Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot2 |
C |
T |
12: 84,039,630 (GRCm39) |
R380C |
possibly damaging |
Het |
Allc |
A |
T |
12: 28,603,993 (GRCm39) |
D363E |
probably damaging |
Het |
Anxa2 |
TCCC |
TCC |
9: 69,397,036 (GRCm39) |
|
probably null |
Het |
App |
C |
A |
16: 84,876,837 (GRCm39) |
V185L |
probably damaging |
Het |
Atp5if1 |
T |
C |
4: 132,258,078 (GRCm39) |
D47G |
probably benign |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Cbr4 |
T |
A |
8: 61,956,192 (GRCm39) |
Y220N |
probably damaging |
Het |
Ccdc6 |
C |
A |
10: 70,002,877 (GRCm39) |
Q203K |
probably damaging |
Het |
Dmxl2 |
A |
G |
9: 54,316,547 (GRCm39) |
I1613T |
possibly damaging |
Het |
Dnah14 |
T |
C |
1: 181,577,742 (GRCm39) |
S3020P |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,392,126 (GRCm39) |
L3829P |
probably damaging |
Het |
Fbxw25 |
C |
T |
9: 109,492,578 (GRCm39) |
C53Y |
probably benign |
Het |
Fndc1 |
G |
T |
17: 7,991,598 (GRCm39) |
H699Q |
unknown |
Het |
Gnaq |
G |
A |
19: 16,360,618 (GRCm39) |
V314M |
possibly damaging |
Het |
Gpr158 |
A |
G |
2: 21,788,104 (GRCm39) |
T582A |
possibly damaging |
Het |
Mapk1 |
T |
C |
16: 16,856,170 (GRCm39) |
|
probably benign |
Het |
Med1 |
T |
A |
11: 98,051,996 (GRCm39) |
H456L |
possibly damaging |
Het |
Myo6 |
G |
A |
9: 80,195,499 (GRCm39) |
|
probably null |
Het |
Nipbl |
A |
G |
15: 8,396,148 (GRCm39) |
Y142H |
probably damaging |
Het |
Or4c113 |
A |
T |
2: 88,885,688 (GRCm39) |
F27L |
probably benign |
Het |
Or8k24 |
A |
G |
2: 86,215,838 (GRCm39) |
I308T |
probably benign |
Het |
Or8k33 |
A |
C |
2: 86,383,949 (GRCm39) |
V173G |
probably damaging |
Het |
Pgbd5 |
T |
C |
8: 125,160,750 (GRCm39) |
D39G |
probably benign |
Het |
Pnisr |
G |
T |
4: 21,871,440 (GRCm39) |
G387* |
probably null |
Het |
Pnpla6 |
T |
C |
8: 3,567,135 (GRCm39) |
L61P |
probably damaging |
Het |
Prkra |
A |
T |
2: 76,463,936 (GRCm39) |
I242N |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,419,424 (GRCm39) |
S563P |
probably damaging |
Het |
Rtp3 |
A |
G |
9: 110,815,085 (GRCm39) |
|
probably benign |
Het |
Sema3d |
A |
G |
5: 12,591,023 (GRCm39) |
T301A |
probably damaging |
Het |
Setmar |
A |
G |
6: 108,053,076 (GRCm39) |
D190G |
probably benign |
Het |
Sf3b2 |
A |
G |
19: 5,345,061 (GRCm39) |
|
probably benign |
Het |
Taf4b |
A |
G |
18: 14,968,938 (GRCm39) |
K692E |
probably damaging |
Het |
Tktl2 |
A |
G |
8: 66,965,504 (GRCm39) |
E354G |
probably benign |
Het |
Tspan4 |
A |
G |
7: 141,071,557 (GRCm39) |
T135A |
probably damaging |
Het |
Vmn1r22 |
G |
T |
6: 57,877,733 (GRCm39) |
Y81* |
probably null |
Het |
Vmn2r31 |
T |
C |
7: 7,387,888 (GRCm39) |
E561G |
probably damaging |
Het |
Xrn1 |
A |
T |
9: 95,856,946 (GRCm39) |
K389N |
probably benign |
Het |
Zfp277 |
A |
T |
12: 40,378,719 (GRCm39) |
N379K |
probably damaging |
Het |
|
Other mutations in Cntnap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00509:Cntnap2
|
APN |
6 |
45,992,197 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00657:Cntnap2
|
APN |
6 |
46,965,721 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00846:Cntnap2
|
APN |
6 |
47,169,972 (GRCm39) |
missense |
probably benign |
0.12 |
IGL00851:Cntnap2
|
APN |
6 |
46,461,006 (GRCm39) |
missense |
probably benign |
|
IGL00857:Cntnap2
|
APN |
6 |
47,026,358 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01290:Cntnap2
|
APN |
6 |
45,992,399 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01445:Cntnap2
|
APN |
6 |
47,169,947 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01468:Cntnap2
|
APN |
6 |
47,248,305 (GRCm39) |
nonsense |
probably null |
|
IGL01859:Cntnap2
|
APN |
6 |
46,965,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02092:Cntnap2
|
APN |
6 |
46,211,137 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02239:Cntnap2
|
APN |
6 |
46,998,588 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02508:Cntnap2
|
APN |
6 |
46,211,254 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02530:Cntnap2
|
APN |
6 |
46,998,670 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL03013:Cntnap2
|
APN |
6 |
47,072,483 (GRCm39) |
missense |
possibly damaging |
0.66 |
BB004:Cntnap2
|
UTSW |
6 |
47,072,621 (GRCm39) |
missense |
possibly damaging |
0.93 |
BB014:Cntnap2
|
UTSW |
6 |
47,072,621 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02802:Cntnap2
|
UTSW |
6 |
46,147,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R0001:Cntnap2
|
UTSW |
6 |
46,507,105 (GRCm39) |
missense |
probably benign |
0.04 |
R0007:Cntnap2
|
UTSW |
6 |
45,969,007 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0007:Cntnap2
|
UTSW |
6 |
45,969,007 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0043:Cntnap2
|
UTSW |
6 |
46,460,917 (GRCm39) |
missense |
probably benign |
0.01 |
R0118:Cntnap2
|
UTSW |
6 |
45,037,326 (GRCm39) |
splice site |
probably null |
|
R0352:Cntnap2
|
UTSW |
6 |
45,969,018 (GRCm39) |
splice site |
probably null |
|
R0389:Cntnap2
|
UTSW |
6 |
45,986,571 (GRCm39) |
missense |
probably benign |
0.06 |
R0482:Cntnap2
|
UTSW |
6 |
45,692,750 (GRCm39) |
missense |
probably benign |
0.00 |
R0530:Cntnap2
|
UTSW |
6 |
46,506,839 (GRCm39) |
nonsense |
probably null |
|
R0611:Cntnap2
|
UTSW |
6 |
47,072,483 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0630:Cntnap2
|
UTSW |
6 |
46,965,694 (GRCm39) |
missense |
probably damaging |
0.99 |
R0636:Cntnap2
|
UTSW |
6 |
47,273,642 (GRCm39) |
splice site |
probably benign |
|
R0976:Cntnap2
|
UTSW |
6 |
47,248,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Cntnap2
|
UTSW |
6 |
46,460,902 (GRCm39) |
missense |
probably benign |
|
R1195:Cntnap2
|
UTSW |
6 |
46,460,902 (GRCm39) |
missense |
probably benign |
|
R1195:Cntnap2
|
UTSW |
6 |
46,460,902 (GRCm39) |
missense |
probably benign |
|
R1387:Cntnap2
|
UTSW |
6 |
47,084,848 (GRCm39) |
missense |
probably benign |
0.19 |
R1524:Cntnap2
|
UTSW |
6 |
46,507,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R1716:Cntnap2
|
UTSW |
6 |
47,084,826 (GRCm39) |
nonsense |
probably null |
|
R1757:Cntnap2
|
UTSW |
6 |
46,736,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R1809:Cntnap2
|
UTSW |
6 |
46,965,609 (GRCm39) |
missense |
probably damaging |
0.99 |
R1813:Cntnap2
|
UTSW |
6 |
46,507,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R2103:Cntnap2
|
UTSW |
6 |
47,275,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Cntnap2
|
UTSW |
6 |
47,275,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R3037:Cntnap2
|
UTSW |
6 |
45,992,200 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3899:Cntnap2
|
UTSW |
6 |
45,968,837 (GRCm39) |
missense |
probably benign |
0.00 |
R4027:Cntnap2
|
UTSW |
6 |
46,833,062 (GRCm39) |
missense |
probably benign |
|
R4030:Cntnap2
|
UTSW |
6 |
46,833,062 (GRCm39) |
missense |
probably benign |
|
R4237:Cntnap2
|
UTSW |
6 |
46,507,324 (GRCm39) |
intron |
probably benign |
|
R4445:Cntnap2
|
UTSW |
6 |
46,736,785 (GRCm39) |
missense |
probably benign |
0.01 |
R4737:Cntnap2
|
UTSW |
6 |
45,037,251 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4740:Cntnap2
|
UTSW |
6 |
45,037,251 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4915:Cntnap2
|
UTSW |
6 |
46,506,969 (GRCm39) |
intron |
probably benign |
|
R4918:Cntnap2
|
UTSW |
6 |
46,506,969 (GRCm39) |
intron |
probably benign |
|
R4999:Cntnap2
|
UTSW |
6 |
45,897,768 (GRCm39) |
missense |
probably damaging |
0.96 |
R5373:Cntnap2
|
UTSW |
6 |
47,084,903 (GRCm39) |
missense |
probably benign |
0.00 |
R5374:Cntnap2
|
UTSW |
6 |
47,084,903 (GRCm39) |
missense |
probably benign |
0.00 |
R5742:Cntnap2
|
UTSW |
6 |
45,897,860 (GRCm39) |
nonsense |
probably null |
|
R5748:Cntnap2
|
UTSW |
6 |
45,692,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R5765:Cntnap2
|
UTSW |
6 |
46,506,749 (GRCm39) |
intron |
probably benign |
|
R6118:Cntnap2
|
UTSW |
6 |
47,170,011 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6181:Cntnap2
|
UTSW |
6 |
46,736,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R6189:Cntnap2
|
UTSW |
6 |
47,248,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R6262:Cntnap2
|
UTSW |
6 |
45,037,046 (GRCm39) |
splice site |
probably null |
|
R6385:Cntnap2
|
UTSW |
6 |
46,833,114 (GRCm39) |
missense |
probably benign |
0.00 |
R6555:Cntnap2
|
UTSW |
6 |
46,736,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R6577:Cntnap2
|
UTSW |
6 |
46,147,206 (GRCm39) |
missense |
probably benign |
0.25 |
R6610:Cntnap2
|
UTSW |
6 |
45,992,191 (GRCm39) |
missense |
probably benign |
0.08 |
R6761:Cntnap2
|
UTSW |
6 |
47,026,307 (GRCm39) |
missense |
probably benign |
0.03 |
R7125:Cntnap2
|
UTSW |
6 |
46,965,580 (GRCm39) |
missense |
probably benign |
0.12 |
R7329:Cntnap2
|
UTSW |
6 |
47,248,205 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7502:Cntnap2
|
UTSW |
6 |
46,460,963 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7927:Cntnap2
|
UTSW |
6 |
47,072,621 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8057:Cntnap2
|
UTSW |
6 |
46,324,079 (GRCm39) |
missense |
probably damaging |
0.98 |
R8261:Cntnap2
|
UTSW |
6 |
47,072,627 (GRCm39) |
missense |
probably damaging |
0.98 |
R8356:Cntnap2
|
UTSW |
6 |
47,026,307 (GRCm39) |
missense |
probably benign |
0.03 |
R8479:Cntnap2
|
UTSW |
6 |
46,736,707 (GRCm39) |
missense |
probably benign |
0.14 |
R8503:Cntnap2
|
UTSW |
6 |
45,968,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R8698:Cntnap2
|
UTSW |
6 |
47,026,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R8719:Cntnap2
|
UTSW |
6 |
45,978,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R8816:Cntnap2
|
UTSW |
6 |
46,833,076 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8987:Cntnap2
|
UTSW |
6 |
46,460,983 (GRCm39) |
missense |
probably benign |
0.01 |
R9000:Cntnap2
|
UTSW |
6 |
46,461,139 (GRCm39) |
intron |
probably benign |
|
R9209:Cntnap2
|
UTSW |
6 |
47,026,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R9253:Cntnap2
|
UTSW |
6 |
45,978,112 (GRCm39) |
missense |
probably benign |
0.00 |
R9310:Cntnap2
|
UTSW |
6 |
45,978,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R9395:Cntnap2
|
UTSW |
6 |
45,978,244 (GRCm39) |
missense |
probably damaging |
0.98 |
R9462:Cntnap2
|
UTSW |
6 |
46,211,217 (GRCm39) |
missense |
probably damaging |
0.99 |
R9526:Cntnap2
|
UTSW |
6 |
45,992,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R9600:Cntnap2
|
UTSW |
6 |
45,969,009 (GRCm39) |
missense |
probably damaging |
0.98 |
R9621:Cntnap2
|
UTSW |
6 |
46,965,726 (GRCm39) |
missense |
probably damaging |
0.98 |
R9738:Cntnap2
|
UTSW |
6 |
45,992,373 (GRCm39) |
frame shift |
probably null |
|
R9745:Cntnap2
|
UTSW |
6 |
46,211,100 (GRCm39) |
missense |
probably benign |
0.01 |
R9775:Cntnap2
|
UTSW |
6 |
47,026,261 (GRCm39) |
missense |
probably damaging |
1.00 |
RF022:Cntnap2
|
UTSW |
6 |
46,998,599 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Cntnap2
|
UTSW |
6 |
45,986,452 (GRCm39) |
missense |
possibly damaging |
0.53 |
X0063:Cntnap2
|
UTSW |
6 |
46,998,688 (GRCm39) |
missense |
possibly damaging |
0.92 |
X0066:Cntnap2
|
UTSW |
6 |
46,211,179 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Cntnap2
|
UTSW |
6 |
47,248,082 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Cntnap2
|
UTSW |
6 |
45,992,233 (GRCm39) |
missense |
possibly damaging |
0.90 |
|