missense |
probably benign |
0.00 |
R9143:Ces1d
|
UTSW |
8 |
93,912,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R9378:Ces1d
|
UTSW |
8 |
93,912,724 (GRCm39) |
missense |
probably damaging |
0.96 |
RF014:Ces1d
|
UTSW |
8 |
93,902,793 (GRCm39) |
critical splice donor site |
probably null |
|
Z1088:Ces1d
|
UTSW |
8 |
93,901,736 (GRCm39) |
missense |
probably benign |
0.00 |
|