Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agbl1 |
A |
G |
7: 76,075,669 (GRCm39) |
Y437C |
probably damaging |
Het |
Apba2 |
T |
A |
7: 64,345,207 (GRCm39) |
D132E |
probably damaging |
Het |
Atp13a4 |
A |
G |
16: 29,288,098 (GRCm39) |
S258P |
probably damaging |
Het |
Bach2 |
T |
A |
4: 32,575,301 (GRCm39) |
M509K |
possibly damaging |
Het |
Ccdc186 |
T |
A |
19: 56,788,561 (GRCm39) |
K549N |
probably damaging |
Het |
Chrna3 |
C |
T |
9: 54,923,094 (GRCm39) |
R238H |
probably damaging |
Het |
Cntnap5b |
G |
A |
1: 99,868,374 (GRCm39) |
C30Y |
probably damaging |
Het |
Cplane1 |
A |
G |
15: 8,216,342 (GRCm39) |
Q520R |
possibly damaging |
Het |
Dnah11 |
T |
C |
12: 117,951,411 (GRCm39) |
|
probably null |
Het |
Ebna1bp2 |
T |
C |
4: 118,478,174 (GRCm39) |
C16R |
probably benign |
Het |
Grin2b |
A |
G |
6: 135,751,826 (GRCm39) |
Y579H |
possibly damaging |
Het |
Ifi206 |
C |
T |
1: 173,309,137 (GRCm39) |
M286I |
probably benign |
Het |
Itpr1 |
G |
A |
6: 108,492,908 (GRCm39) |
V2478I |
probably benign |
Het |
Lrrc37 |
T |
C |
11: 103,511,950 (GRCm39) |
E6G |
unknown |
Het |
Ltbp2 |
T |
C |
12: 84,856,012 (GRCm39) |
S744G |
possibly damaging |
Het |
Magi3 |
T |
A |
3: 103,954,285 (GRCm39) |
N684I |
possibly damaging |
Het |
Muc16 |
A |
G |
9: 18,449,206 (GRCm39) |
|
probably null |
Het |
Nphp4 |
G |
T |
4: 152,622,558 (GRCm39) |
Q614H |
probably benign |
Het |
Nprl3 |
A |
G |
11: 32,217,509 (GRCm39) |
I11T |
probably damaging |
Het |
Or51q1 |
G |
T |
7: 103,628,771 (GRCm39) |
R124L |
possibly damaging |
Het |
Pank2 |
T |
C |
2: 131,104,627 (GRCm39) |
|
probably benign |
Het |
Prss58 |
A |
T |
6: 40,874,666 (GRCm39) |
N58K |
probably damaging |
Het |
Ptk7 |
C |
T |
17: 46,884,454 (GRCm39) |
V759M |
probably damaging |
Het |
Rassf7 |
A |
G |
7: 140,796,722 (GRCm39) |
T28A |
probably damaging |
Het |
Rbm45 |
C |
T |
2: 76,210,804 (GRCm39) |
T445I |
probably benign |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Rsrc2 |
T |
G |
5: 123,877,594 (GRCm39) |
|
probably benign |
Het |
Sh3d19 |
T |
A |
3: 86,011,640 (GRCm39) |
Y409N |
probably damaging |
Het |
Spata31d1a |
A |
T |
13: 59,851,032 (GRCm39) |
N365K |
probably benign |
Het |
Stkld1 |
C |
G |
2: 26,833,922 (GRCm39) |
N136K |
probably benign |
Het |
Tenm4 |
A |
G |
7: 96,461,166 (GRCm39) |
D904G |
possibly damaging |
Het |
Tmf1 |
G |
A |
6: 97,138,408 (GRCm39) |
R837* |
probably null |
Het |
Tnn |
T |
C |
1: 159,948,278 (GRCm39) |
T812A |
possibly damaging |
Het |
Trgj4 |
T |
C |
13: 19,526,365 (GRCm39) |
L15P |
probably damaging |
Het |
Trp53bp1 |
T |
C |
2: 121,059,147 (GRCm39) |
I905V |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 69,786,308 (GRCm39) |
|
probably benign |
Het |
Zfp446 |
T |
C |
7: 12,713,043 (GRCm39) |
L27P |
probably damaging |
Het |
Zfp719 |
A |
G |
7: 43,235,809 (GRCm39) |
D57G |
possibly damaging |
Het |
Zfp747l1 |
T |
C |
7: 126,985,766 (GRCm39) |
|
probably benign |
Het |
Zfp978 |
G |
A |
4: 147,475,284 (GRCm39) |
R277K |
probably benign |
Het |
|
Other mutations in Saxo2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01326:Saxo2
|
APN |
7 |
82,297,613 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01992:Saxo2
|
APN |
7 |
82,284,108 (GRCm39) |
missense |
probably damaging |
0.97 |
R0973:Saxo2
|
UTSW |
7 |
82,284,078 (GRCm39) |
missense |
probably benign |
0.00 |
R0973:Saxo2
|
UTSW |
7 |
82,284,078 (GRCm39) |
missense |
probably benign |
0.00 |
R0974:Saxo2
|
UTSW |
7 |
82,284,078 (GRCm39) |
missense |
probably benign |
0.00 |
R1169:Saxo2
|
UTSW |
7 |
82,284,379 (GRCm39) |
missense |
possibly damaging |
0.77 |
R3113:Saxo2
|
UTSW |
7 |
82,292,949 (GRCm39) |
missense |
probably benign |
0.05 |
R4912:Saxo2
|
UTSW |
7 |
82,283,743 (GRCm39) |
missense |
probably benign |
0.00 |
R5406:Saxo2
|
UTSW |
7 |
82,284,586 (GRCm39) |
missense |
probably benign |
|
R5784:Saxo2
|
UTSW |
7 |
82,284,082 (GRCm39) |
missense |
probably benign |
0.01 |
R6344:Saxo2
|
UTSW |
7 |
82,284,073 (GRCm39) |
missense |
probably damaging |
0.96 |
R6677:Saxo2
|
UTSW |
7 |
82,284,484 (GRCm39) |
missense |
probably benign |
0.01 |
R6912:Saxo2
|
UTSW |
7 |
82,284,402 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6968:Saxo2
|
UTSW |
7 |
82,292,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R7621:Saxo2
|
UTSW |
7 |
82,297,625 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7655:Saxo2
|
UTSW |
7 |
82,284,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R7656:Saxo2
|
UTSW |
7 |
82,284,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R9108:Saxo2
|
UTSW |
7 |
82,284,082 (GRCm39) |
missense |
probably benign |
0.01 |
R9241:Saxo2
|
UTSW |
7 |
82,284,250 (GRCm39) |
missense |
probably benign |
0.00 |
R9682:Saxo2
|
UTSW |
7 |
82,292,881 (GRCm39) |
missense |
probably benign |
0.12 |
|