Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd24 |
A |
G |
10: 81,475,947 (GRCm39) |
H317R |
unknown |
Het |
Aox1 |
A |
T |
1: 58,080,638 (GRCm39) |
Y29F |
probably damaging |
Het |
Bnip2 |
T |
C |
9: 69,910,967 (GRCm39) |
F304S |
possibly damaging |
Het |
Bsn |
G |
A |
9: 107,988,651 (GRCm39) |
A2367V |
probably benign |
Het |
Ccdc18 |
T |
A |
5: 108,363,899 (GRCm39) |
V1198E |
probably damaging |
Het |
Cnot3 |
T |
C |
7: 3,661,687 (GRCm39) |
F660L |
probably benign |
Het |
Cntnap3 |
A |
G |
13: 64,886,479 (GRCm39) |
I1249T |
probably benign |
Het |
Ctnna3 |
A |
G |
10: 63,339,909 (GRCm39) |
I32V |
probably benign |
Het |
Dgkz |
A |
T |
2: 91,770,649 (GRCm39) |
S485T |
possibly damaging |
Het |
Dnaaf6rt |
A |
G |
1: 31,262,564 (GRCm39) |
N182S |
probably benign |
Het |
Dpagt1 |
C |
A |
9: 44,238,482 (GRCm39) |
N49K |
possibly damaging |
Het |
Dsg3 |
A |
T |
18: 20,656,765 (GRCm39) |
S212C |
probably damaging |
Het |
Epb41l1 |
C |
T |
2: 156,368,873 (GRCm39) |
A714V |
probably benign |
Het |
Eppk1 |
A |
G |
15: 75,995,831 (GRCm39) |
V350A |
probably benign |
Het |
Frem1 |
T |
G |
4: 82,918,499 (GRCm39) |
D481A |
probably damaging |
Het |
Git2 |
T |
C |
5: 114,871,989 (GRCm39) |
K532E |
possibly damaging |
Het |
Glyr1 |
T |
C |
16: 4,854,329 (GRCm39) |
H102R |
probably benign |
Het |
Hdgfl2 |
C |
T |
17: 56,400,712 (GRCm39) |
P160L |
probably benign |
Het |
Hivep1 |
T |
C |
13: 42,308,905 (GRCm39) |
S382P |
probably benign |
Het |
Hmcn2 |
C |
A |
2: 31,281,088 (GRCm39) |
L1867I |
probably benign |
Het |
Hydin |
G |
A |
8: 111,178,626 (GRCm39) |
G1074R |
probably damaging |
Het |
Ift140 |
A |
G |
17: 25,311,889 (GRCm39) |
I1271V |
probably damaging |
Het |
Krt28 |
T |
A |
11: 99,265,626 (GRCm39) |
I14L |
probably benign |
Het |
Lrtm2 |
A |
T |
6: 119,294,458 (GRCm39) |
D224E |
probably damaging |
Het |
Map1s |
G |
A |
8: 71,365,910 (GRCm39) |
V272M |
probably damaging |
Het |
Mast3 |
A |
G |
8: 71,233,866 (GRCm39) |
Y960H |
probably damaging |
Het |
Mlh3 |
A |
T |
12: 85,315,854 (GRCm39) |
S111T |
probably benign |
Het |
Muc17 |
A |
G |
5: 137,172,798 (GRCm39) |
L85P |
|
Het |
Myh6 |
C |
G |
14: 55,181,835 (GRCm39) |
R1822P |
probably damaging |
Het |
Myof |
C |
T |
19: 37,983,872 (GRCm39) |
G144E |
probably benign |
Het |
Nat8f2 |
A |
G |
6: 85,845,024 (GRCm39) |
S113P |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,256,925 (GRCm39) |
Y181F |
probably benign |
Het |
Nup85 |
A |
G |
11: 115,457,468 (GRCm39) |
I57V |
probably benign |
Het |
Or4c99 |
T |
A |
2: 88,329,710 (GRCm39) |
C94S |
probably damaging |
Het |
Or5p79 |
C |
T |
7: 108,221,163 (GRCm39) |
T48I |
probably damaging |
Het |
Or7e170 |
T |
A |
9: 19,795,409 (GRCm39) |
Y64F |
possibly damaging |
Het |
Pcdhb2 |
A |
G |
18: 37,429,110 (GRCm39) |
N361S |
probably damaging |
Het |
Peg10 |
T |
TCCA |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Phf20 |
C |
T |
2: 156,129,913 (GRCm39) |
T495M |
probably benign |
Het |
Pitpnm1 |
T |
C |
19: 4,155,454 (GRCm39) |
M368T |
probably benign |
Het |
Pter |
A |
G |
2: 13,005,700 (GRCm39) |
D291G |
probably damaging |
Het |
Rasgrp2 |
T |
G |
19: 6,454,781 (GRCm39) |
V207G |
probably damaging |
Het |
Rnd2 |
A |
T |
11: 101,362,011 (GRCm39) |
Q188L |
probably benign |
Het |
Sh3d19 |
T |
A |
3: 85,992,363 (GRCm39) |
D130E |
probably benign |
Het |
Slc7a2 |
A |
T |
8: 41,369,396 (GRCm39) |
Y617F |
probably damaging |
Het |
Snx29 |
T |
C |
16: 11,265,291 (GRCm39) |
L165P |
probably damaging |
Het |
St7 |
T |
C |
6: 17,848,080 (GRCm39) |
|
probably null |
Het |
Tas2r115 |
A |
G |
6: 132,714,798 (GRCm39) |
L51P |
probably damaging |
Het |
Tead1 |
C |
A |
7: 112,456,135 (GRCm39) |
P164Q |
probably benign |
Het |
Thop1 |
A |
G |
10: 80,914,385 (GRCm39) |
Y224C |
probably damaging |
Het |
Twf1 |
T |
C |
15: 94,477,702 (GRCm39) |
*351W |
probably null |
Het |
Uck1 |
C |
A |
2: 32,150,153 (GRCm39) |
|
probably benign |
Het |
Utp20 |
A |
G |
10: 88,662,466 (GRCm39) |
|
probably null |
Het |
Vmn2r118 |
G |
T |
17: 55,915,057 (GRCm39) |
L530I |
probably benign |
Het |
Vmn2r30 |
A |
T |
7: 7,315,359 (GRCm39) |
C825S |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,818,549 (GRCm39) |
M3106K |
|
Het |
Wfdc15a |
A |
T |
2: 164,041,671 (GRCm39) |
C51S |
probably damaging |
Het |
Zc3hc1 |
T |
C |
6: 30,375,951 (GRCm39) |
D203G |
probably damaging |
Het |
Zfhx2 |
G |
T |
14: 55,308,079 (GRCm39) |
D932E |
probably benign |
Het |
Zfp267 |
G |
A |
3: 36,219,182 (GRCm39) |
G402S |
probably damaging |
Het |
|
Other mutations in Mettl25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00310:Mettl25
|
APN |
10 |
105,662,295 (GRCm39) |
missense |
probably benign |
|
IGL00698:Mettl25
|
APN |
10 |
105,629,201 (GRCm39) |
missense |
probably null |
0.31 |
IGL00766:Mettl25
|
APN |
10 |
105,615,443 (GRCm39) |
splice site |
probably benign |
|
IGL01360:Mettl25
|
APN |
10 |
105,659,058 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01954:Mettl25
|
APN |
10 |
105,659,068 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02088:Mettl25
|
APN |
10 |
105,659,111 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02623:Mettl25
|
APN |
10 |
105,662,185 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03245:Mettl25
|
APN |
10 |
105,662,358 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03134:Mettl25
|
UTSW |
10 |
105,661,888 (GRCm39) |
nonsense |
probably null |
|
R0238:Mettl25
|
UTSW |
10 |
105,662,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Mettl25
|
UTSW |
10 |
105,662,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Mettl25
|
UTSW |
10 |
105,662,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Mettl25
|
UTSW |
10 |
105,662,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1297:Mettl25
|
UTSW |
10 |
105,659,126 (GRCm39) |
missense |
probably benign |
0.11 |
R1482:Mettl25
|
UTSW |
10 |
105,662,451 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1526:Mettl25
|
UTSW |
10 |
105,668,844 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1542:Mettl25
|
UTSW |
10 |
105,661,981 (GRCm39) |
missense |
probably benign |
0.04 |
R1589:Mettl25
|
UTSW |
10 |
105,615,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R1901:Mettl25
|
UTSW |
10 |
105,661,948 (GRCm39) |
missense |
probably damaging |
0.96 |
R1902:Mettl25
|
UTSW |
10 |
105,661,948 (GRCm39) |
missense |
probably damaging |
0.96 |
R2016:Mettl25
|
UTSW |
10 |
105,633,167 (GRCm39) |
missense |
probably benign |
0.00 |
R2355:Mettl25
|
UTSW |
10 |
105,599,316 (GRCm39) |
missense |
probably benign |
0.00 |
R2920:Mettl25
|
UTSW |
10 |
105,601,038 (GRCm39) |
splice site |
probably null |
|
R3149:Mettl25
|
UTSW |
10 |
105,662,214 (GRCm39) |
missense |
probably benign |
0.00 |
R4547:Mettl25
|
UTSW |
10 |
105,661,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R4646:Mettl25
|
UTSW |
10 |
105,662,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R4652:Mettl25
|
UTSW |
10 |
105,615,509 (GRCm39) |
nonsense |
probably null |
|
R5020:Mettl25
|
UTSW |
10 |
105,662,068 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5435:Mettl25
|
UTSW |
10 |
105,615,447 (GRCm39) |
critical splice donor site |
probably null |
|
R6947:Mettl25
|
UTSW |
10 |
105,662,053 (GRCm39) |
missense |
probably benign |
0.00 |
R7075:Mettl25
|
UTSW |
10 |
105,665,785 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7729:Mettl25
|
UTSW |
10 |
105,601,871 (GRCm39) |
missense |
probably benign |
0.03 |
R8074:Mettl25
|
UTSW |
10 |
105,661,941 (GRCm39) |
missense |
probably benign |
0.02 |
R8108:Mettl25
|
UTSW |
10 |
105,659,040 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8937:Mettl25
|
UTSW |
10 |
105,601,122 (GRCm39) |
missense |
probably benign |
0.17 |
R8949:Mettl25
|
UTSW |
10 |
105,668,714 (GRCm39) |
missense |
probably benign |
0.00 |
R9497:Mettl25
|
UTSW |
10 |
105,677,090 (GRCm39) |
missense |
probably damaging |
0.98 |
R9772:Mettl25
|
UTSW |
10 |
105,633,127 (GRCm39) |
missense |
probably benign |
|
RF009:Mettl25
|
UTSW |
10 |
105,669,100 (GRCm39) |
intron |
probably benign |
|
Z1176:Mettl25
|
UTSW |
10 |
105,661,959 (GRCm39) |
missense |
possibly damaging |
0.95 |
|