Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap3b2 |
C |
T |
7: 81,123,598 (GRCm39) |
|
probably benign |
Het |
Arl1 |
C |
T |
10: 88,569,398 (GRCm39) |
|
probably benign |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atp10a |
T |
C |
7: 58,476,852 (GRCm39) |
M1189T |
possibly damaging |
Het |
Bcl2l14 |
A |
G |
6: 134,400,771 (GRCm39) |
D64G |
probably damaging |
Het |
Cdc34b |
G |
A |
11: 94,633,441 (GRCm39) |
V214M |
probably benign |
Het |
Cfap54 |
T |
C |
10: 92,665,619 (GRCm39) |
T2985A |
probably benign |
Het |
Clcc1 |
T |
C |
3: 108,580,682 (GRCm39) |
M332T |
probably damaging |
Het |
Coch |
T |
C |
12: 51,650,121 (GRCm39) |
I370T |
probably damaging |
Het |
Ctdnep1 |
A |
G |
11: 69,880,400 (GRCm39) |
|
probably benign |
Het |
Fam135b |
T |
A |
15: 71,322,280 (GRCm39) |
Q1295L |
probably benign |
Het |
Fam184a |
C |
T |
10: 53,575,397 (GRCm39) |
A71T |
probably damaging |
Het |
Fbxw10 |
A |
G |
11: 62,759,983 (GRCm39) |
|
probably benign |
Het |
Frmd4a |
T |
C |
2: 4,542,071 (GRCm39) |
W247R |
probably damaging |
Het |
Gcn1 |
A |
G |
5: 115,725,893 (GRCm39) |
H553R |
probably benign |
Het |
Grin3a |
C |
T |
4: 49,672,472 (GRCm39) |
|
probably null |
Het |
H2-Q6 |
C |
T |
17: 35,644,542 (GRCm39) |
|
probably benign |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Hspg2 |
T |
C |
4: 137,242,879 (GRCm39) |
V670A |
probably damaging |
Het |
Med10 |
A |
G |
13: 69,958,101 (GRCm39) |
N18D |
probably damaging |
Het |
Mgat4b |
T |
A |
11: 50,124,165 (GRCm39) |
H368Q |
possibly damaging |
Het |
Morn5 |
C |
A |
2: 35,943,035 (GRCm39) |
T45N |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Msl3 |
C |
T |
X: 167,454,813 (GRCm39) |
A87T |
probably damaging |
Het |
Myrf |
T |
C |
19: 10,195,515 (GRCm39) |
T432A |
probably damaging |
Het |
Nalf2 |
G |
A |
X: 98,865,470 (GRCm39) |
V266M |
possibly damaging |
Het |
Nav3 |
T |
A |
10: 109,529,896 (GRCm39) |
E2148D |
probably damaging |
Het |
Nfe2l3 |
A |
G |
6: 51,433,595 (GRCm39) |
T236A |
possibly damaging |
Het |
Odc1 |
T |
A |
12: 17,598,801 (GRCm39) |
F227Y |
probably benign |
Het |
Opa1 |
A |
T |
16: 29,429,698 (GRCm39) |
E401D |
probably damaging |
Het |
Or5b21 |
T |
C |
19: 12,839,994 (GRCm39) |
M285T |
possibly damaging |
Het |
Pdcd1 |
T |
C |
1: 93,968,989 (GRCm39) |
I110V |
probably benign |
Het |
Pde5a |
G |
A |
3: 122,554,545 (GRCm39) |
E212K |
probably damaging |
Het |
Plin4 |
A |
G |
17: 56,413,704 (GRCm39) |
I307T |
probably benign |
Het |
Rag1 |
T |
C |
2: 101,473,384 (GRCm39) |
Y586C |
probably damaging |
Het |
Rgs7bp |
T |
C |
13: 105,189,506 (GRCm39) |
M98V |
probably benign |
Het |
Rgs9 |
A |
G |
11: 109,166,639 (GRCm39) |
|
probably benign |
Het |
Rin3 |
A |
G |
12: 102,356,342 (GRCm39) |
D961G |
probably damaging |
Het |
Rubcn |
A |
G |
16: 32,649,629 (GRCm39) |
|
probably null |
Het |
Slc13a2 |
T |
A |
11: 78,289,226 (GRCm39) |
Y495F |
probably damaging |
Het |
Tfec |
T |
A |
6: 16,845,458 (GRCm39) |
D67V |
probably damaging |
Het |
Tmem94 |
T |
C |
11: 115,680,080 (GRCm39) |
M30T |
probably benign |
Het |
Tsbp1 |
A |
G |
17: 34,662,417 (GRCm39) |
T86A |
possibly damaging |
Het |
Tubgcp6 |
A |
G |
15: 88,988,617 (GRCm39) |
|
probably benign |
Het |
Vmn2r10 |
C |
A |
5: 109,150,088 (GRCm39) |
A319S |
possibly damaging |
Het |
Vmn2r85 |
T |
C |
10: 130,254,336 (GRCm39) |
M783V |
probably damaging |
Het |
Zfp422 |
T |
C |
6: 116,603,420 (GRCm39) |
K193R |
probably benign |
Het |
Zfp94 |
T |
G |
7: 24,003,112 (GRCm39) |
D110A |
probably benign |
Het |
|
Other mutations in Edar |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01306:Edar
|
APN |
10 |
58,464,460 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01551:Edar
|
APN |
10 |
58,441,860 (GRCm39) |
splice site |
probably benign |
|
IGL02207:Edar
|
APN |
10 |
58,446,343 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02391:Edar
|
APN |
10 |
58,464,403 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03152:Edar
|
APN |
10 |
58,445,817 (GRCm39) |
missense |
possibly damaging |
0.88 |
achtung2
|
UTSW |
10 |
58,438,985 (GRCm39) |
missense |
probably damaging |
1.00 |
two-tone
|
UTSW |
10 |
58,439,001 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU23:Edar
|
UTSW |
10 |
58,464,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R0113:Edar
|
UTSW |
10 |
58,465,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R0413:Edar
|
UTSW |
10 |
58,465,262 (GRCm39) |
missense |
probably benign |
0.00 |
R0927:Edar
|
UTSW |
10 |
58,465,313 (GRCm39) |
splice site |
probably null |
|
R1217:Edar
|
UTSW |
10 |
58,464,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R1458:Edar
|
UTSW |
10 |
58,443,188 (GRCm39) |
missense |
probably benign |
0.27 |
R1651:Edar
|
UTSW |
10 |
58,441,875 (GRCm39) |
missense |
possibly damaging |
0.49 |
R3820:Edar
|
UTSW |
10 |
58,457,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R4050:Edar
|
UTSW |
10 |
58,445,769 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4911:Edar
|
UTSW |
10 |
58,457,146 (GRCm39) |
missense |
probably benign |
0.03 |
R4924:Edar
|
UTSW |
10 |
58,465,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R4998:Edar
|
UTSW |
10 |
58,441,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R5311:Edar
|
UTSW |
10 |
58,443,257 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5314:Edar
|
UTSW |
10 |
58,443,182 (GRCm39) |
missense |
probably benign |
0.00 |
R5371:Edar
|
UTSW |
10 |
58,443,274 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5566:Edar
|
UTSW |
10 |
58,464,463 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5847:Edar
|
UTSW |
10 |
58,439,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R7330:Edar
|
UTSW |
10 |
58,446,376 (GRCm39) |
missense |
probably damaging |
0.98 |
R7529:Edar
|
UTSW |
10 |
58,447,830 (GRCm39) |
missense |
probably benign |
|
R7812:Edar
|
UTSW |
10 |
58,465,926 (GRCm39) |
missense |
probably benign |
|
R7872:Edar
|
UTSW |
10 |
58,446,348 (GRCm39) |
missense |
possibly damaging |
0.88 |
|