Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad9 |
T |
C |
3: 36,120,337 (GRCm39) |
F27S |
probably benign |
Het |
AK157302 |
T |
A |
13: 21,679,715 (GRCm39) |
D80E |
probably damaging |
Het |
Amz2 |
T |
C |
11: 109,324,881 (GRCm39) |
|
probably null |
Het |
Ankrd34c |
T |
A |
9: 89,611,817 (GRCm39) |
K175* |
probably null |
Het |
Arid1b |
C |
A |
17: 5,090,938 (GRCm39) |
S546R |
probably damaging |
Het |
Atf6b |
T |
A |
17: 34,871,648 (GRCm39) |
M428K |
probably benign |
Het |
Brpf3 |
G |
A |
17: 29,042,949 (GRCm39) |
V997M |
probably benign |
Het |
Cckar |
A |
G |
5: 53,863,839 (GRCm39) |
S41P |
probably benign |
Het |
Cd96 |
T |
A |
16: 45,892,112 (GRCm39) |
Q292L |
probably damaging |
Het |
Cdh18 |
C |
A |
15: 22,714,637 (GRCm39) |
|
probably benign |
Het |
Cfb |
T |
G |
17: 35,080,114 (GRCm39) |
D122A |
possibly damaging |
Het |
Copa |
G |
T |
1: 171,919,964 (GRCm39) |
|
probably benign |
Het |
Ctnna2 |
T |
A |
6: 76,859,728 (GRCm39) |
K854N |
probably damaging |
Het |
Cwh43 |
G |
A |
5: 73,569,275 (GRCm39) |
V106M |
probably benign |
Het |
Dact2 |
C |
T |
17: 14,416,833 (GRCm39) |
E456K |
probably benign |
Het |
Dnah8 |
T |
C |
17: 30,967,533 (GRCm39) |
S2582P |
probably benign |
Het |
Eef2 |
A |
G |
10: 81,015,414 (GRCm39) |
T312A |
probably benign |
Het |
Enpep |
T |
A |
3: 129,063,966 (GRCm39) |
R934* |
probably null |
Het |
Fam240b |
A |
T |
13: 64,629,627 (GRCm39) |
M63K |
possibly damaging |
Het |
Fhdc1 |
C |
A |
3: 84,352,133 (GRCm39) |
V1031F |
probably benign |
Het |
Gm6124 |
A |
T |
7: 38,872,195 (GRCm39) |
|
noncoding transcript |
Het |
Gsn |
G |
A |
2: 35,180,432 (GRCm39) |
V147I |
probably benign |
Het |
Gucy1a1 |
A |
T |
3: 82,002,066 (GRCm39) |
F671Y |
possibly damaging |
Het |
Hectd3 |
A |
G |
4: 116,852,889 (GRCm39) |
E97G |
probably damaging |
Het |
Kcnv1 |
G |
A |
15: 44,977,840 (GRCm39) |
T66M |
probably damaging |
Het |
Krba1 |
C |
T |
6: 48,392,599 (GRCm39) |
P802S |
possibly damaging |
Het |
Lca5l |
C |
T |
16: 95,979,974 (GRCm39) |
S52N |
probably damaging |
Het |
Lmf1 |
T |
C |
17: 25,873,455 (GRCm39) |
L320P |
probably damaging |
Het |
Map3k4 |
G |
T |
17: 12,474,147 (GRCm39) |
Q845K |
probably benign |
Het |
Mapkapk3 |
T |
C |
9: 107,136,131 (GRCm39) |
|
probably benign |
Het |
Mccc1 |
A |
G |
3: 36,044,217 (GRCm39) |
V203A |
probably damaging |
Het |
Mcm9 |
C |
A |
10: 53,423,668 (GRCm39) |
M677I |
probably benign |
Het |
Mkrn2 |
A |
G |
6: 115,594,395 (GRCm39) |
T369A |
possibly damaging |
Het |
Mthfr |
C |
A |
4: 148,139,949 (GRCm39) |
N623K |
probably damaging |
Het |
Myh2 |
T |
C |
11: 67,071,985 (GRCm39) |
V571A |
probably benign |
Het |
Nom1 |
G |
A |
5: 29,651,370 (GRCm39) |
|
probably null |
Het |
Nucb1 |
T |
A |
7: 45,144,704 (GRCm39) |
D283V |
probably damaging |
Het |
Or12e8 |
G |
A |
2: 87,188,419 (GRCm39) |
M210I |
probably benign |
Het |
Or14c46 |
A |
T |
7: 85,918,968 (GRCm39) |
F10I |
probably damaging |
Het |
Or2v2 |
T |
A |
11: 49,004,254 (GRCm39) |
I100L |
probably benign |
Het |
Pcdhb1 |
A |
C |
18: 37,398,470 (GRCm39) |
L140F |
probably damaging |
Het |
Ptgs2 |
G |
A |
1: 149,976,002 (GRCm39) |
A10T |
probably benign |
Het |
Rfx3 |
C |
T |
19: 27,777,632 (GRCm39) |
R497Q |
probably damaging |
Het |
Rps6kb1 |
A |
T |
11: 86,410,702 (GRCm39) |
|
probably benign |
Het |
Slc22a21 |
T |
C |
11: 53,860,329 (GRCm39) |
D34G |
probably damaging |
Het |
Spata13 |
T |
A |
14: 60,947,004 (GRCm39) |
M684K |
probably damaging |
Het |
Tet3 |
T |
C |
6: 83,350,181 (GRCm39) |
T961A |
probably damaging |
Het |
Ttc27 |
T |
C |
17: 75,163,474 (GRCm39) |
L694P |
probably damaging |
Het |
Vmn1r238 |
G |
A |
18: 3,123,214 (GRCm39) |
Q67* |
probably null |
Het |
Vmn2r101 |
A |
T |
17: 19,832,303 (GRCm39) |
R766S |
probably damaging |
Het |
Vwf |
A |
T |
6: 125,619,285 (GRCm39) |
Y1321F |
probably damaging |
Het |
Wfdc1 |
C |
A |
8: 120,406,194 (GRCm39) |
P103Q |
probably damaging |
Het |
Zfp488 |
C |
A |
14: 33,692,851 (GRCm39) |
C104F |
possibly damaging |
Het |
|
Other mutations in Angel1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01678:Angel1
|
APN |
12 |
86,763,800 (GRCm39) |
missense |
probably benign |
|
IGL02712:Angel1
|
APN |
12 |
86,769,613 (GRCm39) |
splice site |
probably benign |
|
IGL02738:Angel1
|
APN |
12 |
86,752,060 (GRCm39) |
missense |
probably benign |
0.10 |
R0521:Angel1
|
UTSW |
12 |
86,769,681 (GRCm39) |
missense |
probably benign |
0.01 |
R0626:Angel1
|
UTSW |
12 |
86,764,487 (GRCm39) |
critical splice donor site |
probably null |
|
R1929:Angel1
|
UTSW |
12 |
86,749,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R4292:Angel1
|
UTSW |
12 |
86,767,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R4295:Angel1
|
UTSW |
12 |
86,767,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R4450:Angel1
|
UTSW |
12 |
86,768,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R4726:Angel1
|
UTSW |
12 |
86,768,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R7097:Angel1
|
UTSW |
12 |
86,773,158 (GRCm39) |
missense |
probably damaging |
0.98 |
R7284:Angel1
|
UTSW |
12 |
86,767,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R7616:Angel1
|
UTSW |
12 |
86,764,510 (GRCm39) |
missense |
probably benign |
0.00 |
R7984:Angel1
|
UTSW |
12 |
86,767,068 (GRCm39) |
missense |
probably benign |
0.33 |
R9010:Angel1
|
UTSW |
12 |
86,770,153 (GRCm39) |
missense |
possibly damaging |
0.78 |
|