Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930451I11Rik |
A |
T |
7: 126,429,894 (GRCm39) |
F101Y |
possibly damaging |
Het |
Abca17 |
G |
C |
17: 24,508,481 (GRCm39) |
T1018R |
probably damaging |
Het |
Adamts14 |
T |
A |
10: 61,054,214 (GRCm39) |
Q606L |
probably damaging |
Het |
Adgrf5 |
C |
A |
17: 43,733,531 (GRCm39) |
N118K |
possibly damaging |
Het |
Baz2b |
A |
T |
2: 59,755,010 (GRCm39) |
Y1073N |
possibly damaging |
Het |
Celf2 |
T |
C |
2: 6,608,936 (GRCm39) |
R282G |
probably damaging |
Het |
Cntnap5c |
A |
T |
17: 58,183,387 (GRCm39) |
D31V |
probably damaging |
Het |
Cobl |
A |
G |
11: 12,328,342 (GRCm39) |
L81P |
probably damaging |
Het |
Cpsf1 |
A |
T |
15: 76,487,051 (GRCm39) |
L209Q |
probably damaging |
Het |
Crocc |
G |
A |
4: 140,746,067 (GRCm39) |
A1684V |
probably damaging |
Het |
Cyp4f37 |
T |
A |
17: 32,848,099 (GRCm39) |
C206S |
probably damaging |
Het |
Dnah3 |
A |
G |
7: 119,567,161 (GRCm39) |
V2355A |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,106,314 (GRCm39) |
K1756E |
probably benign |
Het |
Fis1 |
T |
C |
5: 136,991,971 (GRCm39) |
I55T |
possibly damaging |
Het |
Gm2381 |
G |
A |
7: 42,469,831 (GRCm39) |
P98S |
probably damaging |
Het |
Gpr37 |
C |
T |
6: 25,666,945 (GRCm39) |
|
probably benign |
Het |
Grin2a |
A |
G |
16: 9,579,829 (GRCm39) |
F145L |
possibly damaging |
Het |
Igkv9-120 |
T |
A |
6: 68,027,128 (GRCm39) |
|
probably benign |
Het |
Il12rb1 |
G |
A |
8: 71,268,446 (GRCm39) |
W396* |
probably null |
Het |
Itga8 |
A |
T |
2: 12,165,215 (GRCm39) |
V798D |
probably damaging |
Het |
Lfng |
T |
A |
5: 140,597,622 (GRCm39) |
D149E |
probably damaging |
Het |
Magi2 |
A |
AG |
5: 20,807,459 (GRCm39) |
|
probably null |
Het |
Mgam |
C |
A |
6: 40,629,649 (GRCm39) |
A86E |
possibly damaging |
Het |
Myh4 |
A |
G |
11: 67,139,459 (GRCm39) |
N592S |
probably benign |
Het |
Naa16 |
A |
G |
14: 79,573,323 (GRCm39) |
C816R |
probably damaging |
Het |
Nek8 |
A |
G |
11: 78,058,967 (GRCm39) |
S513P |
probably damaging |
Het |
Ociad1 |
A |
G |
5: 73,451,694 (GRCm39) |
|
probably null |
Het |
Or1j4 |
A |
G |
2: 36,740,811 (GRCm39) |
Y251C |
probably damaging |
Het |
Or2t35 |
C |
T |
14: 14,407,398 (GRCm38) |
P57S |
probably damaging |
Het |
Or4g7 |
T |
C |
2: 111,309,699 (GRCm39) |
M190T |
probably benign |
Het |
Osbpl8 |
T |
A |
10: 111,105,297 (GRCm39) |
S251T |
probably benign |
Het |
Pcdh7 |
G |
A |
5: 57,877,618 (GRCm39) |
G391E |
probably damaging |
Het |
Pcdhga10 |
T |
A |
18: 37,881,253 (GRCm39) |
V338E |
possibly damaging |
Het |
Pde4b |
C |
T |
4: 102,458,742 (GRCm39) |
A466V |
probably damaging |
Het |
Peg10 |
C |
T |
6: 4,756,912 (GRCm39) |
|
probably benign |
Het |
Poteg |
A |
T |
8: 27,971,704 (GRCm39) |
N406I |
probably benign |
Het |
Ppargc1a |
A |
G |
5: 51,631,151 (GRCm39) |
F493L |
probably benign |
Het |
Ptpra |
C |
A |
2: 130,386,919 (GRCm39) |
H603Q |
probably benign |
Het |
Rnf10 |
T |
C |
5: 115,387,171 (GRCm39) |
D439G |
probably benign |
Het |
Shfl |
A |
T |
9: 20,784,868 (GRCm39) |
H225L |
probably damaging |
Het |
Syt3 |
G |
A |
7: 44,042,866 (GRCm39) |
V383I |
probably benign |
Het |
Tectb |
C |
G |
19: 55,169,431 (GRCm39) |
|
probably benign |
Het |
Try5 |
C |
T |
6: 41,290,410 (GRCm39) |
V25I |
probably benign |
Het |
Ttn |
G |
T |
2: 76,749,551 (GRCm39) |
Q3833K |
probably benign |
Het |
Usp53 |
G |
A |
3: 122,728,140 (GRCm39) |
P814L |
probably benign |
Het |
Utp25 |
A |
T |
1: 192,810,759 (GRCm39) |
N81K |
probably benign |
Het |
Vmn1r181 |
G |
T |
7: 23,683,943 (GRCm39) |
S136I |
possibly damaging |
Het |
Vmn2r114 |
A |
T |
17: 23,509,948 (GRCm39) |
M844K |
probably benign |
Het |
Vwa8 |
G |
T |
14: 79,184,582 (GRCm39) |
R360L |
probably benign |
Het |
Xlr4b |
A |
T |
X: 72,258,938 (GRCm39) |
Q25L |
probably null |
Het |
Zfp532 |
T |
A |
18: 65,789,697 (GRCm39) |
H1045Q |
possibly damaging |
Het |
Zfp985 |
G |
A |
4: 147,667,468 (GRCm39) |
W112* |
probably null |
Het |
|
Other mutations in Htr4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01965:Htr4
|
APN |
18 |
62,570,740 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02822:Htr4
|
APN |
18 |
62,561,255 (GRCm39) |
splice site |
probably benign |
|
IGL03240:Htr4
|
APN |
18 |
62,570,692 (GRCm39) |
missense |
possibly damaging |
0.92 |
P0042:Htr4
|
UTSW |
18 |
62,546,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0485:Htr4
|
UTSW |
18 |
62,561,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R1137:Htr4
|
UTSW |
18 |
62,570,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1661:Htr4
|
UTSW |
18 |
62,545,305 (GRCm39) |
missense |
probably damaging |
0.97 |
R1665:Htr4
|
UTSW |
18 |
62,545,305 (GRCm39) |
missense |
probably damaging |
0.97 |
R1682:Htr4
|
UTSW |
18 |
62,561,137 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1903:Htr4
|
UTSW |
18 |
62,561,193 (GRCm39) |
missense |
probably benign |
0.01 |
R2215:Htr4
|
UTSW |
18 |
62,546,787 (GRCm39) |
nonsense |
probably null |
|
R2847:Htr4
|
UTSW |
18 |
62,561,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R5764:Htr4
|
UTSW |
18 |
62,570,613 (GRCm39) |
missense |
probably damaging |
0.97 |
R5787:Htr4
|
UTSW |
18 |
62,546,693 (GRCm39) |
missense |
probably damaging |
0.98 |
R7184:Htr4
|
UTSW |
18 |
62,570,498 (GRCm39) |
nonsense |
probably null |
|
R7278:Htr4
|
UTSW |
18 |
62,545,247 (GRCm39) |
missense |
probably benign |
0.04 |
R7811:Htr4
|
UTSW |
18 |
62,545,269 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8190:Htr4
|
UTSW |
18 |
62,570,971 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8312:Htr4
|
UTSW |
18 |
62,570,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R8699:Htr4
|
UTSW |
18 |
62,570,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Htr4
|
UTSW |
18 |
62,561,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R8727:Htr4
|
UTSW |
18 |
62,561,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R8757:Htr4
|
UTSW |
18 |
62,545,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R8787:Htr4
|
UTSW |
18 |
62,570,853 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1177:Htr4
|
UTSW |
18 |
62,570,679 (GRCm39) |
missense |
probably benign |
0.29 |
|