Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afap1l1 |
A |
T |
18: 61,891,754 (GRCm39) |
L21Q |
probably damaging |
Het |
Ago1 |
G |
A |
4: 126,335,729 (GRCm39) |
R661C |
probably damaging |
Het |
Albfm1 |
T |
A |
5: 90,740,864 (GRCm39) |
|
probably null |
Het |
Aoc3 |
T |
C |
11: 101,223,132 (GRCm39) |
V456A |
probably benign |
Het |
Aopep |
G |
C |
13: 63,180,921 (GRCm39) |
W294C |
probably damaging |
Het |
Cacna1b |
A |
T |
2: 24,547,311 (GRCm39) |
F1223L |
probably damaging |
Het |
Ccdc40 |
T |
C |
11: 119,122,507 (GRCm39) |
F33S |
possibly damaging |
Het |
Ccnjl |
T |
C |
11: 43,470,538 (GRCm39) |
V102A |
probably damaging |
Het |
Cd48 |
T |
C |
1: 171,526,958 (GRCm39) |
V128A |
probably damaging |
Het |
Cmah |
A |
G |
13: 24,652,601 (GRCm39) |
D577G |
probably benign |
Het |
Cnnm4 |
A |
G |
1: 36,511,174 (GRCm39) |
K134R |
probably benign |
Het |
Col14a1 |
A |
G |
15: 55,318,626 (GRCm39) |
E1375G |
unknown |
Het |
Comtd1 |
T |
A |
14: 21,897,985 (GRCm39) |
E153V |
probably benign |
Het |
Dchs1 |
T |
A |
7: 105,404,395 (GRCm39) |
T2716S |
probably benign |
Het |
Ddx4 |
A |
T |
13: 112,762,928 (GRCm39) |
S143T |
probably benign |
Het |
Dlg1 |
A |
G |
16: 31,656,885 (GRCm39) |
D593G |
possibly damaging |
Het |
Dok6 |
A |
G |
18: 89,578,213 (GRCm39) |
I68T |
possibly damaging |
Het |
Dpysl5 |
A |
G |
5: 30,953,658 (GRCm39) |
I563V |
probably benign |
Het |
Eapp |
A |
G |
12: 54,739,650 (GRCm39) |
S56P |
probably damaging |
Het |
Efcab3 |
T |
G |
11: 104,810,305 (GRCm39) |
D3147E |
unknown |
Het |
Fgd5 |
A |
T |
6: 92,038,837 (GRCm39) |
D1157V |
probably damaging |
Het |
Fmn1 |
T |
A |
2: 113,194,939 (GRCm39) |
L213Q |
unknown |
Het |
Foxo1 |
T |
A |
3: 52,253,044 (GRCm39) |
Y402* |
probably null |
Het |
Fyb2 |
C |
A |
4: 104,857,681 (GRCm39) |
F619L |
possibly damaging |
Het |
Gtf2i |
A |
T |
5: 134,322,599 (GRCm39) |
|
probably null |
Het |
Hrh1 |
G |
A |
6: 114,456,878 (GRCm39) |
R53H |
not run |
Het |
Hydin |
A |
T |
8: 111,301,626 (GRCm39) |
M3786L |
probably benign |
Het |
Ifi207 |
T |
C |
1: 173,555,268 (GRCm39) |
R805G |
possibly damaging |
Het |
Igfn1 |
C |
A |
1: 135,895,797 (GRCm39) |
G1590* |
probably null |
Het |
Jph3 |
A |
C |
8: 122,516,201 (GRCm39) |
I740L |
probably benign |
Het |
Kbtbd7 |
T |
A |
14: 79,666,144 (GRCm39) |
F659I |
probably benign |
Het |
Kcns2 |
A |
T |
15: 34,839,291 (GRCm39) |
Q218L |
probably benign |
Het |
Kcnt2 |
A |
G |
1: 140,537,398 (GRCm39) |
N1119S |
probably benign |
Het |
Krit1 |
A |
T |
5: 3,857,309 (GRCm39) |
H38L |
probably benign |
Het |
Krt20 |
T |
A |
11: 99,328,663 (GRCm39) |
R87S |
probably damaging |
Het |
Ly6g5c |
A |
G |
17: 35,330,808 (GRCm39) |
E110G |
probably damaging |
Het |
Mamdc4 |
A |
G |
2: 25,454,707 (GRCm39) |
F1035S |
probably damaging |
Het |
Mmp13 |
A |
T |
9: 7,280,865 (GRCm39) |
D416V |
probably benign |
Het |
Nadk |
G |
T |
4: 155,661,524 (GRCm39) |
D17Y |
probably benign |
Het |
Nrap |
A |
T |
19: 56,352,768 (GRCm39) |
L566* |
probably null |
Het |
Or12d17 |
T |
C |
17: 37,777,540 (GRCm39) |
F148L |
probably benign |
Het |
Or4b12 |
A |
T |
2: 90,096,488 (GRCm39) |
C95* |
probably null |
Het |
Or51ai2 |
T |
C |
7: 103,586,788 (GRCm39) |
L67P |
probably damaging |
Het |
Or5p69 |
T |
C |
7: 107,966,741 (GRCm39) |
F15L |
probably damaging |
Het |
Pcdhb19 |
T |
C |
18: 37,630,367 (GRCm39) |
L54P |
possibly damaging |
Het |
Pitpnm2 |
A |
G |
5: 124,259,519 (GRCm39) |
F1272S |
probably damaging |
Het |
Pml |
C |
A |
9: 58,141,968 (GRCm39) |
R288L |
probably benign |
Het |
Reep4 |
T |
C |
14: 70,785,627 (GRCm39) |
Y186H |
probably benign |
Het |
Rpgrip1 |
A |
G |
14: 52,356,702 (GRCm39) |
T89A |
possibly damaging |
Het |
Shc1 |
T |
C |
3: 89,330,260 (GRCm39) |
S175P |
probably damaging |
Het |
Sipa1l3 |
A |
G |
7: 29,063,645 (GRCm39) |
S1156P |
probably damaging |
Het |
Slc1a3 |
G |
A |
15: 8,665,683 (GRCm39) |
P522L |
probably benign |
Het |
Slc6a17 |
T |
A |
3: 107,381,744 (GRCm39) |
T446S |
probably damaging |
Het |
Tas1r2 |
A |
T |
4: 139,387,290 (GRCm39) |
N250Y |
possibly damaging |
Het |
Tex15 |
G |
T |
8: 34,065,874 (GRCm39) |
R1768L |
probably damaging |
Het |
Ttll9 |
G |
C |
2: 152,844,956 (GRCm39) |
Q441H |
possibly damaging |
Het |
Unc5c |
T |
A |
3: 141,171,545 (GRCm39) |
V24E |
possibly damaging |
Het |
Unc79 |
A |
G |
12: 103,054,726 (GRCm39) |
E888G |
probably benign |
Het |
Vmn2r19 |
T |
C |
6: 123,312,750 (GRCm39) |
S607P |
possibly damaging |
Het |
Vsig1 |
C |
T |
X: 139,833,875 (GRCm39) |
H232Y |
probably benign |
Het |
Wdfy4 |
A |
G |
14: 32,875,965 (GRCm39) |
|
probably null |
Het |
Zbtb49 |
T |
C |
5: 38,358,198 (GRCm39) |
D685G |
possibly damaging |
Het |
|
Other mutations in Cntnap5a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00763:Cntnap5a
|
APN |
1 |
116,045,407 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL00929:Cntnap5a
|
APN |
1 |
115,988,004 (GRCm39) |
splice site |
probably null |
|
IGL00959:Cntnap5a
|
APN |
1 |
116,112,057 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01721:Cntnap5a
|
APN |
1 |
116,085,367 (GRCm39) |
missense |
probably benign |
|
IGL02009:Cntnap5a
|
APN |
1 |
116,085,224 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02111:Cntnap5a
|
APN |
1 |
116,017,082 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02198:Cntnap5a
|
APN |
1 |
116,508,262 (GRCm39) |
missense |
probably benign |
|
IGL02751:Cntnap5a
|
APN |
1 |
116,112,187 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02752:Cntnap5a
|
APN |
1 |
116,508,261 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02989:Cntnap5a
|
APN |
1 |
116,339,813 (GRCm39) |
splice site |
probably benign |
|
IGL03195:Cntnap5a
|
APN |
1 |
116,085,178 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4142001:Cntnap5a
|
UTSW |
1 |
115,612,686 (GRCm39) |
start gained |
probably benign |
|
R0294:Cntnap5a
|
UTSW |
1 |
115,843,046 (GRCm39) |
missense |
probably benign |
|
R0377:Cntnap5a
|
UTSW |
1 |
116,220,259 (GRCm39) |
missense |
probably benign |
0.04 |
R0597:Cntnap5a
|
UTSW |
1 |
116,112,191 (GRCm39) |
splice site |
probably benign |
|
R0616:Cntnap5a
|
UTSW |
1 |
116,508,279 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0725:Cntnap5a
|
UTSW |
1 |
116,220,206 (GRCm39) |
missense |
probably benign |
0.25 |
R0842:Cntnap5a
|
UTSW |
1 |
116,369,953 (GRCm39) |
missense |
probably damaging |
0.96 |
R1103:Cntnap5a
|
UTSW |
1 |
116,508,399 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1265:Cntnap5a
|
UTSW |
1 |
116,356,248 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1467:Cntnap5a
|
UTSW |
1 |
115,612,898 (GRCm39) |
nonsense |
probably null |
|
R1467:Cntnap5a
|
UTSW |
1 |
115,612,898 (GRCm39) |
nonsense |
probably null |
|
R1470:Cntnap5a
|
UTSW |
1 |
116,187,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Cntnap5a
|
UTSW |
1 |
116,187,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Cntnap5a
|
UTSW |
1 |
116,370,103 (GRCm39) |
nonsense |
probably null |
|
R1476:Cntnap5a
|
UTSW |
1 |
115,828,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1481:Cntnap5a
|
UTSW |
1 |
116,045,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Cntnap5a
|
UTSW |
1 |
115,828,680 (GRCm39) |
missense |
probably benign |
|
R1526:Cntnap5a
|
UTSW |
1 |
116,356,207 (GRCm39) |
missense |
probably benign |
|
R1589:Cntnap5a
|
UTSW |
1 |
115,987,930 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1603:Cntnap5a
|
UTSW |
1 |
116,339,831 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1728:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1728:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1729:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1730:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1739:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1762:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1783:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1816:Cntnap5a
|
UTSW |
1 |
116,356,618 (GRCm39) |
missense |
probably benign |
0.19 |
R1872:Cntnap5a
|
UTSW |
1 |
116,016,940 (GRCm39) |
missense |
probably benign |
0.02 |
R2095:Cntnap5a
|
UTSW |
1 |
116,369,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R2113:Cntnap5a
|
UTSW |
1 |
116,116,095 (GRCm39) |
missense |
probably damaging |
0.98 |
R2144:Cntnap5a
|
UTSW |
1 |
116,029,440 (GRCm39) |
missense |
probably benign |
0.14 |
R2171:Cntnap5a
|
UTSW |
1 |
116,116,132 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2219:Cntnap5a
|
UTSW |
1 |
116,508,369 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2220:Cntnap5a
|
UTSW |
1 |
116,508,369 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2571:Cntnap5a
|
UTSW |
1 |
116,112,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R3019:Cntnap5a
|
UTSW |
1 |
116,029,299 (GRCm39) |
missense |
probably benign |
|
R3827:Cntnap5a
|
UTSW |
1 |
116,045,409 (GRCm39) |
missense |
probably benign |
0.14 |
R3870:Cntnap5a
|
UTSW |
1 |
115,987,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R3871:Cntnap5a
|
UTSW |
1 |
115,987,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R4041:Cntnap5a
|
UTSW |
1 |
116,112,129 (GRCm39) |
missense |
probably benign |
0.00 |
R4080:Cntnap5a
|
UTSW |
1 |
116,029,304 (GRCm39) |
missense |
probably benign |
0.01 |
R4260:Cntnap5a
|
UTSW |
1 |
116,374,325 (GRCm39) |
missense |
probably benign |
0.31 |
R4685:Cntnap5a
|
UTSW |
1 |
116,374,410 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4781:Cntnap5a
|
UTSW |
1 |
116,339,931 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4785:Cntnap5a
|
UTSW |
1 |
116,029,295 (GRCm39) |
missense |
probably benign |
0.00 |
R5057:Cntnap5a
|
UTSW |
1 |
115,612,943 (GRCm39) |
missense |
probably benign |
0.10 |
R5059:Cntnap5a
|
UTSW |
1 |
116,356,224 (GRCm39) |
missense |
probably benign |
0.44 |
R5101:Cntnap5a
|
UTSW |
1 |
116,370,026 (GRCm39) |
missense |
probably benign |
0.00 |
R5302:Cntnap5a
|
UTSW |
1 |
116,085,300 (GRCm39) |
missense |
probably benign |
0.15 |
R5451:Cntnap5a
|
UTSW |
1 |
115,612,873 (GRCm39) |
missense |
probably benign |
|
R5473:Cntnap5a
|
UTSW |
1 |
116,016,986 (GRCm39) |
missense |
probably benign |
0.12 |
R5886:Cntnap5a
|
UTSW |
1 |
116,499,402 (GRCm39) |
critical splice donor site |
probably null |
|
R6311:Cntnap5a
|
UTSW |
1 |
116,339,836 (GRCm39) |
nonsense |
probably null |
|
R6464:Cntnap5a
|
UTSW |
1 |
116,112,138 (GRCm39) |
missense |
probably benign |
|
R6497:Cntnap5a
|
UTSW |
1 |
116,505,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R6781:Cntnap5a
|
UTSW |
1 |
116,220,127 (GRCm39) |
missense |
probably benign |
0.05 |
R7137:Cntnap5a
|
UTSW |
1 |
116,017,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R7290:Cntnap5a
|
UTSW |
1 |
116,149,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R7342:Cntnap5a
|
UTSW |
1 |
115,987,852 (GRCm39) |
missense |
probably benign |
0.00 |
R7367:Cntnap5a
|
UTSW |
1 |
116,370,025 (GRCm39) |
missense |
probably benign |
0.00 |
R7373:Cntnap5a
|
UTSW |
1 |
116,508,367 (GRCm39) |
missense |
probably benign |
0.20 |
R7426:Cntnap5a
|
UTSW |
1 |
116,370,110 (GRCm39) |
missense |
probably benign |
0.03 |
R7444:Cntnap5a
|
UTSW |
1 |
116,220,079 (GRCm39) |
missense |
probably benign |
|
R7582:Cntnap5a
|
UTSW |
1 |
116,374,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R7745:Cntnap5a
|
UTSW |
1 |
116,370,013 (GRCm39) |
missense |
probably benign |
|
R7948:Cntnap5a
|
UTSW |
1 |
116,508,258 (GRCm39) |
missense |
probably benign |
0.01 |
R7995:Cntnap5a
|
UTSW |
1 |
116,499,277 (GRCm39) |
missense |
probably damaging |
0.99 |
R8262:Cntnap5a
|
UTSW |
1 |
116,116,140 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8273:Cntnap5a
|
UTSW |
1 |
116,499,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R8320:Cntnap5a
|
UTSW |
1 |
116,374,466 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9242:Cntnap5a
|
UTSW |
1 |
116,220,109 (GRCm39) |
missense |
probably benign |
0.06 |
R9470:Cntnap5a
|
UTSW |
1 |
116,374,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R9601:Cntnap5a
|
UTSW |
1 |
116,508,217 (GRCm39) |
missense |
probably damaging |
0.96 |
R9616:Cntnap5a
|
UTSW |
1 |
116,029,323 (GRCm39) |
missense |
probably benign |
|
R9623:Cntnap5a
|
UTSW |
1 |
116,369,985 (GRCm39) |
nonsense |
probably null |
|
Z1088:Cntnap5a
|
UTSW |
1 |
115,987,981 (GRCm39) |
missense |
probably benign |
0.08 |
Z1176:Cntnap5a
|
UTSW |
1 |
116,356,246 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cntnap5a
|
UTSW |
1 |
116,339,898 (GRCm39) |
missense |
probably benign |
0.03 |
Z1188:Cntnap5a
|
UTSW |
1 |
116,445,935 (GRCm39) |
missense |
possibly damaging |
0.70 |
|