Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alkbh8 |
T |
A |
9: 3,385,343 |
I580N |
probably damaging |
Het |
Ankrd35 |
C |
T |
3: 96,684,900 |
T834M |
probably damaging |
Het |
Astn2 |
C |
T |
4: 65,644,866 |
V893I |
possibly damaging |
Het |
B4galt1 |
A |
G |
4: 40,823,501 |
Y197H |
probably benign |
Het |
Brdt |
T |
C |
5: 107,359,933 |
S676P |
possibly damaging |
Het |
Chrdl2 |
T |
C |
7: 100,029,250 |
V343A |
possibly damaging |
Het |
Clcn3 |
A |
T |
8: 60,941,399 |
M59K |
probably benign |
Het |
Cpne4 |
A |
T |
9: 105,032,791 |
N529I |
probably damaging |
Het |
Crcp |
G |
T |
5: 130,037,870 |
K32N |
possibly damaging |
Het |
Ddx54 |
C |
T |
5: 120,627,203 |
R846C |
probably damaging |
Het |
Dennd6a |
T |
C |
14: 26,599,657 |
S118P |
possibly damaging |
Het |
Egr3 |
A |
G |
14: 70,079,202 |
Y116C |
probably damaging |
Het |
Fbxw25 |
A |
G |
9: 109,649,594 |
|
probably null |
Het |
Focad |
T |
G |
4: 88,182,616 |
I313M |
probably damaging |
Het |
Gm10272 |
C |
T |
10: 77,706,945 |
P107L |
probably benign |
Het |
Gpr26 |
A |
C |
7: 131,966,973 |
I16L |
probably benign |
Het |
Gpr39 |
C |
A |
1: 125,677,542 |
T69K |
probably damaging |
Het |
Hacl1 |
C |
T |
14: 31,634,227 |
G97S |
probably damaging |
Het |
Idh3b |
A |
C |
2: 130,281,758 |
D136E |
probably damaging |
Het |
Irf6 |
G |
A |
1: 193,167,732 |
V321M |
probably damaging |
Het |
Klrg2 |
T |
A |
6: 38,636,571 |
T166S |
probably damaging |
Het |
Lnx2 |
T |
C |
5: 147,019,043 |
I648V |
probably damaging |
Het |
Mecr |
A |
G |
4: 131,860,866 |
|
probably null |
Het |
Mnat1 |
T |
A |
12: 73,188,191 |
S205T |
probably benign |
Het |
Mpnd |
G |
A |
17: 56,011,097 |
G204D |
probably benign |
Het |
Myh7 |
C |
T |
14: 54,983,662 |
E935K |
possibly damaging |
Het |
Nid1 |
G |
T |
13: 13,499,733 |
R899L |
possibly damaging |
Het |
Nisch |
C |
T |
14: 31,176,695 |
W664* |
probably null |
Het |
Nudt6 |
C |
T |
3: 37,412,380 |
V157I |
possibly damaging |
Het |
Olfr1156 |
T |
C |
2: 87,949,880 |
M118V |
probably damaging |
Het |
Olfr573-ps1 |
A |
C |
7: 102,942,151 |
L142R |
possibly damaging |
Het |
Olfr949-ps1 |
A |
T |
9: 39,364,879 |
M107L |
unknown |
Het |
Onecut2 |
T |
A |
18: 64,340,975 |
M180K |
possibly damaging |
Het |
Parg |
T |
A |
14: 32,217,662 |
D548E |
possibly damaging |
Het |
Pclo |
GTCTAT |
GTCTATTCTAT |
5: 14,714,190 |
|
probably null |
Het |
Phf11d |
A |
G |
14: 59,359,580 |
Y57H |
probably damaging |
Het |
Prkaca |
T |
C |
8: 83,986,895 |
V99A |
probably benign |
Het |
Rnf144b |
T |
A |
13: 47,239,811 |
C209S |
probably damaging |
Het |
Scly |
G |
A |
1: 91,300,641 |
|
probably null |
Het |
Selplg |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
5: 113,819,695 |
|
probably benign |
Het |
Sphkap |
T |
C |
1: 83,277,412 |
Y872C |
probably benign |
Het |
Ssh1 |
C |
T |
5: 113,961,349 |
|
probably null |
Het |
Strap |
T |
G |
6: 137,739,809 |
L129V |
possibly damaging |
Het |
Sympk |
T |
C |
7: 19,034,439 |
I111T |
possibly damaging |
Het |
Tprn |
C |
A |
2: 25,264,012 |
A442E |
probably damaging |
Het |
Tsen34 |
T |
C |
7: 3,694,708 |
L36P |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,407,810 |
F818L |
probably damaging |
Het |
Uggt1 |
T |
C |
1: 36,208,034 |
Y294C |
probably damaging |
Het |
Usp20 |
A |
G |
2: 31,020,894 |
K862E |
probably benign |
Het |
Vmn1r201 |
A |
T |
13: 22,474,786 |
I57F |
probably damaging |
Het |
|