Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
C |
A |
7: 40,643,968 (GRCm39) |
P546T |
possibly damaging |
Het |
Abca13 |
T |
C |
11: 9,241,599 (GRCm39) |
I1154T |
possibly damaging |
Het |
Abca8a |
A |
G |
11: 109,969,641 (GRCm39) |
|
probably benign |
Het |
Acsm5 |
A |
T |
7: 119,136,509 (GRCm39) |
Q360L |
probably benign |
Het |
Adamtsl5 |
T |
C |
10: 80,177,612 (GRCm39) |
E350G |
probably benign |
Het |
Adgrl2 |
A |
T |
3: 148,534,125 (GRCm39) |
L1017* |
probably null |
Het |
Aqr |
T |
C |
2: 113,940,417 (GRCm39) |
D1243G |
probably damaging |
Het |
Arhgef17 |
G |
T |
7: 100,578,650 (GRCm39) |
P766Q |
possibly damaging |
Het |
Bclaf1 |
T |
C |
10: 20,201,113 (GRCm39) |
V413A |
possibly damaging |
Het |
Bcr |
A |
G |
10: 75,011,131 (GRCm39) |
D14G |
probably benign |
Het |
Cadps2 |
C |
T |
6: 23,287,731 (GRCm39) |
V1190I |
probably benign |
Het |
Cdh9 |
A |
G |
15: 16,856,086 (GRCm39) |
I709V |
possibly damaging |
Het |
Cnbd1 |
C |
A |
4: 18,887,748 (GRCm39) |
|
probably null |
Het |
Cnbd1 |
T |
A |
4: 18,887,749 (GRCm39) |
|
probably null |
Het |
Col4a3 |
T |
C |
1: 82,650,509 (GRCm39) |
|
probably benign |
Het |
Coro1a |
T |
A |
7: 126,302,288 (GRCm39) |
K20* |
probably null |
Het |
Crb2 |
T |
A |
2: 37,673,447 (GRCm39) |
D114E |
probably damaging |
Het |
Dnah6 |
C |
A |
6: 73,053,623 (GRCm39) |
K2870N |
probably benign |
Het |
Fpr3 |
A |
G |
17: 18,191,254 (GRCm39) |
H175R |
probably benign |
Het |
Gk5 |
T |
G |
9: 96,032,533 (GRCm39) |
S248A |
possibly damaging |
Het |
Grm4 |
T |
A |
17: 27,653,635 (GRCm39) |
I772F |
probably damaging |
Het |
Gstt4 |
A |
G |
10: 75,653,073 (GRCm39) |
I163T |
possibly damaging |
Het |
Hr |
A |
G |
14: 70,795,201 (GRCm39) |
R278G |
probably damaging |
Het |
Igfbp5 |
T |
A |
1: 72,903,108 (GRCm39) |
R156* |
probably null |
Het |
Ighv1-4 |
G |
A |
12: 114,450,753 (GRCm39) |
|
probably benign |
Het |
Kcna2 |
A |
C |
3: 107,012,274 (GRCm39) |
Q285P |
probably benign |
Het |
Klf5 |
A |
T |
14: 99,538,894 (GRCm39) |
R102S |
possibly damaging |
Het |
Ldb1 |
A |
T |
19: 46,022,929 (GRCm39) |
M252K |
possibly damaging |
Het |
Lrrc66 |
T |
C |
5: 73,787,009 (GRCm39) |
I114V |
possibly damaging |
Het |
Map1b |
A |
T |
13: 99,567,651 (GRCm39) |
I1690N |
unknown |
Het |
Myo1a |
A |
G |
10: 127,550,354 (GRCm39) |
T565A |
probably benign |
Het |
Nt5c |
T |
C |
11: 115,382,127 (GRCm39) |
D84G |
possibly damaging |
Het |
Pde1b |
A |
G |
15: 103,428,417 (GRCm39) |
N51S |
possibly damaging |
Het |
Pikfyve |
T |
A |
1: 65,295,180 (GRCm39) |
L1437Q |
probably damaging |
Het |
Pld5 |
C |
T |
1: 175,967,610 (GRCm39) |
V82I |
probably damaging |
Het |
Psmb6 |
T |
A |
11: 70,416,737 (GRCm39) |
N42K |
probably benign |
Het |
Slco3a1 |
G |
A |
7: 74,204,238 (GRCm39) |
S34F |
probably damaging |
Het |
Slfn9 |
A |
G |
11: 82,872,046 (GRCm39) |
Y897H |
probably benign |
Het |
Spag6l |
T |
C |
16: 16,581,033 (GRCm39) |
|
probably null |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Tmem215 |
A |
T |
4: 40,474,534 (GRCm39) |
I204F |
probably benign |
Het |
Txnl1 |
A |
G |
18: 63,807,114 (GRCm39) |
|
probably null |
Het |
Ube2q2 |
T |
A |
9: 55,070,296 (GRCm39) |
D79E |
probably benign |
Het |
Ugt2a3 |
T |
C |
5: 87,484,658 (GRCm39) |
D122G |
probably benign |
Het |
Vmn2r73 |
A |
T |
7: 85,507,383 (GRCm39) |
I643K |
probably benign |
Het |
Xkrx |
T |
A |
X: 133,051,388 (GRCm39) |
H421L |
probably benign |
Het |
|
Other mutations in Insyn2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01504:Insyn2a
|
APN |
7 |
134,519,669 (GRCm39) |
missense |
probably benign |
0.15 |
R0557:Insyn2a
|
UTSW |
7 |
134,520,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R1421:Insyn2a
|
UTSW |
7 |
134,500,960 (GRCm39) |
splice site |
probably benign |
|
R1691:Insyn2a
|
UTSW |
7 |
134,520,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R1726:Insyn2a
|
UTSW |
7 |
134,500,867 (GRCm39) |
splice site |
probably benign |
|
R2045:Insyn2a
|
UTSW |
7 |
134,520,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R2259:Insyn2a
|
UTSW |
7 |
134,519,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R3078:Insyn2a
|
UTSW |
7 |
134,519,750 (GRCm39) |
missense |
probably benign |
0.15 |
R3851:Insyn2a
|
UTSW |
7 |
134,486,255 (GRCm39) |
missense |
probably benign |
0.23 |
R4619:Insyn2a
|
UTSW |
7 |
134,520,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R4663:Insyn2a
|
UTSW |
7 |
134,500,877 (GRCm39) |
nonsense |
probably null |
|
R5024:Insyn2a
|
UTSW |
7 |
134,520,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R5067:Insyn2a
|
UTSW |
7 |
134,520,284 (GRCm39) |
missense |
probably benign |
0.01 |
R5195:Insyn2a
|
UTSW |
7 |
134,486,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R5708:Insyn2a
|
UTSW |
7 |
134,520,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R6195:Insyn2a
|
UTSW |
7 |
134,520,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R7151:Insyn2a
|
UTSW |
7 |
134,520,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R7414:Insyn2a
|
UTSW |
7 |
134,519,738 (GRCm39) |
missense |
probably benign |
0.06 |
R7988:Insyn2a
|
UTSW |
7 |
134,519,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R8930:Insyn2a
|
UTSW |
7 |
134,500,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R8932:Insyn2a
|
UTSW |
7 |
134,500,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R9230:Insyn2a
|
UTSW |
7 |
134,520,439 (GRCm39) |
nonsense |
probably null |
|
R9586:Insyn2a
|
UTSW |
7 |
134,520,180 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Insyn2a
|
UTSW |
7 |
134,520,435 (GRCm39) |
missense |
probably damaging |
1.00 |
|