Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
G |
7: 120,030,383 (GRCm39) |
D165G |
probably benign |
Het |
Abca8a |
A |
C |
11: 109,917,718 (GRCm39) |
F1574V |
probably damaging |
Het |
Adh6a |
A |
T |
3: 138,034,857 (GRCm39) |
I329L |
probably benign |
Het |
Agap2 |
T |
A |
10: 126,918,297 (GRCm39) |
|
probably benign |
Het |
Ager |
A |
T |
17: 34,818,124 (GRCm39) |
I185F |
probably damaging |
Het |
Agrn |
C |
T |
4: 156,263,675 (GRCm39) |
G173R |
probably damaging |
Het |
Arhgef16 |
T |
A |
4: 154,369,490 (GRCm39) |
H329L |
probably damaging |
Het |
Astn1 |
T |
C |
1: 158,329,669 (GRCm39) |
Y175H |
probably damaging |
Het |
Banp |
A |
G |
8: 122,702,662 (GRCm39) |
T70A |
probably benign |
Het |
Bcl11b |
T |
C |
12: 107,881,910 (GRCm39) |
T802A |
possibly damaging |
Het |
Ces2a |
A |
T |
8: 105,466,822 (GRCm39) |
I65F |
probably benign |
Het |
Cflar |
G |
A |
1: 58,780,206 (GRCm39) |
|
probably null |
Het |
Clec16a |
G |
A |
16: 10,462,650 (GRCm39) |
R656H |
probably damaging |
Het |
Cntn1 |
A |
G |
15: 92,192,863 (GRCm39) |
|
probably benign |
Het |
Coasy |
A |
G |
11: 100,976,708 (GRCm39) |
T493A |
probably benign |
Het |
Col16a1 |
C |
A |
4: 129,946,711 (GRCm39) |
H111Q |
probably benign |
Het |
Commd8 |
A |
G |
5: 72,322,765 (GRCm39) |
W51R |
probably damaging |
Het |
Cyp3a41b |
A |
T |
5: 145,514,976 (GRCm39) |
V83D |
probably benign |
Het |
D2hgdh |
C |
T |
1: 93,763,157 (GRCm39) |
A314V |
probably damaging |
Het |
Dcun1d4 |
T |
A |
5: 73,638,618 (GRCm39) |
|
probably benign |
Het |
Decr2 |
C |
A |
17: 26,302,858 (GRCm39) |
V173L |
probably benign |
Het |
Defb11 |
A |
G |
8: 22,395,444 (GRCm39) |
*78Q |
probably null |
Het |
Dock3 |
C |
A |
9: 106,818,525 (GRCm39) |
V1190F |
probably damaging |
Het |
Dusp1 |
A |
T |
17: 26,726,093 (GRCm39) |
I200N |
probably damaging |
Het |
Efna1 |
G |
A |
3: 89,183,646 (GRCm39) |
A60V |
possibly damaging |
Het |
Egfl8 |
C |
T |
17: 34,832,832 (GRCm39) |
V253M |
probably damaging |
Het |
Epb41 |
T |
A |
4: 131,691,458 (GRCm39) |
N623I |
probably benign |
Het |
Fbxw22 |
C |
T |
9: 109,213,062 (GRCm39) |
R295K |
probably benign |
Het |
Foxn4 |
T |
C |
5: 114,393,662 (GRCm39) |
T486A |
probably damaging |
Het |
Gbe1 |
C |
T |
16: 70,233,840 (GRCm39) |
A239V |
probably damaging |
Het |
Gpc6 |
A |
T |
14: 118,125,932 (GRCm39) |
|
probably null |
Het |
Hdhd2 |
C |
T |
18: 77,052,866 (GRCm39) |
T172M |
probably benign |
Het |
Heatr5a |
T |
C |
12: 51,940,528 (GRCm39) |
D1444G |
possibly damaging |
Het |
Hnrnpul1 |
A |
G |
7: 25,450,299 (GRCm39) |
Y138H |
probably damaging |
Het |
Itgal |
A |
G |
7: 126,905,873 (GRCm39) |
I352V |
possibly damaging |
Het |
Klhl31 |
A |
G |
9: 77,557,440 (GRCm39) |
D52G |
possibly damaging |
Het |
Klk1b21 |
T |
C |
7: 43,753,863 (GRCm39) |
I49T |
possibly damaging |
Het |
Lama2 |
T |
A |
10: 26,868,932 (GRCm39) |
I2838F |
probably damaging |
Het |
Lrrc43 |
A |
T |
5: 123,641,354 (GRCm39) |
T513S |
probably damaging |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Mamdc2 |
A |
T |
19: 23,281,267 (GRCm39) |
|
probably benign |
Het |
Mpdz |
A |
G |
4: 81,301,628 (GRCm39) |
S266P |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Mroh5 |
T |
C |
15: 73,664,997 (GRCm39) |
N258D |
probably benign |
Het |
Mrpl28 |
T |
C |
17: 26,345,285 (GRCm39) |
V235A |
probably benign |
Het |
Mtbp |
G |
A |
15: 55,432,556 (GRCm39) |
|
probably null |
Het |
Mtss2 |
A |
G |
8: 111,455,362 (GRCm39) |
K92E |
possibly damaging |
Het |
Muc4 |
C |
A |
16: 32,754,529 (GRCm38) |
H1468N |
probably benign |
Het |
Nav1 |
A |
T |
1: 135,399,974 (GRCm39) |
L532* |
probably null |
Het |
Or10ak16 |
A |
T |
4: 118,751,071 (GRCm39) |
R264W |
probably damaging |
Het |
Or1e23 |
A |
G |
11: 73,407,309 (GRCm39) |
S239P |
probably damaging |
Het |
Or51f1d |
G |
A |
7: 102,701,344 (GRCm39) |
V280I |
probably benign |
Het |
Pappa2 |
A |
G |
1: 158,684,841 (GRCm39) |
M766T |
probably damaging |
Het |
Pkhd1 |
C |
T |
1: 20,604,759 (GRCm39) |
|
probably null |
Het |
Plch2 |
T |
C |
4: 155,077,461 (GRCm39) |
E423G |
probably benign |
Het |
Prrc1 |
G |
T |
18: 57,514,718 (GRCm39) |
D312Y |
probably damaging |
Het |
Pxdn |
T |
A |
12: 30,055,774 (GRCm39) |
V1220E |
probably damaging |
Het |
Robo1 |
T |
A |
16: 72,775,660 (GRCm39) |
F728L |
probably benign |
Het |
Rtel1 |
G |
T |
2: 180,977,796 (GRCm39) |
Q292H |
probably benign |
Het |
Sh3bp4 |
G |
A |
1: 89,073,314 (GRCm39) |
V721I |
possibly damaging |
Het |
Slc2a10 |
T |
A |
2: 165,356,701 (GRCm39) |
C120* |
probably null |
Het |
Srd5a2 |
T |
C |
17: 74,331,485 (GRCm39) |
R171G |
probably damaging |
Het |
Srsf4 |
T |
C |
4: 131,624,993 (GRCm39) |
V130A |
probably damaging |
Het |
Styk1 |
T |
C |
6: 131,289,539 (GRCm39) |
E25G |
probably benign |
Het |
Taar8b |
T |
C |
10: 23,967,270 (GRCm39) |
N308S |
probably damaging |
Het |
Tbc1d14 |
A |
G |
5: 36,700,561 (GRCm39) |
L269P |
possibly damaging |
Het |
Tbx1 |
T |
C |
16: 18,400,744 (GRCm39) |
|
probably null |
Het |
Tmem233 |
G |
C |
5: 116,189,517 (GRCm39) |
|
probably benign |
Het |
Tmem252 |
T |
C |
19: 24,651,455 (GRCm39) |
I8T |
probably benign |
Het |
Vcp |
G |
A |
4: 42,980,833 (GRCm39) |
A759V |
possibly damaging |
Het |
Vmn2r107 |
T |
C |
17: 20,595,817 (GRCm39) |
I790T |
possibly damaging |
Het |
Vmn2r77 |
T |
C |
7: 86,460,897 (GRCm39) |
V741A |
probably benign |
Het |
Vps13c |
T |
C |
9: 67,828,229 (GRCm39) |
V1461A |
possibly damaging |
Het |
Ylpm1 |
T |
A |
12: 85,061,824 (GRCm39) |
V575E |
unknown |
Het |
Zbp1 |
T |
A |
2: 173,060,616 (GRCm39) |
|
probably benign |
Het |
Zfp280d |
C |
A |
9: 72,209,052 (GRCm39) |
|
probably benign |
Het |
Zkscan5 |
A |
G |
5: 145,142,277 (GRCm39) |
Y58C |
probably damaging |
Het |
|
Other mutations in Gpatch3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01590:Gpatch3
|
APN |
4 |
133,308,028 (GRCm39) |
unclassified |
probably benign |
|
IGL02876:Gpatch3
|
APN |
4 |
133,307,995 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03181:Gpatch3
|
APN |
4 |
133,305,433 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU23:Gpatch3
|
UTSW |
4 |
133,305,613 (GRCm39) |
small deletion |
probably benign |
|
PIT4585001:Gpatch3
|
UTSW |
4 |
133,310,397 (GRCm39) |
missense |
probably damaging |
0.99 |
R0358:Gpatch3
|
UTSW |
4 |
133,305,215 (GRCm39) |
splice site |
probably null |
|
R0383:Gpatch3
|
UTSW |
4 |
133,305,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1706:Gpatch3
|
UTSW |
4 |
133,302,484 (GRCm39) |
nonsense |
probably null |
|
R3788:Gpatch3
|
UTSW |
4 |
133,302,479 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4030:Gpatch3
|
UTSW |
4 |
133,305,458 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4334:Gpatch3
|
UTSW |
4 |
133,309,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R4718:Gpatch3
|
UTSW |
4 |
133,309,855 (GRCm39) |
missense |
probably benign |
0.37 |
R5036:Gpatch3
|
UTSW |
4 |
133,305,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:Gpatch3
|
UTSW |
4 |
133,305,617 (GRCm39) |
missense |
probably benign |
0.06 |
R6032:Gpatch3
|
UTSW |
4 |
133,305,617 (GRCm39) |
missense |
probably benign |
0.06 |
R6572:Gpatch3
|
UTSW |
4 |
133,302,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R6923:Gpatch3
|
UTSW |
4 |
133,309,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R7106:Gpatch3
|
UTSW |
4 |
133,305,514 (GRCm39) |
missense |
probably benign |
0.05 |
R7572:Gpatch3
|
UTSW |
4 |
133,302,117 (GRCm39) |
missense |
probably benign |
0.01 |
R7737:Gpatch3
|
UTSW |
4 |
133,302,407 (GRCm39) |
missense |
probably benign |
0.01 |
R7937:Gpatch3
|
UTSW |
4 |
133,310,308 (GRCm39) |
missense |
probably damaging |
0.98 |
R8300:Gpatch3
|
UTSW |
4 |
133,307,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R9541:Gpatch3
|
UTSW |
4 |
133,305,595 (GRCm39) |
missense |
probably benign |
0.01 |
RF025:Gpatch3
|
UTSW |
4 |
133,305,621 (GRCm39) |
frame shift |
probably null |
|
|