Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730049H05Rik |
T |
A |
6: 92,804,997 (GRCm39) |
|
probably benign |
Het |
Ace2 |
T |
A |
X: 162,946,996 (GRCm39) |
V293D |
probably damaging |
Het |
Adgrg6 |
T |
C |
10: 14,317,185 (GRCm39) |
Y545C |
probably damaging |
Het |
Arhgap40 |
A |
G |
2: 158,376,742 (GRCm39) |
T293A |
probably damaging |
Het |
Arhgef19 |
A |
G |
4: 140,973,707 (GRCm39) |
T65A |
probably damaging |
Het |
Brf1 |
A |
G |
12: 112,956,682 (GRCm39) |
|
probably null |
Het |
Cbfb |
T |
C |
8: 105,905,252 (GRCm39) |
S65P |
possibly damaging |
Het |
Chsy1 |
T |
C |
7: 65,821,576 (GRCm39) |
S604P |
possibly damaging |
Het |
Ckmt1 |
T |
C |
2: 121,191,643 (GRCm39) |
V271A |
probably damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Csmd2 |
T |
C |
4: 128,371,263 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
A |
G |
2: 104,038,559 (GRCm39) |
|
probably benign |
Het |
Fam3a |
G |
A |
X: 73,430,241 (GRCm39) |
T156I |
probably damaging |
Het |
Fbn2 |
A |
T |
18: 58,229,087 (GRCm39) |
C708S |
probably damaging |
Het |
Fgf5 |
G |
A |
5: 98,409,831 (GRCm39) |
G127R |
probably damaging |
Het |
Fhip1a |
T |
G |
3: 85,637,939 (GRCm39) |
K120T |
probably damaging |
Het |
Fn3k |
A |
T |
11: 121,325,909 (GRCm39) |
Y32F |
probably benign |
Het |
Frem3 |
T |
C |
8: 81,338,118 (GRCm39) |
I137T |
probably benign |
Het |
Hc |
T |
C |
2: 34,903,531 (GRCm39) |
D1041G |
probably benign |
Het |
Heatr6 |
T |
A |
11: 83,655,708 (GRCm39) |
|
probably benign |
Het |
Hivep1 |
G |
A |
13: 42,309,553 (GRCm39) |
A598T |
probably benign |
Het |
Ifngr1 |
T |
C |
10: 19,483,007 (GRCm39) |
S254P |
probably benign |
Het |
Kel |
T |
C |
6: 41,674,408 (GRCm39) |
S341G |
probably benign |
Het |
Klra6 |
A |
C |
6: 129,990,439 (GRCm39) |
M224R |
probably benign |
Het |
Mis18bp1 |
A |
G |
12: 65,183,522 (GRCm39) |
|
probably null |
Het |
Mpeg1 |
C |
T |
19: 12,440,660 (GRCm39) |
T706I |
probably benign |
Het |
Mrpl41 |
T |
C |
2: 24,864,429 (GRCm39) |
D81G |
possibly damaging |
Het |
Or5al7 |
G |
T |
2: 85,993,181 (GRCm39) |
F37L |
probably benign |
Het |
Palld |
T |
C |
8: 61,978,148 (GRCm39) |
R881G |
probably damaging |
Het |
Pdha2 |
A |
T |
3: 140,916,662 (GRCm39) |
V282E |
probably damaging |
Het |
Pga5 |
C |
T |
19: 10,654,065 (GRCm39) |
R46Q |
probably benign |
Het |
Plekhg2 |
T |
C |
7: 28,068,122 (GRCm39) |
Y189C |
probably damaging |
Het |
Rnf43 |
A |
G |
11: 87,622,479 (GRCm39) |
T527A |
probably benign |
Het |
Rplp0 |
G |
A |
5: 115,699,174 (GRCm39) |
R73Q |
probably benign |
Het |
Smco3 |
A |
G |
6: 136,808,197 (GRCm39) |
*226R |
probably null |
Het |
Sugp2 |
T |
C |
8: 70,712,324 (GRCm39) |
|
probably benign |
Het |
Tsga10 |
T |
C |
1: 37,846,098 (GRCm39) |
I343V |
probably benign |
Het |
Ube2q2 |
A |
G |
9: 55,075,502 (GRCm39) |
K104E |
probably damaging |
Het |
Ube3a |
C |
T |
7: 58,925,506 (GRCm39) |
|
probably benign |
Het |
Usp11 |
T |
C |
X: 20,585,381 (GRCm39) |
I785T |
probably damaging |
Het |
Vmn2r22 |
A |
T |
6: 123,626,026 (GRCm39) |
C137S |
probably damaging |
Het |
Zfp281 |
T |
C |
1: 136,555,185 (GRCm39) |
V721A |
possibly damaging |
Het |
Zfp946 |
T |
C |
17: 22,672,469 (GRCm39) |
S23P |
probably damaging |
Het |
Zfyve1 |
A |
G |
12: 83,594,694 (GRCm39) |
V766A |
probably damaging |
Het |
|
Other mutations in Dsg1c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00567:Dsg1c
|
APN |
18 |
20,407,733 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00596:Dsg1c
|
APN |
18 |
20,414,899 (GRCm39) |
splice site |
probably benign |
|
IGL01412:Dsg1c
|
APN |
18 |
20,380,518 (GRCm39) |
missense |
probably benign |
|
IGL02247:Dsg1c
|
APN |
18 |
20,397,373 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02386:Dsg1c
|
APN |
18 |
20,410,056 (GRCm39) |
missense |
probably benign |
|
IGL02408:Dsg1c
|
APN |
18 |
20,407,776 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02519:Dsg1c
|
APN |
18 |
20,416,790 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02591:Dsg1c
|
APN |
18 |
20,408,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02730:Dsg1c
|
APN |
18 |
20,407,887 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02836:Dsg1c
|
APN |
18 |
20,400,986 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03335:Dsg1c
|
APN |
18 |
20,416,754 (GRCm39) |
missense |
probably benign |
0.01 |
Nancy
|
UTSW |
18 |
20,416,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R0385:Dsg1c
|
UTSW |
18 |
20,416,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R0561:Dsg1c
|
UTSW |
18 |
20,407,832 (GRCm39) |
missense |
probably benign |
0.04 |
R0570:Dsg1c
|
UTSW |
18 |
20,403,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Dsg1c
|
UTSW |
18 |
20,412,298 (GRCm39) |
missense |
probably benign |
0.02 |
R0621:Dsg1c
|
UTSW |
18 |
20,412,752 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0632:Dsg1c
|
UTSW |
18 |
20,405,403 (GRCm39) |
splice site |
probably benign |
|
R1183:Dsg1c
|
UTSW |
18 |
20,416,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R1529:Dsg1c
|
UTSW |
18 |
20,415,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R1596:Dsg1c
|
UTSW |
18 |
20,415,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Dsg1c
|
UTSW |
18 |
20,397,899 (GRCm39) |
missense |
probably benign |
0.36 |
R1623:Dsg1c
|
UTSW |
18 |
20,408,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1844:Dsg1c
|
UTSW |
18 |
20,416,096 (GRCm39) |
splice site |
probably null |
|
R1881:Dsg1c
|
UTSW |
18 |
20,405,597 (GRCm39) |
splice site |
probably benign |
|
R2017:Dsg1c
|
UTSW |
18 |
20,399,253 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2072:Dsg1c
|
UTSW |
18 |
20,408,309 (GRCm39) |
missense |
probably benign |
0.09 |
R2319:Dsg1c
|
UTSW |
18 |
20,408,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R2340:Dsg1c
|
UTSW |
18 |
20,400,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R3403:Dsg1c
|
UTSW |
18 |
20,403,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R3407:Dsg1c
|
UTSW |
18 |
20,415,115 (GRCm39) |
critical splice donor site |
probably null |
|
R3874:Dsg1c
|
UTSW |
18 |
20,410,109 (GRCm39) |
missense |
probably benign |
0.02 |
R3910:Dsg1c
|
UTSW |
18 |
20,399,253 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4535:Dsg1c
|
UTSW |
18 |
20,408,322 (GRCm39) |
missense |
probably benign |
0.01 |
R4739:Dsg1c
|
UTSW |
18 |
20,408,246 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5038:Dsg1c
|
UTSW |
18 |
20,397,901 (GRCm39) |
missense |
probably benign |
0.00 |
R5165:Dsg1c
|
UTSW |
18 |
20,410,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R5210:Dsg1c
|
UTSW |
18 |
20,407,758 (GRCm39) |
missense |
probably damaging |
0.97 |
R5253:Dsg1c
|
UTSW |
18 |
20,405,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R5327:Dsg1c
|
UTSW |
18 |
20,400,994 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5361:Dsg1c
|
UTSW |
18 |
20,416,703 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5475:Dsg1c
|
UTSW |
18 |
20,415,088 (GRCm39) |
missense |
probably damaging |
0.99 |
R5512:Dsg1c
|
UTSW |
18 |
20,405,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R5681:Dsg1c
|
UTSW |
18 |
20,416,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R5710:Dsg1c
|
UTSW |
18 |
20,405,408 (GRCm39) |
missense |
probably benign |
0.06 |
R5889:Dsg1c
|
UTSW |
18 |
20,416,658 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6513:Dsg1c
|
UTSW |
18 |
20,407,687 (GRCm39) |
missense |
probably benign |
0.01 |
R6596:Dsg1c
|
UTSW |
18 |
20,403,581 (GRCm39) |
splice site |
probably null |
|
R6941:Dsg1c
|
UTSW |
18 |
20,400,980 (GRCm39) |
missense |
probably damaging |
0.96 |
R7041:Dsg1c
|
UTSW |
18 |
20,399,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R7061:Dsg1c
|
UTSW |
18 |
20,410,066 (GRCm39) |
missense |
probably benign |
|
R7240:Dsg1c
|
UTSW |
18 |
20,416,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R8048:Dsg1c
|
UTSW |
18 |
20,407,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R8092:Dsg1c
|
UTSW |
18 |
20,415,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:Dsg1c
|
UTSW |
18 |
20,416,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R8117:Dsg1c
|
UTSW |
18 |
20,410,016 (GRCm39) |
missense |
probably benign |
|
R8192:Dsg1c
|
UTSW |
18 |
20,399,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R8801:Dsg1c
|
UTSW |
18 |
20,410,022 (GRCm39) |
missense |
probably benign |
0.00 |
R9059:Dsg1c
|
UTSW |
18 |
20,408,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R9152:Dsg1c
|
UTSW |
18 |
20,416,329 (GRCm39) |
missense |
probably benign |
0.06 |
R9292:Dsg1c
|
UTSW |
18 |
20,416,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R9469:Dsg1c
|
UTSW |
18 |
20,400,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R9596:Dsg1c
|
UTSW |
18 |
20,416,361 (GRCm39) |
missense |
probably benign |
0.17 |
R9619:Dsg1c
|
UTSW |
18 |
20,416,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R9628:Dsg1c
|
UTSW |
18 |
20,397,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R9710:Dsg1c
|
UTSW |
18 |
20,410,044 (GRCm39) |
missense |
probably benign |
|
X0026:Dsg1c
|
UTSW |
18 |
20,416,315 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dsg1c
|
UTSW |
18 |
20,416,630 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dsg1c
|
UTSW |
18 |
20,398,006 (GRCm39) |
missense |
probably damaging |
1.00 |
|