Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700111E14Rik |
A |
T |
6: 36,914,152 (GRCm39) |
|
probably benign |
Het |
Actn2 |
A |
T |
13: 12,324,479 (GRCm39) |
|
probably null |
Het |
Apom |
C |
T |
17: 35,350,208 (GRCm39) |
A78T |
probably benign |
Het |
Bambi |
A |
G |
18: 3,508,229 (GRCm39) |
Y7C |
possibly damaging |
Het |
Cdc42bpb |
T |
C |
12: 111,289,576 (GRCm39) |
M418V |
probably benign |
Het |
Clptm1 |
T |
C |
7: 19,389,701 (GRCm39) |
N43D |
probably benign |
Het |
Cspp1 |
T |
C |
1: 10,136,886 (GRCm39) |
V241A |
probably benign |
Het |
Ctnna3 |
T |
A |
10: 63,339,910 (GRCm39) |
I32N |
probably benign |
Het |
Elp2 |
A |
G |
18: 24,752,576 (GRCm39) |
|
probably benign |
Het |
Frmd4a |
A |
G |
2: 4,608,844 (GRCm39) |
D893G |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
H2-M10.1 |
C |
A |
17: 36,635,971 (GRCm39) |
G154* |
probably null |
Het |
Igdcc3 |
C |
T |
9: 65,051,819 (GRCm39) |
R141W |
probably damaging |
Het |
Igkv14-130 |
A |
G |
6: 67,768,323 (GRCm39) |
K60E |
possibly damaging |
Het |
Kcnmb2 |
A |
G |
3: 32,252,512 (GRCm39) |
|
probably benign |
Het |
Lrp4 |
T |
C |
2: 91,324,529 (GRCm39) |
L1288P |
possibly damaging |
Het |
Mavs |
T |
A |
2: 131,087,441 (GRCm39) |
M313K |
probably benign |
Het |
Mia2 |
A |
G |
12: 59,154,731 (GRCm39) |
E148G |
possibly damaging |
Het |
Or6c76b |
A |
T |
10: 129,692,950 (GRCm39) |
T188S |
probably damaging |
Het |
Or8b12b |
T |
A |
9: 37,684,159 (GRCm39) |
I68K |
possibly damaging |
Het |
Or8d1 |
T |
A |
9: 38,767,013 (GRCm39) |
Y218* |
probably null |
Het |
Plekha3 |
C |
T |
2: 76,517,047 (GRCm39) |
T133M |
probably damaging |
Het |
Plxna1 |
A |
T |
6: 89,309,066 (GRCm39) |
|
probably null |
Het |
Septin2 |
A |
G |
1: 93,426,823 (GRCm39) |
N144S |
probably damaging |
Het |
Slc9a4 |
T |
C |
1: 40,651,451 (GRCm39) |
|
probably benign |
Het |
Slco1b2 |
T |
A |
6: 141,594,312 (GRCm39) |
I59K |
probably damaging |
Het |
Sp140l2 |
A |
G |
1: 85,231,907 (GRCm39) |
|
probably benign |
Het |
Tnrc6b |
A |
G |
15: 80,786,184 (GRCm39) |
S1243G |
possibly damaging |
Het |
Unc13a |
T |
A |
8: 72,091,854 (GRCm39) |
|
probably benign |
Het |
Vmn2r105 |
T |
C |
17: 20,444,918 (GRCm39) |
R525G |
probably damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r37 |
T |
A |
7: 9,219,032 (GRCm39) |
K451* |
probably null |
Het |
Vmn2r71 |
C |
T |
7: 85,270,001 (GRCm39) |
T504I |
probably benign |
Het |
Zfp668 |
A |
T |
7: 127,465,994 (GRCm39) |
C397S |
probably damaging |
Het |
|
Other mutations in Gm5862 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01606:Gm5862
|
APN |
5 |
26,224,514 (GRCm39) |
missense |
probably benign |
|
IGL01863:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01868:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01873:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01881:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01902:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01905:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01917:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01924:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01927:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL01951:Gm5862
|
APN |
5 |
26,227,769 (GRCm39) |
missense |
probably benign |
|
IGL03374:Gm5862
|
APN |
5 |
26,224,510 (GRCm39) |
missense |
probably damaging |
0.98 |
R2475:Gm5862
|
UTSW |
5 |
26,224,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R3828:Gm5862
|
UTSW |
5 |
26,224,345 (GRCm39) |
missense |
probably benign |
0.27 |
R4591:Gm5862
|
UTSW |
5 |
26,224,486 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6916:Gm5862
|
UTSW |
5 |
26,224,346 (GRCm39) |
missense |
probably benign |
|
R8291:Gm5862
|
UTSW |
5 |
26,224,444 (GRCm39) |
missense |
probably benign |
0.32 |
R8927:Gm5862
|
UTSW |
5 |
26,226,678 (GRCm39) |
missense |
probably damaging |
0.98 |
R8928:Gm5862
|
UTSW |
5 |
26,226,678 (GRCm39) |
missense |
probably damaging |
0.98 |
R9074:Gm5862
|
UTSW |
5 |
26,226,624 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Gm5862
|
UTSW |
5 |
26,223,485 (GRCm39) |
frame shift |
probably null |
|
|