Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
T |
C |
13: 77,471,655 (GRCm39) |
I1020T |
probably benign |
Het |
2310057N15Rik |
A |
T |
16: 88,570,523 (GRCm39) |
Y172* |
probably null |
Het |
4930558K02Rik |
T |
A |
1: 161,770,092 (GRCm39) |
Y139F |
possibly damaging |
Het |
A830018L16Rik |
T |
G |
1: 11,658,695 (GRCm39) |
M202R |
probably damaging |
Het |
Abca12 |
T |
C |
1: 71,287,591 (GRCm39) |
E2450G |
probably damaging |
Het |
Ank2 |
C |
T |
3: 126,736,782 (GRCm39) |
R3034H |
unknown |
Het |
Anxa9 |
A |
G |
3: 95,213,184 (GRCm39) |
I54T |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,961,941 (GRCm39) |
|
probably null |
Het |
Aspm |
T |
C |
1: 139,386,066 (GRCm39) |
I570T |
probably benign |
Het |
Bcar3 |
A |
T |
3: 122,302,045 (GRCm39) |
I247F |
possibly damaging |
Het |
Cep350 |
A |
G |
1: 155,829,334 (GRCm39) |
V130A |
probably damaging |
Het |
Cep89 |
A |
T |
7: 35,137,888 (GRCm39) |
R757S |
probably benign |
Het |
Cryga |
A |
T |
1: 65,142,381 (GRCm39) |
I4N |
probably damaging |
Het |
Cyp2d26 |
T |
A |
15: 82,676,764 (GRCm39) |
Y194F |
probably benign |
Het |
Edn2 |
G |
A |
4: 120,019,143 (GRCm39) |
R44H |
probably damaging |
Het |
Ep400 |
G |
A |
5: 110,903,511 (GRCm39) |
Q363* |
probably null |
Het |
Ice2 |
T |
A |
9: 69,324,365 (GRCm39) |
S763T |
possibly damaging |
Het |
Itgad |
C |
A |
7: 127,804,245 (GRCm39) |
F1169L |
probably damaging |
Het |
Kcnv1 |
A |
G |
15: 44,976,576 (GRCm39) |
L237P |
probably benign |
Het |
Kctd18 |
T |
C |
1: 57,995,710 (GRCm39) |
E356G |
probably damaging |
Het |
Krt33a |
C |
T |
11: 99,902,837 (GRCm39) |
R329Q |
probably damaging |
Het |
Lama2 |
C |
A |
10: 27,000,552 (GRCm39) |
G1657C |
probably damaging |
Het |
Marchf3 |
T |
G |
18: 56,895,593 (GRCm39) |
R217S |
probably benign |
Het |
Mmel1 |
A |
T |
4: 154,978,547 (GRCm39) |
T660S |
probably damaging |
Het |
Ms4a7 |
T |
A |
19: 11,310,642 (GRCm39) |
K59* |
probably null |
Het |
Mss51 |
G |
A |
14: 20,534,981 (GRCm39) |
T263I |
probably damaging |
Het |
Ncaph2 |
A |
G |
15: 89,248,385 (GRCm39) |
M199V |
probably benign |
Het |
Ndufa4 |
G |
A |
6: 11,905,209 (GRCm39) |
Q62* |
probably null |
Het |
Nectin4 |
A |
G |
1: 171,214,212 (GRCm39) |
T456A |
probably damaging |
Het |
Nek1 |
T |
C |
8: 61,578,120 (GRCm39) |
M1214T |
probably benign |
Het |
Nsf |
T |
A |
11: 103,718,064 (GRCm39) |
L710F |
probably damaging |
Het |
Nynrin |
G |
T |
14: 56,107,872 (GRCm39) |
G993V |
probably damaging |
Het |
Or1e31 |
T |
A |
11: 73,689,695 (GRCm39) |
D296V |
probably damaging |
Het |
Pbk |
T |
A |
14: 66,052,621 (GRCm39) |
Y155N |
probably damaging |
Het |
Plec |
T |
C |
15: 76,059,153 (GRCm39) |
I3595V |
possibly damaging |
Het |
Pom121 |
G |
A |
5: 135,409,941 (GRCm39) |
T1072I |
unknown |
Het |
Sdc1 |
T |
A |
12: 8,840,554 (GRCm39) |
H106Q |
probably benign |
Het |
Slc44a3 |
T |
C |
3: 121,254,764 (GRCm39) |
D618G |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,401,878 (GRCm39) |
D755G |
possibly damaging |
Het |
Slfn9 |
T |
C |
11: 82,872,387 (GRCm39) |
Y783C |
probably benign |
Het |
Sorl1 |
C |
T |
9: 41,975,006 (GRCm39) |
|
probably null |
Het |
Spindoc |
C |
T |
19: 7,360,085 (GRCm39) |
E28K |
possibly damaging |
Het |
Sptbn1 |
T |
C |
11: 30,064,859 (GRCm39) |
D1880G |
possibly damaging |
Het |
Sspn |
T |
A |
6: 145,907,200 (GRCm39) |
D210E |
probably benign |
Het |
Stx12 |
A |
T |
4: 132,584,687 (GRCm39) |
I219K |
possibly damaging |
Het |
Syne2 |
T |
C |
12: 76,095,417 (GRCm39) |
V508A |
probably benign |
Het |
Tkt |
G |
T |
14: 30,287,564 (GRCm39) |
R186L |
probably damaging |
Het |
Trmt10a |
T |
A |
3: 137,860,527 (GRCm39) |
M241K |
probably damaging |
Het |
Vgll2 |
C |
A |
10: 51,903,758 (GRCm39) |
A207E |
possibly damaging |
Het |
Vmn1r114 |
A |
G |
7: 20,545,543 (GRCm39) |
F190S |
probably damaging |
Het |
Xpot |
C |
T |
10: 121,453,094 (GRCm39) |
|
probably null |
Het |
Yrdc |
G |
A |
4: 124,744,820 (GRCm39) |
A85T |
probably benign |
Het |
Zfp385c |
C |
T |
11: 100,520,865 (GRCm39) |
R265K |
possibly damaging |
Het |
Zgrf1 |
A |
T |
3: 127,392,409 (GRCm39) |
I1310F |
probably damaging |
Het |
|
Other mutations in Gpr33 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01655:Gpr33
|
APN |
12 |
52,070,343 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02177:Gpr33
|
APN |
12 |
52,070,863 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03090:Gpr33
|
APN |
12 |
52,070,809 (GRCm39) |
missense |
probably damaging |
0.99 |
R0883:Gpr33
|
UTSW |
12 |
52,070,418 (GRCm39) |
missense |
probably benign |
0.17 |
R1112:Gpr33
|
UTSW |
12 |
52,070,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R1127:Gpr33
|
UTSW |
12 |
52,070,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R1742:Gpr33
|
UTSW |
12 |
52,071,045 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1967:Gpr33
|
UTSW |
12 |
52,070,991 (GRCm39) |
missense |
probably benign |
|
R2208:Gpr33
|
UTSW |
12 |
52,070,236 (GRCm39) |
missense |
probably benign |
0.00 |
R2917:Gpr33
|
UTSW |
12 |
52,070,379 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4308:Gpr33
|
UTSW |
12 |
52,070,423 (GRCm39) |
nonsense |
probably null |
|
R4725:Gpr33
|
UTSW |
12 |
52,070,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R5616:Gpr33
|
UTSW |
12 |
52,070,377 (GRCm39) |
missense |
probably damaging |
0.99 |
R7055:Gpr33
|
UTSW |
12 |
52,071,036 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R7419:Gpr33
|
UTSW |
12 |
52,070,050 (GRCm39) |
missense |
probably benign |
0.00 |
R8313:Gpr33
|
UTSW |
12 |
52,070,907 (GRCm39) |
missense |
probably benign |
0.00 |
R8514:Gpr33
|
UTSW |
12 |
52,070,181 (GRCm39) |
missense |
probably benign |
0.06 |
|