Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830005F24Rik |
T |
C |
13: 48,667,937 (GRCm39) |
|
probably benign |
Het |
Adamts16 |
G |
A |
13: 70,927,637 (GRCm39) |
|
probably benign |
Het |
Adamts17 |
A |
T |
7: 66,677,641 (GRCm39) |
E518D |
probably damaging |
Het |
Cdk5rap2 |
A |
G |
4: 70,157,549 (GRCm39) |
S1601P |
probably damaging |
Het |
Erc2 |
A |
C |
14: 28,024,861 (GRCm39) |
D580A |
probably damaging |
Het |
Fbxo4 |
A |
G |
15: 3,995,187 (GRCm39) |
*386R |
probably null |
Het |
Fbxo42 |
T |
A |
4: 140,926,321 (GRCm39) |
H334Q |
probably damaging |
Het |
Gdf5 |
A |
G |
2: 155,783,782 (GRCm39) |
R24G |
probably benign |
Het |
Lama3 |
G |
T |
18: 12,612,816 (GRCm39) |
R1200L |
possibly damaging |
Het |
Lxn |
T |
A |
3: 67,365,953 (GRCm39) |
I182F |
possibly damaging |
Het |
Mbd5 |
G |
A |
2: 49,169,406 (GRCm39) |
G1526R |
probably damaging |
Het |
Mcub |
G |
A |
3: 129,709,384 (GRCm39) |
Q310* |
probably null |
Het |
Ndufaf7 |
T |
C |
17: 79,249,516 (GRCm39) |
S138P |
probably benign |
Het |
Nktr |
A |
G |
9: 121,570,189 (GRCm39) |
T90A |
probably damaging |
Het |
Nr1h5 |
G |
A |
3: 102,853,457 (GRCm39) |
A350V |
probably benign |
Het |
Or1e29 |
G |
A |
11: 73,667,307 (GRCm39) |
T282I |
possibly damaging |
Het |
Or7e174 |
T |
C |
9: 20,012,619 (GRCm39) |
L188P |
possibly damaging |
Het |
Pros1 |
A |
G |
16: 62,721,036 (GRCm39) |
K197R |
possibly damaging |
Het |
Rmnd5b |
G |
T |
11: 51,517,732 (GRCm39) |
|
probably null |
Het |
Rnf25 |
A |
T |
1: 74,638,264 (GRCm39) |
I26N |
probably damaging |
Het |
Scn4a |
T |
C |
11: 106,211,272 (GRCm39) |
I1582V |
probably benign |
Het |
Sh2d3c |
A |
G |
2: 32,643,021 (GRCm39) |
T583A |
possibly damaging |
Het |
Sh3tc1 |
T |
C |
5: 35,864,426 (GRCm39) |
Y587C |
probably damaging |
Het |
Slc6a11 |
A |
G |
6: 114,221,773 (GRCm39) |
S488G |
probably benign |
Het |
Smim22 |
T |
A |
16: 4,825,730 (GRCm39) |
F38L |
possibly damaging |
Het |
Stab2 |
T |
G |
10: 86,803,543 (GRCm39) |
E335D |
possibly damaging |
Het |
Tas2r102 |
T |
C |
6: 132,739,878 (GRCm39) |
F262S |
probably damaging |
Het |
Thap12 |
A |
G |
7: 98,365,052 (GRCm39) |
N407D |
probably benign |
Het |
Vmn1r229 |
T |
A |
17: 21,034,953 (GRCm39) |
V66E |
possibly damaging |
Het |
Vmn1r27 |
A |
G |
6: 58,192,804 (GRCm39) |
S67P |
possibly damaging |
Het |
Xrcc4 |
A |
T |
13: 90,140,623 (GRCm39) |
H195Q |
probably benign |
Het |
|
Other mutations in Tmem225 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01833:Tmem225
|
APN |
9 |
40,059,725 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03094:Tmem225
|
APN |
9 |
40,059,682 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0599:Tmem225
|
UTSW |
9 |
40,061,043 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1134:Tmem225
|
UTSW |
9 |
40,061,143 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2842:Tmem225
|
UTSW |
9 |
40,061,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R5024:Tmem225
|
UTSW |
9 |
40,060,639 (GRCm39) |
missense |
probably benign |
0.01 |
R5526:Tmem225
|
UTSW |
9 |
40,062,002 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5540:Tmem225
|
UTSW |
9 |
40,060,681 (GRCm39) |
missense |
probably damaging |
0.99 |
R5597:Tmem225
|
UTSW |
9 |
40,060,726 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6267:Tmem225
|
UTSW |
9 |
40,059,731 (GRCm39) |
missense |
probably damaging |
0.97 |
R6314:Tmem225
|
UTSW |
9 |
40,062,016 (GRCm39) |
missense |
probably benign |
|
R7153:Tmem225
|
UTSW |
9 |
40,059,664 (GRCm39) |
missense |
probably benign |
0.01 |
R8031:Tmem225
|
UTSW |
9 |
40,060,689 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8245:Tmem225
|
UTSW |
9 |
40,061,955 (GRCm39) |
missense |
probably damaging |
0.99 |
X0064:Tmem225
|
UTSW |
9 |
40,061,082 (GRCm39) |
missense |
possibly damaging |
0.85 |
|