Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503E14Rik |
A |
G |
14: 44,407,899 (GRCm39) |
S45P |
probably damaging |
Het |
Adgrg4 |
C |
T |
X: 55,961,802 (GRCm39) |
R1124C |
possibly damaging |
Het |
Anxa13 |
T |
C |
15: 58,228,052 (GRCm39) |
|
noncoding transcript |
Het |
Arhgap32 |
C |
A |
9: 32,093,135 (GRCm39) |
|
probably null |
Het |
Carm1 |
T |
C |
9: 21,480,822 (GRCm39) |
F99L |
probably damaging |
Het |
Dennd1b |
A |
G |
1: 139,013,665 (GRCm39) |
E253G |
possibly damaging |
Het |
Dstyk |
A |
G |
1: 132,362,127 (GRCm39) |
T186A |
possibly damaging |
Het |
Ear1 |
A |
T |
14: 44,056,721 (GRCm39) |
V49D |
probably benign |
Het |
Epha10 |
A |
G |
4: 124,809,480 (GRCm39) |
|
probably benign |
Het |
Fbh1 |
A |
G |
2: 11,753,828 (GRCm39) |
V838A |
possibly damaging |
Het |
Fndc8 |
T |
A |
11: 82,783,226 (GRCm39) |
M69K |
probably benign |
Het |
Golga1 |
T |
C |
2: 38,913,466 (GRCm39) |
I482V |
probably benign |
Het |
Hivep3 |
G |
A |
4: 119,590,990 (GRCm39) |
|
probably benign |
Het |
Igkv13-85 |
A |
G |
6: 68,907,356 (GRCm39) |
F82L |
probably damaging |
Het |
Itih1 |
G |
A |
14: 30,657,842 (GRCm39) |
R410C |
probably damaging |
Het |
Kcnc2 |
T |
C |
10: 112,291,699 (GRCm39) |
W296R |
probably damaging |
Het |
Kcnq3 |
A |
T |
15: 65,867,191 (GRCm39) |
Y817* |
probably null |
Het |
Kif3b |
T |
C |
2: 153,165,564 (GRCm39) |
|
probably null |
Het |
Krtcap2 |
A |
G |
3: 89,153,563 (GRCm39) |
|
probably benign |
Het |
Lhx5 |
C |
A |
5: 120,578,073 (GRCm39) |
H298N |
possibly damaging |
Het |
Notch1 |
A |
G |
2: 26,362,189 (GRCm39) |
V1022A |
probably benign |
Het |
Npc1l1 |
A |
G |
11: 6,178,741 (GRCm39) |
L223S |
possibly damaging |
Het |
Or11m3 |
T |
C |
15: 98,396,015 (GRCm39) |
F221L |
probably benign |
Het |
Or4c10 |
C |
T |
2: 89,760,695 (GRCm39) |
P181S |
possibly damaging |
Het |
Or8a1b |
C |
T |
9: 37,622,760 (GRCm39) |
V272I |
probably benign |
Het |
Pbxip1 |
A |
G |
3: 89,353,690 (GRCm39) |
D281G |
possibly damaging |
Het |
Pcdhga8 |
G |
C |
18: 37,949,816 (GRCm39) |
V411L |
probably damaging |
Het |
Pcsk5 |
C |
T |
19: 17,429,319 (GRCm39) |
C1553Y |
probably damaging |
Het |
Pdgfc |
A |
C |
3: 81,082,298 (GRCm39) |
M164L |
probably benign |
Het |
Pdzd8 |
T |
C |
19: 59,333,880 (GRCm39) |
Y47C |
probably damaging |
Het |
Pip5k1c |
T |
A |
10: 81,150,945 (GRCm39) |
I633N |
probably damaging |
Het |
Pkn1 |
G |
A |
8: 84,419,556 (GRCm39) |
R16* |
probably null |
Het |
Pole2 |
A |
G |
12: 69,269,242 (GRCm39) |
V85A |
probably benign |
Het |
Ppp4c |
A |
C |
7: 126,386,637 (GRCm39) |
L150R |
probably damaging |
Het |
Pramel25 |
G |
C |
4: 143,520,553 (GRCm39) |
E102Q |
probably benign |
Het |
Ric8a |
A |
G |
7: 140,438,429 (GRCm39) |
I223V |
probably benign |
Het |
Rnf144a |
T |
A |
12: 26,377,302 (GRCm39) |
R92S |
probably benign |
Het |
Sbno2 |
C |
A |
10: 79,896,326 (GRCm39) |
R898L |
possibly damaging |
Het |
Scnn1b |
A |
C |
7: 121,511,698 (GRCm39) |
N370T |
probably damaging |
Het |
Taar3 |
A |
G |
10: 23,825,471 (GRCm39) |
I6V |
possibly damaging |
Het |
Vps13a |
T |
C |
19: 16,672,866 (GRCm39) |
E1302G |
possibly damaging |
Het |
|
Other mutations in Dsg4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00708:Dsg4
|
APN |
18 |
20,594,383 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01723:Dsg4
|
APN |
18 |
20,599,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02249:Dsg4
|
APN |
18 |
20,594,361 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02445:Dsg4
|
APN |
18 |
20,579,307 (GRCm39) |
splice site |
probably benign |
|
IGL02553:Dsg4
|
APN |
18 |
20,595,577 (GRCm39) |
missense |
probably benign |
|
IGL02578:Dsg4
|
APN |
18 |
20,604,250 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02634:Dsg4
|
APN |
18 |
20,591,637 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02677:Dsg4
|
APN |
18 |
20,597,933 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02741:Dsg4
|
APN |
18 |
20,604,553 (GRCm39) |
missense |
probably benign |
|
IGL02747:Dsg4
|
APN |
18 |
20,579,995 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03342:Dsg4
|
APN |
18 |
20,584,880 (GRCm39) |
missense |
probably damaging |
1.00 |
burrito
|
UTSW |
18 |
20,584,919 (GRCm39) |
missense |
possibly damaging |
0.81 |
woodshed
|
UTSW |
18 |
20,584,929 (GRCm39) |
nonsense |
probably null |
|
R0043:Dsg4
|
UTSW |
18 |
20,586,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R0375:Dsg4
|
UTSW |
18 |
20,603,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R0537:Dsg4
|
UTSW |
18 |
20,591,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R0619:Dsg4
|
UTSW |
18 |
20,594,416 (GRCm39) |
missense |
probably benign |
0.00 |
R0622:Dsg4
|
UTSW |
18 |
20,582,845 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0765:Dsg4
|
UTSW |
18 |
20,587,703 (GRCm39) |
splice site |
probably benign |
|
R0786:Dsg4
|
UTSW |
18 |
20,582,429 (GRCm39) |
critical splice donor site |
probably null |
|
R1114:Dsg4
|
UTSW |
18 |
20,599,540 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1249:Dsg4
|
UTSW |
18 |
20,579,929 (GRCm39) |
nonsense |
probably null |
|
R1372:Dsg4
|
UTSW |
18 |
20,582,733 (GRCm39) |
splice site |
probably null |
|
R1382:Dsg4
|
UTSW |
18 |
20,598,181 (GRCm39) |
missense |
probably benign |
0.00 |
R1392:Dsg4
|
UTSW |
18 |
20,579,304 (GRCm39) |
splice site |
probably benign |
|
R1442:Dsg4
|
UTSW |
18 |
20,595,717 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1503:Dsg4
|
UTSW |
18 |
20,582,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R1704:Dsg4
|
UTSW |
18 |
20,604,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R1716:Dsg4
|
UTSW |
18 |
20,595,518 (GRCm39) |
nonsense |
probably null |
|
R1765:Dsg4
|
UTSW |
18 |
20,589,888 (GRCm39) |
missense |
probably benign |
0.01 |
R1817:Dsg4
|
UTSW |
18 |
20,604,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R1982:Dsg4
|
UTSW |
18 |
20,604,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R2025:Dsg4
|
UTSW |
18 |
20,599,693 (GRCm39) |
nonsense |
probably null |
|
R2097:Dsg4
|
UTSW |
18 |
20,604,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R2198:Dsg4
|
UTSW |
18 |
20,594,499 (GRCm39) |
missense |
probably benign |
|
R3551:Dsg4
|
UTSW |
18 |
20,584,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R3742:Dsg4
|
UTSW |
18 |
20,604,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R3853:Dsg4
|
UTSW |
18 |
20,582,291 (GRCm39) |
missense |
probably benign |
|
R3955:Dsg4
|
UTSW |
18 |
20,582,432 (GRCm39) |
splice site |
probably null |
|
R4006:Dsg4
|
UTSW |
18 |
20,604,022 (GRCm39) |
missense |
probably damaging |
0.97 |
R4012:Dsg4
|
UTSW |
18 |
20,584,919 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4171:Dsg4
|
UTSW |
18 |
20,591,636 (GRCm39) |
nonsense |
probably null |
|
R4254:Dsg4
|
UTSW |
18 |
20,604,595 (GRCm39) |
missense |
probably benign |
0.07 |
R4559:Dsg4
|
UTSW |
18 |
20,603,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R4607:Dsg4
|
UTSW |
18 |
20,604,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Dsg4
|
UTSW |
18 |
20,595,470 (GRCm39) |
missense |
probably benign |
0.10 |
R4683:Dsg4
|
UTSW |
18 |
20,594,466 (GRCm39) |
missense |
probably benign |
|
R4700:Dsg4
|
UTSW |
18 |
20,589,965 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4749:Dsg4
|
UTSW |
18 |
20,579,888 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4775:Dsg4
|
UTSW |
18 |
20,604,184 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4809:Dsg4
|
UTSW |
18 |
20,599,678 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5276:Dsg4
|
UTSW |
18 |
20,579,896 (GRCm39) |
missense |
probably benign |
0.21 |
R5426:Dsg4
|
UTSW |
18 |
20,591,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R5767:Dsg4
|
UTSW |
18 |
20,595,549 (GRCm39) |
nonsense |
probably null |
|
R5982:Dsg4
|
UTSW |
18 |
20,598,226 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6280:Dsg4
|
UTSW |
18 |
20,599,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6305:Dsg4
|
UTSW |
18 |
20,582,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R6489:Dsg4
|
UTSW |
18 |
20,604,420 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7013:Dsg4
|
UTSW |
18 |
20,591,578 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7040:Dsg4
|
UTSW |
18 |
20,584,909 (GRCm39) |
missense |
probably benign |
0.01 |
R7196:Dsg4
|
UTSW |
18 |
20,599,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R7432:Dsg4
|
UTSW |
18 |
20,579,323 (GRCm39) |
nonsense |
probably null |
|
R7438:Dsg4
|
UTSW |
18 |
20,599,685 (GRCm39) |
missense |
probably damaging |
0.96 |
R7490:Dsg4
|
UTSW |
18 |
20,584,993 (GRCm39) |
splice site |
probably null |
|
R7612:Dsg4
|
UTSW |
18 |
20,604,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R7639:Dsg4
|
UTSW |
18 |
20,582,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R7905:Dsg4
|
UTSW |
18 |
20,587,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R8251:Dsg4
|
UTSW |
18 |
20,604,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R8326:Dsg4
|
UTSW |
18 |
20,582,788 (GRCm39) |
missense |
probably benign |
0.31 |
R8554:Dsg4
|
UTSW |
18 |
20,586,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R8911:Dsg4
|
UTSW |
18 |
20,584,929 (GRCm39) |
nonsense |
probably null |
|
R9059:Dsg4
|
UTSW |
18 |
20,604,182 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9508:Dsg4
|
UTSW |
18 |
20,604,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R9607:Dsg4
|
UTSW |
18 |
20,586,047 (GRCm39) |
missense |
probably benign |
0.00 |
R9765:Dsg4
|
UTSW |
18 |
20,604,334 (GRCm39) |
missense |
probably benign |
0.02 |
|