Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
T |
C |
9: 57,165,040 (GRCm39) |
K445E |
probably damaging |
Het |
Abca15 |
A |
T |
7: 119,932,081 (GRCm39) |
|
probably benign |
Het |
Acsbg3 |
C |
T |
17: 57,189,203 (GRCm39) |
Q204* |
probably null |
Het |
Acvr1c |
A |
T |
2: 58,170,254 (GRCm39) |
C371* |
probably null |
Het |
Brs3 |
T |
C |
X: 56,092,727 (GRCm39) |
|
probably benign |
Het |
Car14 |
C |
T |
3: 95,806,871 (GRCm39) |
V198M |
possibly damaging |
Het |
Cenpc1 |
G |
A |
5: 86,170,313 (GRCm39) |
R704* |
probably null |
Het |
Crybg1 |
C |
T |
10: 43,868,490 (GRCm39) |
R1396H |
possibly damaging |
Het |
Cubn |
A |
G |
2: 13,315,377 (GRCm39) |
S3019P |
probably damaging |
Het |
Cyp2j9 |
T |
C |
4: 96,471,665 (GRCm39) |
E222G |
probably benign |
Het |
Defb50 |
C |
A |
8: 22,321,187 (GRCm39) |
T59K |
probably benign |
Het |
Dlg3 |
T |
C |
X: 99,850,848 (GRCm39) |
I587T |
possibly damaging |
Het |
Doc2a |
C |
T |
7: 126,450,173 (GRCm39) |
R204C |
probably damaging |
Het |
Galc |
T |
C |
12: 98,212,503 (GRCm39) |
|
probably benign |
Het |
Gm8257 |
A |
T |
14: 44,892,800 (GRCm39) |
F67I |
probably damaging |
Het |
Hnrnpul1 |
A |
T |
7: 25,426,323 (GRCm39) |
N509K |
probably damaging |
Het |
Iars2 |
T |
A |
1: 185,028,625 (GRCm39) |
I678F |
possibly damaging |
Het |
Ifit1 |
A |
G |
19: 34,625,533 (GRCm39) |
E223G |
possibly damaging |
Het |
Krt81 |
G |
A |
15: 101,361,269 (GRCm39) |
H104Y |
probably benign |
Het |
Lrp4 |
C |
A |
2: 91,304,293 (GRCm39) |
D157E |
probably damaging |
Het |
Ltk |
T |
A |
2: 119,586,186 (GRCm39) |
T21S |
probably benign |
Het |
Lvrn |
A |
T |
18: 46,997,733 (GRCm39) |
|
probably benign |
Het |
Maob |
G |
A |
X: 16,578,881 (GRCm39) |
A424V |
probably damaging |
Het |
Myo1g |
C |
A |
11: 6,465,856 (GRCm39) |
V410F |
possibly damaging |
Het |
Myorg |
T |
A |
4: 41,498,923 (GRCm39) |
I236F |
possibly damaging |
Het |
Naxe |
T |
C |
3: 87,963,981 (GRCm39) |
H250R |
probably damaging |
Het |
Nek5 |
T |
C |
8: 22,601,199 (GRCm39) |
N174S |
possibly damaging |
Het |
Or2y3 |
G |
T |
17: 38,392,998 (GRCm39) |
N290K |
probably damaging |
Het |
Or51l14 |
C |
T |
7: 103,101,002 (GRCm39) |
R153W |
probably damaging |
Het |
Or9m2 |
A |
G |
2: 87,821,288 (GRCm39) |
T278A |
probably benign |
Het |
Pex1 |
A |
G |
5: 3,656,027 (GRCm39) |
T285A |
probably benign |
Het |
Pfas |
A |
G |
11: 68,892,086 (GRCm39) |
S141P |
probably benign |
Het |
Pmm1 |
T |
C |
15: 81,839,945 (GRCm39) |
T127A |
probably damaging |
Het |
Proc |
C |
A |
18: 32,256,873 (GRCm39) |
|
probably benign |
Het |
Ranbp9 |
T |
C |
13: 43,633,980 (GRCm39) |
E142G |
probably damaging |
Het |
Recql4 |
C |
A |
15: 76,594,112 (GRCm39) |
|
probably benign |
Het |
Robo4 |
C |
T |
9: 37,324,336 (GRCm39) |
P955S |
possibly damaging |
Het |
Ryr3 |
T |
A |
2: 112,539,418 (GRCm39) |
N3274I |
probably damaging |
Het |
Serpinb10 |
T |
C |
1: 107,468,612 (GRCm39) |
|
probably benign |
Het |
Slc9c1 |
A |
T |
16: 45,404,811 (GRCm39) |
K848* |
probably null |
Het |
Slfn5 |
A |
G |
11: 82,847,807 (GRCm39) |
T231A |
probably damaging |
Het |
Syncrip |
T |
C |
9: 88,338,660 (GRCm39) |
|
probably benign |
Het |
Taf1c |
G |
A |
8: 120,327,931 (GRCm39) |
T293M |
probably benign |
Het |
Tbc1d5 |
T |
C |
17: 51,120,826 (GRCm39) |
D430G |
possibly damaging |
Het |
Tbx18 |
T |
C |
9: 87,606,384 (GRCm39) |
T254A |
probably damaging |
Het |
Tpm1 |
C |
T |
9: 66,943,337 (GRCm39) |
R105H |
probably damaging |
Het |
Usp17la |
T |
C |
7: 104,510,522 (GRCm39) |
S376P |
probably benign |
Het |
Vmn1r19 |
A |
G |
6: 57,382,179 (GRCm39) |
D244G |
probably damaging |
Het |
Vmn1r58 |
A |
T |
7: 5,414,054 (GRCm39) |
F59I |
probably benign |
Het |
Vmn2r45 |
A |
T |
7: 8,488,622 (GRCm39) |
M136K |
probably benign |
Het |
Vmn2r70 |
T |
A |
7: 85,218,227 (GRCm39) |
R24* |
probably null |
Het |
Vmn2r75 |
T |
A |
7: 85,797,801 (GRCm39) |
I671F |
probably damaging |
Het |
|
Other mutations in Syt16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00984:Syt16
|
APN |
12 |
74,269,604 (GRCm39) |
nonsense |
probably null |
|
IGL01401:Syt16
|
APN |
12 |
74,269,437 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01780:Syt16
|
APN |
12 |
74,313,616 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02350:Syt16
|
APN |
12 |
74,313,616 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02353:Syt16
|
APN |
12 |
74,176,245 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02357:Syt16
|
APN |
12 |
74,313,616 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02360:Syt16
|
APN |
12 |
74,176,245 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02558:Syt16
|
APN |
12 |
74,281,832 (GRCm39) |
nonsense |
probably null |
|
IGL02696:Syt16
|
APN |
12 |
74,176,185 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0701:Syt16
|
UTSW |
12 |
74,281,886 (GRCm39) |
missense |
probably benign |
0.01 |
R1103:Syt16
|
UTSW |
12 |
74,313,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R2002:Syt16
|
UTSW |
12 |
74,281,977 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2079:Syt16
|
UTSW |
12 |
74,285,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R2124:Syt16
|
UTSW |
12 |
74,285,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R3806:Syt16
|
UTSW |
12 |
74,276,172 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3807:Syt16
|
UTSW |
12 |
74,276,172 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4887:Syt16
|
UTSW |
12 |
74,176,160 (GRCm39) |
missense |
probably damaging |
0.96 |
R4889:Syt16
|
UTSW |
12 |
74,176,269 (GRCm39) |
missense |
probably damaging |
0.98 |
R5153:Syt16
|
UTSW |
12 |
74,269,542 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6038:Syt16
|
UTSW |
12 |
74,269,309 (GRCm39) |
splice site |
probably null |
|
R6042:Syt16
|
UTSW |
12 |
74,313,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R6328:Syt16
|
UTSW |
12 |
74,313,467 (GRCm39) |
nonsense |
probably null |
|
R6752:Syt16
|
UTSW |
12 |
74,275,987 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7248:Syt16
|
UTSW |
12 |
74,313,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R7275:Syt16
|
UTSW |
12 |
74,313,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R7276:Syt16
|
UTSW |
12 |
74,313,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R9058:Syt16
|
UTSW |
12 |
74,282,019 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Syt16
|
UTSW |
12 |
74,269,563 (GRCm39) |
missense |
possibly damaging |
0.92 |
|