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 |
Htr4 |
T |
C |
18: 62,561,197 (GRCm39) |
S153P |
probably 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 |
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 Syt3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01487:Syt3
|
APN |
7 |
44,040,423 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02738:Syt3
|
APN |
7 |
44,035,447 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02751:Syt3
|
APN |
7 |
44,035,486 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0129:Syt3
|
UTSW |
7 |
44,042,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R0749:Syt3
|
UTSW |
7 |
44,048,571 (GRCm39) |
missense |
probably benign |
0.41 |
R1022:Syt3
|
UTSW |
7 |
44,040,106 (GRCm39) |
missense |
probably damaging |
0.99 |
R1024:Syt3
|
UTSW |
7 |
44,040,106 (GRCm39) |
missense |
probably damaging |
0.99 |
R1204:Syt3
|
UTSW |
7 |
44,042,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Syt3
|
UTSW |
7 |
44,045,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Syt3
|
UTSW |
7 |
44,045,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R1902:Syt3
|
UTSW |
7 |
44,039,940 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2849:Syt3
|
UTSW |
7 |
44,042,866 (GRCm39) |
missense |
probably benign |
0.43 |
R2924:Syt3
|
UTSW |
7 |
44,045,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R2925:Syt3
|
UTSW |
7 |
44,045,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R4560:Syt3
|
UTSW |
7 |
44,045,368 (GRCm39) |
missense |
probably benign |
0.13 |
R5161:Syt3
|
UTSW |
7 |
44,045,439 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5430:Syt3
|
UTSW |
7 |
44,040,337 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5570:Syt3
|
UTSW |
7 |
44,040,043 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5572:Syt3
|
UTSW |
7 |
44,040,142 (GRCm39) |
missense |
probably benign |
0.07 |
R5975:Syt3
|
UTSW |
7 |
44,042,187 (GRCm39) |
nonsense |
probably null |
|
R6370:Syt3
|
UTSW |
7 |
44,045,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R7291:Syt3
|
UTSW |
7 |
44,045,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7319:Syt3
|
UTSW |
7 |
44,041,953 (GRCm39) |
nonsense |
probably null |
|
R7382:Syt3
|
UTSW |
7 |
44,042,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R7579:Syt3
|
UTSW |
7 |
44,040,272 (GRCm39) |
nonsense |
probably null |
|
R7705:Syt3
|
UTSW |
7 |
44,042,083 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7743:Syt3
|
UTSW |
7 |
44,042,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Syt3
|
UTSW |
7 |
44,045,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R9134:Syt3
|
UTSW |
7 |
44,042,791 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9705:Syt3
|
UTSW |
7 |
44,045,225 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Syt3
|
UTSW |
7 |
44,045,071 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Syt3
|
UTSW |
7 |
44,040,097 (GRCm39) |
missense |
probably damaging |
0.99 |
|