Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
A |
T |
4: 53,068,739 (GRCm39) |
L1333* |
probably null |
Het |
Adcy6 |
C |
A |
15: 98,497,795 (GRCm39) |
M452I |
probably damaging |
Het |
Adsl |
G |
A |
15: 80,844,676 (GRCm39) |
R173H |
probably benign |
Het |
Ank3 |
A |
G |
10: 69,718,200 (GRCm39) |
T484A |
probably damaging |
Het |
Apol10a |
A |
G |
15: 77,372,709 (GRCm39) |
D115G |
probably damaging |
Het |
Bard1 |
A |
G |
1: 71,092,828 (GRCm39) |
S529P |
probably damaging |
Het |
C2 |
A |
G |
17: 35,083,484 (GRCm39) |
|
probably benign |
Het |
Cftr |
T |
A |
6: 18,277,870 (GRCm39) |
I956N |
possibly damaging |
Het |
Cwc15 |
A |
G |
9: 14,414,977 (GRCm39) |
T110A |
probably benign |
Het |
Dsg4 |
A |
T |
18: 20,594,361 (GRCm39) |
I497F |
possibly damaging |
Het |
Gadd45b |
A |
G |
10: 80,766,967 (GRCm39) |
D69G |
possibly damaging |
Het |
Glb1l3 |
A |
T |
9: 26,742,564 (GRCm39) |
S307R |
possibly damaging |
Het |
Greb1l |
G |
A |
18: 10,532,961 (GRCm39) |
G843R |
probably damaging |
Het |
H2-M11 |
A |
T |
17: 36,858,829 (GRCm39) |
Y123F |
probably benign |
Het |
Hal |
G |
A |
10: 93,333,400 (GRCm39) |
A323T |
probably damaging |
Het |
Il4ra |
T |
C |
7: 125,166,396 (GRCm39) |
F47L |
probably benign |
Het |
Klra10 |
T |
A |
6: 130,256,367 (GRCm39) |
N96Y |
probably benign |
Het |
Maco1 |
T |
C |
4: 134,555,623 (GRCm39) |
I283M |
possibly damaging |
Het |
Mki67 |
T |
A |
7: 135,302,251 (GRCm39) |
M928L |
possibly damaging |
Het |
Myh15 |
T |
A |
16: 48,930,847 (GRCm39) |
V607D |
probably damaging |
Het |
Ndufaf2 |
A |
G |
13: 108,217,925 (GRCm39) |
W74R |
probably damaging |
Het |
Noc4l |
C |
A |
5: 110,801,081 (GRCm39) |
|
probably benign |
Het |
Or51b6b |
T |
A |
7: 103,309,573 (GRCm39) |
I295F |
probably damaging |
Het |
Papss1 |
T |
A |
3: 131,307,772 (GRCm39) |
W274R |
probably damaging |
Het |
Pax3 |
C |
T |
1: 78,171,962 (GRCm39) |
V83I |
probably damaging |
Het |
Prmt5 |
C |
T |
14: 54,747,322 (GRCm39) |
R485H |
probably damaging |
Het |
Ptprq |
A |
G |
10: 107,418,220 (GRCm39) |
Y1719H |
probably damaging |
Het |
Ranbp2 |
A |
T |
10: 58,315,900 (GRCm39) |
I2207F |
possibly damaging |
Het |
Rock2 |
T |
A |
12: 17,021,042 (GRCm39) |
|
probably benign |
Het |
Sema3c |
G |
A |
5: 17,867,961 (GRCm39) |
R124H |
probably damaging |
Het |
Serpina1e |
G |
A |
12: 103,917,393 (GRCm39) |
T92M |
probably benign |
Het |
Sgip1 |
T |
C |
4: 102,768,667 (GRCm39) |
L83P |
probably benign |
Het |
Tm9sf2 |
C |
T |
14: 122,361,162 (GRCm39) |
S68L |
probably damaging |
Het |
Tmem178 |
A |
G |
17: 81,297,235 (GRCm39) |
T206A |
probably damaging |
Het |
Tmem207 |
A |
T |
16: 26,336,617 (GRCm39) |
Y46N |
possibly damaging |
Het |
Tyk2 |
A |
G |
9: 21,031,703 (GRCm39) |
L429P |
probably damaging |
Het |
|
Other mutations in 1700019A02Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01728:1700019A02Rik
|
APN |
1 |
53,221,668 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02727:1700019A02Rik
|
APN |
1 |
53,226,724 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02970:1700019A02Rik
|
APN |
1 |
53,226,748 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03402:1700019A02Rik
|
APN |
1 |
53,216,972 (GRCm39) |
missense |
probably benign |
0.00 |
R1557:1700019A02Rik
|
UTSW |
1 |
53,221,025 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1955:1700019A02Rik
|
UTSW |
1 |
53,202,400 (GRCm39) |
missense |
probably benign |
0.09 |
R4030:1700019A02Rik
|
UTSW |
1 |
53,221,668 (GRCm39) |
missense |
probably benign |
0.03 |
R4060:1700019A02Rik
|
UTSW |
1 |
53,197,928 (GRCm39) |
missense |
probably damaging |
0.97 |
R4061:1700019A02Rik
|
UTSW |
1 |
53,197,928 (GRCm39) |
missense |
probably damaging |
0.97 |
R4062:1700019A02Rik
|
UTSW |
1 |
53,197,928 (GRCm39) |
missense |
probably damaging |
0.97 |
R4327:1700019A02Rik
|
UTSW |
1 |
53,221,664 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6018:1700019A02Rik
|
UTSW |
1 |
53,202,405 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7490:1700019A02Rik
|
UTSW |
1 |
53,202,389 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7715:1700019A02Rik
|
UTSW |
1 |
53,221,659 (GRCm39) |
missense |
probably benign |
|
R9487:1700019A02Rik
|
UTSW |
1 |
53,221,665 (GRCm39) |
missense |
possibly damaging |
0.90 |
|