Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
A |
G |
7: 78,749,447 (GRCm39) |
D1406G |
possibly damaging |
Het |
Aebp2 |
T |
C |
6: 140,579,624 (GRCm39) |
|
probably null |
Het |
Ap5m1 |
T |
A |
14: 49,321,339 (GRCm39) |
Y49* |
probably null |
Het |
Atp8b5 |
T |
C |
4: 43,361,953 (GRCm39) |
|
probably benign |
Het |
Baz1a |
A |
G |
12: 54,970,224 (GRCm39) |
S518P |
probably damaging |
Het |
Ces1c |
T |
A |
8: 93,830,821 (GRCm39) |
D445V |
probably benign |
Het |
Ctnnbl1 |
C |
T |
2: 157,713,106 (GRCm39) |
H464Y |
probably benign |
Het |
Cyp2j6 |
T |
C |
4: 96,420,018 (GRCm39) |
K238E |
probably benign |
Het |
Gdf10 |
G |
A |
14: 33,646,148 (GRCm39) |
R99H |
probably damaging |
Het |
Gm4779 |
G |
A |
X: 100,836,568 (GRCm39) |
P116L |
possibly damaging |
Het |
Gucy2g |
A |
G |
19: 55,198,708 (GRCm39) |
S812P |
probably damaging |
Het |
Irgm1 |
A |
T |
11: 48,757,417 (GRCm39) |
Y131* |
probably null |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Myh7b |
A |
G |
2: 155,474,175 (GRCm39) |
N1630S |
probably benign |
Het |
Myo5a |
T |
C |
9: 75,023,484 (GRCm39) |
I15T |
probably damaging |
Het |
Naip6 |
C |
T |
13: 100,437,108 (GRCm39) |
A472T |
probably benign |
Het |
Nme6 |
A |
G |
9: 109,671,159 (GRCm39) |
|
probably benign |
Het |
Or11g25 |
T |
A |
14: 50,723,065 (GRCm39) |
I50N |
probably damaging |
Het |
Or5al6 |
T |
C |
2: 85,976,908 (GRCm39) |
T57A |
probably damaging |
Het |
Plch2 |
T |
G |
4: 155,075,224 (GRCm39) |
M797L |
probably benign |
Het |
Plscr2 |
G |
T |
9: 92,172,724 (GRCm39) |
E128* |
probably null |
Het |
Plxna2 |
T |
A |
1: 194,480,039 (GRCm39) |
D1403E |
probably damaging |
Het |
Pou6f2 |
T |
C |
13: 18,556,552 (GRCm39) |
T25A |
unknown |
Het |
Psmb11 |
T |
C |
14: 54,862,800 (GRCm39) |
V6A |
possibly damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Ptprd |
T |
G |
4: 76,025,561 (GRCm39) |
S546R |
probably benign |
Het |
Rbp3 |
A |
G |
14: 33,676,411 (GRCm39) |
N120D |
probably benign |
Het |
Skint1 |
C |
A |
4: 111,878,527 (GRCm39) |
P153H |
possibly damaging |
Het |
Slc15a4 |
A |
G |
5: 127,681,600 (GRCm39) |
|
probably null |
Het |
Tmem201 |
A |
G |
4: 149,806,902 (GRCm39) |
|
probably benign |
Het |
Ube2v1 |
T |
C |
2: 167,452,256 (GRCm39) |
N89D |
probably damaging |
Het |
Zfp282 |
A |
T |
6: 47,874,866 (GRCm39) |
|
probably null |
Het |
Zfp560 |
C |
A |
9: 20,260,240 (GRCm39) |
M207I |
probably benign |
Het |
Zfp697 |
T |
C |
3: 98,335,617 (GRCm39) |
Y461H |
probably damaging |
Het |
|
Other mutations in Ifit3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
Galilee
|
UTSW |
19 |
34,588,925 (GRCm39) |
missense |
probably benign |
|
negev
|
UTSW |
19 |
34,588,860 (GRCm39) |
missense |
probably benign |
0.14 |
R1528:Ifit3b
|
UTSW |
19 |
34,589,072 (GRCm39) |
missense |
probably benign |
0.05 |
R1996:Ifit3b
|
UTSW |
19 |
34,588,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R2680:Ifit3b
|
UTSW |
19 |
34,589,705 (GRCm39) |
missense |
probably benign |
0.01 |
R4395:Ifit3b
|
UTSW |
19 |
34,589,951 (GRCm39) |
nonsense |
probably null |
|
R4719:Ifit3b
|
UTSW |
19 |
34,590,030 (GRCm39) |
missense |
probably damaging |
0.96 |
R4726:Ifit3b
|
UTSW |
19 |
34,588,860 (GRCm39) |
missense |
probably benign |
0.14 |
R5094:Ifit3b
|
UTSW |
19 |
34,589,948 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5958:Ifit3b
|
UTSW |
19 |
34,589,142 (GRCm39) |
missense |
probably benign |
0.02 |
R5987:Ifit3b
|
UTSW |
19 |
34,589,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R6381:Ifit3b
|
UTSW |
19 |
34,589,871 (GRCm39) |
missense |
probably benign |
0.00 |
R6614:Ifit3b
|
UTSW |
19 |
34,588,919 (GRCm39) |
missense |
probably benign |
0.01 |
R6662:Ifit3b
|
UTSW |
19 |
34,589,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R6804:Ifit3b
|
UTSW |
19 |
34,588,947 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6847:Ifit3b
|
UTSW |
19 |
34,588,925 (GRCm39) |
missense |
probably benign |
|
R7685:Ifit3b
|
UTSW |
19 |
34,589,955 (GRCm39) |
missense |
possibly damaging |
0.94 |
|