Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr5 |
A |
C |
2: 158,474,321 (GRCm39) |
I375L |
probably benign |
Het |
Adgrl2 |
G |
T |
3: 148,544,761 (GRCm39) |
T778K |
possibly damaging |
Het |
Ccn3 |
A |
T |
15: 54,615,687 (GRCm39) |
Y284F |
probably damaging |
Het |
Cdc73 |
A |
T |
1: 143,485,234 (GRCm39) |
L478H |
probably damaging |
Het |
Cdh20 |
C |
A |
1: 110,027,843 (GRCm39) |
H529Q |
probably benign |
Het |
Cep55 |
T |
C |
19: 38,059,592 (GRCm39) |
|
probably null |
Het |
Chd9 |
G |
A |
8: 91,683,198 (GRCm39) |
R546Q |
unknown |
Het |
Ddit4 |
A |
T |
10: 59,786,515 (GRCm39) |
L178Q |
probably damaging |
Het |
Dgke |
A |
T |
11: 88,941,237 (GRCm39) |
N315K |
possibly damaging |
Het |
Dsg1a |
A |
G |
18: 20,473,549 (GRCm39) |
D874G |
probably damaging |
Het |
Dsp |
T |
A |
13: 38,352,673 (GRCm39) |
Y184N |
probably damaging |
Het |
Dynlt1c |
A |
G |
17: 6,870,916 (GRCm39) |
I20V |
probably benign |
Het |
Epx |
A |
T |
11: 87,763,470 (GRCm39) |
M250K |
probably benign |
Het |
Fan1 |
T |
C |
7: 64,022,761 (GRCm39) |
Y164C |
probably benign |
Het |
Fer1l6 |
A |
T |
15: 58,502,594 (GRCm39) |
Y1365F |
probably damaging |
Het |
Fndc8 |
A |
G |
11: 82,789,522 (GRCm39) |
T227A |
probably benign |
Het |
Gbp7 |
T |
C |
3: 142,243,798 (GRCm39) |
I115T |
probably damaging |
Het |
Gm5145 |
A |
G |
17: 20,791,270 (GRCm39) |
E216G |
probably benign |
Het |
Gm94 |
A |
T |
18: 43,914,326 (GRCm39) |
F77L |
possibly damaging |
Het |
Grik3 |
C |
A |
4: 125,526,185 (GRCm39) |
H139Q |
probably benign |
Het |
Gucy2e |
T |
C |
11: 69,115,827 (GRCm39) |
T852A |
probably damaging |
Het |
Hif1a |
T |
C |
12: 73,983,010 (GRCm39) |
S274P |
probably damaging |
Het |
Hmcn1 |
T |
A |
1: 150,692,870 (GRCm39) |
I268L |
probably benign |
Het |
Klk15 |
C |
T |
7: 43,587,790 (GRCm39) |
H73Y |
possibly damaging |
Het |
Lin52 |
T |
A |
12: 84,592,681 (GRCm39) |
S87T |
|
Het |
Lrrc74b |
A |
G |
16: 17,367,640 (GRCm39) |
|
probably null |
Het |
Mapk10 |
T |
C |
5: 103,144,499 (GRCm39) |
K136R |
probably damaging |
Het |
Nlrp2 |
A |
T |
7: 5,325,457 (GRCm39) |
N738K |
probably null |
Het |
Nlrp5 |
A |
T |
7: 23,129,573 (GRCm39) |
Q880L |
possibly damaging |
Het |
Or2y11 |
T |
A |
11: 49,442,808 (GRCm39) |
V78E |
probably damaging |
Het |
Or5d39 |
A |
T |
2: 87,979,718 (GRCm39) |
I215N |
possibly damaging |
Het |
Or6c215 |
G |
T |
10: 129,637,926 (GRCm39) |
P156Q |
probably damaging |
Het |
P4htm |
G |
A |
9: 108,474,627 (GRCm39) |
P46L |
probably benign |
Het |
Pcsk4 |
A |
T |
10: 80,164,858 (GRCm39) |
H69Q |
probably damaging |
Het |
Pdzd2 |
A |
G |
15: 12,374,385 (GRCm39) |
S1917P |
probably benign |
Het |
Pnpla5 |
A |
G |
15: 83,998,087 (GRCm39) |
V385A |
possibly damaging |
Het |
Prorp |
T |
C |
12: 55,426,192 (GRCm39) |
F514S |
probably damaging |
Het |
Rims2 |
C |
T |
15: 39,339,873 (GRCm39) |
R856C |
probably damaging |
Het |
Rprd2 |
A |
G |
3: 95,691,622 (GRCm39) |
Y218H |
probably benign |
Het |
Sat2 |
T |
A |
11: 69,513,069 (GRCm39) |
|
probably benign |
Het |
Sf1 |
C |
T |
19: 6,426,336 (GRCm39) |
R186C |
|
Het |
Snrnp200 |
A |
G |
2: 127,053,466 (GRCm39) |
|
probably benign |
Het |
Sqor |
A |
T |
2: 122,629,514 (GRCm39) |
D124V |
probably benign |
Het |
Ssh2 |
A |
G |
11: 77,312,062 (GRCm39) |
H191R |
possibly damaging |
Het |
Stac |
C |
A |
9: 111,519,320 (GRCm39) |
|
probably benign |
Het |
Svs4 |
T |
C |
2: 164,119,058 (GRCm39) |
M93V |
unknown |
Het |
Tbc1d32 |
A |
T |
10: 56,037,241 (GRCm39) |
S668T |
possibly damaging |
Het |
Tex10 |
A |
G |
4: 48,452,056 (GRCm39) |
F690S |
probably damaging |
Het |
Tex30 |
A |
G |
1: 44,130,356 (GRCm39) |
M88T |
|
Het |
Tgfbrap1 |
T |
C |
1: 43,095,837 (GRCm39) |
T534A |
probably benign |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tnrc18 |
T |
C |
5: 142,711,818 (GRCm39) |
E2647G |
probably damaging |
Het |
Trim43a |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
9: 88,465,042 (GRCm39) |
|
probably benign |
Het |
Tubb3 |
A |
T |
8: 124,145,696 (GRCm39) |
R62W |
probably damaging |
Het |
Vmn2r108 |
A |
G |
17: 20,690,312 (GRCm39) |
S507P |
probably benign |
Het |
Vmn2r116 |
A |
G |
17: 23,603,864 (GRCm39) |
K30E |
possibly damaging |
Het |
Vmn2r14 |
G |
A |
5: 109,368,054 (GRCm39) |
H313Y |
probably damaging |
Het |
Wdr37 |
C |
T |
13: 8,885,424 (GRCm39) |
V340M |
probably damaging |
Het |
Zfp799 |
A |
G |
17: 33,039,565 (GRCm39) |
F234L |
possibly damaging |
Het |
|
Other mutations in Ephx4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00885:Ephx4
|
APN |
5 |
107,553,991 (GRCm39) |
splice site |
probably benign |
|
IGL01382:Ephx4
|
APN |
5 |
107,577,585 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01916:Ephx4
|
APN |
5 |
107,553,896 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03301:Ephx4
|
APN |
5 |
107,574,730 (GRCm39) |
missense |
probably benign |
|
G5030:Ephx4
|
UTSW |
5 |
107,577,693 (GRCm39) |
missense |
probably damaging |
0.99 |
R0055:Ephx4
|
UTSW |
5 |
107,560,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Ephx4
|
UTSW |
5 |
107,560,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R0408:Ephx4
|
UTSW |
5 |
107,561,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R0413:Ephx4
|
UTSW |
5 |
107,551,601 (GRCm39) |
missense |
probably benign |
0.00 |
R0471:Ephx4
|
UTSW |
5 |
107,561,379 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1570:Ephx4
|
UTSW |
5 |
107,567,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R3700:Ephx4
|
UTSW |
5 |
107,550,673 (GRCm39) |
missense |
probably benign |
0.00 |
R4366:Ephx4
|
UTSW |
5 |
107,551,679 (GRCm39) |
unclassified |
probably benign |
|
R5895:Ephx4
|
UTSW |
5 |
107,577,518 (GRCm39) |
splice site |
probably null |
|
R5933:Ephx4
|
UTSW |
5 |
107,551,631 (GRCm39) |
splice site |
probably null |
|
R6326:Ephx4
|
UTSW |
5 |
107,553,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R6505:Ephx4
|
UTSW |
5 |
107,551,522 (GRCm39) |
nonsense |
probably null |
|
R6606:Ephx4
|
UTSW |
5 |
107,560,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R6848:Ephx4
|
UTSW |
5 |
107,574,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R6901:Ephx4
|
UTSW |
5 |
107,561,427 (GRCm39) |
missense |
probably benign |
0.29 |
R7017:Ephx4
|
UTSW |
5 |
107,553,980 (GRCm39) |
missense |
probably damaging |
0.98 |
R7484:Ephx4
|
UTSW |
5 |
107,577,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R7999:Ephx4
|
UTSW |
5 |
107,567,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R8371:Ephx4
|
UTSW |
5 |
107,561,384 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9712:Ephx4
|
UTSW |
5 |
107,567,647 (GRCm39) |
missense |
probably benign |
0.12 |
X0019:Ephx4
|
UTSW |
5 |
107,567,726 (GRCm39) |
missense |
possibly damaging |
0.88 |
|