Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp6ap1 |
A |
G |
X: 73,340,924 (GRCm39) |
D47G |
probably benign |
Het |
Atr |
T |
C |
9: 95,747,314 (GRCm39) |
F199L |
probably benign |
Het |
Bivm |
C |
A |
1: 44,182,120 (GRCm39) |
H443N |
probably benign |
Het |
Btnl2 |
A |
T |
17: 34,580,043 (GRCm39) |
H192L |
probably benign |
Het |
Ccdc178 |
A |
T |
18: 22,253,775 (GRCm39) |
C155S |
probably benign |
Het |
Celsr1 |
C |
A |
15: 85,785,673 (GRCm39) |
V2934L |
probably benign |
Het |
Celsr3 |
T |
C |
9: 108,726,652 (GRCm39) |
S3294P |
probably damaging |
Het |
Ddx10 |
T |
A |
9: 53,115,579 (GRCm39) |
E585V |
possibly damaging |
Het |
Elapor2 |
T |
C |
5: 9,511,478 (GRCm39) |
Y947H |
probably damaging |
Het |
Eps15l1 |
A |
T |
8: 73,138,606 (GRCm39) |
|
probably benign |
Het |
Erlin1 |
G |
T |
19: 44,051,491 (GRCm39) |
T70K |
probably damaging |
Het |
Ext2 |
A |
T |
2: 93,534,964 (GRCm39) |
|
probably null |
Het |
Fam124a |
G |
A |
14: 62,793,368 (GRCm39) |
|
probably null |
Het |
Fam53a |
T |
C |
5: 33,765,103 (GRCm39) |
D201G |
probably damaging |
Het |
Fgf14 |
C |
T |
14: 124,369,891 (GRCm39) |
G136D |
possibly damaging |
Het |
Gdi2 |
A |
T |
13: 3,614,623 (GRCm39) |
T323S |
probably benign |
Het |
Gemin5 |
A |
T |
11: 58,047,556 (GRCm39) |
N339K |
probably damaging |
Het |
Golga4 |
A |
G |
9: 118,364,522 (GRCm39) |
E286G |
probably benign |
Het |
Golga4 |
A |
C |
9: 118,363,700 (GRCm39) |
K233T |
probably damaging |
Het |
Gosr1 |
A |
G |
11: 76,641,732 (GRCm39) |
|
probably benign |
Het |
Haus8 |
A |
G |
8: 71,708,361 (GRCm39) |
|
probably benign |
Het |
Itgb3bp |
T |
C |
4: 99,690,373 (GRCm39) |
T49A |
probably null |
Het |
Lpo |
A |
G |
11: 87,706,004 (GRCm39) |
M273T |
possibly damaging |
Het |
Map3k4 |
T |
A |
17: 12,491,036 (GRCm39) |
S132C |
probably damaging |
Het |
Mycbp2 |
T |
G |
14: 103,414,715 (GRCm39) |
T2566P |
probably benign |
Het |
Nalcn |
T |
C |
14: 123,536,284 (GRCm39) |
E1255G |
probably null |
Het |
Nop56 |
A |
T |
2: 130,120,117 (GRCm39) |
K157N |
probably damaging |
Het |
Or10g9 |
C |
T |
9: 39,912,194 (GRCm39) |
E110K |
probably benign |
Het |
Or6c1 |
A |
T |
10: 129,517,857 (GRCm39) |
Y250* |
probably null |
Het |
Pcdh15 |
A |
G |
10: 74,340,648 (GRCm39) |
|
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,172,074 (GRCm39) |
H557R |
probably damaging |
Het |
Plekha4 |
C |
T |
7: 45,181,787 (GRCm39) |
Q64* |
probably null |
Het |
Ppp2r3c |
G |
A |
12: 55,345,192 (GRCm39) |
|
probably benign |
Het |
Rgmb |
C |
T |
17: 16,027,755 (GRCm39) |
M321I |
probably benign |
Het |
Rnf31 |
T |
C |
14: 55,833,131 (GRCm39) |
S363P |
probably benign |
Het |
Sap18b |
T |
A |
8: 96,552,329 (GRCm39) |
M113K |
probably benign |
Het |
Scara3 |
T |
A |
14: 66,169,105 (GRCm39) |
M171L |
probably benign |
Het |
Slc9a2 |
T |
G |
1: 40,781,863 (GRCm39) |
M364R |
probably damaging |
Het |
Sorcs1 |
C |
T |
19: 50,666,368 (GRCm39) |
W180* |
probably null |
Het |
Stat6 |
T |
A |
10: 127,482,809 (GRCm39) |
M10K |
probably benign |
Het |
Sun1 |
T |
C |
5: 139,221,243 (GRCm39) |
|
probably benign |
Het |
Tead2 |
T |
C |
7: 44,869,858 (GRCm39) |
|
probably benign |
Het |
Tjp1 |
T |
G |
7: 64,964,638 (GRCm39) |
E844D |
probably damaging |
Het |
Tmtc2 |
A |
G |
10: 105,206,411 (GRCm39) |
S295P |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,612,756 (GRCm39) |
R17108C |
probably damaging |
Het |
Ubr1 |
T |
C |
2: 120,711,664 (GRCm39) |
|
probably null |
Het |
Vmn2r108 |
T |
A |
17: 20,691,545 (GRCm39) |
H326L |
probably benign |
Het |
Xdh |
A |
G |
17: 74,250,840 (GRCm39) |
|
probably null |
Het |
Zfp385b |
A |
G |
2: 77,242,403 (GRCm39) |
S439P |
probably benign |
Het |
Zfp597 |
G |
A |
16: 3,683,805 (GRCm39) |
S317L |
probably benign |
Het |
Zfp638 |
A |
G |
6: 83,946,214 (GRCm39) |
D1081G |
probably damaging |
Het |
Zfp93 |
C |
T |
7: 23,974,509 (GRCm39) |
H165Y |
possibly damaging |
Het |
|
Other mutations in Ldlrad4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03140:Ldlrad4
|
APN |
18 |
68,387,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R1566:Ldlrad4
|
UTSW |
18 |
68,383,669 (GRCm39) |
missense |
probably benign |
|
R1750:Ldlrad4
|
UTSW |
18 |
68,239,758 (GRCm39) |
missense |
probably benign |
0.11 |
R6347:Ldlrad4
|
UTSW |
18 |
68,368,851 (GRCm39) |
missense |
probably benign |
0.00 |
R7774:Ldlrad4
|
UTSW |
18 |
68,368,863 (GRCm39) |
nonsense |
probably null |
|
R7775:Ldlrad4
|
UTSW |
18 |
68,368,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R7775:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7777:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7778:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7812:Ldlrad4
|
UTSW |
18 |
68,239,742 (GRCm39) |
missense |
probably benign |
0.07 |
R7827:Ldlrad4
|
UTSW |
18 |
68,387,495 (GRCm39) |
missense |
probably damaging |
0.97 |
R7977:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7983:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7984:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7986:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7987:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8017:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8018:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8019:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8020:Ldlrad4
|
UTSW |
18 |
68,368,740 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8151:Ldlrad4
|
UTSW |
18 |
68,383,643 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8154:Ldlrad4
|
UTSW |
18 |
68,387,293 (GRCm39) |
nonsense |
probably null |
|
R8157:Ldlrad4
|
UTSW |
18 |
68,387,293 (GRCm39) |
nonsense |
probably null |
|
R9083:Ldlrad4
|
UTSW |
18 |
68,197,746 (GRCm39) |
missense |
probably benign |
0.34 |
R9563:Ldlrad4
|
UTSW |
18 |
68,387,551 (GRCm39) |
missense |
probably benign |
|
|