Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd6 |
T |
C |
14: 8,049,808 (GRCm38) |
L246S |
possibly damaging |
Het |
Ahcyl |
A |
G |
16: 45,975,035 (GRCm39) |
I114T |
probably benign |
Het |
Arhgap22 |
C |
A |
14: 33,020,727 (GRCm39) |
H107N |
probably damaging |
Het |
Atp6v0a2 |
G |
A |
5: 124,790,257 (GRCm39) |
G480D |
probably damaging |
Het |
Baz2b |
T |
C |
2: 59,731,847 (GRCm39) |
T2064A |
possibly damaging |
Het |
Bop1 |
T |
A |
15: 76,338,688 (GRCm39) |
N449I |
probably benign |
Het |
C8g |
C |
T |
2: 25,388,916 (GRCm39) |
|
probably null |
Het |
Camp |
T |
G |
9: 109,677,504 (GRCm39) |
T110P |
|
Het |
Ccdc141 |
T |
C |
2: 76,885,073 (GRCm39) |
T523A |
possibly damaging |
Het |
Ccdc157 |
A |
T |
11: 4,094,598 (GRCm39) |
I578N |
probably damaging |
Het |
Ccdc187 |
C |
T |
2: 26,143,445 (GRCm39) |
A1298T |
possibly damaging |
Het |
Cdc20 |
C |
T |
4: 118,290,716 (GRCm39) |
W428* |
probably null |
Het |
Chd9 |
A |
T |
8: 91,732,360 (GRCm39) |
R1293* |
probably null |
Het |
Clca3a1 |
C |
T |
3: 144,453,310 (GRCm39) |
G505S |
probably benign |
Het |
Clptm1 |
C |
A |
7: 19,369,763 (GRCm39) |
W382C |
probably damaging |
Het |
Cnot1 |
A |
T |
8: 96,482,835 (GRCm39) |
N739K |
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,508,217 (GRCm39) |
I1243T |
probably damaging |
Het |
Col12a1 |
T |
G |
9: 79,525,034 (GRCm39) |
D2709A |
probably damaging |
Het |
Cpm |
T |
C |
10: 117,511,999 (GRCm39) |
|
probably null |
Het |
Ctsd |
C |
A |
7: 141,936,373 (GRCm39) |
G143C |
probably damaging |
Het |
Cux2 |
A |
G |
5: 122,025,461 (GRCm39) |
V69A |
possibly damaging |
Het |
Cyp2c66 |
A |
T |
19: 39,175,054 (GRCm39) |
I485L |
probably benign |
Het |
Cyp4a29 |
T |
C |
4: 115,105,772 (GRCm39) |
V158A |
probably damaging |
Het |
Dbx1 |
A |
T |
7: 49,282,403 (GRCm39) |
D267E |
probably damaging |
Het |
Dop1b |
A |
G |
16: 93,544,531 (GRCm39) |
Y224C |
possibly damaging |
Het |
Dsg3 |
T |
A |
18: 20,666,578 (GRCm39) |
C596S |
probably damaging |
Het |
Fcgbpl1 |
G |
A |
7: 27,853,805 (GRCm39) |
V1590I |
possibly damaging |
Het |
Gabra1 |
A |
T |
11: 42,026,401 (GRCm39) |
I297N |
probably damaging |
Het |
Grid1 |
A |
G |
14: 35,167,814 (GRCm39) |
E446G |
probably damaging |
Het |
H2bc12 |
T |
C |
13: 22,220,393 (GRCm39) |
S113P |
probably benign |
Het |
Hmmr |
A |
T |
11: 40,598,210 (GRCm39) |
Y667* |
probably null |
Het |
Katnip |
A |
G |
7: 125,442,092 (GRCm39) |
Q693R |
probably benign |
Het |
Klhl25 |
A |
G |
7: 75,515,757 (GRCm39) |
D221G |
probably damaging |
Het |
Krtcap2 |
T |
C |
3: 89,156,449 (GRCm39) |
|
probably null |
Het |
Lipi |
T |
A |
16: 75,352,706 (GRCm39) |
N377I |
possibly damaging |
Het |
Lrp2 |
C |
A |
2: 69,289,928 (GRCm39) |
C3637F |
probably damaging |
Het |
Mrgprh |
T |
C |
17: 13,096,264 (GRCm39) |
F168S |
possibly damaging |
Het |
Naip6 |
T |
C |
13: 100,436,961 (GRCm39) |
T521A |
probably benign |
Het |
Nkpd1 |
A |
T |
7: 19,257,462 (GRCm39) |
I414F |
probably damaging |
Het |
Or4c99 |
T |
A |
2: 88,330,314 (GRCm39) |
M295K |
probably damaging |
Het |
Or52z13 |
A |
T |
7: 103,246,598 (GRCm39) |
D25V |
probably benign |
Het |
Pcdhb21 |
A |
T |
18: 37,648,385 (GRCm39) |
I505F |
probably damaging |
Het |
Plxna1 |
C |
T |
6: 89,308,253 (GRCm39) |
R1278Q |
probably damaging |
Het |
Pofut2 |
T |
C |
10: 77,095,220 (GRCm39) |
S22P |
possibly damaging |
Het |
Prrc2b |
C |
A |
2: 32,090,953 (GRCm39) |
R442S |
probably damaging |
Het |
Sema3e |
T |
A |
5: 14,302,397 (GRCm39) |
F641I |
possibly damaging |
Het |
Sfswap |
G |
A |
5: 129,618,463 (GRCm39) |
V466I |
possibly damaging |
Het |
Slc22a21 |
A |
T |
11: 53,850,051 (GRCm39) |
V268E |
possibly damaging |
Het |
Slc6a17 |
T |
C |
3: 107,380,930 (GRCm39) |
D525G |
possibly damaging |
Het |
Spata21 |
C |
T |
4: 140,822,467 (GRCm39) |
T91I |
possibly damaging |
Het |
Spryd7 |
T |
G |
14: 61,783,228 (GRCm39) |
H98P |
probably benign |
Het |
Sptb |
G |
T |
12: 76,667,763 (GRCm39) |
T778K |
probably damaging |
Het |
Syne1 |
C |
T |
10: 5,209,270 (GRCm39) |
R3411Q |
probably benign |
Het |
Trank1 |
A |
G |
9: 111,202,193 (GRCm39) |
I1607V |
probably benign |
Het |
Ttll1 |
T |
C |
15: 83,380,516 (GRCm39) |
D283G |
probably benign |
Het |
Ufl1 |
G |
A |
4: 25,275,807 (GRCm39) |
R199W |
probably benign |
Het |
Vmn1r159 |
A |
G |
7: 22,542,616 (GRCm39) |
S139P |
probably damaging |
Het |
Vmn2r97 |
A |
G |
17: 19,134,770 (GRCm39) |
I63V |
probably benign |
Het |
Vps13a |
T |
C |
19: 16,623,337 (GRCm39) |
S2775G |
possibly damaging |
Het |
Zfp992 |
C |
T |
4: 146,551,976 (GRCm39) |
H566Y |
probably damaging |
Het |
|
Other mutations in Fgd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01397:Fgd2
|
APN |
17 |
29,586,949 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01505:Fgd2
|
APN |
17 |
29,585,971 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03240:Fgd2
|
APN |
17 |
29,580,135 (GRCm39) |
splice site |
probably benign |
|
ceci
|
UTSW |
17 |
29,587,350 (GRCm39) |
splice site |
probably null |
|
R0046:Fgd2
|
UTSW |
17 |
29,593,964 (GRCm39) |
splice site |
probably benign |
|
R0271:Fgd2
|
UTSW |
17 |
29,585,982 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0594:Fgd2
|
UTSW |
17 |
29,584,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R0612:Fgd2
|
UTSW |
17 |
29,597,321 (GRCm39) |
missense |
probably benign |
0.45 |
R1470:Fgd2
|
UTSW |
17 |
29,593,082 (GRCm39) |
splice site |
probably benign |
|
R1551:Fgd2
|
UTSW |
17 |
29,597,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R1596:Fgd2
|
UTSW |
17 |
29,595,904 (GRCm39) |
missense |
probably benign |
0.43 |
R1664:Fgd2
|
UTSW |
17 |
29,588,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R1689:Fgd2
|
UTSW |
17 |
29,582,696 (GRCm39) |
missense |
probably benign |
|
R1691:Fgd2
|
UTSW |
17 |
29,597,918 (GRCm39) |
nonsense |
probably null |
|
R1695:Fgd2
|
UTSW |
17 |
29,587,219 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2697:Fgd2
|
UTSW |
17 |
29,595,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R3500:Fgd2
|
UTSW |
17 |
29,584,575 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3689:Fgd2
|
UTSW |
17 |
29,597,924 (GRCm39) |
missense |
probably benign |
0.00 |
R4583:Fgd2
|
UTSW |
17 |
29,586,052 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4871:Fgd2
|
UTSW |
17 |
29,592,223 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5011:Fgd2
|
UTSW |
17 |
29,593,954 (GRCm39) |
critical splice donor site |
probably null |
|
R5209:Fgd2
|
UTSW |
17 |
29,587,350 (GRCm39) |
splice site |
probably null |
|
R7106:Fgd2
|
UTSW |
17 |
29,595,944 (GRCm39) |
nonsense |
probably null |
|
R7139:Fgd2
|
UTSW |
17 |
29,592,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R7712:Fgd2
|
UTSW |
17 |
29,595,886 (GRCm39) |
missense |
probably benign |
0.01 |
R7833:Fgd2
|
UTSW |
17 |
29,586,369 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7834:Fgd2
|
UTSW |
17 |
29,583,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R7913:Fgd2
|
UTSW |
17 |
29,593,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R8547:Fgd2
|
UTSW |
17 |
29,583,934 (GRCm39) |
missense |
probably damaging |
0.99 |
R8686:Fgd2
|
UTSW |
17 |
29,597,997 (GRCm39) |
missense |
probably benign |
|
R9088:Fgd2
|
UTSW |
17 |
29,583,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R9525:Fgd2
|
UTSW |
17 |
29,583,955 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fgd2
|
UTSW |
17 |
29,597,300 (GRCm39) |
missense |
probably benign |
0.05 |
|