Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438A13Rik |
G |
T |
3: 37,006,984 |
|
probably null |
Het |
9930022D16Rik |
T |
C |
11: 109,417,911 |
|
probably benign |
Het |
Aatk |
T |
C |
11: 120,012,275 |
S375G |
probably benign |
Het |
Abcg8 |
T |
C |
17: 84,691,995 |
M173T |
probably benign |
Het |
B3galt2 |
A |
C |
1: 143,646,757 |
R210S |
probably benign |
Het |
Capn5 |
C |
T |
7: 98,135,764 |
A168T |
probably damaging |
Het |
Cbx7 |
C |
T |
15: 79,930,628 |
G24D |
probably damaging |
Het |
Ccdc7a |
A |
T |
8: 129,061,618 |
S77T |
probably benign |
Het |
Cd200r2 |
T |
A |
16: 44,909,469 |
|
probably benign |
Het |
Cdh11 |
T |
C |
8: 102,679,745 |
H32R |
probably benign |
Het |
Chdh |
A |
T |
14: 30,031,332 |
N66I |
probably benign |
Het |
Clca3a2 |
G |
A |
3: 144,813,627 |
Q263* |
probably null |
Het |
Dcc |
T |
C |
18: 71,809,090 |
I319V |
probably benign |
Het |
Depdc5 |
G |
T |
5: 32,893,401 |
M170I |
probably damaging |
Het |
Dopey2 |
T |
A |
16: 93,810,229 |
L2140Q |
probably benign |
Het |
Frem3 |
G |
A |
8: 80,615,134 |
G1352E |
probably benign |
Het |
Fsd1l |
T |
A |
4: 53,694,742 |
C389S |
probably damaging |
Het |
Grin2c |
C |
T |
11: 115,258,110 |
A221T |
possibly damaging |
Het |
Gstz1 |
C |
A |
12: 87,163,801 |
P153T |
probably damaging |
Het |
Itgb2 |
T |
C |
10: 77,542,403 |
S22P |
possibly damaging |
Het |
Krt87 |
G |
T |
15: 101,438,431 |
Q114K |
possibly damaging |
Het |
Krtap5-4 |
A |
C |
7: 142,303,910 |
S106R |
unknown |
Het |
Lats1 |
T |
C |
10: 7,705,671 |
V740A |
probably damaging |
Het |
Mcm9 |
C |
A |
10: 53,629,945 |
G78C |
probably damaging |
Het |
Mn1 |
G |
A |
5: 111,421,547 |
E1128K |
possibly damaging |
Het |
Myo1f |
G |
A |
17: 33,593,003 |
R592H |
possibly damaging |
Het |
Nfat5 |
G |
T |
8: 107,367,514 |
A277S |
probably damaging |
Het |
Nfkbia |
T |
A |
12: 55,490,542 |
Y254F |
probably damaging |
Het |
Nr3c2 |
A |
T |
8: 76,909,214 |
N315Y |
probably damaging |
Het |
Otof |
T |
C |
5: 30,405,216 |
M258V |
probably benign |
Het |
Panx3 |
C |
T |
9: 37,661,471 |
C261Y |
probably damaging |
Het |
Pdia2 |
C |
A |
17: 26,198,922 |
G38W |
probably damaging |
Het |
Psg19 |
G |
T |
7: 18,794,046 |
Y257* |
probably null |
Het |
Ptpre |
A |
T |
7: 135,678,325 |
K586* |
probably null |
Het |
Reps1 |
A |
G |
10: 18,124,895 |
R752G |
probably damaging |
Het |
Rpgrip1 |
T |
A |
14: 52,131,176 |
D277E |
possibly damaging |
Het |
Rpl21-ps6 |
A |
G |
17: 55,915,671 |
|
noncoding transcript |
Het |
Serpinf2 |
T |
A |
11: 75,436,507 |
E198V |
possibly damaging |
Het |
Sh3tc1 |
A |
G |
5: 35,703,375 |
L1046P |
probably damaging |
Het |
Snw1 |
T |
C |
12: 87,450,941 |
E426G |
probably benign |
Het |
Sord |
T |
A |
2: 122,264,083 |
N317K |
probably benign |
Het |
Tdrd3 |
C |
A |
14: 87,472,182 |
T94K |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,856,821 |
E736* |
probably null |
Het |
Usp32 |
A |
G |
11: 85,039,265 |
V562A |
probably damaging |
Het |
Vmn1r169 |
T |
G |
7: 23,577,186 |
M1R |
probably null |
Het |
Vmn2r3 |
C |
T |
3: 64,259,883 |
C609Y |
probably damaging |
Het |
Vmn2r69 |
T |
C |
7: 85,406,531 |
T800A |
probably benign |
Het |
Vmn2r72 |
G |
A |
7: 85,738,334 |
T674I |
probably benign |
Het |
Zfp160 |
T |
A |
17: 21,020,826 |
M52K |
possibly damaging |
Het |
Zfp607a |
T |
A |
7: 27,878,617 |
C371S |
probably damaging |
Het |
|