Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430550D23Rik |
A |
T |
2: 155,845,787 (GRCm39) |
H23Q |
unknown |
Het |
9530068E07Rik |
A |
T |
11: 52,297,821 (GRCm39) |
K233I |
probably damaging |
Het |
Aldh1l2 |
T |
C |
10: 83,350,408 (GRCm39) |
M320V |
possibly damaging |
Het |
C2cd3 |
A |
G |
7: 100,079,310 (GRCm39) |
N838S |
|
Het |
Cacna1s |
T |
C |
1: 135,998,759 (GRCm39) |
F218S |
probably damaging |
Het |
Carmil3 |
G |
T |
14: 55,728,590 (GRCm39) |
|
probably benign |
Het |
Cd300a |
A |
T |
11: 114,784,153 (GRCm39) |
T54S |
probably benign |
Het |
Celf3 |
G |
A |
3: 94,387,637 (GRCm39) |
E70K |
probably damaging |
Het |
Celsr1 |
A |
C |
15: 85,914,715 (GRCm39) |
M1086R |
probably benign |
Het |
Chrdl2 |
G |
A |
7: 99,678,414 (GRCm39) |
V329I |
probably benign |
Het |
Ctc1 |
T |
A |
11: 68,925,568 (GRCm39) |
L1035Q |
probably benign |
Het |
Dbi |
A |
G |
1: 120,047,623 (GRCm39) |
|
probably null |
Het |
Dock3 |
A |
G |
9: 106,882,568 (GRCm39) |
I405T |
probably benign |
Het |
Dpp4 |
A |
T |
2: 62,217,421 (GRCm39) |
W59R |
probably benign |
Het |
Dsg3 |
T |
A |
18: 20,672,840 (GRCm39) |
I837N |
probably damaging |
Het |
Fbxw15 |
A |
G |
9: 109,387,308 (GRCm39) |
V229A |
probably benign |
Het |
Fermt3 |
T |
C |
19: 6,980,211 (GRCm39) |
T395A |
probably benign |
Het |
Focad |
A |
T |
4: 88,147,572 (GRCm39) |
I404F |
probably benign |
Het |
Gm8104 |
T |
C |
14: 42,959,068 (GRCm39) |
I86T |
probably damaging |
Het |
Gm9857 |
A |
C |
3: 108,847,478 (GRCm39) |
L95R |
unknown |
Het |
Hoxa1 |
A |
T |
6: 52,133,929 (GRCm39) |
S266T |
probably benign |
Het |
Kif19b |
A |
G |
5: 140,480,806 (GRCm39) |
R979G |
possibly damaging |
Het |
Leng8 |
T |
A |
7: 4,147,932 (GRCm39) |
Y625* |
probably null |
Het |
Mast3 |
A |
G |
8: 71,237,503 (GRCm39) |
V557A |
probably damaging |
Het |
Morc1 |
T |
C |
16: 48,442,953 (GRCm39) |
F813L |
probably benign |
Het |
Ntf3 |
T |
A |
6: 126,078,961 (GRCm39) |
I182F |
probably damaging |
Het |
Nup153 |
G |
T |
13: 46,870,642 (GRCm39) |
A91E |
probably benign |
Het |
Or13l2 |
G |
C |
3: 97,317,971 (GRCm39) |
N175K |
probably damaging |
Het |
Or52h1 |
A |
T |
7: 103,828,978 (GRCm39) |
D212E |
probably damaging |
Het |
Pamr1 |
G |
A |
2: 102,417,049 (GRCm39) |
W120* |
probably null |
Het |
Pcsk1 |
A |
G |
13: 75,274,079 (GRCm39) |
N436S |
probably damaging |
Het |
Pde4dip |
T |
C |
3: 97,622,857 (GRCm39) |
K1451E |
probably benign |
Het |
Pebp4 |
G |
A |
14: 70,285,864 (GRCm39) |
V176I |
possibly damaging |
Het |
Phgdh |
G |
A |
3: 98,247,138 (GRCm39) |
A4V |
probably benign |
Het |
Pik3c2g |
T |
C |
6: 139,610,791 (GRCm39) |
|
probably null |
Het |
Ppic |
T |
C |
18: 53,544,139 (GRCm39) |
Y82C |
probably damaging |
Het |
Ppip5k2 |
A |
G |
1: 97,686,941 (GRCm39) |
V94A |
possibly damaging |
Het |
Ppp1r9b |
T |
C |
11: 94,895,424 (GRCm39) |
V704A |
probably benign |
Het |
Pramel6 |
G |
T |
2: 87,340,856 (GRCm39) |
R396L |
not run |
Het |
Prss48 |
A |
T |
3: 85,904,528 (GRCm39) |
D223E |
probably damaging |
Het |
Psd3 |
T |
C |
8: 68,574,149 (GRCm39) |
K11E |
probably benign |
Het |
Rabgap1l |
T |
C |
1: 160,169,608 (GRCm39) |
K780E |
probably damaging |
Het |
Retreg1 |
A |
T |
15: 25,972,029 (GRCm39) |
D323V |
probably damaging |
Het |
Samd11 |
A |
T |
4: 156,340,067 (GRCm39) |
|
probably null |
Het |
Sec14l3 |
T |
A |
11: 4,020,127 (GRCm39) |
F188Y |
probably benign |
Het |
Serpina5 |
A |
T |
12: 104,069,639 (GRCm39) |
T284S |
possibly damaging |
Het |
Setx |
A |
G |
2: 29,020,313 (GRCm39) |
D100G |
probably benign |
Het |
Sis |
A |
T |
3: 72,832,404 (GRCm39) |
V1035D |
probably damaging |
Het |
Slco4a1 |
A |
G |
2: 180,113,930 (GRCm39) |
I456V |
probably benign |
Het |
Snx14 |
A |
T |
9: 88,286,369 (GRCm39) |
C393S |
possibly damaging |
Het |
Stil |
T |
C |
4: 114,871,423 (GRCm39) |
|
probably null |
Het |
Sult6b1 |
A |
G |
17: 79,202,059 (GRCm39) |
S148P |
probably damaging |
Het |
Sycp2 |
G |
T |
2: 178,045,597 (GRCm39) |
|
probably null |
Het |
Tesmin |
T |
C |
19: 3,447,042 (GRCm39) |
I273T |
probably benign |
Het |
Tmem39a |
T |
A |
16: 38,406,592 (GRCm39) |
Y310N |
probably damaging |
Het |
Trp53bp1 |
A |
T |
2: 121,041,781 (GRCm39) |
D1258E |
probably damaging |
Het |
Ttc12 |
A |
C |
9: 49,349,687 (GRCm39) |
D703E |
probably benign |
Het |
Unc13c |
TATAA |
TATAATAA |
9: 73,840,810 (GRCm39) |
|
probably benign |
Het |
Unc13c |
ATA |
ATAGTA |
9: 73,840,811 (GRCm39) |
|
probably benign |
Het |
Usp18 |
T |
C |
6: 121,230,808 (GRCm39) |
I79T |
possibly damaging |
Het |
Usp9y |
A |
T |
Y: 1,333,656 (GRCm39) |
D1596E |
possibly damaging |
Het |
Vmn2r109 |
A |
T |
17: 20,761,536 (GRCm39) |
V607E |
probably damaging |
Het |
Vwa8 |
G |
A |
14: 79,275,641 (GRCm39) |
R808K |
probably null |
Het |
Zfp248 |
A |
G |
6: 118,406,618 (GRCm39) |
Y324H |
probably damaging |
Het |
Zfp513 |
G |
A |
5: 31,357,132 (GRCm39) |
P387S |
possibly damaging |
Het |
|
Other mutations in Ces2f |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00160:Ces2f
|
APN |
8 |
105,676,604 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00160:Ces2f
|
APN |
8 |
105,676,605 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01680:Ces2f
|
APN |
8 |
105,680,705 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01683:Ces2f
|
APN |
8 |
105,679,733 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02685:Ces2f
|
APN |
8 |
105,679,730 (GRCm39) |
nonsense |
probably null |
|
R0545:Ces2f
|
UTSW |
8 |
105,676,668 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0707:Ces2f
|
UTSW |
8 |
105,677,618 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1170:Ces2f
|
UTSW |
8 |
105,680,178 (GRCm39) |
missense |
probably damaging |
0.99 |
R1476:Ces2f
|
UTSW |
8 |
105,679,134 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4105:Ces2f
|
UTSW |
8 |
105,677,824 (GRCm39) |
splice site |
probably null |
|
R4394:Ces2f
|
UTSW |
8 |
105,677,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R4436:Ces2f
|
UTSW |
8 |
105,679,788 (GRCm39) |
missense |
probably benign |
0.00 |
R4601:Ces2f
|
UTSW |
8 |
105,676,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R4986:Ces2f
|
UTSW |
8 |
105,678,657 (GRCm39) |
missense |
probably benign |
0.39 |
R5502:Ces2f
|
UTSW |
8 |
105,679,155 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6610:Ces2f
|
UTSW |
8 |
105,676,738 (GRCm39) |
critical splice donor site |
probably null |
|
R7078:Ces2f
|
UTSW |
8 |
105,681,284 (GRCm39) |
missense |
probably damaging |
0.98 |
R7480:Ces2f
|
UTSW |
8 |
105,681,338 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7497:Ces2f
|
UTSW |
8 |
105,681,330 (GRCm39) |
missense |
probably benign |
0.00 |
R8403:Ces2f
|
UTSW |
8 |
105,674,808 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8558:Ces2f
|
UTSW |
8 |
105,679,758 (GRCm39) |
nonsense |
probably null |
|
R8826:Ces2f
|
UTSW |
8 |
105,679,734 (GRCm39) |
missense |
probably benign |
0.39 |
R8869:Ces2f
|
UTSW |
8 |
105,676,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R8937:Ces2f
|
UTSW |
8 |
105,677,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R8982:Ces2f
|
UTSW |
8 |
105,679,667 (GRCm39) |
missense |
probably benign |
0.04 |
R9000:Ces2f
|
UTSW |
8 |
105,677,661 (GRCm39) |
missense |
probably benign |
0.01 |
R9057:Ces2f
|
UTSW |
8 |
105,674,744 (GRCm39) |
missense |
probably benign |
0.21 |
R9505:Ces2f
|
UTSW |
8 |
105,676,669 (GRCm39) |
missense |
probably benign |
0.10 |
R9723:Ces2f
|
UTSW |
8 |
105,677,463 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9765:Ces2f
|
UTSW |
8 |
105,676,678 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ces2f
|
UTSW |
8 |
105,674,867 (GRCm39) |
missense |
probably damaging |
1.00 |
|