Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
A |
G |
5: 88,119,621 (GRCm39) |
K126R |
possibly damaging |
Het |
Adam7 |
A |
T |
14: 68,748,206 (GRCm39) |
C548S |
probably damaging |
Het |
Adar |
C |
A |
3: 89,652,897 (GRCm39) |
H260N |
probably benign |
Het |
Ak9 |
A |
G |
10: 41,258,828 (GRCm39) |
E775G |
probably benign |
Het |
Arhgap35 |
T |
C |
7: 16,297,568 (GRCm39) |
Y499C |
probably damaging |
Het |
Bank1 |
A |
G |
3: 135,772,190 (GRCm39) |
L480P |
probably damaging |
Het |
Cep135 |
G |
T |
5: 76,763,638 (GRCm39) |
|
probably null |
Het |
Cnga1 |
G |
T |
5: 72,768,155 (GRCm39) |
A177E |
probably damaging |
Het |
Cubn |
T |
A |
2: 13,432,658 (GRCm39) |
D1221V |
probably damaging |
Het |
Cyp2d40 |
T |
C |
15: 82,648,205 (GRCm39) |
Y36C |
possibly damaging |
Het |
Dock8 |
C |
A |
19: 25,138,438 (GRCm39) |
N1254K |
probably benign |
Het |
Elapor2 |
T |
C |
5: 9,449,255 (GRCm39) |
S128P |
probably damaging |
Het |
Fam13b |
C |
T |
18: 34,620,192 (GRCm39) |
V231I |
possibly damaging |
Het |
Fbxo8 |
T |
A |
8: 57,022,353 (GRCm39) |
Y122N |
probably damaging |
Het |
Fmo2 |
T |
A |
1: 162,708,002 (GRCm39) |
I378F |
probably benign |
Het |
Golga3 |
A |
T |
5: 110,352,812 (GRCm39) |
Q861L |
probably damaging |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Ighv3-8 |
G |
T |
12: 114,286,000 (GRCm39) |
A114E |
probably damaging |
Het |
Itga3 |
C |
T |
11: 94,943,269 (GRCm39) |
|
probably null |
Het |
Kank1 |
G |
A |
19: 25,387,088 (GRCm39) |
V254I |
probably benign |
Het |
Lrfn2 |
A |
G |
17: 49,378,154 (GRCm39) |
S412G |
probably benign |
Het |
Lrrn3 |
T |
C |
12: 41,503,534 (GRCm39) |
N261S |
possibly damaging |
Het |
Mical2 |
C |
T |
7: 111,917,692 (GRCm39) |
Q350* |
probably null |
Het |
Nras |
T |
C |
3: 102,967,637 (GRCm39) |
F78L |
probably damaging |
Het |
Nudt9 |
A |
G |
5: 104,198,679 (GRCm39) |
I65V |
probably benign |
Het |
Or10ag59 |
A |
G |
2: 87,406,259 (GRCm39) |
D277G |
probably benign |
Het |
Or4f17-ps1 |
A |
T |
2: 111,358,526 (GRCm39) |
E289V |
possibly damaging |
Het |
Oscar |
G |
A |
7: 3,614,311 (GRCm39) |
P143S |
probably benign |
Het |
Pla2g4d |
C |
T |
2: 120,100,487 (GRCm39) |
G615D |
probably damaging |
Het |
Plekha1 |
T |
G |
7: 130,502,301 (GRCm39) |
S175A |
probably benign |
Het |
Psg27 |
T |
C |
7: 18,290,869 (GRCm39) |
K445E |
probably benign |
Het |
Rad51c |
A |
G |
11: 87,271,705 (GRCm39) |
Y318H |
probably benign |
Het |
Ret |
G |
T |
6: 118,153,252 (GRCm39) |
T472K |
possibly damaging |
Het |
Tarbp1 |
T |
C |
8: 127,155,709 (GRCm39) |
D1343G |
probably benign |
Het |
Top2b |
C |
A |
14: 16,409,864 (GRCm38) |
R844S |
probably benign |
Het |
Vmn1r171 |
T |
A |
7: 23,332,429 (GRCm39) |
M218K |
probably damaging |
Het |
Vmn2r89 |
A |
T |
14: 51,695,033 (GRCm39) |
|
probably null |
Het |
Zc3h13 |
T |
A |
14: 75,568,149 (GRCm39) |
D1147E |
probably damaging |
Het |
Zgrf1 |
T |
A |
3: 127,409,135 (GRCm39) |
L1703H |
probably damaging |
Het |
|
Other mutations in Lipo5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02162:Lipo5
|
APN |
19 |
33,446,163 (GRCm39) |
splice site |
probably benign |
|
IGL02210:Lipo5
|
APN |
19 |
33,445,277 (GRCm39) |
missense |
unknown |
|
IGL02689:Lipo5
|
APN |
19 |
33,445,186 (GRCm39) |
missense |
unknown |
|
IGL03276:Lipo5
|
APN |
19 |
33,445,242 (GRCm39) |
missense |
unknown |
|
bradybunch
|
UTSW |
19 |
33,445,317 (GRCm39) |
missense |
unknown |
|
PIT4382001:Lipo5
|
UTSW |
19 |
33,443,339 (GRCm39) |
missense |
probably null |
|
R1456:Lipo5
|
UTSW |
19 |
33,443,273 (GRCm39) |
splice site |
probably benign |
|
R1820:Lipo5
|
UTSW |
19 |
33,441,995 (GRCm39) |
splice site |
probably null |
|
R3770:Lipo5
|
UTSW |
19 |
33,445,200 (GRCm39) |
missense |
unknown |
|
R4658:Lipo5
|
UTSW |
19 |
33,441,922 (GRCm39) |
missense |
unknown |
|
R4906:Lipo5
|
UTSW |
19 |
33,443,348 (GRCm39) |
missense |
unknown |
|
R4951:Lipo5
|
UTSW |
19 |
33,446,251 (GRCm39) |
missense |
probably damaging |
0.98 |
R5304:Lipo5
|
UTSW |
19 |
33,445,149 (GRCm39) |
missense |
unknown |
|
R5526:Lipo5
|
UTSW |
19 |
33,445,284 (GRCm39) |
missense |
unknown |
|
R6110:Lipo5
|
UTSW |
19 |
33,445,317 (GRCm39) |
missense |
unknown |
|
R7077:Lipo5
|
UTSW |
19 |
33,445,170 (GRCm39) |
missense |
|
|
R7094:Lipo5
|
UTSW |
19 |
33,446,249 (GRCm39) |
missense |
probably damaging |
0.99 |
R8500:Lipo5
|
UTSW |
19 |
33,441,849 (GRCm39) |
critical splice donor site |
probably null |
|
R8955:Lipo5
|
UTSW |
19 |
33,450,530 (GRCm39) |
missense |
|
|
|