Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
C |
T |
11: 109,853,406 (GRCm39) |
|
probably null |
Het |
Ank3 |
T |
C |
10: 69,840,810 (GRCm39) |
S1937P |
possibly damaging |
Het |
Atg5 |
T |
A |
10: 44,162,115 (GRCm39) |
D10E |
probably benign |
Het |
Car12 |
A |
G |
9: 66,654,879 (GRCm39) |
D103G |
probably benign |
Het |
Cpa3 |
A |
G |
3: 20,276,316 (GRCm39) |
Y306H |
probably damaging |
Het |
Cyp2c40 |
A |
G |
19: 39,796,066 (GRCm39) |
V104A |
probably damaging |
Het |
Cyp2c66 |
A |
T |
19: 39,165,078 (GRCm39) |
H353L |
probably damaging |
Het |
Cyp2d22 |
A |
G |
15: 82,256,021 (GRCm39) |
|
probably null |
Het |
Exph5 |
A |
G |
9: 53,287,776 (GRCm39) |
E1619G |
possibly damaging |
Het |
Frmd5 |
T |
A |
2: 121,378,060 (GRCm39) |
T435S |
unknown |
Het |
Gm3371 |
T |
C |
14: 44,641,181 (GRCm39) |
R128G |
|
Het |
Gper1 |
A |
G |
5: 139,412,030 (GRCm39) |
D125G |
probably benign |
Het |
Il17re |
C |
A |
6: 113,443,280 (GRCm39) |
S340* |
probably null |
Het |
Kazald1 |
T |
A |
19: 45,065,278 (GRCm39) |
L53Q |
probably damaging |
Het |
Kdm3b |
A |
T |
18: 34,967,388 (GRCm39) |
H1731L |
probably damaging |
Het |
Kif20a |
T |
C |
18: 34,765,030 (GRCm39) |
S755P |
probably damaging |
Het |
Lrch1 |
T |
C |
14: 75,032,772 (GRCm39) |
N526S |
probably benign |
Het |
Map3k8 |
T |
C |
18: 4,334,064 (GRCm39) |
I343V |
probably damaging |
Het |
Nabp1 |
A |
T |
1: 51,511,498 (GRCm39) |
F140L |
probably benign |
Het |
Ncor1 |
A |
G |
11: 62,224,681 (GRCm39) |
S860P |
probably benign |
Het |
Ndufaf5 |
T |
A |
2: 140,030,698 (GRCm39) |
Y195N |
possibly damaging |
Het |
Nsfl1c |
T |
C |
2: 151,346,056 (GRCm39) |
L157P |
probably damaging |
Het |
Or2aj5 |
T |
A |
16: 19,425,116 (GRCm39) |
I100L |
probably benign |
Het |
Or4c104 |
T |
A |
2: 88,586,987 (GRCm39) |
I11F |
possibly damaging |
Het |
Or5ak24 |
T |
A |
2: 85,260,430 (GRCm39) |
T248S |
possibly damaging |
Het |
Pcdh10 |
A |
G |
3: 45,335,933 (GRCm39) |
Y749C |
probably damaging |
Het |
Plcz1 |
T |
A |
6: 139,974,163 (GRCm39) |
K93I |
probably damaging |
Het |
Plpbp |
T |
C |
8: 27,539,216 (GRCm39) |
S109P |
|
Het |
Prkdc |
G |
A |
16: 15,653,946 (GRCm39) |
R3901H |
probably damaging |
Het |
Psma6 |
A |
T |
12: 55,456,966 (GRCm39) |
Y103F |
probably benign |
Het |
Ptpn3 |
A |
G |
4: 57,218,514 (GRCm39) |
F650L |
probably benign |
Het |
Pxk |
T |
C |
14: 8,164,094 (GRCm38) |
F562S |
probably damaging |
Het |
Rbl2 |
A |
G |
8: 91,812,073 (GRCm39) |
D214G |
probably damaging |
Het |
Rgs17 |
C |
T |
10: 5,812,525 (GRCm39) |
C58Y |
possibly damaging |
Het |
Rnf6 |
A |
T |
5: 146,148,334 (GRCm39) |
V228E |
probably benign |
Het |
Sardh |
T |
C |
2: 27,105,122 (GRCm39) |
D667G |
probably benign |
Het |
Slc12a1 |
T |
A |
2: 125,032,209 (GRCm39) |
V620D |
probably damaging |
Het |
Slc39a7 |
A |
G |
17: 34,249,686 (GRCm39) |
I153T |
probably damaging |
Het |
Slc5a11 |
T |
C |
7: 122,847,162 (GRCm39) |
V125A |
probably damaging |
Het |
Slc9c1 |
T |
C |
16: 45,368,058 (GRCm39) |
F216L |
probably benign |
Het |
Strip1 |
A |
T |
3: 107,533,024 (GRCm39) |
I208N |
probably damaging |
Het |
Top1 |
T |
C |
2: 160,545,496 (GRCm39) |
M288T |
probably damaging |
Het |
Tpbgl |
G |
T |
7: 99,274,774 (GRCm39) |
A361E |
probably damaging |
Het |
Trmt2a |
T |
C |
16: 18,067,813 (GRCm39) |
V162A |
probably damaging |
Het |
Wdr35 |
T |
C |
12: 9,078,110 (GRCm39) |
I1167T |
probably benign |
Het |
Wdr76 |
C |
A |
2: 121,341,044 (GRCm39) |
H30N |
probably benign |
Het |
Zan |
A |
G |
5: 137,407,923 (GRCm39) |
S3624P |
unknown |
Het |
Zc3h7a |
T |
C |
16: 10,955,249 (GRCm39) |
K942E |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,810,893 (GRCm39) |
V722A |
possibly damaging |
Het |
Zfp943 |
A |
G |
17: 22,211,091 (GRCm39) |
H59R |
probably benign |
Het |
|
Other mutations in Dcp1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01653:Dcp1a
|
APN |
14 |
30,227,528 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02698:Dcp1a
|
APN |
14 |
30,227,499 (GRCm39) |
splice site |
probably benign |
|
IGL02799:Dcp1a
|
UTSW |
14 |
30,241,636 (GRCm39) |
critical splice donor site |
probably null |
|
R0240:Dcp1a
|
UTSW |
14 |
30,206,551 (GRCm39) |
splice site |
probably benign |
|
R0387:Dcp1a
|
UTSW |
14 |
30,241,636 (GRCm39) |
critical splice donor site |
probably null |
|
R0646:Dcp1a
|
UTSW |
14 |
30,224,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R1781:Dcp1a
|
UTSW |
14 |
30,235,032 (GRCm39) |
missense |
probably benign |
0.37 |
R1843:Dcp1a
|
UTSW |
14 |
30,240,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R2111:Dcp1a
|
UTSW |
14 |
30,241,327 (GRCm39) |
missense |
probably benign |
0.00 |
R3176:Dcp1a
|
UTSW |
14 |
30,227,499 (GRCm39) |
splice site |
probably benign |
|
R4948:Dcp1a
|
UTSW |
14 |
30,201,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:Dcp1a
|
UTSW |
14 |
30,224,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R6178:Dcp1a
|
UTSW |
14 |
30,245,261 (GRCm39) |
makesense |
probably null |
|
R7767:Dcp1a
|
UTSW |
14 |
30,201,775 (GRCm39) |
critical splice donor site |
probably null |
|
R7818:Dcp1a
|
UTSW |
14 |
30,201,678 (GRCm39) |
missense |
probably damaging |
0.99 |
R8248:Dcp1a
|
UTSW |
14 |
30,244,883 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8248:Dcp1a
|
UTSW |
14 |
30,201,555 (GRCm39) |
intron |
probably benign |
|
R8250:Dcp1a
|
UTSW |
14 |
30,244,883 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8271:Dcp1a
|
UTSW |
14 |
30,244,883 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8297:Dcp1a
|
UTSW |
14 |
30,244,883 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8326:Dcp1a
|
UTSW |
14 |
30,241,527 (GRCm39) |
nonsense |
probably null |
|
R8333:Dcp1a
|
UTSW |
14 |
30,244,883 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8818:Dcp1a
|
UTSW |
14 |
30,240,899 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9554:Dcp1a
|
UTSW |
14 |
30,201,691 (GRCm39) |
missense |
probably benign |
0.01 |
R9599:Dcp1a
|
UTSW |
14 |
30,241,497 (GRCm39) |
missense |
probably benign |
|
R9641:Dcp1a
|
UTSW |
14 |
30,241,132 (GRCm39) |
missense |
probably damaging |
1.00 |
|