Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abt1 |
T |
C |
13: 23,607,938 (GRCm39) |
E22G |
unknown |
Het |
Aoc1l2 |
T |
A |
6: 48,908,582 (GRCm39) |
D527E |
probably damaging |
Het |
Atp11b |
T |
G |
3: 35,885,612 (GRCm39) |
H668Q |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,938,715 (GRCm39) |
V2687D |
probably benign |
Het |
Cadm3 |
T |
C |
1: 173,168,675 (GRCm39) |
T298A |
possibly damaging |
Het |
Car12 |
G |
A |
9: 66,670,552 (GRCm39) |
A174T |
possibly damaging |
Het |
Ccdc180 |
T |
C |
4: 45,904,544 (GRCm39) |
L380P |
probably damaging |
Het |
Col7a1 |
A |
T |
9: 108,784,813 (GRCm39) |
R214W |
unknown |
Het |
Cyp2d26 |
T |
G |
15: 82,674,450 (GRCm39) |
R477S |
probably benign |
Het |
Dip2b |
T |
A |
15: 100,076,392 (GRCm39) |
F797I |
probably damaging |
Het |
Dot1l |
A |
T |
10: 80,616,728 (GRCm39) |
N63I |
probably damaging |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
Ints5 |
T |
C |
19: 8,874,357 (GRCm39) |
I772T |
probably benign |
Het |
Nosip |
T |
A |
7: 44,726,283 (GRCm39) |
I230N |
probably damaging |
Het |
Or2r3 |
A |
T |
6: 42,448,223 (GRCm39) |
D296E |
probably benign |
Het |
Or4d11 |
A |
T |
19: 12,013,461 (GRCm39) |
L215Q |
probably damaging |
Het |
Or5ac22 |
T |
A |
16: 59,135,473 (GRCm39) |
Q99L |
probably damaging |
Het |
Or6c210 |
G |
A |
10: 129,496,519 (GRCm39) |
M281I |
probably benign |
Het |
Orc5 |
A |
T |
5: 22,727,381 (GRCm39) |
|
probably benign |
Het |
Parp1 |
A |
G |
1: 180,425,907 (GRCm39) |
I879M |
probably damaging |
Het |
Pcdh18 |
A |
G |
3: 49,699,370 (GRCm39) |
S1031P |
probably benign |
Het |
Pdzd2 |
A |
G |
15: 12,371,725 (GRCm39) |
S2557P |
probably damaging |
Het |
Rccd1 |
T |
C |
7: 79,969,966 (GRCm39) |
|
probably benign |
Het |
Rsad1 |
A |
G |
11: 94,439,803 (GRCm39) |
|
probably null |
Het |
Samd9l |
A |
T |
6: 3,373,864 (GRCm39) |
C1132* |
probably null |
Het |
Sema6d |
A |
G |
2: 124,500,491 (GRCm39) |
|
probably benign |
Het |
Slc10a5 |
T |
C |
3: 10,400,580 (GRCm39) |
N27D |
probably damaging |
Het |
Slco1a5 |
C |
T |
6: 142,189,599 (GRCm39) |
M462I |
probably benign |
Het |
Tyw5 |
T |
C |
1: 57,440,628 (GRCm39) |
T45A |
probably damaging |
Het |
Usp21 |
T |
A |
1: 171,110,307 (GRCm39) |
Q489L |
possibly damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r20 |
A |
G |
6: 123,370,924 (GRCm39) |
S519P |
possibly damaging |
Het |
|
Other mutations in Dgkd |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01529:Dgkd
|
APN |
1 |
87,808,133 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01531:Dgkd
|
APN |
1 |
87,808,133 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01627:Dgkd
|
APN |
1 |
87,808,150 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01720:Dgkd
|
APN |
1 |
87,864,487 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01941:Dgkd
|
APN |
1 |
87,852,281 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01951:Dgkd
|
APN |
1 |
87,844,638 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02244:Dgkd
|
APN |
1 |
87,842,863 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02581:Dgkd
|
APN |
1 |
87,845,724 (GRCm39) |
splice site |
probably benign |
|
IGL02852:Dgkd
|
APN |
1 |
87,863,135 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02893:Dgkd
|
APN |
1 |
87,842,930 (GRCm39) |
splice site |
probably benign |
|
IGL03367:Dgkd
|
APN |
1 |
87,868,030 (GRCm39) |
critical splice donor site |
probably null |
|
R0014:Dgkd
|
UTSW |
1 |
87,809,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Dgkd
|
UTSW |
1 |
87,845,674 (GRCm39) |
missense |
probably benign |
0.02 |
R0219:Dgkd
|
UTSW |
1 |
87,865,996 (GRCm39) |
splice site |
probably benign |
|
R0496:Dgkd
|
UTSW |
1 |
87,864,622 (GRCm39) |
missense |
probably null |
0.83 |
R0559:Dgkd
|
UTSW |
1 |
87,842,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R0591:Dgkd
|
UTSW |
1 |
87,842,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R1270:Dgkd
|
UTSW |
1 |
87,861,847 (GRCm39) |
missense |
probably damaging |
0.96 |
R1599:Dgkd
|
UTSW |
1 |
87,809,608 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1658:Dgkd
|
UTSW |
1 |
87,853,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R1745:Dgkd
|
UTSW |
1 |
87,859,766 (GRCm39) |
critical splice donor site |
probably null |
|
R1959:Dgkd
|
UTSW |
1 |
87,857,549 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1960:Dgkd
|
UTSW |
1 |
87,857,549 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2044:Dgkd
|
UTSW |
1 |
87,855,413 (GRCm39) |
missense |
probably benign |
|
R2148:Dgkd
|
UTSW |
1 |
87,809,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R2232:Dgkd
|
UTSW |
1 |
87,857,464 (GRCm39) |
missense |
probably benign |
0.05 |
R2266:Dgkd
|
UTSW |
1 |
87,855,540 (GRCm39) |
unclassified |
probably benign |
|
R3774:Dgkd
|
UTSW |
1 |
87,864,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R4004:Dgkd
|
UTSW |
1 |
87,863,145 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4005:Dgkd
|
UTSW |
1 |
87,863,145 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4133:Dgkd
|
UTSW |
1 |
87,869,223 (GRCm39) |
critical splice donor site |
probably null |
|
R4235:Dgkd
|
UTSW |
1 |
87,859,704 (GRCm39) |
nonsense |
probably null |
|
R4644:Dgkd
|
UTSW |
1 |
87,864,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R4747:Dgkd
|
UTSW |
1 |
87,861,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Dgkd
|
UTSW |
1 |
87,844,560 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5334:Dgkd
|
UTSW |
1 |
87,865,989 (GRCm39) |
critical splice donor site |
probably null |
|
R5365:Dgkd
|
UTSW |
1 |
87,863,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R5495:Dgkd
|
UTSW |
1 |
87,854,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R5514:Dgkd
|
UTSW |
1 |
87,861,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R5729:Dgkd
|
UTSW |
1 |
87,864,054 (GRCm39) |
nonsense |
probably null |
|
R5766:Dgkd
|
UTSW |
1 |
87,808,171 (GRCm39) |
nonsense |
probably null |
|
R6133:Dgkd
|
UTSW |
1 |
87,865,962 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6137:Dgkd
|
UTSW |
1 |
87,864,103 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6198:Dgkd
|
UTSW |
1 |
87,851,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R6297:Dgkd
|
UTSW |
1 |
87,853,866 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6577:Dgkd
|
UTSW |
1 |
87,867,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R6846:Dgkd
|
UTSW |
1 |
87,853,413 (GRCm39) |
splice site |
probably null |
|
R6905:Dgkd
|
UTSW |
1 |
87,863,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R7369:Dgkd
|
UTSW |
1 |
87,849,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:Dgkd
|
UTSW |
1 |
87,854,671 (GRCm39) |
missense |
probably benign |
|
R7921:Dgkd
|
UTSW |
1 |
87,851,806 (GRCm39) |
missense |
probably damaging |
0.98 |
R8087:Dgkd
|
UTSW |
1 |
87,844,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R8119:Dgkd
|
UTSW |
1 |
87,845,689 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8731:Dgkd
|
UTSW |
1 |
87,844,535 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8813:Dgkd
|
UTSW |
1 |
87,843,266 (GRCm39) |
missense |
probably damaging |
0.99 |
R8849:Dgkd
|
UTSW |
1 |
87,846,365 (GRCm39) |
missense |
probably damaging |
0.99 |
R8906:Dgkd
|
UTSW |
1 |
87,869,157 (GRCm39) |
missense |
probably damaging |
0.97 |
R9496:Dgkd
|
UTSW |
1 |
87,857,464 (GRCm39) |
missense |
probably benign |
0.05 |
R9743:Dgkd
|
UTSW |
1 |
87,861,850 (GRCm39) |
missense |
|
|
Z1176:Dgkd
|
UTSW |
1 |
87,855,532 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Dgkd
|
UTSW |
1 |
87,844,608 (GRCm39) |
missense |
probably damaging |
0.99 |
|