Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agtr1a |
C |
A |
13: 30,565,901 (GRCm39) |
P322Q |
probably damaging |
Het |
Amh |
AGCGCCTTGG |
AG |
10: 80,641,419 (GRCm39) |
|
probably null |
Het |
Brd1 |
T |
C |
15: 88,585,014 (GRCm39) |
E940G |
probably benign |
Het |
Cd163 |
T |
A |
6: 124,302,209 (GRCm39) |
|
probably benign |
Het |
Cd28 |
C |
T |
1: 60,802,303 (GRCm39) |
T74I |
possibly damaging |
Het |
Cyb5d1 |
C |
T |
11: 69,285,797 (GRCm39) |
|
probably null |
Het |
D6Ertd527e |
C |
G |
6: 87,088,506 (GRCm39) |
T223S |
unknown |
Het |
Dab2ip |
T |
C |
2: 35,608,757 (GRCm39) |
|
probably benign |
Het |
Dnajc25 |
C |
T |
4: 59,003,415 (GRCm39) |
A62V |
probably damaging |
Het |
Dst |
A |
G |
1: 34,250,235 (GRCm39) |
D4063G |
probably damaging |
Het |
Elmod1 |
T |
C |
9: 53,843,052 (GRCm39) |
Y42C |
probably damaging |
Het |
Hdac5 |
T |
C |
11: 102,096,332 (GRCm39) |
I310V |
probably damaging |
Het |
Hpx |
A |
G |
7: 105,248,856 (GRCm39) |
|
probably benign |
Het |
Ighv10-1 |
A |
T |
12: 114,443,015 (GRCm39) |
|
probably benign |
Het |
Igsf3 |
A |
G |
3: 101,365,419 (GRCm39) |
D1130G |
probably benign |
Het |
Katnip |
A |
G |
7: 125,465,654 (GRCm39) |
R1343G |
probably damaging |
Het |
Kdm4d |
A |
G |
9: 14,374,395 (GRCm39) |
S488P |
probably benign |
Het |
Lingo2 |
A |
G |
4: 35,708,538 (GRCm39) |
Y481H |
probably damaging |
Het |
Ltbp1 |
A |
G |
17: 75,532,280 (GRCm39) |
Q118R |
possibly damaging |
Het |
Map3k20 |
C |
T |
2: 72,268,562 (GRCm39) |
P523L |
probably damaging |
Het |
Msx1 |
A |
G |
5: 37,978,625 (GRCm39) |
Y297H |
probably damaging |
Het |
Myo9a |
A |
G |
9: 59,802,483 (GRCm39) |
D1990G |
probably damaging |
Het |
Niban2 |
T |
C |
2: 32,809,815 (GRCm39) |
V304A |
probably benign |
Het |
Perp |
C |
A |
10: 18,731,483 (GRCm39) |
Y147* |
probably null |
Het |
Prr16 |
A |
T |
18: 51,435,755 (GRCm39) |
D78V |
probably damaging |
Het |
Rfx7 |
C |
T |
9: 72,525,228 (GRCm39) |
T806M |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,713,016 (GRCm39) |
|
probably null |
Het |
Sema5b |
A |
T |
16: 35,472,030 (GRCm39) |
E496V |
probably null |
Het |
Shf |
G |
A |
2: 122,199,163 (GRCm39) |
P51S |
probably damaging |
Het |
Spdl1 |
T |
C |
11: 34,710,644 (GRCm39) |
Y368C |
probably damaging |
Het |
Sptbn2 |
G |
C |
19: 4,795,921 (GRCm39) |
R1700P |
possibly damaging |
Het |
Tenm2 |
C |
T |
11: 35,954,004 (GRCm39) |
G1236R |
possibly damaging |
Het |
Tln2 |
T |
G |
9: 67,165,848 (GRCm39) |
K1000Q |
probably damaging |
Het |
Tmbim7 |
A |
G |
5: 3,711,943 (GRCm39) |
T63A |
probably benign |
Het |
Tmed11 |
T |
C |
5: 108,926,885 (GRCm39) |
D129G |
possibly damaging |
Het |
Ttc28 |
G |
A |
5: 111,373,543 (GRCm39) |
S962N |
probably damaging |
Het |
Ttll6 |
T |
C |
11: 96,026,555 (GRCm39) |
I113T |
probably damaging |
Het |
Uso1 |
T |
A |
5: 92,318,606 (GRCm39) |
F210L |
probably damaging |
Het |
Uspl1 |
T |
A |
5: 149,131,131 (GRCm39) |
V224E |
probably benign |
Het |
Zfp639 |
G |
A |
3: 32,573,345 (GRCm39) |
V86I |
possibly 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 |
|
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 |
R1609:Cntnap2
|
UTSW |
6 |
45,992,264 (GRCm39) |
missense |
probably benign |
0.13 |
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 |
|