Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610002M06Rik |
C |
A |
X: 107,788,283 |
V180F |
possibly damaging |
Het |
Actrt1 |
T |
C |
X: 46,329,747 |
V213A |
probably benign |
Het |
Adam28 |
A |
T |
14: 68,634,803 |
|
probably benign |
Het |
Apeh |
T |
C |
9: 108,086,445 |
H557R |
probably benign |
Het |
Atmin |
T |
A |
8: 116,957,425 |
L608* |
probably null |
Het |
B3gnt5 |
A |
T |
16: 19,769,153 |
M41L |
probably benign |
Het |
Best3 |
T |
C |
10: 116,993,105 |
F97L |
possibly damaging |
Het |
Col7a1 |
G |
A |
9: 108,978,160 |
V2486M |
unknown |
Het |
Crym |
T |
C |
7: 120,199,313 |
|
probably null |
Het |
Cubn |
T |
C |
2: 13,478,057 |
|
probably null |
Het |
Eea1 |
T |
C |
10: 96,042,212 |
|
probably benign |
Het |
Emc1 |
C |
T |
4: 139,371,593 |
|
probably benign |
Het |
Eps8 |
T |
C |
6: 137,512,145 |
|
probably benign |
Het |
Ereg |
A |
G |
5: 91,088,581 |
|
probably benign |
Het |
Faah |
G |
A |
4: 116,002,528 |
P369S |
probably benign |
Het |
Fam135a |
A |
T |
1: 24,029,168 |
N703K |
possibly damaging |
Het |
Frmpd1 |
T |
C |
4: 45,279,140 |
S622P |
probably damaging |
Het |
Gm10030 |
A |
G |
9: 111,006,773 |
|
noncoding transcript |
Het |
Gpr179 |
A |
T |
11: 97,337,608 |
S1240R |
possibly damaging |
Het |
Hax1 |
A |
T |
3: 89,997,447 |
H146Q |
possibly damaging |
Het |
Ift46 |
A |
G |
9: 44,782,148 |
N31D |
possibly damaging |
Het |
Kel |
C |
T |
6: 41,698,887 |
|
probably null |
Het |
Khk |
A |
T |
5: 30,929,560 |
I108L |
probably benign |
Het |
Morc4 |
T |
C |
X: 139,849,682 |
N375S |
probably null |
Het |
Mta3 |
A |
T |
17: 83,800,045 |
|
probably benign |
Het |
Nacc2 |
T |
C |
2: 26,062,237 |
K369R |
probably damaging |
Het |
Nkap |
T |
C |
X: 37,139,670 |
|
probably benign |
Het |
Obscn |
A |
T |
11: 59,037,792 |
L6016Q |
probably damaging |
Het |
Olfr25 |
A |
T |
9: 38,329,656 |
Q20L |
probably benign |
Het |
Olfr589 |
T |
C |
7: 103,155,201 |
E182G |
probably damaging |
Het |
Pde4c |
T |
A |
8: 70,746,595 |
L182Q |
probably damaging |
Het |
Pla2g10 |
G |
T |
16: 13,730,420 |
|
probably null |
Het |
Rap1gap2 |
T |
A |
11: 74,412,344 |
I426F |
probably damaging |
Het |
Rbm33 |
C |
A |
5: 28,391,061 |
|
probably benign |
Het |
Rnf139 |
C |
A |
15: 58,900,032 |
D635E |
probably benign |
Het |
Sar1a |
T |
C |
10: 61,684,939 |
V15A |
possibly damaging |
Het |
Scarb1 |
A |
C |
5: 125,289,702 |
S56A |
probably benign |
Het |
Scn3a |
T |
C |
2: 65,460,568 |
K1945E |
possibly damaging |
Het |
Sec62 |
G |
A |
3: 30,809,922 |
G118R |
unknown |
Het |
Sgce |
T |
A |
6: 4,689,738 |
Q356L |
probably damaging |
Het |
Slco4c1 |
A |
T |
1: 96,842,507 |
Y277* |
probably null |
Het |
Smarca4 |
C |
T |
9: 21,635,836 |
T219I |
probably benign |
Het |
Sphkap |
A |
T |
1: 83,280,503 |
I173N |
probably damaging |
Het |
Spred3 |
C |
T |
7: 29,161,572 |
C394Y |
unknown |
Het |
Stra6l |
A |
G |
4: 45,873,689 |
D283G |
probably benign |
Het |
Tipin |
A |
T |
9: 64,288,124 |
Q4L |
probably benign |
Het |
Tmprss11c |
T |
A |
5: 86,231,871 |
I380F |
probably benign |
Het |
Tymp |
T |
C |
15: 89,375,016 |
D195G |
possibly damaging |
Het |
Ugt2b34 |
T |
A |
5: 86,906,685 |
Y79F |
probably benign |
Het |
Vmn2r16 |
T |
A |
5: 109,363,714 |
S596T |
possibly damaging |
Het |
Wdhd1 |
A |
G |
14: 47,243,889 |
S1024P |
possibly damaging |
Het |
|