Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
G |
T |
18: 6,630,166 (GRCm39) |
|
probably null |
Het |
Aarsd1 |
T |
A |
11: 101,301,971 (GRCm39) |
I332F |
probably damaging |
Het |
Abcd2 |
C |
T |
15: 91,058,908 (GRCm39) |
G512D |
probably damaging |
Het |
Adam6a |
T |
C |
12: 113,507,798 (GRCm39) |
I57T |
probably benign |
Het |
Adam6b |
C |
T |
12: 113,453,984 (GRCm39) |
T267I |
probably benign |
Het |
Ap1g2 |
G |
A |
14: 55,338,030 (GRCm39) |
|
probably benign |
Het |
Arhgap22 |
G |
A |
14: 33,089,378 (GRCm39) |
E455K |
probably benign |
Het |
Bltp1 |
G |
A |
3: 37,094,583 (GRCm39) |
V917I |
probably damaging |
Het |
Ccdc93 |
T |
C |
1: 121,389,969 (GRCm39) |
I253T |
probably damaging |
Het |
Cd44 |
T |
C |
2: 102,731,738 (GRCm39) |
|
probably null |
Het |
Cnot6 |
A |
T |
11: 49,579,999 (GRCm39) |
S98T |
probably benign |
Het |
Dnah9 |
C |
A |
11: 65,741,829 (GRCm39) |
|
probably null |
Het |
Eif5 |
A |
T |
12: 111,506,618 (GRCm39) |
R43* |
probably null |
Het |
Eml4 |
C |
A |
17: 83,780,494 (GRCm39) |
T667K |
probably damaging |
Het |
Fchsd1 |
A |
G |
18: 38,102,510 (GRCm39) |
|
probably benign |
Het |
Flt1 |
A |
G |
5: 147,636,827 (GRCm39) |
|
probably benign |
Het |
Frem2 |
T |
A |
3: 53,424,270 (GRCm39) |
I3056F |
probably damaging |
Het |
Hivep1 |
A |
T |
13: 42,337,787 (GRCm39) |
H2622L |
possibly damaging |
Het |
Ido2 |
T |
C |
8: 25,023,771 (GRCm39) |
I356V |
probably benign |
Het |
Insyn2b |
T |
C |
11: 34,353,007 (GRCm39) |
S350P |
probably benign |
Het |
Itgb3 |
C |
A |
11: 104,524,438 (GRCm39) |
Y191* |
probably null |
Het |
Kcnma1 |
T |
C |
14: 23,350,006 (GRCm39) |
T1178A |
possibly damaging |
Het |
Kcnt1 |
A |
G |
2: 25,790,904 (GRCm39) |
H486R |
probably damaging |
Het |
Kif21a |
T |
C |
15: 90,852,277 (GRCm39) |
N950S |
probably benign |
Het |
Lama1 |
C |
A |
17: 68,086,041 (GRCm39) |
|
probably null |
Het |
Lrrc4b |
T |
A |
7: 44,111,982 (GRCm39) |
V618E |
probably damaging |
Het |
Micall2 |
C |
T |
5: 139,701,611 (GRCm39) |
G461D |
possibly damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Ncoa6 |
T |
A |
2: 155,248,858 (GRCm39) |
N1482I |
probably damaging |
Het |
Pcdhga10 |
A |
G |
18: 37,880,995 (GRCm39) |
N252S |
probably damaging |
Het |
Pcdhgb7 |
C |
A |
18: 37,885,286 (GRCm39) |
T152K |
possibly damaging |
Het |
Pds5a |
A |
G |
5: 65,811,419 (GRCm39) |
V338A |
possibly damaging |
Het |
Pds5b |
T |
C |
5: 150,659,802 (GRCm39) |
V255A |
possibly damaging |
Het |
Prkar2a |
T |
G |
9: 108,624,155 (GRCm39) |
F391V |
probably damaging |
Het |
Prr14l |
A |
G |
5: 32,986,328 (GRCm39) |
C1056R |
probably damaging |
Het |
Ptpn23 |
A |
G |
9: 110,218,862 (GRCm39) |
|
probably benign |
Het |
Serpinb5 |
T |
A |
1: 106,802,802 (GRCm39) |
Y112* |
probably null |
Het |
Slc17a4 |
C |
T |
13: 24,085,752 (GRCm39) |
R387H |
probably benign |
Het |
Tdrd5 |
A |
G |
1: 156,113,053 (GRCm39) |
V409A |
probably benign |
Het |
Tenm2 |
A |
T |
11: 35,915,147 (GRCm39) |
I2129N |
probably damaging |
Het |
Tmem8b |
C |
A |
4: 43,689,745 (GRCm39) |
H800N |
probably damaging |
Het |
Trpm3 |
A |
T |
19: 22,964,813 (GRCm39) |
N1436I |
probably benign |
Het |
Unc13c |
A |
T |
9: 73,838,240 (GRCm39) |
S870R |
probably benign |
Het |
Vmn2r16 |
C |
T |
5: 109,510,143 (GRCm39) |
P509S |
probably benign |
Het |
Vmn2r60 |
A |
T |
7: 41,785,125 (GRCm39) |
E112D |
probably damaging |
Het |
Xpnpep1 |
G |
A |
19: 52,992,250 (GRCm39) |
|
probably benign |
Het |
Zfp729a |
A |
T |
13: 67,769,438 (GRCm39) |
C264S |
probably damaging |
Het |
Zmynd8 |
T |
A |
2: 165,657,381 (GRCm39) |
K521* |
probably null |
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 |
R3932:Edar
|
UTSW |
10 |
58,446,164 (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 |
|