Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd8 |
T |
A |
8: 71,914,359 (GRCm39) |
N90Y |
probably damaging |
Het |
Alkal1 |
T |
C |
1: 6,459,670 (GRCm39) |
V82A |
probably damaging |
Het |
Ascc3 |
T |
C |
10: 50,624,932 (GRCm39) |
S1607P |
probably benign |
Het |
Ccny |
A |
T |
18: 9,345,427 (GRCm39) |
L149H |
probably damaging |
Het |
Clptm1 |
T |
C |
7: 19,369,762 (GRCm39) |
N383D |
possibly damaging |
Het |
Clrn2 |
T |
A |
5: 45,621,074 (GRCm39) |
M156K |
probably benign |
Het |
Coro2b |
T |
A |
9: 62,333,910 (GRCm39) |
H328L |
probably benign |
Het |
Echs1 |
A |
T |
7: 139,688,055 (GRCm39) |
M250K |
probably benign |
Het |
Ecsit |
A |
G |
9: 21,985,981 (GRCm39) |
V145A |
possibly damaging |
Het |
Fas |
G |
A |
19: 34,293,969 (GRCm39) |
G108D |
probably damaging |
Het |
Folh1 |
A |
G |
7: 86,424,964 (GRCm39) |
W2R |
probably damaging |
Het |
Gba1 |
C |
T |
3: 89,111,388 (GRCm39) |
P51L |
probably benign |
Het |
Grik2 |
C |
T |
10: 49,008,776 (GRCm39) |
M770I |
probably benign |
Het |
Hcst |
T |
C |
7: 30,117,250 (GRCm39) |
N74S |
probably damaging |
Het |
Hdac9 |
T |
A |
12: 34,481,990 (GRCm39) |
|
probably null |
Het |
Htt |
T |
C |
5: 34,982,239 (GRCm39) |
V941A |
probably benign |
Het |
Naip5 |
A |
G |
13: 100,351,171 (GRCm39) |
V1279A |
possibly damaging |
Het |
Neb |
T |
A |
2: 52,170,624 (GRCm39) |
M1683L |
probably benign |
Het |
Nudt21 |
C |
T |
8: 94,746,282 (GRCm39) |
V139I |
probably benign |
Het |
Or5e1 |
T |
C |
7: 108,354,236 (GRCm39) |
Y58H |
probably damaging |
Het |
Pex2 |
A |
G |
3: 5,626,191 (GRCm39) |
F206S |
probably damaging |
Het |
Plek2 |
C |
A |
12: 78,943,065 (GRCm39) |
R77L |
probably benign |
Het |
Ppfia1 |
A |
T |
7: 144,059,942 (GRCm39) |
D623E |
possibly damaging |
Het |
Ppm1l |
T |
A |
3: 69,460,374 (GRCm39) |
I317N |
probably damaging |
Het |
Prkacb |
T |
A |
3: 146,461,479 (GRCm39) |
T36S |
probably damaging |
Het |
Sphkap |
T |
A |
1: 83,256,544 (GRCm39) |
I115F |
probably damaging |
Het |
Sprtn |
G |
T |
8: 125,625,873 (GRCm39) |
E95* |
probably null |
Het |
St3gal1 |
A |
G |
15: 66,983,195 (GRCm39) |
V187A |
possibly damaging |
Het |
Tcap |
C |
A |
11: 98,275,003 (GRCm39) |
Q46K |
probably benign |
Het |
Thada |
T |
C |
17: 84,751,339 (GRCm39) |
I546V |
possibly damaging |
Het |
Tubal3 |
T |
A |
13: 3,983,107 (GRCm39) |
S296T |
probably benign |
Het |
Ube3a |
A |
G |
7: 58,936,772 (GRCm39) |
N683D |
probably damaging |
Het |
Vmn2r82 |
T |
G |
10: 79,214,871 (GRCm39) |
L285V |
possibly damaging |
Het |
Zfp871 |
T |
C |
17: 32,994,647 (GRCm39) |
D157G |
possibly damaging |
Het |
|
Other mutations in Hsfy2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1618:Hsfy2
|
UTSW |
1 |
56,676,388 (GRCm39) |
missense |
probably benign |
0.41 |
R1670:Hsfy2
|
UTSW |
1 |
56,675,548 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1687:Hsfy2
|
UTSW |
1 |
56,676,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R1843:Hsfy2
|
UTSW |
1 |
56,675,791 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1954:Hsfy2
|
UTSW |
1 |
56,676,342 (GRCm39) |
missense |
probably benign |
0.01 |
R2031:Hsfy2
|
UTSW |
1 |
56,675,476 (GRCm39) |
missense |
probably benign |
0.18 |
R3117:Hsfy2
|
UTSW |
1 |
56,676,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R3778:Hsfy2
|
UTSW |
1 |
56,675,847 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4760:Hsfy2
|
UTSW |
1 |
56,676,349 (GRCm39) |
missense |
probably benign |
|
R5065:Hsfy2
|
UTSW |
1 |
56,675,626 (GRCm39) |
nonsense |
probably null |
|
R5192:Hsfy2
|
UTSW |
1 |
56,675,894 (GRCm39) |
missense |
probably benign |
0.41 |
R5378:Hsfy2
|
UTSW |
1 |
56,675,827 (GRCm39) |
missense |
probably benign |
0.41 |
R6296:Hsfy2
|
UTSW |
1 |
56,676,351 (GRCm39) |
missense |
probably benign |
0.00 |
R6813:Hsfy2
|
UTSW |
1 |
56,675,461 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6996:Hsfy2
|
UTSW |
1 |
56,675,569 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7486:Hsfy2
|
UTSW |
1 |
56,676,130 (GRCm39) |
nonsense |
probably null |
|
R7609:Hsfy2
|
UTSW |
1 |
56,676,310 (GRCm39) |
missense |
probably benign |
0.37 |
R7819:Hsfy2
|
UTSW |
1 |
56,675,418 (GRCm39) |
missense |
probably benign |
|
R8208:Hsfy2
|
UTSW |
1 |
56,676,310 (GRCm39) |
missense |
probably benign |
0.00 |
R9058:Hsfy2
|
UTSW |
1 |
56,676,504 (GRCm39) |
missense |
probably benign |
0.00 |
R9129:Hsfy2
|
UTSW |
1 |
56,675,752 (GRCm39) |
missense |
probably benign |
0.41 |
|