Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg2 |
A |
G |
6: 58,662,681 (GRCm39) |
I508V |
probably benign |
Het |
Adgrb2 |
T |
C |
4: 129,913,075 (GRCm39) |
|
probably null |
Het |
Api5 |
T |
A |
2: 94,260,184 (GRCm39) |
H24L |
possibly damaging |
Het |
Apoh |
T |
C |
11: 108,302,968 (GRCm39) |
V311A |
probably benign |
Het |
Atp2a3 |
C |
A |
11: 72,866,165 (GRCm39) |
H262N |
probably benign |
Het |
Brca2 |
G |
T |
5: 150,484,255 (GRCm39) |
V2994L |
possibly damaging |
Het |
Brd1 |
A |
T |
15: 88,585,080 (GRCm39) |
V918D |
probably damaging |
Het |
Calr3 |
T |
G |
8: 73,197,304 (GRCm39) |
D43A |
possibly damaging |
Het |
Cdh16 |
T |
C |
8: 105,348,737 (GRCm39) |
|
probably null |
Het |
Cep192 |
T |
C |
18: 67,995,548 (GRCm39) |
S2033P |
probably damaging |
Het |
Dnah7a |
G |
A |
1: 53,564,194 (GRCm39) |
T1955M |
probably damaging |
Het |
Dock10 |
T |
A |
1: 80,551,840 (GRCm39) |
Y665F |
probably damaging |
Het |
Dync1i1 |
A |
G |
6: 5,767,034 (GRCm39) |
D86G |
probably benign |
Het |
Eri2 |
T |
C |
7: 119,385,331 (GRCm39) |
D390G |
possibly damaging |
Het |
Fank1 |
C |
T |
7: 133,481,758 (GRCm39) |
|
probably benign |
Het |
Hoxb7 |
A |
T |
11: 96,177,570 (GRCm39) |
Y6F |
possibly damaging |
Het |
Hspg2 |
A |
C |
4: 137,279,159 (GRCm39) |
S3081R |
possibly damaging |
Het |
Kcnt1 |
T |
A |
2: 25,790,892 (GRCm39) |
|
probably benign |
Het |
Med13 |
A |
G |
11: 86,174,212 (GRCm39) |
I1762T |
probably benign |
Het |
Mia2 |
A |
G |
12: 59,155,622 (GRCm39) |
D445G |
probably damaging |
Het |
Or8h9 |
T |
C |
2: 86,789,697 (GRCm39) |
Y35C |
probably damaging |
Het |
Plcg2 |
A |
T |
8: 118,330,622 (GRCm39) |
I827F |
possibly damaging |
Het |
Poglut3 |
A |
G |
9: 53,295,551 (GRCm39) |
D51G |
probably benign |
Het |
Rnls |
C |
A |
19: 33,115,684 (GRCm39) |
|
probably benign |
Het |
Scn1a |
A |
T |
2: 66,129,962 (GRCm39) |
|
probably null |
Het |
Sec22b |
T |
A |
3: 97,828,561 (GRCm39) |
V208E |
possibly damaging |
Het |
Slc8a3 |
A |
T |
12: 81,361,868 (GRCm39) |
I317N |
probably damaging |
Het |
Snx33 |
A |
G |
9: 56,834,043 (GRCm39) |
Y9H |
probably damaging |
Het |
Stard9 |
C |
A |
2: 120,529,473 (GRCm39) |
T1910N |
probably damaging |
Het |
Tas2r122 |
T |
A |
6: 132,688,753 (GRCm39) |
I47F |
probably damaging |
Het |
Tedc1 |
T |
G |
12: 113,120,921 (GRCm39) |
L118V |
possibly damaging |
Het |
Tln2 |
A |
T |
9: 67,163,278 (GRCm39) |
S1090T |
probably benign |
Het |
Tpcn2 |
T |
C |
7: 144,812,311 (GRCm39) |
D511G |
probably benign |
Het |
Usp21 |
T |
C |
1: 171,110,669 (GRCm39) |
|
probably benign |
Het |
Vmn2r17 |
T |
A |
5: 109,600,946 (GRCm39) |
L748Q |
probably damaging |
Het |
Zp2 |
T |
C |
7: 119,734,564 (GRCm39) |
D495G |
possibly damaging |
Het |
|
Other mutations in 1700013G24Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01547:1700013G24Rik
|
APN |
4 |
137,182,573 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0526:1700013G24Rik
|
UTSW |
4 |
137,182,535 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1449:1700013G24Rik
|
UTSW |
4 |
137,182,666 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3743:1700013G24Rik
|
UTSW |
4 |
137,182,348 (GRCm39) |
missense |
probably damaging |
0.96 |
R5357:1700013G24Rik
|
UTSW |
4 |
137,182,463 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6265:1700013G24Rik
|
UTSW |
4 |
137,181,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R6586:1700013G24Rik
|
UTSW |
4 |
137,182,639 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6720:1700013G24Rik
|
UTSW |
4 |
137,181,997 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6988:1700013G24Rik
|
UTSW |
4 |
137,181,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R7640:1700013G24Rik
|
UTSW |
4 |
137,181,905 (GRCm39) |
missense |
probably damaging |
0.99 |
R7825:1700013G24Rik
|
UTSW |
4 |
137,182,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:1700013G24Rik
|
UTSW |
4 |
137,182,553 (GRCm39) |
missense |
probably benign |
|
R9536:1700013G24Rik
|
UTSW |
4 |
137,182,623 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:1700013G24Rik
|
UTSW |
4 |
137,182,303 (GRCm39) |
missense |
probably damaging |
1.00 |
|