Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
A |
G |
5: 64,055,459 (GRCm39) |
E65G |
probably benign |
Het |
Abcc8 |
G |
A |
7: 45,756,431 (GRCm39) |
R1425C |
probably damaging |
Het |
Adcy3 |
A |
T |
12: 4,259,407 (GRCm39) |
|
probably null |
Het |
AI661453 |
T |
G |
17: 47,778,263 (GRCm39) |
|
probably benign |
Het |
Arhgef10 |
A |
T |
8: 15,004,819 (GRCm39) |
Y445F |
probably benign |
Het |
Atrx |
G |
T |
X: 104,874,587 (GRCm39) |
S1924R |
possibly damaging |
Het |
Clca3a1 |
T |
C |
3: 144,733,763 (GRCm39) |
T58A |
possibly damaging |
Het |
Clec1b |
A |
G |
6: 129,378,804 (GRCm39) |
Y97C |
probably damaging |
Het |
Cobll1 |
A |
G |
2: 64,928,084 (GRCm39) |
S1080P |
probably damaging |
Het |
Crb1 |
C |
A |
1: 139,176,213 (GRCm39) |
C529F |
probably damaging |
Het |
Crim1 |
C |
T |
17: 78,642,763 (GRCm39) |
R494* |
probably null |
Het |
Cyp3a25 |
A |
T |
5: 145,938,257 (GRCm39) |
|
probably benign |
Het |
Dntt |
T |
A |
19: 41,041,424 (GRCm39) |
|
probably null |
Het |
Gjb1 |
T |
C |
X: 100,428,611 (GRCm39) |
C280R |
probably damaging |
Het |
Glp1r |
T |
A |
17: 31,143,485 (GRCm39) |
C174S |
probably damaging |
Het |
Gm5414 |
A |
T |
15: 101,536,269 (GRCm39) |
Y119N |
probably benign |
Het |
Gm9631 |
G |
A |
11: 121,834,478 (GRCm39) |
|
|
Het |
Gm9796 |
G |
T |
11: 95,588,756 (GRCm39) |
|
noncoding transcript |
Het |
Gm9956 |
T |
C |
10: 56,621,388 (GRCm39) |
F17L |
unknown |
Het |
Il1rap |
A |
T |
16: 26,529,366 (GRCm39) |
D396V |
probably damaging |
Het |
Impa1 |
T |
C |
3: 10,388,018 (GRCm39) |
K135E |
possibly damaging |
Het |
Iqub |
G |
A |
6: 24,449,810 (GRCm39) |
A685V |
probably damaging |
Het |
Jade3 |
T |
C |
X: 20,379,063 (GRCm39) |
V512A |
probably benign |
Het |
Kif3a |
C |
A |
11: 53,461,525 (GRCm39) |
P57T |
probably damaging |
Het |
Kndc1 |
G |
T |
7: 139,501,829 (GRCm39) |
|
probably null |
Het |
Lyst |
G |
A |
13: 13,835,541 (GRCm39) |
C1741Y |
probably benign |
Het |
Maged2 |
G |
T |
X: 149,592,755 (GRCm39) |
D343E |
probably benign |
Het |
Magi2 |
T |
C |
5: 19,883,707 (GRCm39) |
S120P |
probably damaging |
Het |
Nxph3 |
A |
T |
11: 95,401,656 (GRCm39) |
*253R |
probably null |
Het |
Oog2 |
A |
T |
4: 143,921,618 (GRCm39) |
H194L |
probably damaging |
Het |
Pcbd2 |
T |
G |
13: 55,880,764 (GRCm39) |
W7G |
probably benign |
Het |
Pcdhb14 |
T |
G |
18: 37,582,823 (GRCm39) |
L643R |
possibly damaging |
Het |
Plch1 |
G |
T |
3: 63,605,177 (GRCm39) |
|
probably null |
Het |
Poln |
G |
T |
5: 34,270,666 (GRCm39) |
S455* |
probably null |
Het |
Ppp2r1a |
T |
C |
17: 21,171,596 (GRCm39) |
|
probably benign |
Het |
Rsu1 |
T |
G |
2: 13,082,308 (GRCm39) |
|
probably benign |
Het |
Serpina10 |
A |
T |
12: 103,583,202 (GRCm39) |
M360K |
possibly damaging |
Het |
Thbs1 |
T |
C |
2: 117,945,451 (GRCm39) |
V310A |
probably benign |
Het |
Tie1 |
C |
A |
4: 118,343,760 (GRCm39) |
E61* |
probably null |
Het |
Tm2d1 |
G |
T |
4: 98,268,911 (GRCm39) |
P62Q |
probably damaging |
Het |
Tpp1 |
G |
T |
7: 105,398,826 (GRCm39) |
P201Q |
probably damaging |
Het |
Trim13 |
A |
G |
14: 61,842,598 (GRCm39) |
E205G |
probably damaging |
Het |
|
Other mutations in Sox30 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00898:Sox30
|
APN |
11 |
45,882,727 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01449:Sox30
|
APN |
11 |
45,872,169 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02601:Sox30
|
APN |
11 |
45,875,589 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02747:Sox30
|
APN |
11 |
45,871,772 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03403:Sox30
|
APN |
11 |
45,908,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R0104:Sox30
|
UTSW |
11 |
45,872,141 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1450:Sox30
|
UTSW |
11 |
45,908,098 (GRCm39) |
missense |
probably damaging |
0.99 |
R2109:Sox30
|
UTSW |
11 |
45,882,595 (GRCm39) |
missense |
probably damaging |
0.99 |
R2213:Sox30
|
UTSW |
11 |
45,875,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R3715:Sox30
|
UTSW |
11 |
45,875,619 (GRCm39) |
missense |
probably damaging |
0.99 |
R4111:Sox30
|
UTSW |
11 |
45,908,041 (GRCm39) |
missense |
probably benign |
0.09 |
R4723:Sox30
|
UTSW |
11 |
45,875,592 (GRCm39) |
missense |
probably benign |
0.03 |
R5014:Sox30
|
UTSW |
11 |
45,882,736 (GRCm39) |
missense |
probably benign |
0.01 |
R5408:Sox30
|
UTSW |
11 |
45,882,694 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5974:Sox30
|
UTSW |
11 |
45,871,900 (GRCm39) |
missense |
probably damaging |
0.99 |
R6063:Sox30
|
UTSW |
11 |
45,882,769 (GRCm39) |
missense |
probably benign |
0.04 |
R6948:Sox30
|
UTSW |
11 |
45,908,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R7242:Sox30
|
UTSW |
11 |
45,875,347 (GRCm39) |
splice site |
probably null |
|
R7258:Sox30
|
UTSW |
11 |
45,871,379 (GRCm39) |
missense |
unknown |
|
R8195:Sox30
|
UTSW |
11 |
45,882,592 (GRCm39) |
missense |
probably benign |
0.00 |
R9205:Sox30
|
UTSW |
11 |
45,908,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R9605:Sox30
|
UTSW |
11 |
45,875,640 (GRCm39) |
missense |
possibly damaging |
0.90 |
|