Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts2 |
T |
A |
11: 50,683,548 (GRCm39) |
C943* |
probably null |
Het |
Arhgef28 |
A |
T |
13: 98,187,566 (GRCm39) |
V243D |
probably benign |
Het |
Arrdc3 |
T |
A |
13: 81,038,884 (GRCm39) |
I62K |
probably damaging |
Het |
Atm |
T |
C |
9: 53,427,863 (GRCm39) |
T416A |
probably benign |
Het |
AW209491 |
A |
G |
13: 14,812,268 (GRCm39) |
T374A |
probably damaging |
Het |
Brcc3 |
T |
C |
X: 74,479,704 (GRCm39) |
|
probably benign |
Het |
Ccdc181 |
T |
G |
1: 164,107,514 (GRCm39) |
S66A |
probably benign |
Het |
Ccdc62 |
T |
C |
5: 124,092,320 (GRCm39) |
I435T |
probably benign |
Het |
Cdc14b |
C |
A |
13: 64,364,117 (GRCm39) |
|
probably benign |
Het |
Chst5 |
A |
G |
8: 112,617,477 (GRCm39) |
S48P |
probably damaging |
Het |
Ciita |
C |
A |
16: 10,326,577 (GRCm39) |
S253Y |
probably damaging |
Het |
Dock7 |
C |
T |
4: 98,877,533 (GRCm39) |
R1005H |
probably damaging |
Het |
Enpep |
T |
C |
3: 129,103,506 (GRCm39) |
E361G |
probably damaging |
Het |
Fblim1 |
T |
C |
4: 141,310,422 (GRCm39) |
D280G |
probably benign |
Het |
Fignl1 |
G |
A |
11: 11,752,756 (GRCm39) |
R100* |
probably null |
Het |
Ggcx |
G |
T |
6: 72,395,286 (GRCm39) |
A126S |
probably damaging |
Het |
Hdgfl1 |
A |
G |
13: 26,953,786 (GRCm39) |
S96P |
probably benign |
Het |
Iqgap2 |
G |
A |
13: 95,764,622 (GRCm39) |
L1541F |
probably damaging |
Het |
Itga8 |
T |
C |
2: 12,145,289 (GRCm39) |
E888G |
possibly damaging |
Het |
Kank4 |
T |
A |
4: 98,667,064 (GRCm39) |
Q461L |
probably benign |
Het |
Klhl20 |
C |
T |
1: 160,925,935 (GRCm39) |
V438M |
probably damaging |
Het |
Klrc3 |
A |
T |
6: 129,620,171 (GRCm39) |
S27R |
probably damaging |
Het |
Ksr2 |
T |
C |
5: 117,901,394 (GRCm39) |
|
probably benign |
Het |
Lrrc37a |
C |
T |
11: 103,389,938 (GRCm39) |
S1829N |
probably benign |
Het |
Obscn |
A |
G |
11: 58,945,611 (GRCm39) |
L4585P |
probably damaging |
Het |
Or5p57 |
T |
C |
7: 107,665,978 (GRCm39) |
N9S |
probably benign |
Het |
Palm3 |
T |
G |
8: 84,755,494 (GRCm39) |
S335R |
probably damaging |
Het |
Pcsk7 |
C |
T |
9: 45,830,560 (GRCm39) |
A446V |
possibly damaging |
Het |
Penk |
A |
G |
4: 4,134,065 (GRCm39) |
L194P |
possibly damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,403,063 (GRCm39) |
F2255S |
probably damaging |
Het |
Plcd3 |
G |
A |
11: 102,968,653 (GRCm39) |
S31F |
probably damaging |
Het |
Pou2af2 |
A |
G |
9: 51,203,055 (GRCm39) |
L33P |
possibly damaging |
Het |
Ppp6r2 |
C |
T |
15: 89,159,680 (GRCm39) |
Q456* |
probably null |
Het |
Rbbp8nl |
T |
C |
2: 179,922,688 (GRCm39) |
D235G |
probably benign |
Het |
Ror1 |
T |
A |
4: 100,283,307 (GRCm39) |
N457K |
probably benign |
Het |
Rpgrip1l |
C |
A |
8: 91,951,972 (GRCm39) |
|
probably benign |
Het |
Sdk1 |
T |
C |
5: 141,595,787 (GRCm39) |
F148L |
probably benign |
Het |
Slc45a2 |
A |
T |
15: 11,023,440 (GRCm39) |
H348L |
probably benign |
Het |
Smg8 |
C |
T |
11: 86,977,498 (GRCm39) |
A28T |
probably benign |
Het |
Snx14 |
A |
G |
9: 88,285,356 (GRCm39) |
I436T |
probably damaging |
Het |
Synj2 |
G |
A |
17: 6,080,035 (GRCm39) |
R1088H |
probably damaging |
Het |
Tubb6 |
T |
C |
18: 67,535,366 (GRCm39) |
Y422H |
probably damaging |
Het |
Unc13a |
T |
A |
8: 72,108,345 (GRCm39) |
I503F |
probably benign |
Het |
Unc13d |
A |
G |
11: 115,961,382 (GRCm39) |
|
probably benign |
Het |
Zp1 |
T |
C |
19: 10,896,871 (GRCm39) |
|
probably benign |
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 |
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 |
R4504:Dsg4
|
UTSW |
18 |
20,594,493 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|