Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acer2 |
G |
T |
4: 86,835,692 (GRCm39) |
A235S |
probably benign |
Het |
Add2 |
A |
G |
6: 86,084,388 (GRCm39) |
I479V |
possibly damaging |
Het |
Anapc11 |
T |
A |
11: 120,490,168 (GRCm39) |
M28K |
probably benign |
Het |
Anapc15-ps |
T |
C |
10: 95,508,993 (GRCm39) |
S87G |
probably benign |
Het |
Atraid |
T |
C |
5: 31,209,826 (GRCm39) |
L46P |
probably damaging |
Het |
Ccdc80 |
T |
A |
16: 44,916,772 (GRCm39) |
Y509* |
probably null |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cecr2 |
T |
A |
6: 120,739,128 (GRCm39) |
L1257Q |
probably damaging |
Het |
Csn1s2b |
A |
G |
5: 87,957,780 (GRCm39) |
I5V |
probably benign |
Het |
Dhps |
T |
C |
8: 85,800,379 (GRCm39) |
Y221H |
possibly damaging |
Het |
Dmxl1 |
T |
C |
18: 49,997,962 (GRCm39) |
S717P |
probably damaging |
Het |
Dppa5a |
G |
T |
9: 78,275,113 (GRCm39) |
S63Y |
probably damaging |
Het |
Eif3l |
A |
T |
15: 78,970,719 (GRCm39) |
D331V |
possibly damaging |
Het |
Folh1 |
G |
T |
7: 86,412,253 (GRCm39) |
|
probably null |
Het |
Gbp9 |
G |
T |
5: 105,253,662 (GRCm39) |
Q18K |
probably benign |
Het |
Grm5 |
A |
G |
7: 87,251,918 (GRCm39) |
K56R |
probably damaging |
Het |
H2-M3 |
T |
A |
17: 37,581,432 (GRCm39) |
Y31* |
probably null |
Het |
Herc2 |
T |
C |
7: 55,815,031 (GRCm39) |
|
probably benign |
Het |
Itga7 |
G |
T |
10: 128,782,687 (GRCm39) |
A675S |
possibly damaging |
Het |
Or2bd2 |
T |
C |
7: 6,443,574 (GRCm39) |
L225P |
possibly damaging |
Het |
Or5b121 |
A |
G |
19: 13,507,171 (GRCm39) |
I89V |
probably benign |
Het |
Pdk4 |
C |
T |
6: 5,487,408 (GRCm39) |
V281I |
probably benign |
Het |
Pkn3 |
G |
A |
2: 29,970,858 (GRCm39) |
G202D |
probably damaging |
Het |
Rcbtb1 |
A |
G |
14: 59,462,149 (GRCm39) |
N260S |
probably damaging |
Het |
Sipa1l1 |
T |
C |
12: 82,487,594 (GRCm39) |
F1623L |
probably benign |
Het |
Slfn8 |
A |
G |
11: 82,907,934 (GRCm39) |
F203S |
probably damaging |
Het |
St6gal2 |
T |
C |
17: 55,789,596 (GRCm39) |
L210S |
probably damaging |
Het |
Taf5 |
T |
C |
19: 47,065,704 (GRCm39) |
|
probably benign |
Het |
Taok2 |
A |
G |
7: 126,475,270 (GRCm39) |
F226S |
probably damaging |
Het |
Timm10b |
A |
G |
7: 105,289,839 (GRCm39) |
|
probably benign |
Het |
Tmx3 |
A |
G |
18: 90,555,240 (GRCm39) |
N319S |
possibly damaging |
Het |
Trmt1 |
G |
T |
8: 85,426,385 (GRCm39) |
|
probably benign |
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 |
|
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 |
|
R6087:Lipo5
|
UTSW |
19 |
33,443,375 (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 |
|
|
|