Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
C |
1: 71,306,764 (GRCm39) |
I1981V |
probably benign |
Het |
Actr3b |
A |
G |
5: 26,027,440 (GRCm39) |
Y37C |
probably damaging |
Het |
Adgrd1 |
A |
T |
5: 129,206,169 (GRCm39) |
I248F |
probably benign |
Het |
Alg10b |
T |
C |
15: 90,112,139 (GRCm39) |
S328P |
probably benign |
Het |
C5ar2 |
G |
A |
7: 15,971,349 (GRCm39) |
R193C |
probably damaging |
Het |
Cct8 |
A |
G |
16: 87,285,765 (GRCm39) |
V231A |
possibly damaging |
Het |
Clca4a |
C |
T |
3: 144,674,014 (GRCm39) |
M240I |
probably damaging |
Het |
Cmya5 |
A |
T |
13: 93,185,435 (GRCm39) |
I3520N |
probably damaging |
Het |
Dock6 |
G |
T |
9: 21,757,050 (GRCm39) |
|
probably benign |
Het |
Dynlrb1 |
T |
A |
2: 155,091,865 (GRCm39) |
I99N |
probably damaging |
Het |
Ebf4 |
G |
A |
2: 130,148,419 (GRCm39) |
D77N |
probably damaging |
Het |
Fbxw10 |
C |
T |
11: 62,758,339 (GRCm39) |
|
probably benign |
Het |
Gm10801 |
T |
C |
2: 98,494,197 (GRCm39) |
I113T |
probably damaging |
Het |
Gm5499 |
T |
C |
17: 87,386,314 (GRCm39) |
|
noncoding transcript |
Het |
Gm9913 |
A |
G |
2: 125,348,459 (GRCm39) |
|
probably benign |
Het |
Herc2 |
A |
G |
7: 55,786,991 (GRCm39) |
N1612S |
probably benign |
Het |
Ifnar2 |
T |
C |
16: 91,182,889 (GRCm39) |
S53P |
possibly damaging |
Het |
Inpp5j |
T |
A |
11: 3,453,124 (GRCm39) |
|
probably null |
Het |
Iqca1l |
G |
C |
5: 24,751,664 (GRCm39) |
T528S |
probably benign |
Het |
Kif14 |
T |
G |
1: 136,447,383 (GRCm39) |
I1396S |
possibly damaging |
Het |
Med28 |
A |
G |
5: 45,679,820 (GRCm39) |
T68A |
possibly damaging |
Het |
Meis1 |
A |
T |
11: 18,961,254 (GRCm39) |
N206K |
probably benign |
Het |
Mfsd14a |
T |
C |
3: 116,441,566 (GRCm39) |
|
probably benign |
Het |
Mnt |
G |
C |
11: 74,733,936 (GRCm39) |
|
probably benign |
Het |
Mto1 |
A |
G |
9: 78,365,310 (GRCm39) |
Y413C |
probably damaging |
Het |
Myo7b |
T |
C |
18: 32,100,237 (GRCm39) |
D1599G |
probably benign |
Het |
Myoz1 |
T |
C |
14: 20,703,685 (GRCm39) |
|
probably benign |
Het |
Nhsl2 |
C |
T |
X: 101,121,201 (GRCm39) |
R62W |
probably damaging |
Het |
Npr2 |
T |
A |
4: 43,640,182 (GRCm39) |
Y306N |
probably damaging |
Het |
Nrxn3 |
T |
G |
12: 89,227,186 (GRCm39) |
C274G |
probably damaging |
Het |
Or1e29 |
G |
A |
11: 73,667,466 (GRCm39) |
P229L |
possibly damaging |
Het |
Or5ac22 |
A |
T |
16: 59,135,089 (GRCm39) |
M227K |
probably benign |
Het |
Phldb2 |
T |
C |
16: 45,645,373 (GRCm39) |
T403A |
probably benign |
Het |
Plaa |
T |
C |
4: 94,458,042 (GRCm39) |
I643V |
probably benign |
Het |
Slc28a2b |
T |
C |
2: 122,344,895 (GRCm39) |
L167P |
possibly damaging |
Het |
Stau1 |
T |
C |
2: 166,796,936 (GRCm39) |
I154V |
possibly damaging |
Het |
Ugcg |
T |
G |
4: 59,213,922 (GRCm39) |
V168G |
probably damaging |
Het |
Vmn2r2 |
T |
C |
3: 64,042,053 (GRCm39) |
I221V |
probably benign |
Het |
Wdr93 |
T |
C |
7: 79,402,241 (GRCm39) |
I180T |
possibly damaging |
Het |
Whamm |
G |
C |
7: 81,221,532 (GRCm39) |
G155R |
probably damaging |
Het |
Wnt5a |
T |
A |
14: 28,235,140 (GRCm39) |
Y41* |
probably null |
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 |
IGL02380:Insyn2a
|
APN |
7 |
134,500,873 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
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 |
|