Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022A10Rik |
T |
A |
7: 27,271,076 (GRCm39) |
I157N |
probably damaging |
Het |
Adgrl3 |
T |
C |
5: 81,908,571 (GRCm39) |
Y1165H |
probably damaging |
Het |
Adra2a |
A |
G |
19: 54,034,926 (GRCm39) |
D94G |
probably damaging |
Het |
Akr1c20 |
T |
A |
13: 4,558,174 (GRCm39) |
K197* |
probably null |
Het |
Ankrd65 |
C |
T |
4: 155,877,493 (GRCm39) |
H335Y |
possibly damaging |
Het |
Axin2 |
T |
A |
11: 108,834,682 (GRCm39) |
L636Q |
probably damaging |
Het |
Camk1g |
G |
T |
1: 193,038,652 (GRCm39) |
T90N |
probably benign |
Het |
Cd177 |
C |
A |
7: 24,450,051 (GRCm39) |
C528F |
probably damaging |
Het |
Crtap |
T |
C |
9: 114,215,304 (GRCm39) |
D195G |
probably benign |
Het |
Csn1s2b |
A |
G |
5: 87,966,952 (GRCm39) |
S74G |
possibly damaging |
Het |
Cyp3a16 |
T |
C |
5: 145,392,922 (GRCm39) |
R128G |
possibly damaging |
Het |
Dnah7a |
A |
G |
1: 53,464,367 (GRCm39) |
F3675L |
probably benign |
Het |
Dram2 |
T |
A |
3: 106,478,992 (GRCm39) |
W195R |
probably damaging |
Het |
E130308A19Rik |
C |
T |
4: 59,691,057 (GRCm39) |
P297L |
probably benign |
Het |
Eif3i |
T |
C |
4: 129,489,066 (GRCm39) |
S83G |
probably benign |
Het |
Gabra1 |
G |
A |
11: 42,024,488 (GRCm39) |
P396S |
probably damaging |
Het |
Gipr |
T |
A |
7: 18,891,300 (GRCm39) |
Y459F |
possibly damaging |
Het |
Gm11677 |
C |
T |
11: 111,615,537 (GRCm39) |
|
noncoding transcript |
Het |
Gm6981 |
T |
C |
9: 51,914,056 (GRCm39) |
|
noncoding transcript |
Het |
Grin2d |
T |
C |
7: 45,511,905 (GRCm39) |
D180G |
probably damaging |
Het |
Hectd4 |
T |
G |
5: 121,444,170 (GRCm39) |
|
probably null |
Het |
Hhat |
T |
C |
1: 192,369,287 (GRCm39) |
|
probably benign |
Het |
Hoxa6 |
A |
G |
6: 52,183,400 (GRCm39) |
L215P |
possibly damaging |
Het |
Hsf4 |
G |
A |
8: 106,001,384 (GRCm39) |
|
probably null |
Het |
Igf1r |
G |
A |
7: 67,814,947 (GRCm39) |
A283T |
possibly damaging |
Het |
Ighv15-2 |
A |
G |
12: 114,528,476 (GRCm39) |
S25P |
probably damaging |
Het |
Inpp5a |
C |
T |
7: 139,057,921 (GRCm39) |
T43I |
probably benign |
Het |
Kmt2c |
T |
A |
5: 25,648,823 (GRCm39) |
E82V |
probably damaging |
Het |
Lrrc31 |
A |
G |
3: 30,741,526 (GRCm39) |
|
probably benign |
Het |
Mdga2 |
A |
G |
12: 66,844,396 (GRCm39) |
|
probably null |
Het |
Mefv |
G |
A |
16: 3,533,198 (GRCm39) |
P358S |
probably benign |
Het |
Mrgpra9 |
A |
G |
7: 46,884,795 (GRCm39) |
F291L |
possibly damaging |
Het |
Mtmr3 |
A |
G |
11: 4,438,435 (GRCm39) |
L673P |
probably benign |
Het |
Muc19 |
T |
C |
15: 91,787,360 (GRCm39) |
|
noncoding transcript |
Het |
Myo5b |
A |
T |
18: 74,877,752 (GRCm39) |
T1584S |
possibly damaging |
Het |
Or1x6 |
A |
T |
11: 50,939,307 (GRCm39) |
R124S |
probably damaging |
Het |
Or4z4 |
T |
C |
19: 12,076,731 (GRCm39) |
T91A |
probably benign |
Het |
Palld |
G |
T |
8: 62,330,062 (GRCm39) |
R272S |
probably benign |
Het |
Pcnx3 |
T |
A |
19: 5,737,158 (GRCm39) |
N144Y |
probably damaging |
Het |
Prf1 |
A |
G |
10: 61,136,203 (GRCm39) |
K160E |
probably damaging |
Het |
Rasgrp1 |
G |
A |
2: 117,122,190 (GRCm39) |
A400V |
probably benign |
Het |
Rnf150 |
A |
G |
8: 83,590,781 (GRCm39) |
Y48C |
probably damaging |
Het |
Rpl11 |
G |
T |
4: 135,777,599 (GRCm39) |
Q170K |
probably benign |
Het |
Scin |
G |
A |
12: 40,131,763 (GRCm39) |
A257V |
possibly damaging |
Het |
Scn7a |
C |
A |
2: 66,534,104 (GRCm39) |
A524S |
possibly damaging |
Het |
Sim1 |
T |
C |
10: 50,859,881 (GRCm39) |
L581S |
probably benign |
Het |
Skor1 |
T |
C |
9: 63,051,741 (GRCm39) |
T715A |
probably benign |
Het |
Slc22a26 |
A |
G |
19: 7,767,500 (GRCm39) |
V301A |
probably benign |
Het |
Sorcs1 |
T |
C |
19: 50,171,119 (GRCm39) |
Y923C |
probably damaging |
Het |
Src |
T |
A |
2: 157,309,405 (GRCm39) |
M304K |
possibly damaging |
Het |
Srgap3 |
A |
T |
6: 112,734,386 (GRCm39) |
|
probably benign |
Het |
Stard3 |
G |
A |
11: 98,263,160 (GRCm39) |
E72K |
possibly damaging |
Het |
Svep1 |
T |
A |
4: 58,070,340 (GRCm39) |
N2482I |
probably damaging |
Het |
Tbc1d23 |
T |
C |
16: 57,038,778 (GRCm39) |
K20R |
possibly damaging |
Het |
Tcstv4 |
A |
C |
13: 120,769,698 (GRCm39) |
K6T |
possibly damaging |
Het |
Tfip11 |
G |
A |
5: 112,481,265 (GRCm39) |
E414K |
probably damaging |
Het |
Tinag |
G |
T |
9: 76,904,232 (GRCm39) |
T397K |
possibly damaging |
Het |
Traf7 |
C |
G |
17: 24,729,412 (GRCm39) |
|
probably benign |
Het |
Trmt10b |
T |
A |
4: 45,305,817 (GRCm39) |
I164N |
probably damaging |
Het |
Trpm1 |
A |
G |
7: 63,884,800 (GRCm39) |
D827G |
probably benign |
Het |
Ube2u |
A |
T |
4: 100,343,855 (GRCm39) |
T85S |
probably benign |
Het |
Ulk4 |
T |
C |
9: 120,932,642 (GRCm39) |
D1066G |
probably benign |
Het |
Vmn2r72 |
T |
A |
7: 85,387,069 (GRCm39) |
I832F |
probably benign |
Het |
Yipf1 |
A |
C |
4: 107,193,355 (GRCm39) |
E80D |
probably benign |
Het |
Zfp40 |
T |
A |
17: 23,394,629 (GRCm39) |
R653W |
probably damaging |
Het |
Zxdc |
A |
G |
6: 90,349,535 (GRCm39) |
T308A |
probably 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 |
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 |
R8041:Cntnap5a
|
UTSW |
1 |
116,187,209 (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 |
|