Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap21 |
A |
T |
2: 20,886,397 (GRCm39) |
V270E |
probably damaging |
Het |
Blvrb |
A |
G |
7: 27,158,786 (GRCm39) |
D62G |
probably benign |
Het |
Ccdc68 |
T |
A |
18: 70,089,113 (GRCm39) |
S219T |
probably damaging |
Het |
Celf2 |
G |
A |
2: 6,590,886 (GRCm39) |
T303I |
possibly damaging |
Het |
Cep290 |
T |
C |
10: 100,372,729 (GRCm39) |
S1176P |
probably damaging |
Het |
Cpeb2 |
C |
A |
5: 43,391,584 (GRCm39) |
S260* |
probably null |
Het |
Dscam |
A |
T |
16: 96,857,857 (GRCm39) |
I51N |
probably benign |
Het |
Erbb4 |
G |
A |
1: 68,779,642 (GRCm39) |
Q45* |
probably null |
Het |
Hipk3 |
T |
C |
2: 104,301,850 (GRCm39) |
N114S |
probably benign |
Het |
Hnrnph3 |
T |
C |
10: 62,853,957 (GRCm39) |
M54V |
probably benign |
Het |
Map7d1 |
T |
C |
4: 126,127,429 (GRCm39) |
E720G |
unknown |
Het |
Mark2 |
G |
T |
19: 7,263,263 (GRCm39) |
T201N |
possibly damaging |
Het |
Mef2c |
A |
G |
13: 83,810,461 (GRCm39) |
N371S |
probably benign |
Het |
Mgst3 |
T |
C |
1: 167,205,871 (GRCm39) |
Y36C |
probably damaging |
Het |
Mtor |
C |
T |
4: 148,599,397 (GRCm39) |
R1482C |
probably damaging |
Het |
Ndst1 |
G |
T |
18: 60,845,931 (GRCm39) |
T126K |
probably damaging |
Het |
Nkain3 |
C |
A |
4: 20,778,431 (GRCm39) |
|
probably benign |
Het |
Obscn |
T |
C |
11: 58,922,787 (GRCm39) |
I5850V |
possibly damaging |
Het |
Or11g1 |
C |
T |
14: 50,651,625 (GRCm39) |
S208F |
probably benign |
Het |
Or5d14 |
C |
T |
2: 87,880,509 (GRCm39) |
W153* |
probably null |
Het |
Or6k4 |
A |
T |
1: 173,964,885 (GRCm39) |
T192S |
probably benign |
Het |
Pbx1 |
T |
C |
1: 168,258,910 (GRCm39) |
D55G |
possibly damaging |
Het |
Pi4ka |
T |
C |
16: 17,125,574 (GRCm39) |
E1187G |
|
Het |
Pkn1 |
A |
T |
8: 84,404,367 (GRCm39) |
N543K |
probably benign |
Het |
Plin1 |
T |
C |
7: 79,372,544 (GRCm39) |
N343D |
probably benign |
Het |
Prpf4 |
T |
C |
4: 62,336,131 (GRCm39) |
V286A |
probably benign |
Het |
Pyroxd2 |
A |
G |
19: 42,719,756 (GRCm39) |
|
probably null |
Het |
Rbpms |
A |
G |
8: 34,294,173 (GRCm39) |
F190S |
possibly damaging |
Het |
Rpl10a |
T |
A |
17: 28,548,006 (GRCm39) |
F49Y |
possibly damaging |
Het |
Slc32a1 |
A |
G |
2: 158,455,995 (GRCm39) |
T217A |
probably damaging |
Het |
Slco6c1 |
T |
C |
1: 97,055,827 (GRCm39) |
S25G |
probably benign |
Het |
Slitrk5 |
C |
T |
14: 111,916,496 (GRCm39) |
T40I |
probably benign |
Het |
Smchd1 |
T |
C |
17: 71,718,843 (GRCm39) |
N842S |
possibly damaging |
Het |
Sorbs1 |
G |
A |
19: 40,361,923 (GRCm39) |
R154* |
probably null |
Het |
Stc2 |
A |
G |
11: 31,310,332 (GRCm39) |
S235P |
probably benign |
Het |
Tcaf2 |
C |
T |
6: 42,619,728 (GRCm39) |
A100T |
probably benign |
Het |
Tcerg1l |
T |
C |
7: 137,995,998 (GRCm39) |
D170G |
possibly damaging |
Het |
Tcf15 |
T |
C |
2: 151,986,039 (GRCm39) |
L165P |
probably damaging |
Het |
Tle5 |
T |
C |
10: 81,399,988 (GRCm39) |
V62A |
probably damaging |
Het |
Tmem200c |
G |
T |
17: 69,148,682 (GRCm39) |
G422W |
probably damaging |
Het |
Tnfsf13b |
A |
G |
8: 10,085,391 (GRCm39) |
I294V |
possibly damaging |
Het |
Tns3 |
T |
A |
11: 8,442,606 (GRCm39) |
T586S |
probably damaging |
Het |
Unc80 |
A |
T |
1: 66,629,460 (GRCm39) |
E1319V |
possibly damaging |
Het |
Vegfc |
A |
G |
8: 54,622,180 (GRCm39) |
I221V |
possibly damaging |
Het |
Vmn1r86 |
A |
T |
7: 12,836,781 (GRCm39) |
Y32N |
possibly damaging |
Het |
Vmn2r111 |
T |
A |
17: 22,787,859 (GRCm39) |
L497F |
probably benign |
Het |
Wdr49 |
T |
C |
3: 75,230,931 (GRCm39) |
D577G |
probably benign |
Het |
Xpo4 |
A |
G |
14: 57,828,512 (GRCm39) |
F783L |
possibly damaging |
Het |
|
Other mutations in Fam124a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01556:Fam124a
|
APN |
14 |
62,825,181 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02010:Fam124a
|
APN |
14 |
62,824,728 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Fam124a
|
APN |
14 |
62,793,368 (GRCm39) |
splice site |
probably null |
|
IGL03060:Fam124a
|
APN |
14 |
62,843,353 (GRCm39) |
missense |
probably benign |
|
P0026:Fam124a
|
UTSW |
14 |
62,843,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R0133:Fam124a
|
UTSW |
14 |
62,843,782 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2044:Fam124a
|
UTSW |
14 |
62,824,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R5397:Fam124a
|
UTSW |
14 |
62,843,838 (GRCm39) |
missense |
probably benign |
|
R5753:Fam124a
|
UTSW |
14 |
62,843,988 (GRCm39) |
missense |
probably benign |
0.01 |
R5988:Fam124a
|
UTSW |
14 |
62,824,986 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7170:Fam124a
|
UTSW |
14 |
62,824,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R7583:Fam124a
|
UTSW |
14 |
62,844,008 (GRCm39) |
nonsense |
probably null |
|
R7790:Fam124a
|
UTSW |
14 |
62,843,526 (GRCm39) |
missense |
probably benign |
|
R8039:Fam124a
|
UTSW |
14 |
62,843,325 (GRCm39) |
nonsense |
probably null |
|
R8873:Fam124a
|
UTSW |
14 |
62,844,024 (GRCm39) |
missense |
probably benign |
0.09 |
R9483:Fam124a
|
UTSW |
14 |
62,844,100 (GRCm39) |
missense |
probably damaging |
0.99 |
R9518:Fam124a
|
UTSW |
14 |
62,824,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R9551:Fam124a
|
UTSW |
14 |
62,843,988 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9628:Fam124a
|
UTSW |
14 |
62,825,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R9765:Fam124a
|
UTSW |
14 |
62,824,883 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Fam124a
|
UTSW |
14 |
62,843,439 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Fam124a
|
UTSW |
14 |
62,843,857 (GRCm39) |
missense |
probably benign |
|
|