Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc8 |
A |
G |
7: 45,757,858 (GRCm39) |
V1297A |
possibly damaging |
Het |
Agbl2 |
C |
T |
2: 90,614,442 (GRCm39) |
H25Y |
probably damaging |
Het |
Akap11 |
A |
T |
14: 78,750,990 (GRCm39) |
W466R |
probably benign |
Het |
Ccdc66 |
T |
A |
14: 27,213,890 (GRCm39) |
Q471L |
probably damaging |
Het |
Dennd1c |
G |
A |
17: 57,380,822 (GRCm39) |
A210V |
probably damaging |
Het |
F13b |
A |
G |
1: 139,438,597 (GRCm39) |
K334E |
probably damaging |
Het |
Fam186a |
A |
C |
15: 99,840,055 (GRCm39) |
I2063R |
probably damaging |
Het |
Fcrl5 |
T |
C |
3: 87,353,767 (GRCm39) |
Y371H |
probably damaging |
Het |
Fnbp1 |
C |
T |
2: 30,923,041 (GRCm39) |
G549D |
probably benign |
Het |
Fndc3a |
A |
G |
14: 72,794,067 (GRCm39) |
Y869H |
probably benign |
Het |
Gm7592 |
A |
G |
1: 85,454,437 (GRCm39) |
|
noncoding transcript |
Het |
Gucy2d |
C |
A |
7: 98,108,209 (GRCm39) |
|
probably null |
Het |
Hmcn1 |
C |
T |
1: 150,479,562 (GRCm39) |
C4634Y |
probably damaging |
Het |
Kctd5 |
A |
G |
17: 24,278,194 (GRCm39) |
|
probably null |
Het |
Kics2 |
T |
C |
10: 121,581,280 (GRCm39) |
Y94H |
probably damaging |
Het |
Mitf |
A |
G |
6: 97,970,104 (GRCm39) |
E17G |
probably damaging |
Het |
Mmut |
T |
A |
17: 41,248,149 (GRCm39) |
W59R |
probably benign |
Het |
Mrc1 |
G |
A |
2: 14,312,720 (GRCm39) |
D881N |
probably benign |
Het |
Mrm1 |
T |
C |
11: 84,709,509 (GRCm39) |
T183A |
possibly damaging |
Het |
Mylk |
G |
A |
16: 34,605,344 (GRCm39) |
|
probably null |
Het |
Nab2 |
G |
A |
10: 127,500,936 (GRCm39) |
A19V |
probably damaging |
Het |
Ntsr2 |
T |
A |
12: 16,709,719 (GRCm39) |
Y333* |
probably null |
Het |
Sephs1 |
A |
G |
2: 4,904,371 (GRCm39) |
T250A |
probably benign |
Het |
Sypl2 |
T |
C |
3: 108,133,473 (GRCm39) |
E32G |
possibly damaging |
Het |
Tasp1 |
T |
C |
2: 139,793,403 (GRCm39) |
K258E |
probably damaging |
Het |
Tcam1 |
G |
A |
11: 106,174,904 (GRCm39) |
E120K |
probably benign |
Het |
Tenm4 |
G |
T |
7: 96,555,088 (GRCm39) |
V2561F |
probably damaging |
Het |
Tmc1 |
T |
C |
19: 20,776,409 (GRCm39) |
Y650C |
probably damaging |
Het |
Trim34b |
T |
C |
7: 103,979,062 (GRCm39) |
L103P |
probably damaging |
Het |
Usp47 |
T |
C |
7: 111,662,600 (GRCm39) |
|
probably null |
Het |
Vmn1r201 |
T |
A |
13: 22,659,193 (GRCm39) |
W136R |
probably damaging |
Het |
Vmn2r104 |
A |
T |
17: 20,268,264 (GRCm39) |
Y68* |
probably null |
Het |
Wscd2 |
T |
A |
5: 113,689,192 (GRCm39) |
L66Q |
probably damaging |
Het |
|
Other mutations in Mettl24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00517:Mettl24
|
APN |
10 |
40,686,496 (GRCm39) |
missense |
probably benign |
0.05 |
R0961:Mettl24
|
UTSW |
10 |
40,686,615 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1172:Mettl24
|
UTSW |
10 |
40,613,704 (GRCm39) |
missense |
probably benign |
0.01 |
R1430:Mettl24
|
UTSW |
10 |
40,613,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Mettl24
|
UTSW |
10 |
40,613,812 (GRCm39) |
critical splice donor site |
probably null |
|
R1940:Mettl24
|
UTSW |
10 |
40,613,722 (GRCm39) |
missense |
probably benign |
0.01 |
R3424:Mettl24
|
UTSW |
10 |
40,559,637 (GRCm39) |
nonsense |
probably null |
|
R4831:Mettl24
|
UTSW |
10 |
40,559,413 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5430:Mettl24
|
UTSW |
10 |
40,613,780 (GRCm39) |
missense |
probably benign |
0.07 |
R5889:Mettl24
|
UTSW |
10 |
40,622,486 (GRCm39) |
missense |
probably benign |
0.27 |
R6893:Mettl24
|
UTSW |
10 |
40,613,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R7072:Mettl24
|
UTSW |
10 |
40,559,509 (GRCm39) |
missense |
probably benign |
|
R7177:Mettl24
|
UTSW |
10 |
40,686,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R7309:Mettl24
|
UTSW |
10 |
40,686,496 (GRCm39) |
missense |
probably benign |
0.05 |
R7898:Mettl24
|
UTSW |
10 |
40,686,478 (GRCm39) |
missense |
probably benign |
0.02 |
X0022:Mettl24
|
UTSW |
10 |
40,622,383 (GRCm39) |
missense |
probably damaging |
1.00 |
|