Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adap1 |
C |
T |
5: 139,293,541 (GRCm39) |
V57M |
probably damaging |
Het |
Agap3 |
A |
G |
5: 24,688,369 (GRCm39) |
K23E |
possibly damaging |
Het |
Anln |
A |
T |
9: 22,249,331 (GRCm39) |
I132K |
probably damaging |
Het |
Anxa4 |
T |
C |
6: 86,737,683 (GRCm39) |
T13A |
probably benign |
Het |
Bdp1 |
A |
T |
13: 100,235,022 (GRCm39) |
Y191N |
possibly damaging |
Het |
Carm1 |
G |
A |
9: 21,498,204 (GRCm39) |
V403M |
probably damaging |
Het |
Cbx7 |
A |
G |
15: 79,807,671 (GRCm39) |
|
probably null |
Het |
Chd8 |
A |
C |
14: 52,451,757 (GRCm39) |
N16K |
possibly damaging |
Het |
Crtc3 |
A |
T |
7: 80,242,315 (GRCm39) |
D499E |
probably damaging |
Het |
Cul3 |
A |
G |
1: 80,249,432 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
T |
C |
2: 104,060,631 (GRCm39) |
D1421G |
probably damaging |
Het |
Fgb |
T |
A |
3: 82,952,367 (GRCm39) |
E167D |
probably benign |
Het |
Gimap6 |
T |
A |
6: 48,679,409 (GRCm39) |
Q209L |
probably damaging |
Het |
Gm3604 |
G |
A |
13: 62,517,990 (GRCm39) |
H123Y |
possibly damaging |
Het |
Gm5884 |
A |
T |
6: 128,622,749 (GRCm39) |
|
noncoding transcript |
Het |
Lyst |
G |
A |
13: 13,835,541 (GRCm39) |
C1741Y |
probably benign |
Het |
Obox3 |
T |
C |
7: 15,360,848 (GRCm39) |
E97G |
probably damaging |
Het |
Obsl1 |
T |
C |
1: 75,466,264 (GRCm39) |
H1488R |
probably benign |
Het |
Or4e1 |
A |
T |
14: 52,700,802 (GRCm39) |
Y221* |
probably null |
Het |
Or6c75 |
A |
G |
10: 129,337,723 (GRCm39) |
*323W |
probably null |
Het |
Pak5 |
T |
A |
2: 135,958,855 (GRCm39) |
K78* |
probably null |
Het |
Paqr9 |
A |
G |
9: 95,442,877 (GRCm39) |
N289S |
probably damaging |
Het |
Pde3b |
G |
A |
7: 114,122,577 (GRCm39) |
R715H |
probably damaging |
Het |
Pglyrp2 |
T |
C |
17: 32,634,835 (GRCm39) |
H509R |
probably benign |
Het |
Pik3ap1 |
A |
C |
19: 41,290,881 (GRCm39) |
N550K |
probably benign |
Het |
Pon3 |
A |
G |
6: 5,221,671 (GRCm39) |
Y320H |
probably damaging |
Het |
Ptprt |
T |
A |
2: 161,608,227 (GRCm39) |
T690S |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,000,686 (GRCm39) |
D925E |
probably benign |
Het |
Rag1 |
T |
C |
2: 101,473,018 (GRCm39) |
D708G |
probably damaging |
Het |
Rbm12 |
C |
T |
2: 155,937,480 (GRCm39) |
|
probably benign |
Het |
Rbmy1b |
A |
G |
Y: 3,774,885 (GRCm39) |
I27M |
probably benign |
Het |
Rfx2 |
G |
A |
17: 57,092,354 (GRCm39) |
H315Y |
possibly damaging |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Sis |
T |
C |
3: 72,820,543 (GRCm39) |
N1407S |
probably benign |
Het |
Slco1c1 |
T |
A |
6: 141,490,555 (GRCm39) |
L261Q |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Ssu72 |
A |
G |
4: 155,789,882 (GRCm39) |
N15S |
possibly damaging |
Het |
Stat4 |
C |
T |
1: 52,137,574 (GRCm39) |
S455F |
probably damaging |
Het |
Stk4 |
T |
A |
2: 163,928,462 (GRCm39) |
L97Q |
probably damaging |
Het |
Sulf1 |
A |
T |
1: 12,856,869 (GRCm39) |
N40I |
probably damaging |
Het |
Sympk |
G |
A |
7: 18,782,794 (GRCm39) |
V877I |
probably benign |
Het |
Taar7b |
A |
T |
10: 23,876,204 (GRCm39) |
H123L |
probably damaging |
Het |
Teddm1b |
A |
G |
1: 153,750,362 (GRCm39) |
Y57C |
probably damaging |
Het |
Tep1 |
A |
T |
14: 51,070,935 (GRCm39) |
C2121* |
probably null |
Het |
Tnfsf11 |
T |
A |
14: 78,537,385 (GRCm39) |
R93* |
probably null |
Het |
Tspan12 |
A |
C |
6: 21,835,378 (GRCm39) |
|
probably benign |
Het |
Tyrp1 |
A |
G |
4: 80,759,012 (GRCm39) |
E295G |
probably null |
Het |
Vps4a |
T |
C |
8: 107,769,693 (GRCm39) |
I334T |
probably damaging |
Het |
Zfhx3 |
T |
C |
8: 109,583,462 (GRCm39) |
S1110P |
probably damaging |
Het |
Zfp507 |
A |
G |
7: 35,491,136 (GRCm39) |
S716P |
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 |
IGL02411:Sox30
|
APN |
11 |
45,871,951 (GRCm39) |
nonsense |
probably null |
|
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 |
|