Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930519G04Rik |
T |
C |
5: 115,012,341 (GRCm39) |
V86A |
probably benign |
Het |
Abcc3 |
A |
T |
11: 94,255,243 (GRCm39) |
I601N |
probably damaging |
Het |
Abl2 |
T |
A |
1: 156,448,397 (GRCm39) |
|
probably null |
Het |
Adgrf4 |
C |
T |
17: 42,977,789 (GRCm39) |
R518Q |
possibly damaging |
Het |
Ahi1 |
C |
T |
10: 20,835,895 (GRCm39) |
T76I |
probably damaging |
Het |
Arhgap42 |
C |
T |
9: 9,035,601 (GRCm39) |
G247D |
probably damaging |
Het |
Arid2 |
C |
T |
15: 96,260,471 (GRCm39) |
L407F |
probably damaging |
Het |
Atp13a1 |
T |
C |
8: 70,252,423 (GRCm39) |
F606L |
probably benign |
Het |
Avl9 |
T |
A |
6: 56,713,420 (GRCm39) |
|
probably benign |
Het |
B3glct |
C |
T |
5: 149,632,845 (GRCm39) |
A65V |
probably damaging |
Het |
Bcorl1 |
T |
C |
X: 47,490,794 (GRCm39) |
|
probably benign |
Het |
Bdp1 |
T |
C |
13: 100,187,496 (GRCm39) |
T1624A |
probably benign |
Het |
Bmp15 |
A |
G |
X: 6,228,075 (GRCm39) |
M263T |
probably benign |
Het |
Brd8 |
T |
C |
18: 34,747,532 (GRCm39) |
K110E |
probably damaging |
Het |
Cachd1 |
A |
G |
4: 100,848,041 (GRCm39) |
D1052G |
probably damaging |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Ccdc113 |
G |
A |
8: 96,283,924 (GRCm39) |
E333K |
probably benign |
Het |
Ccnl2 |
A |
T |
4: 155,896,938 (GRCm39) |
|
probably null |
Het |
Ccr9 |
T |
C |
9: 123,608,429 (GRCm39) |
F37S |
probably benign |
Het |
Cdh20 |
A |
T |
1: 110,065,889 (GRCm39) |
D721V |
probably damaging |
Het |
Ceacam10 |
A |
T |
7: 24,477,797 (GRCm39) |
N104I |
probably damaging |
Het |
Cenpk |
T |
A |
13: 104,372,684 (GRCm39) |
|
probably benign |
Het |
Cfi |
A |
G |
3: 129,652,453 (GRCm39) |
|
probably null |
Het |
Chd1 |
T |
C |
17: 15,962,556 (GRCm39) |
F771S |
probably damaging |
Het |
Chil4 |
G |
A |
3: 106,126,771 (GRCm39) |
L4F |
probably benign |
Het |
Cilp |
G |
A |
9: 65,185,372 (GRCm39) |
R489Q |
possibly damaging |
Het |
Coq8b |
A |
G |
7: 26,956,802 (GRCm39) |
E485G |
probably damaging |
Het |
Cse1l |
A |
G |
2: 166,783,412 (GRCm39) |
S733G |
probably benign |
Het |
Dnah5 |
G |
A |
15: 28,312,534 (GRCm39) |
|
probably null |
Het |
Dnmt3l |
T |
C |
10: 77,888,566 (GRCm39) |
V156A |
probably damaging |
Het |
Duox1 |
A |
T |
2: 122,163,543 (GRCm39) |
T792S |
probably benign |
Het |
Duox2 |
T |
C |
2: 122,117,589 (GRCm39) |
D915G |
probably benign |
Het |
Efcab5 |
A |
T |
11: 77,063,147 (GRCm39) |
M115K |
probably benign |
Het |
Eif2s1 |
G |
A |
12: 78,923,959 (GRCm39) |
D139N |
probably benign |
Het |
Erg |
A |
G |
16: 95,161,937 (GRCm39) |
F390L |
probably damaging |
Het |
Fam193b |
A |
T |
13: 55,690,811 (GRCm39) |
S650R |
probably damaging |
Het |
Fbp2 |
T |
A |
13: 63,001,875 (GRCm39) |
K113N |
possibly damaging |
Het |
Fnbp4 |
T |
G |
2: 90,588,716 (GRCm39) |
S496A |
probably damaging |
Het |
Gab3 |
C |
A |
X: 74,043,701 (GRCm39) |
R475L |
probably damaging |
Het |
Gsap |
T |
C |
5: 21,431,837 (GRCm39) |
|
probably benign |
Het |
Gucy1a2 |
C |
T |
9: 3,582,697 (GRCm39) |
L160F |
probably damaging |
Het |
Hivep1 |
C |
T |
13: 42,337,262 (GRCm39) |
A2447V |
possibly damaging |
Het |
Insc |
G |
T |
7: 114,403,828 (GRCm39) |
|
probably null |
Het |
Jph2 |
A |
G |
2: 163,181,605 (GRCm39) |
S520P |
possibly damaging |
Het |
Kidins220 |
T |
A |
12: 25,037,005 (GRCm39) |
|
probably benign |
Het |
Krtap29-1 |
A |
G |
11: 99,869,438 (GRCm39) |
S148P |
probably damaging |
Het |
Ltbp2 |
A |
C |
12: 84,840,507 (GRCm39) |
C1000G |
probably damaging |
Het |
Map2k3 |
T |
C |
11: 60,840,853 (GRCm39) |
F294S |
probably damaging |
Het |
Map4k2 |
C |
A |
19: 6,392,768 (GRCm39) |
|
probably benign |
Het |
Mboat2 |
T |
C |
12: 25,001,442 (GRCm39) |
V281A |
probably benign |
Het |
Mdga2 |
G |
A |
12: 66,615,691 (GRCm39) |
R570* |
probably null |
Het |
Mlxipl |
A |
G |
5: 135,135,859 (GRCm39) |
D28G |
probably damaging |
Het |
Morc2b |
T |
C |
17: 33,355,734 (GRCm39) |
I679M |
probably benign |
Het |
Myh4 |
T |
C |
11: 67,137,192 (GRCm39) |
|
probably benign |
Het |
Nfib |
A |
C |
4: 82,416,852 (GRCm39) |
L61R |
probably damaging |
Het |
Noc2l |
C |
A |
4: 156,325,907 (GRCm39) |
Y227* |
probably null |
Het |
Nrde2 |
A |
G |
12: 100,108,491 (GRCm39) |
S367P |
probably damaging |
Het |
Nup93 |
C |
A |
8: 94,970,367 (GRCm39) |
P89T |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Or10a2 |
A |
T |
7: 106,673,826 (GRCm39) |
K264* |
probably null |
Het |
Or11h4 |
T |
A |
14: 50,974,033 (GRCm39) |
E195D |
possibly damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or4k77 |
A |
G |
2: 111,199,440 (GRCm39) |
I154M |
probably benign |
Het |
Or6b9 |
A |
T |
7: 106,555,494 (GRCm39) |
Y216* |
probably null |
Het |
Or9r7 |
A |
G |
10: 129,962,074 (GRCm39) |
I284T |
possibly damaging |
Het |
Oxct1 |
G |
T |
15: 4,122,007 (GRCm39) |
A319S |
probably null |
Het |
P2ry10 |
A |
G |
X: 106,146,859 (GRCm39) |
S265G |
probably benign |
Het |
Peak1 |
A |
T |
9: 56,166,043 (GRCm39) |
N628K |
probably damaging |
Het |
Pkdrej |
T |
A |
15: 85,705,432 (GRCm39) |
Q168L |
probably benign |
Het |
Plaat5 |
T |
C |
19: 7,590,003 (GRCm39) |
S10P |
possibly damaging |
Het |
Plec |
A |
G |
15: 76,073,126 (GRCm39) |
M604T |
probably benign |
Het |
Pmfbp1 |
A |
T |
8: 110,258,735 (GRCm39) |
N680I |
possibly damaging |
Het |
Pnma8b |
T |
C |
7: 16,679,714 (GRCm39) |
W233R |
probably damaging |
Het |
Pxn |
A |
G |
5: 115,683,726 (GRCm39) |
N186S |
probably benign |
Het |
Rsad1 |
A |
C |
11: 94,439,951 (GRCm39) |
|
probably benign |
Het |
Runx2 |
A |
G |
17: 45,046,229 (GRCm39) |
I112T |
probably benign |
Het |
S1pr2 |
A |
T |
9: 20,878,790 (GRCm39) |
L346Q |
probably damaging |
Het |
Skint6 |
A |
G |
4: 113,095,329 (GRCm39) |
I110T |
probably damaging |
Het |
Slc36a4 |
T |
A |
9: 15,638,276 (GRCm39) |
F234Y |
probably damaging |
Het |
Slitrk2 |
T |
A |
X: 65,698,235 (GRCm39) |
V242D |
probably damaging |
Het |
Sp100 |
A |
G |
1: 85,608,863 (GRCm39) |
|
probably null |
Het |
Spryd3 |
A |
C |
15: 102,026,616 (GRCm39) |
L352V |
probably benign |
Het |
Ssc4d |
A |
C |
5: 135,999,171 (GRCm39) |
W11G |
possibly damaging |
Het |
Stx17 |
T |
A |
4: 48,158,870 (GRCm39) |
D83E |
probably damaging |
Het |
Tlk2 |
A |
T |
11: 105,131,266 (GRCm39) |
Q204L |
probably benign |
Het |
Tnfrsf21 |
A |
T |
17: 43,348,829 (GRCm39) |
H147L |
possibly damaging |
Het |
Tnrc18 |
A |
T |
5: 142,751,842 (GRCm39) |
D1154E |
unknown |
Het |
Trap1 |
A |
G |
16: 3,886,200 (GRCm39) |
S86P |
probably benign |
Het |
Trim32 |
T |
A |
4: 65,533,013 (GRCm39) |
C523* |
probably null |
Het |
Ttc38 |
G |
T |
15: 85,722,989 (GRCm39) |
D146Y |
probably damaging |
Het |
Ttc9 |
T |
A |
12: 81,678,570 (GRCm39) |
L131Q |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,557,192 (GRCm39) |
|
probably benign |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Ubash3b |
G |
A |
9: 40,954,869 (GRCm39) |
P92S |
possibly damaging |
Het |
Ube4a |
T |
C |
9: 44,859,397 (GRCm39) |
N367S |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,206,851 (GRCm39) |
H4899Q |
possibly damaging |
Het |
Ufl1 |
C |
T |
4: 25,269,036 (GRCm39) |
G265D |
possibly damaging |
Het |
Vmn2r27 |
T |
A |
6: 124,201,442 (GRCm39) |
I172F |
probably damaging |
Het |
Vmn2r6 |
A |
T |
3: 64,463,519 (GRCm39) |
H438Q |
possibly damaging |
Het |
Vmn2r61 |
A |
G |
7: 41,949,425 (GRCm39) |
D615G |
probably benign |
Het |
Wdr24 |
T |
A |
17: 26,045,256 (GRCm39) |
D330E |
probably damaging |
Het |
Zbbx |
A |
T |
3: 74,985,719 (GRCm39) |
N444K |
probably benign |
Het |
Zc3h7b |
A |
T |
15: 81,676,529 (GRCm39) |
Q757L |
probably damaging |
Het |
Zpld2 |
T |
G |
4: 133,929,252 (GRCm39) |
N351T |
possibly damaging |
Het |
|
Other mutations in Cntnap5b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00417:Cntnap5b
|
APN |
1 |
99,978,479 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00477:Cntnap5b
|
APN |
1 |
100,141,468 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00505:Cntnap5b
|
APN |
1 |
100,306,886 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00596:Cntnap5b
|
APN |
1 |
100,306,886 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00846:Cntnap5b
|
APN |
1 |
100,091,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00895:Cntnap5b
|
APN |
1 |
100,311,310 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00948:Cntnap5b
|
APN |
1 |
100,069,082 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01073:Cntnap5b
|
APN |
1 |
100,003,755 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01523:Cntnap5b
|
APN |
1 |
100,359,504 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01779:Cntnap5b
|
APN |
1 |
99,895,064 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02253:Cntnap5b
|
APN |
1 |
100,091,936 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02628:Cntnap5b
|
APN |
1 |
99,999,794 (GRCm39) |
missense |
probably damaging |
0.97 |
R0166:Cntnap5b
|
UTSW |
1 |
100,202,086 (GRCm39) |
missense |
probably benign |
0.41 |
R0211:Cntnap5b
|
UTSW |
1 |
100,406,099 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0281:Cntnap5b
|
UTSW |
1 |
99,999,878 (GRCm39) |
missense |
probably benign |
0.22 |
R0363:Cntnap5b
|
UTSW |
1 |
100,202,193 (GRCm39) |
missense |
probably benign |
0.01 |
R0514:Cntnap5b
|
UTSW |
1 |
99,700,511 (GRCm39) |
missense |
probably benign |
|
R0645:Cntnap5b
|
UTSW |
1 |
99,999,767 (GRCm39) |
splice site |
probably benign |
|
R0848:Cntnap5b
|
UTSW |
1 |
100,182,888 (GRCm39) |
missense |
probably benign |
0.22 |
R1006:Cntnap5b
|
UTSW |
1 |
100,311,342 (GRCm39) |
missense |
probably benign |
0.00 |
R1349:Cntnap5b
|
UTSW |
1 |
100,091,813 (GRCm39) |
missense |
probably benign |
0.09 |
R1372:Cntnap5b
|
UTSW |
1 |
100,091,813 (GRCm39) |
missense |
probably benign |
0.09 |
R1474:Cntnap5b
|
UTSW |
1 |
99,999,814 (GRCm39) |
missense |
probably benign |
0.25 |
R1681:Cntnap5b
|
UTSW |
1 |
100,003,832 (GRCm39) |
missense |
probably damaging |
0.98 |
R1727:Cntnap5b
|
UTSW |
1 |
100,141,469 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1760:Cntnap5b
|
UTSW |
1 |
99,700,535 (GRCm39) |
missense |
probably benign |
0.05 |
R1777:Cntnap5b
|
UTSW |
1 |
100,297,803 (GRCm39) |
missense |
probably benign |
0.10 |
R1939:Cntnap5b
|
UTSW |
1 |
99,895,073 (GRCm39) |
missense |
probably benign |
|
R1988:Cntnap5b
|
UTSW |
1 |
99,999,865 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2113:Cntnap5b
|
UTSW |
1 |
100,202,140 (GRCm39) |
missense |
probably benign |
|
R2148:Cntnap5b
|
UTSW |
1 |
100,311,199 (GRCm39) |
missense |
probably benign |
0.01 |
R2158:Cntnap5b
|
UTSW |
1 |
100,318,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R2223:Cntnap5b
|
UTSW |
1 |
100,141,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R2350:Cntnap5b
|
UTSW |
1 |
100,306,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R3840:Cntnap5b
|
UTSW |
1 |
100,311,202 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4329:Cntnap5b
|
UTSW |
1 |
99,999,888 (GRCm39) |
missense |
probably damaging |
0.99 |
R4609:Cntnap5b
|
UTSW |
1 |
99,700,572 (GRCm39) |
critical splice donor site |
probably null |
|
R4799:Cntnap5b
|
UTSW |
1 |
100,286,450 (GRCm39) |
missense |
probably benign |
0.04 |
R5129:Cntnap5b
|
UTSW |
1 |
100,306,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R5323:Cntnap5b
|
UTSW |
1 |
100,311,275 (GRCm39) |
nonsense |
probably null |
|
R5434:Cntnap5b
|
UTSW |
1 |
99,999,926 (GRCm39) |
missense |
probably benign |
0.02 |
R5579:Cntnap5b
|
UTSW |
1 |
100,311,124 (GRCm39) |
missense |
probably benign |
0.27 |
R5579:Cntnap5b
|
UTSW |
1 |
100,311,120 (GRCm39) |
nonsense |
probably null |
|
R5630:Cntnap5b
|
UTSW |
1 |
99,999,794 (GRCm39) |
missense |
probably damaging |
0.99 |
R5644:Cntnap5b
|
UTSW |
1 |
100,311,326 (GRCm39) |
missense |
probably benign |
0.00 |
R5761:Cntnap5b
|
UTSW |
1 |
100,374,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R6042:Cntnap5b
|
UTSW |
1 |
100,318,317 (GRCm39) |
missense |
probably benign |
|
R6147:Cntnap5b
|
UTSW |
1 |
99,978,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Cntnap5b
|
UTSW |
1 |
100,306,800 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6248:Cntnap5b
|
UTSW |
1 |
99,999,827 (GRCm39) |
missense |
probably benign |
0.30 |
R6286:Cntnap5b
|
UTSW |
1 |
100,182,798 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6306:Cntnap5b
|
UTSW |
1 |
100,091,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R6336:Cntnap5b
|
UTSW |
1 |
100,286,394 (GRCm39) |
missense |
probably benign |
0.00 |
R6360:Cntnap5b
|
UTSW |
1 |
100,359,461 (GRCm39) |
nonsense |
probably null |
|
R6722:Cntnap5b
|
UTSW |
1 |
100,406,211 (GRCm39) |
missense |
probably damaging |
0.98 |
R6750:Cntnap5b
|
UTSW |
1 |
100,202,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R6806:Cntnap5b
|
UTSW |
1 |
99,868,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R6933:Cntnap5b
|
UTSW |
1 |
100,311,175 (GRCm39) |
missense |
probably benign |
0.01 |
R6957:Cntnap5b
|
UTSW |
1 |
100,202,197 (GRCm39) |
missense |
probably benign |
0.08 |
R6958:Cntnap5b
|
UTSW |
1 |
100,202,197 (GRCm39) |
missense |
probably benign |
0.08 |
R6959:Cntnap5b
|
UTSW |
1 |
100,202,197 (GRCm39) |
missense |
probably benign |
0.08 |
R6961:Cntnap5b
|
UTSW |
1 |
100,202,197 (GRCm39) |
missense |
probably benign |
0.08 |
R6962:Cntnap5b
|
UTSW |
1 |
100,202,197 (GRCm39) |
missense |
probably benign |
0.08 |
R7088:Cntnap5b
|
UTSW |
1 |
100,087,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R7146:Cntnap5b
|
UTSW |
1 |
99,978,519 (GRCm39) |
splice site |
probably null |
|
R7165:Cntnap5b
|
UTSW |
1 |
100,003,887 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7190:Cntnap5b
|
UTSW |
1 |
100,359,574 (GRCm39) |
splice site |
probably null |
|
R7376:Cntnap5b
|
UTSW |
1 |
99,894,994 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7385:Cntnap5b
|
UTSW |
1 |
100,306,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Cntnap5b
|
UTSW |
1 |
100,318,402 (GRCm39) |
missense |
probably damaging |
0.98 |
R8080:Cntnap5b
|
UTSW |
1 |
99,999,928 (GRCm39) |
missense |
probably benign |
0.16 |
R8082:Cntnap5b
|
UTSW |
1 |
100,306,941 (GRCm39) |
missense |
probably benign |
0.00 |
R8271:Cntnap5b
|
UTSW |
1 |
99,999,832 (GRCm39) |
missense |
probably benign |
0.00 |
R8303:Cntnap5b
|
UTSW |
1 |
100,069,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R8428:Cntnap5b
|
UTSW |
1 |
100,311,310 (GRCm39) |
missense |
probably damaging |
0.98 |
R9131:Cntnap5b
|
UTSW |
1 |
99,978,368 (GRCm39) |
missense |
probably benign |
0.22 |
R9144:Cntnap5b
|
UTSW |
1 |
99,978,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R9522:Cntnap5b
|
UTSW |
1 |
100,412,347 (GRCm39) |
missense |
probably benign |
0.00 |
R9611:Cntnap5b
|
UTSW |
1 |
99,894,935 (GRCm39) |
missense |
probably damaging |
1.00 |
RF007:Cntnap5b
|
UTSW |
1 |
100,091,795 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Cntnap5b
|
UTSW |
1 |
100,359,573 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Cntnap5b
|
UTSW |
1 |
100,374,565 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Cntnap5b
|
UTSW |
1 |
100,091,953 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1176:Cntnap5b
|
UTSW |
1 |
99,894,995 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Cntnap5b
|
UTSW |
1 |
99,978,431 (GRCm39) |
missense |
probably damaging |
0.96 |
|