Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
T |
C |
18: 6,638,653 (GRCm39) |
S351P |
possibly damaging |
Het |
Abca2 |
T |
C |
2: 25,332,015 (GRCm39) |
S1376P |
probably damaging |
Het |
Ablim3 |
A |
G |
18: 62,004,754 (GRCm39) |
Y12H |
probably damaging |
Het |
Akr1b7 |
A |
G |
6: 34,398,052 (GRCm39) |
R294G |
possibly damaging |
Het |
Aldh3b1 |
A |
C |
19: 3,971,205 (GRCm39) |
V153G |
probably benign |
Het |
Alk |
A |
T |
17: 72,181,173 (GRCm39) |
H1372Q |
probably damaging |
Het |
Ano9 |
A |
C |
7: 140,681,955 (GRCm39) |
Y731* |
probably null |
Het |
Apol11b |
G |
A |
15: 77,522,219 (GRCm39) |
T26M |
probably damaging |
Het |
Asl |
T |
C |
5: 130,048,645 (GRCm39) |
E43G |
probably damaging |
Het |
Cd4 |
G |
A |
6: 124,856,341 (GRCm39) |
T50I |
probably benign |
Het |
Cfap43 |
T |
C |
19: 47,784,105 (GRCm39) |
D476G |
probably benign |
Het |
Cpa1 |
A |
G |
6: 30,645,275 (GRCm39) |
H417R |
possibly damaging |
Het |
Cpeb3 |
T |
C |
19: 37,065,948 (GRCm39) |
D407G |
probably benign |
Het |
Dcaf15 |
A |
T |
8: 84,825,026 (GRCm39) |
C469S |
probably damaging |
Het |
Dpy19l4 |
C |
A |
4: 11,273,006 (GRCm39) |
|
probably null |
Het |
E4f1 |
A |
T |
17: 24,663,208 (GRCm39) |
L699Q |
probably damaging |
Het |
Eif4g2 |
A |
G |
7: 110,676,234 (GRCm39) |
F349S |
possibly damaging |
Het |
Ermap |
T |
C |
4: 119,044,355 (GRCm39) |
Y147C |
probably damaging |
Het |
Frk |
A |
C |
10: 34,423,381 (GRCm39) |
E153A |
probably damaging |
Het |
Fubp3 |
G |
A |
2: 31,494,733 (GRCm39) |
|
probably null |
Het |
Gdi2 |
A |
G |
13: 3,614,611 (GRCm39) |
T319A |
probably benign |
Het |
Gjc3 |
A |
G |
5: 137,956,120 (GRCm39) |
F55S |
probably damaging |
Het |
Gm10762 |
C |
T |
2: 128,809,005 (GRCm39) |
|
probably benign |
Het |
Got1 |
A |
G |
19: 43,493,048 (GRCm39) |
I291T |
possibly damaging |
Het |
Gpr179 |
C |
A |
11: 97,229,012 (GRCm39) |
G1048* |
probably null |
Het |
Hectd3 |
G |
T |
4: 116,853,262 (GRCm39) |
R163L |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,477,480 (GRCm39) |
|
probably benign |
Het |
Ifnb1 |
T |
C |
4: 88,440,480 (GRCm39) |
R178G |
probably benign |
Het |
Ino80 |
T |
A |
2: 119,287,199 (GRCm39) |
D56V |
possibly damaging |
Het |
Kctd1 |
T |
A |
18: 15,102,610 (GRCm39) |
Q857L |
probably damaging |
Het |
Kdm5a |
T |
A |
6: 120,367,640 (GRCm39) |
L445* |
probably null |
Het |
Lins1 |
G |
A |
7: 66,363,676 (GRCm39) |
V524I |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,430,901 (GRCm39) |
Y383N |
probably damaging |
Het |
Malrd1 |
G |
A |
2: 16,106,768 (GRCm39) |
|
probably null |
Het |
Mgam |
A |
C |
6: 40,621,879 (GRCm39) |
K84Q |
probably benign |
Het |
Mlh3 |
A |
T |
12: 85,314,703 (GRCm39) |
F494L |
probably benign |
Het |
Mpped1 |
T |
C |
15: 83,676,414 (GRCm39) |
F60S |
possibly damaging |
Het |
Myo1e |
A |
G |
9: 70,245,048 (GRCm39) |
Y382C |
probably benign |
Het |
Ncor1 |
C |
A |
11: 62,231,300 (GRCm39) |
V836F |
probably damaging |
Het |
Nktr |
G |
A |
9: 121,570,218 (GRCm39) |
|
probably null |
Het |
Or10al4 |
A |
G |
17: 38,037,193 (GRCm39) |
T93A |
probably benign |
Het |
Or4d5 |
A |
G |
9: 40,012,558 (GRCm39) |
I76T |
probably benign |
Het |
Or5k8 |
G |
A |
16: 58,644,958 (GRCm39) |
T38I |
probably damaging |
Het |
Rnf144a |
T |
A |
12: 26,377,300 (GRCm39) |
Y93F |
probably benign |
Het |
Rubcn |
G |
A |
16: 32,647,666 (GRCm39) |
T636M |
probably damaging |
Het |
Scn5a |
A |
C |
9: 119,315,536 (GRCm39) |
L1724R |
probably damaging |
Het |
Sel1l |
A |
G |
12: 91,808,607 (GRCm39) |
S45P |
possibly damaging |
Het |
Serpina3k |
A |
G |
12: 104,306,882 (GRCm39) |
D38G |
probably benign |
Het |
Sh3bgr |
A |
C |
16: 96,007,690 (GRCm39) |
K18N |
probably damaging |
Het |
Slc28a2 |
T |
G |
2: 122,282,538 (GRCm39) |
I287M |
probably damaging |
Het |
St8sia6 |
T |
C |
2: 13,670,318 (GRCm39) |
N214S |
probably damaging |
Het |
Syt11 |
A |
G |
3: 88,669,523 (GRCm39) |
I123T |
probably benign |
Het |
Tcerg1l |
A |
T |
7: 137,861,568 (GRCm39) |
I387N |
probably damaging |
Het |
Tgm4 |
A |
G |
9: 122,880,519 (GRCm39) |
K307E |
possibly damaging |
Het |
Tmem177 |
T |
C |
1: 119,837,791 (GRCm39) |
D296G |
probably damaging |
Het |
Tmem270 |
C |
T |
5: 134,930,763 (GRCm39) |
|
probably benign |
Het |
Tnrc6b |
G |
T |
15: 80,764,745 (GRCm39) |
G749V |
possibly damaging |
Het |
Trp63 |
C |
A |
16: 25,639,135 (GRCm39) |
|
probably benign |
Het |
Ugt1a8 |
T |
C |
1: 88,015,617 (GRCm39) |
L10P |
probably benign |
Het |
Vmn2r107 |
A |
T |
17: 20,596,009 (GRCm39) |
K854M |
probably damaging |
Het |
Vmn2r45 |
T |
C |
7: 8,484,467 (GRCm39) |
N446S |
probably damaging |
Het |
Vps13c |
A |
T |
9: 67,820,486 (GRCm39) |
|
probably null |
Het |
Wdr91 |
G |
A |
6: 34,865,998 (GRCm39) |
P518L |
probably benign |
Het |
Yap1 |
G |
A |
9: 7,934,742 (GRCm39) |
|
probably benign |
Het |
Zfp282 |
A |
C |
6: 47,874,770 (GRCm39) |
D325A |
probably damaging |
Het |
|
Other mutations in Tfg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01404:Tfg
|
APN |
16 |
56,514,856 (GRCm39) |
splice site |
probably benign |
|
IGL01548:Tfg
|
APN |
16 |
56,521,465 (GRCm39) |
missense |
probably damaging |
1.00 |
trafalgar
|
UTSW |
16 |
56,532,997 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0003:Tfg
|
UTSW |
16 |
56,511,351 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0003:Tfg
|
UTSW |
16 |
56,511,351 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0036:Tfg
|
UTSW |
16 |
56,511,358 (GRCm39) |
missense |
probably benign |
0.18 |
R1730:Tfg
|
UTSW |
16 |
56,533,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R2025:Tfg
|
UTSW |
16 |
56,525,988 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4629:Tfg
|
UTSW |
16 |
56,533,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R4676:Tfg
|
UTSW |
16 |
56,514,854 (GRCm39) |
splice site |
probably null |
|
R4879:Tfg
|
UTSW |
16 |
56,521,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4916:Tfg
|
UTSW |
16 |
56,514,759 (GRCm39) |
splice site |
probably null |
|
R5237:Tfg
|
UTSW |
16 |
56,533,071 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5568:Tfg
|
UTSW |
16 |
56,521,450 (GRCm39) |
missense |
probably benign |
0.14 |
R5698:Tfg
|
UTSW |
16 |
56,521,467 (GRCm39) |
missense |
probably damaging |
0.98 |
R5887:Tfg
|
UTSW |
16 |
56,514,779 (GRCm39) |
nonsense |
probably null |
|
R7213:Tfg
|
UTSW |
16 |
56,521,516 (GRCm39) |
missense |
probably benign |
0.03 |
R7392:Tfg
|
UTSW |
16 |
56,532,972 (GRCm39) |
critical splice donor site |
probably null |
|
R7514:Tfg
|
UTSW |
16 |
56,525,972 (GRCm39) |
critical splice donor site |
probably null |
|
R7632:Tfg
|
UTSW |
16 |
56,532,997 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8304:Tfg
|
UTSW |
16 |
56,521,581 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9254:Tfg
|
UTSW |
16 |
56,526,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R9432:Tfg
|
UTSW |
16 |
56,524,868 (GRCm39) |
nonsense |
probably null |
|
|