Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap1 |
A |
G |
11: 69,775,162 (GRCm39) |
V367A |
probably benign |
Het |
Adam26b |
T |
C |
8: 43,973,310 (GRCm39) |
E564G |
possibly damaging |
Het |
Akap1 |
A |
G |
11: 88,725,486 (GRCm39) |
|
probably null |
Het |
Akap5 |
T |
A |
12: 76,374,619 (GRCm39) |
V10E |
possibly damaging |
Het |
Atad2 |
A |
T |
15: 57,961,910 (GRCm39) |
L887* |
probably null |
Het |
Brd10 |
T |
C |
19: 29,696,677 (GRCm39) |
I939V |
probably benign |
Het |
C1qbp |
A |
G |
11: 70,873,008 (GRCm39) |
V122A |
probably benign |
Het |
C1qtnf7 |
G |
A |
5: 43,772,998 (GRCm39) |
G92D |
probably damaging |
Het |
Cacna1a |
T |
C |
8: 85,249,651 (GRCm39) |
I219T |
probably damaging |
Het |
Capn12 |
A |
G |
7: 28,587,030 (GRCm39) |
N333S |
probably benign |
Het |
Ccdc154 |
C |
T |
17: 25,390,792 (GRCm39) |
T644I |
probably benign |
Het |
Cd200r1 |
T |
C |
16: 44,610,566 (GRCm39) |
S225P |
possibly damaging |
Het |
Coq4 |
A |
T |
2: 29,680,626 (GRCm39) |
|
probably benign |
Het |
Cubn |
A |
T |
2: 13,324,834 (GRCm39) |
|
probably benign |
Het |
Cyp4f17 |
A |
T |
17: 32,743,013 (GRCm39) |
S229C |
possibly damaging |
Het |
Cysltr2 |
T |
C |
14: 73,266,931 (GRCm39) |
K260E |
probably benign |
Het |
D930007J09Rik |
C |
A |
13: 32,986,819 (GRCm39) |
A200E |
probably benign |
Het |
Dnah8 |
C |
T |
17: 31,013,691 (GRCm39) |
P3811S |
probably damaging |
Het |
Duoxa1 |
A |
T |
2: 122,134,291 (GRCm39) |
S276T |
possibly damaging |
Het |
Efcab15 |
A |
G |
11: 103,098,947 (GRCm39) |
|
probably null |
Het |
Efhb |
T |
C |
17: 53,758,582 (GRCm39) |
I351M |
probably benign |
Het |
Fat1 |
G |
A |
8: 45,480,718 (GRCm39) |
|
probably null |
Het |
Fat1 |
A |
T |
8: 45,486,432 (GRCm39) |
T3329S |
probably damaging |
Het |
Gad1-ps |
G |
A |
10: 99,281,009 (GRCm39) |
|
noncoding transcript |
Het |
Gm973 |
T |
A |
1: 59,597,409 (GRCm39) |
|
probably benign |
Het |
Gpr156 |
T |
A |
16: 37,799,375 (GRCm39) |
L124Q |
probably damaging |
Het |
Hars2 |
T |
A |
18: 36,923,150 (GRCm39) |
|
probably benign |
Het |
Hcrt |
G |
A |
11: 100,652,759 (GRCm39) |
A85V |
probably damaging |
Het |
Hivep1 |
A |
G |
13: 42,310,088 (GRCm39) |
D776G |
probably damaging |
Het |
Hmgcr |
A |
T |
13: 96,796,691 (GRCm39) |
S200T |
probably damaging |
Het |
Krt40 |
C |
T |
11: 99,430,907 (GRCm39) |
A201T |
probably benign |
Het |
Lca5 |
G |
A |
9: 83,281,734 (GRCm39) |
A350V |
probably benign |
Het |
Lrig2 |
T |
A |
3: 104,370,014 (GRCm39) |
M515L |
probably benign |
Het |
Mbd5 |
A |
G |
2: 49,162,464 (GRCm39) |
D90G |
probably damaging |
Het |
Mfsd4a |
C |
T |
1: 131,995,465 (GRCm39) |
V56I |
probably damaging |
Het |
Mpi |
A |
G |
9: 57,455,745 (GRCm39) |
|
probably benign |
Het |
Mroh4 |
G |
T |
15: 74,478,296 (GRCm39) |
D935E |
possibly damaging |
Het |
Mtg1 |
G |
T |
7: 139,729,778 (GRCm39) |
|
probably null |
Het |
Nanos1 |
T |
A |
19: 60,745,268 (GRCm39) |
C189S |
probably damaging |
Het |
Naprt |
A |
C |
15: 75,763,324 (GRCm39) |
|
probably null |
Het |
Nubpl |
T |
A |
12: 52,228,092 (GRCm39) |
|
probably null |
Het |
Or10ad1b |
T |
C |
15: 98,124,672 (GRCm39) |
T285A |
possibly damaging |
Het |
Or10d4 |
G |
T |
9: 39,581,252 (GRCm39) |
V300L |
probably benign |
Het |
Or8g23 |
T |
A |
9: 38,971,678 (GRCm39) |
T95S |
probably benign |
Het |
Or9g20 |
A |
G |
2: 85,630,147 (GRCm39) |
S156P |
probably damaging |
Het |
Otud4 |
T |
A |
8: 80,399,436 (GRCm39) |
Y717N |
probably damaging |
Het |
Pakap |
T |
A |
4: 57,856,295 (GRCm39) |
D582E |
probably damaging |
Het |
Pnpla1 |
T |
C |
17: 29,095,837 (GRCm39) |
F86S |
possibly damaging |
Het |
Prlhr |
C |
T |
19: 60,456,014 (GRCm39) |
W184* |
probably null |
Het |
Rtp3 |
A |
G |
9: 110,816,204 (GRCm39) |
S116P |
probably damaging |
Het |
Sema3c |
T |
C |
5: 17,886,984 (GRCm39) |
I345T |
possibly damaging |
Het |
Skor2 |
T |
C |
18: 76,947,124 (GRCm39) |
L282P |
unknown |
Het |
Slc24a4 |
T |
C |
12: 102,226,674 (GRCm39) |
V468A |
probably damaging |
Het |
Slfn8 |
C |
T |
11: 82,894,160 (GRCm39) |
M826I |
probably benign |
Het |
Tacc2 |
A |
G |
7: 130,330,850 (GRCm39) |
D378G |
probably benign |
Het |
Thbs3 |
C |
A |
3: 89,127,470 (GRCm39) |
D370E |
probably damaging |
Het |
Tk1 |
CC |
GA |
11: 117,707,948 (GRCm39) |
|
probably benign |
Het |
Tm7sf2 |
A |
G |
19: 6,116,572 (GRCm39) |
|
probably benign |
Het |
Trappc8 |
T |
C |
18: 21,007,737 (GRCm39) |
Y126C |
probably damaging |
Het |
Trim35 |
C |
G |
14: 66,541,502 (GRCm39) |
L209V |
possibly damaging |
Het |
Trim35 |
T |
C |
14: 66,541,503 (GRCm39) |
L209P |
probably damaging |
Het |
Trip12 |
C |
T |
1: 84,708,179 (GRCm39) |
|
probably benign |
Het |
Trp53bp1 |
A |
G |
2: 121,035,502 (GRCm39) |
V1583A |
probably damaging |
Het |
Tuba5-ps |
A |
G |
1: 134,447,937 (GRCm39) |
|
noncoding transcript |
Het |
Tubgcp6 |
A |
T |
15: 88,987,450 (GRCm39) |
N1166K |
possibly damaging |
Het |
Usp54 |
C |
T |
14: 20,611,910 (GRCm39) |
D969N |
probably benign |
Het |
Vldlr |
C |
A |
19: 27,221,171 (GRCm39) |
S612R |
probably benign |
Het |
Vps13a |
T |
C |
19: 16,641,926 (GRCm39) |
T2234A |
probably benign |
Het |
Vps39 |
A |
G |
2: 120,152,053 (GRCm39) |
|
probably benign |
Het |
Zdhhc3 |
A |
T |
9: 122,920,146 (GRCm39) |
C120S |
probably benign |
Het |
Zfp37 |
A |
G |
4: 62,109,471 (GRCm39) |
F531S |
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 |
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 |
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 |
|