Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
G |
A |
6: 92,784,156 (GRCm39) |
T985M |
probably damaging |
Het |
Alpk1 |
A |
G |
3: 127,473,592 (GRCm39) |
S804P |
possibly damaging |
Het |
Ap3b1 |
A |
G |
13: 94,664,835 (GRCm39) |
I925V |
unknown |
Het |
Cep135 |
T |
A |
5: 76,788,796 (GRCm39) |
S1130T |
probably damaging |
Het |
Cers3 |
A |
T |
7: 66,431,573 (GRCm39) |
M183L |
probably benign |
Het |
Col5a1 |
A |
G |
2: 27,842,352 (GRCm39) |
E409G |
unknown |
Het |
Cyp4a32 |
G |
T |
4: 115,471,818 (GRCm39) |
V410F |
probably damaging |
Het |
Ddx1 |
G |
A |
12: 13,277,318 (GRCm39) |
Q528* |
probably null |
Het |
Dio2 |
G |
A |
12: 90,696,178 (GRCm39) |
|
probably benign |
Het |
Dnah9 |
G |
T |
11: 65,931,172 (GRCm39) |
A2008E |
probably damaging |
Het |
Dnajc2 |
A |
G |
5: 21,965,408 (GRCm39) |
V457A |
probably benign |
Het |
Dytn |
T |
C |
1: 63,682,532 (GRCm39) |
T372A |
probably benign |
Het |
Fam135a |
T |
C |
1: 24,067,714 (GRCm39) |
I152V |
probably benign |
Het |
Fmnl2 |
C |
T |
2: 52,748,261 (GRCm39) |
A36V |
possibly damaging |
Het |
Galnt7 |
G |
A |
8: 58,005,531 (GRCm39) |
T234I |
probably damaging |
Het |
Gba1 |
A |
C |
3: 89,110,809 (GRCm39) |
I6L |
probably benign |
Het |
Gja10 |
A |
G |
4: 32,602,147 (GRCm39) |
V79A |
probably damaging |
Het |
Gpd2 |
T |
A |
2: 57,228,991 (GRCm39) |
V265E |
probably damaging |
Het |
Gpld1 |
T |
C |
13: 25,136,861 (GRCm39) |
Y60H |
probably damaging |
Het |
H2bc27 |
A |
G |
11: 58,839,869 (GRCm39) |
K35R |
probably benign |
Het |
Krt75 |
T |
A |
15: 101,476,508 (GRCm39) |
D419V |
probably benign |
Het |
Lrig3 |
A |
T |
10: 125,842,871 (GRCm39) |
I599F |
probably benign |
Het |
Lrp4 |
A |
G |
2: 91,341,925 (GRCm39) |
D1846G |
probably damaging |
Het |
Mamdc2 |
C |
T |
19: 23,281,215 (GRCm39) |
A653T |
probably damaging |
Het |
Myo7a |
A |
T |
7: 97,740,227 (GRCm39) |
|
probably null |
Het |
Notch2 |
A |
G |
3: 98,044,689 (GRCm39) |
D1537G |
probably benign |
Het |
Or10k2 |
G |
A |
8: 84,268,100 (GRCm39) |
C109Y |
probably damaging |
Het |
Or51a25 |
G |
T |
7: 102,372,858 (GRCm39) |
H280N |
probably benign |
Het |
Or52ae7 |
A |
T |
7: 103,119,905 (GRCm39) |
I220L |
probably benign |
Het |
Papss1 |
A |
C |
3: 131,288,280 (GRCm39) |
D84A |
probably damaging |
Het |
Pcdhb16 |
T |
A |
18: 37,611,527 (GRCm39) |
D162E |
probably damaging |
Het |
Rab11fip1 |
C |
T |
8: 27,642,840 (GRCm39) |
R653Q |
possibly damaging |
Het |
Rap1gap2 |
A |
T |
11: 74,303,281 (GRCm39) |
|
probably benign |
Het |
Rasal2 |
T |
C |
1: 156,984,777 (GRCm39) |
D990G |
probably damaging |
Het |
Rnf32 |
T |
C |
5: 29,410,701 (GRCm39) |
|
probably null |
Het |
Rp1 |
T |
C |
1: 4,419,936 (GRCm39) |
D392G |
probably benign |
Het |
Scn9a |
T |
C |
2: 66,398,373 (GRCm39) |
D79G |
probably damaging |
Het |
Selenon |
A |
T |
4: 134,268,219 (GRCm39) |
V438D |
probably damaging |
Het |
Slc47a1 |
G |
A |
11: 61,254,239 (GRCm39) |
H158Y |
probably benign |
Het |
Slc5a12 |
A |
T |
2: 110,471,160 (GRCm39) |
E463D |
probably benign |
Het |
Taf2 |
C |
T |
15: 54,879,959 (GRCm39) |
V1126M |
probably benign |
Het |
Tas2r143 |
G |
T |
6: 42,377,259 (GRCm39) |
V30L |
possibly damaging |
Het |
Tcea3 |
G |
A |
4: 135,995,424 (GRCm39) |
V256M |
probably damaging |
Het |
Thy1 |
A |
G |
9: 43,958,111 (GRCm39) |
T80A |
probably benign |
Het |
Tmem9 |
A |
G |
1: 135,947,469 (GRCm39) |
N47S |
probably damaging |
Het |
Tmprss11g |
T |
C |
5: 86,645,128 (GRCm39) |
Q101R |
probably benign |
Het |
Trim66 |
C |
T |
7: 109,059,704 (GRCm39) |
C792Y |
probably damaging |
Het |
Tstd2 |
A |
T |
4: 46,124,949 (GRCm39) |
M226K |
probably damaging |
Het |
Utrn |
G |
T |
10: 12,613,937 (GRCm39) |
T378K |
possibly damaging |
Het |
Vmn2r23 |
A |
G |
6: 123,681,355 (GRCm39) |
I88V |
probably benign |
Het |
|
Other mutations in Heatr9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02160:Heatr9
|
APN |
11 |
83,409,651 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03325:Heatr9
|
APN |
11 |
83,404,085 (GRCm39) |
splice site |
probably null |
|
R0084:Heatr9
|
UTSW |
11 |
83,403,721 (GRCm39) |
splice site |
probably benign |
|
R0243:Heatr9
|
UTSW |
11 |
83,404,164 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0326:Heatr9
|
UTSW |
11 |
83,405,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R0589:Heatr9
|
UTSW |
11 |
83,405,516 (GRCm39) |
splice site |
probably benign |
|
R1386:Heatr9
|
UTSW |
11 |
83,409,651 (GRCm39) |
missense |
probably benign |
0.00 |
R1914:Heatr9
|
UTSW |
11 |
83,409,035 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1915:Heatr9
|
UTSW |
11 |
83,409,035 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4078:Heatr9
|
UTSW |
11 |
83,403,254 (GRCm39) |
missense |
probably benign |
0.24 |
R4756:Heatr9
|
UTSW |
11 |
83,407,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R4789:Heatr9
|
UTSW |
11 |
83,410,018 (GRCm39) |
missense |
probably benign |
0.06 |
R4999:Heatr9
|
UTSW |
11 |
83,409,618 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5060:Heatr9
|
UTSW |
11 |
83,403,258 (GRCm39) |
missense |
probably benign |
0.20 |
R5506:Heatr9
|
UTSW |
11 |
83,405,592 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5874:Heatr9
|
UTSW |
11 |
83,405,426 (GRCm39) |
missense |
probably benign |
0.36 |
R5922:Heatr9
|
UTSW |
11 |
83,403,193 (GRCm39) |
critical splice donor site |
probably null |
|
R6322:Heatr9
|
UTSW |
11 |
83,407,538 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7007:Heatr9
|
UTSW |
11 |
83,411,446 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7431:Heatr9
|
UTSW |
11 |
83,410,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R7790:Heatr9
|
UTSW |
11 |
83,409,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Heatr9
|
UTSW |
11 |
83,403,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R8154:Heatr9
|
UTSW |
11 |
83,402,703 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9248:Heatr9
|
UTSW |
11 |
83,409,281 (GRCm39) |
missense |
possibly damaging |
0.80 |
|