Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg3 |
A |
G |
17: 57,188,062 (GRCm39) |
N190S |
probably benign |
Het |
Adamts18 |
T |
A |
8: 114,469,728 (GRCm39) |
Y658F |
probably benign |
Het |
Camsap3 |
T |
A |
8: 3,658,508 (GRCm39) |
L1151Q |
probably damaging |
Het |
Casp14 |
T |
A |
10: 78,551,237 (GRCm39) |
Y16F |
probably damaging |
Het |
Clip2 |
A |
T |
5: 134,526,938 (GRCm39) |
|
probably benign |
Het |
Clip4 |
G |
A |
17: 72,134,785 (GRCm39) |
|
probably benign |
Het |
Cyb5r4 |
G |
A |
9: 86,941,505 (GRCm39) |
|
probably null |
Het |
Ep400 |
A |
T |
5: 110,827,874 (GRCm39) |
N2329K |
unknown |
Het |
Fam163a |
T |
A |
1: 155,955,742 (GRCm39) |
I17F |
probably damaging |
Het |
Galnt1 |
T |
A |
18: 24,400,617 (GRCm39) |
I241N |
probably damaging |
Het |
Galnt14 |
T |
G |
17: 73,811,899 (GRCm39) |
I441L |
probably benign |
Het |
Gpr45 |
T |
C |
1: 43,071,402 (GRCm39) |
L15P |
probably benign |
Het |
Hivep1 |
A |
T |
13: 42,308,464 (GRCm39) |
K235* |
probably null |
Het |
Kcnip2 |
T |
C |
19: 45,782,746 (GRCm39) |
|
probably null |
Het |
Kpna3 |
T |
C |
14: 61,607,894 (GRCm39) |
N437S |
possibly damaging |
Het |
Lmtk2 |
A |
T |
5: 144,112,753 (GRCm39) |
R1158* |
probably null |
Het |
Lpo |
A |
G |
11: 87,698,159 (GRCm39) |
V612A |
possibly damaging |
Het |
Myh15 |
T |
C |
16: 48,934,421 (GRCm39) |
C663R |
probably damaging |
Het |
Nacad |
G |
A |
11: 6,555,700 (GRCm39) |
R17C |
unknown |
Het |
Or7a35 |
A |
T |
10: 78,853,770 (GRCm39) |
M205L |
probably benign |
Het |
Pcsk2 |
A |
G |
2: 143,529,500 (GRCm39) |
Q99R |
possibly damaging |
Het |
Pkd1l2 |
T |
C |
8: 117,787,264 (GRCm39) |
N593S |
probably benign |
Het |
Plce1 |
G |
A |
19: 38,709,425 (GRCm39) |
S1093N |
probably damaging |
Het |
Prxl2b |
G |
T |
4: 154,981,059 (GRCm39) |
|
probably benign |
Het |
Rhpn2 |
T |
A |
7: 35,075,596 (GRCm39) |
Y258N |
probably benign |
Het |
Serpinb9d |
T |
C |
13: 33,384,688 (GRCm39) |
Y222H |
probably damaging |
Het |
Shprh |
T |
C |
10: 11,066,806 (GRCm39) |
L1401P |
probably damaging |
Het |
Slc5a7 |
A |
G |
17: 54,588,861 (GRCm39) |
L262P |
probably damaging |
Het |
Stat2 |
T |
G |
10: 128,117,045 (GRCm39) |
F293V |
probably benign |
Het |
Stpg4 |
T |
A |
17: 87,702,585 (GRCm39) |
|
probably null |
Het |
Styk1 |
G |
T |
6: 131,279,329 (GRCm39) |
|
probably benign |
Het |
Sult2a2 |
T |
A |
7: 13,468,721 (GRCm39) |
D62E |
probably damaging |
Het |
Sytl2 |
G |
A |
7: 90,045,745 (GRCm39) |
V632M |
probably damaging |
Het |
Themis |
C |
T |
10: 28,658,307 (GRCm39) |
Q445* |
probably null |
Het |
Vmn1r48 |
T |
A |
6: 90,013,265 (GRCm39) |
T187S |
probably damaging |
Het |
Xpnpep1 |
A |
G |
19: 52,988,824 (GRCm39) |
Y463H |
probably damaging |
Het |
|
Other mutations in Tmem225 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
R4556:Tmem225
|
UTSW |
9 |
40,060,762 (GRCm39) |
missense |
probably damaging |
0.96 |
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 |
|