Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
C |
1: 71,330,501 (GRCm39) |
T1385A |
probably damaging |
Het |
Apc2 |
T |
A |
10: 80,149,972 (GRCm39) |
D1646E |
probably damaging |
Het |
Aspm |
G |
A |
1: 139,407,407 (GRCm39) |
R2098H |
probably benign |
Het |
Atl3 |
C |
A |
19: 7,509,592 (GRCm39) |
T435N |
possibly damaging |
Het |
Cdh22 |
G |
T |
2: 164,958,200 (GRCm39) |
T589K |
probably damaging |
Het |
Cnot3 |
T |
C |
7: 3,661,082 (GRCm39) |
L561S |
probably benign |
Het |
Col5a1 |
A |
G |
2: 27,841,468 (GRCm39) |
D363G |
unknown |
Het |
Cyp24a1 |
T |
C |
2: 170,338,229 (GRCm39) |
D105G |
possibly damaging |
Het |
Dennd4a |
C |
A |
9: 64,758,491 (GRCm39) |
|
probably null |
Het |
Dnah8 |
A |
G |
17: 31,019,561 (GRCm39) |
K3878R |
probably benign |
Het |
Dock4 |
T |
C |
12: 40,894,539 (GRCm39) |
S1900P |
probably benign |
Het |
Fancg |
A |
G |
4: 43,008,736 (GRCm39) |
L167P |
probably damaging |
Het |
Ighd2-8 |
A |
G |
12: 113,414,487 (GRCm39) |
S1P |
possibly damaging |
Het |
Kif28 |
A |
G |
1: 179,525,336 (GRCm39) |
|
probably null |
Het |
Mrpl55 |
T |
A |
11: 59,095,397 (GRCm39) |
C20* |
probably null |
Het |
Myo5a |
A |
G |
9: 75,079,001 (GRCm39) |
K920E |
possibly damaging |
Het |
Naa35 |
G |
A |
13: 59,770,680 (GRCm39) |
|
probably benign |
Het |
Olfm3 |
A |
G |
3: 114,890,573 (GRCm39) |
R76G |
probably damaging |
Het |
Or14a258 |
T |
C |
7: 86,035,521 (GRCm39) |
M116V |
probably damaging |
Het |
Or2ag1 |
T |
C |
7: 106,313,373 (GRCm39) |
R172G |
possibly damaging |
Het |
Pcdha12 |
A |
T |
18: 37,155,468 (GRCm39) |
D729V |
probably benign |
Het |
Phf11c |
T |
C |
14: 59,622,981 (GRCm39) |
|
probably null |
Het |
Phf20 |
T |
A |
2: 156,093,688 (GRCm39) |
|
probably null |
Het |
Plbd1 |
T |
A |
6: 136,593,987 (GRCm39) |
Y376F |
probably benign |
Het |
Poglut1 |
A |
G |
16: 38,352,173 (GRCm39) |
V257A |
probably damaging |
Het |
Reln |
A |
G |
5: 22,106,623 (GRCm39) |
I3249T |
probably benign |
Het |
Rgsl1 |
G |
A |
1: 153,701,639 (GRCm39) |
P272S |
possibly damaging |
Het |
Slc15a2 |
A |
T |
16: 36,592,472 (GRCm39) |
Y197* |
probably null |
Het |
Slc45a2 |
C |
T |
15: 11,012,693 (GRCm39) |
T232I |
probably benign |
Het |
Ssc5d |
T |
A |
7: 4,929,517 (GRCm39) |
|
probably null |
Het |
Thbs2 |
T |
C |
17: 14,910,215 (GRCm39) |
Y128C |
probably damaging |
Het |
Them4 |
A |
T |
3: 94,238,851 (GRCm39) |
L219F |
possibly damaging |
Het |
Trappc2b |
T |
C |
11: 51,576,799 (GRCm39) |
E33G |
probably benign |
Het |
Ttc29 |
G |
A |
8: 78,972,942 (GRCm39) |
E131K |
possibly damaging |
Het |
Vmn1r29 |
C |
G |
6: 58,284,676 (GRCm39) |
S132C |
probably benign |
Het |
Vmn1r53 |
G |
A |
6: 90,200,742 (GRCm39) |
A194V |
probably benign |
Het |
Wdr86 |
A |
T |
5: 24,923,085 (GRCm39) |
H202Q |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,347,239 (GRCm39) |
D3160G |
probably benign |
Het |
Xkr5 |
T |
C |
8: 18,983,982 (GRCm39) |
D520G |
probably benign |
Het |
Zfp607b |
T |
G |
7: 27,403,406 (GRCm39) |
C621G |
probably damaging |
Het |
|
Other mutations in Tmem30b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0034:Tmem30b
|
UTSW |
12 |
73,592,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Tmem30b
|
UTSW |
12 |
73,592,942 (GRCm39) |
missense |
probably benign |
0.24 |
R0707:Tmem30b
|
UTSW |
12 |
73,592,942 (GRCm39) |
missense |
probably benign |
0.24 |
R2135:Tmem30b
|
UTSW |
12 |
73,592,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R3615:Tmem30b
|
UTSW |
12 |
73,592,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R3616:Tmem30b
|
UTSW |
12 |
73,592,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R4858:Tmem30b
|
UTSW |
12 |
73,592,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R4922:Tmem30b
|
UTSW |
12 |
73,592,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R7391:Tmem30b
|
UTSW |
12 |
73,592,702 (GRCm39) |
missense |
probably benign |
0.00 |
R7521:Tmem30b
|
UTSW |
12 |
73,592,092 (GRCm39) |
missense |
probably benign |
0.07 |
R9054:Tmem30b
|
UTSW |
12 |
73,592,923 (GRCm39) |
missense |
probably benign |
0.11 |
|