Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610009L18Rik |
T |
C |
11: 120,241,773 (GRCm39) |
|
probably benign |
Het |
Alpk2 |
A |
T |
18: 65,424,605 (GRCm39) |
|
probably benign |
Het |
Angptl8 |
T |
C |
9: 21,748,349 (GRCm39) |
|
probably benign |
Het |
AU040320 |
T |
A |
4: 126,722,632 (GRCm39) |
D383E |
probably benign |
Het |
Cep97 |
C |
T |
16: 55,745,323 (GRCm39) |
|
probably benign |
Het |
Clcn4 |
A |
T |
7: 7,290,672 (GRCm39) |
L649H |
probably damaging |
Het |
Col5a2 |
T |
C |
1: 45,415,899 (GRCm39) |
N1416S |
probably benign |
Het |
Erbb2 |
C |
T |
11: 98,326,456 (GRCm39) |
P1027S |
probably damaging |
Het |
Eya1 |
A |
G |
1: 14,340,925 (GRCm39) |
|
probably benign |
Het |
Gfm2 |
T |
C |
13: 97,299,485 (GRCm39) |
I402T |
probably benign |
Het |
Gmeb2 |
A |
T |
2: 180,900,836 (GRCm39) |
V187E |
probably benign |
Het |
Hectd1 |
T |
C |
12: 51,838,173 (GRCm39) |
H662R |
possibly damaging |
Het |
Kidins220 |
A |
G |
12: 25,107,473 (GRCm39) |
D1642G |
probably damaging |
Het |
Klhl32 |
T |
A |
4: 24,682,245 (GRCm39) |
D146V |
probably damaging |
Het |
Krt36 |
T |
C |
11: 99,993,774 (GRCm39) |
I355V |
probably damaging |
Het |
Lrrcc1 |
T |
A |
3: 14,601,188 (GRCm39) |
S73R |
possibly damaging |
Het |
Ltbp3 |
A |
T |
19: 5,804,047 (GRCm39) |
H853L |
probably benign |
Het |
Map3k5 |
G |
A |
10: 20,017,313 (GRCm39) |
R1369Q |
probably damaging |
Het |
Mcm8 |
A |
G |
2: 132,663,326 (GRCm39) |
N148S |
probably benign |
Het |
Mylk3 |
A |
T |
8: 86,082,155 (GRCm39) |
L211* |
probably null |
Het |
Nras |
T |
C |
3: 102,966,232 (GRCm39) |
|
probably benign |
Het |
Or2n1c |
A |
T |
17: 38,519,873 (GRCm39) |
I246F |
probably damaging |
Het |
Or52e18 |
A |
T |
7: 104,609,923 (GRCm39) |
N5K |
probably damaging |
Het |
Os9 |
A |
T |
10: 126,956,378 (GRCm39) |
Y66N |
probably damaging |
Het |
Pitpnm1 |
A |
G |
19: 4,151,228 (GRCm39) |
D15G |
possibly damaging |
Het |
Reg3a |
A |
T |
6: 78,359,284 (GRCm39) |
R95* |
probably null |
Het |
Rnf17 |
C |
T |
14: 56,749,728 (GRCm39) |
P1425S |
probably damaging |
Het |
Smad2 |
T |
C |
18: 76,432,846 (GRCm39) |
|
probably benign |
Het |
Ttll5 |
C |
T |
12: 85,980,256 (GRCm39) |
Q76* |
probably null |
Het |
Uri1 |
A |
T |
7: 37,696,156 (GRCm39) |
|
probably benign |
Het |
Vmn2r102 |
G |
T |
17: 19,899,185 (GRCm39) |
|
probably null |
Het |
Vmn2r70 |
T |
G |
7: 85,213,007 (GRCm39) |
M467L |
probably benign |
Het |
Zfp318 |
T |
A |
17: 46,724,652 (GRCm39) |
D2218E |
possibly damaging |
Het |
Zfp692 |
T |
C |
11: 58,204,855 (GRCm39) |
I405T |
possibly damaging |
Het |
Zfp692 |
A |
G |
11: 58,200,824 (GRCm39) |
H235R |
possibly damaging |
Het |
|
Other mutations in Ifne |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00594:Ifne
|
APN |
4 |
88,798,041 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02167:Ifne
|
APN |
4 |
88,798,065 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0212:Ifne
|
UTSW |
4 |
88,797,972 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0699:Ifne
|
UTSW |
4 |
88,798,014 (GRCm39) |
missense |
probably benign |
0.00 |
R1868:Ifne
|
UTSW |
4 |
88,797,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R4480:Ifne
|
UTSW |
4 |
88,797,838 (GRCm39) |
makesense |
probably null |
|
R4865:Ifne
|
UTSW |
4 |
88,797,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R6752:Ifne
|
UTSW |
4 |
88,798,319 (GRCm39) |
missense |
probably benign |
0.06 |
R7319:Ifne
|
UTSW |
4 |
88,798,243 (GRCm39) |
missense |
probably damaging |
0.98 |
R7413:Ifne
|
UTSW |
4 |
88,797,840 (GRCm39) |
makesense |
probably null |
|
|