Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
A |
T |
5: 138,564,192 |
Y96N |
probably damaging |
Het |
Abca15 |
C |
T |
7: 120,402,979 |
Q1572* |
probably null |
Het |
Ajuba |
T |
C |
14: 54,569,526 |
R490G |
probably damaging |
Het |
Akap6 |
T |
A |
12: 53,139,671 |
N1289K |
probably damaging |
Het |
Ankfy1 |
G |
A |
11: 72,714,484 |
|
probably null |
Het |
Aph1c |
A |
G |
9: 66,833,321 |
F41S |
probably damaging |
Het |
Arhgap21 |
A |
G |
2: 20,887,137 |
V161A |
probably damaging |
Het |
Arhgef18 |
T |
C |
8: 3,450,317 |
I541T |
possibly damaging |
Het |
Arhgef40 |
T |
C |
14: 51,990,171 |
V458A |
possibly damaging |
Het |
Atg14 |
T |
C |
14: 47,551,345 |
K184E |
probably benign |
Het |
Casp8 |
T |
C |
1: 58,844,770 |
V432A |
probably damaging |
Het |
Ccar2 |
T |
C |
14: 70,151,091 |
T169A |
possibly damaging |
Het |
Cfap58 |
G |
A |
19: 47,975,555 |
V541M |
possibly damaging |
Het |
Coro2b |
T |
C |
9: 62,426,185 |
E376G |
possibly damaging |
Het |
Dnah11 |
T |
C |
12: 117,916,791 |
T3865A |
probably damaging |
Het |
Dync2h1 |
T |
C |
9: 7,134,360 |
E1549G |
probably benign |
Het |
Ercc6l2 |
T |
C |
13: 63,872,168 |
|
probably benign |
Het |
Fam160b2 |
A |
C |
14: 70,586,878 |
V473G |
probably damaging |
Het |
Fbxo32 |
G |
T |
15: 58,192,333 |
T135K |
possibly damaging |
Het |
Fras1 |
A |
T |
5: 96,714,376 |
I2205F |
possibly damaging |
Het |
Gm26678 |
T |
C |
3: 54,633,083 |
|
noncoding transcript |
Het |
Gm5108 |
C |
A |
5: 67,975,153 |
T55K |
unknown |
Het |
Gpa33 |
A |
T |
1: 166,146,771 |
D59V |
probably damaging |
Het |
Gpn2 |
T |
A |
4: 133,584,705 |
Y83N |
probably damaging |
Het |
Gzf1 |
C |
T |
2: 148,686,533 |
P460S |
possibly damaging |
Het |
Ifi203 |
A |
T |
1: 173,936,533 |
S124R |
possibly damaging |
Het |
Impg1 |
A |
G |
9: 80,345,329 |
L523P |
probably damaging |
Het |
Ldlrap1 |
T |
A |
4: 134,757,338 |
|
probably null |
Het |
Madd |
T |
C |
2: 91,178,236 |
E107G |
probably benign |
Het |
Med12l |
T |
G |
3: 59,257,223 |
|
probably null |
Het |
Nxpe4 |
A |
T |
9: 48,398,837 |
T467S |
probably damaging |
Het |
Olfr658 |
A |
G |
7: 104,644,988 |
V126A |
probably benign |
Het |
Olfr849 |
T |
A |
9: 19,441,590 |
L226I |
probably damaging |
Het |
Pam |
A |
T |
1: 97,864,394 |
V434D |
possibly damaging |
Het |
Plxnd1 |
T |
C |
6: 115,965,953 |
N1257D |
probably benign |
Het |
Prkdc |
C |
T |
16: 15,835,919 |
A3870V |
probably benign |
Het |
Ralgapa1 |
C |
T |
12: 55,640,644 |
R2019Q |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,147,663 |
C537R |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,750,725 |
D1375G |
probably benign |
Het |
Skint11 |
C |
A |
4: 114,244,659 |
Q99K |
probably benign |
Het |
Slc13a2 |
A |
G |
11: 78,403,535 |
|
probably benign |
Het |
Slc7a13 |
T |
C |
4: 19,819,070 |
F90S |
probably damaging |
Het |
Spc24 |
T |
C |
9: 21,756,202 |
|
probably null |
Het |
Stard13 |
A |
G |
5: 151,062,699 |
S331P |
probably benign |
Het |
Sult2a8 |
T |
A |
7: 14,413,683 |
I228L |
probably benign |
Het |
Tas2r140 |
A |
T |
6: 133,054,952 |
V281D |
probably damaging |
Het |
Tmem38b |
T |
C |
4: 53,840,710 |
C66R |
probably damaging |
Het |
Tshz1 |
C |
A |
18: 84,016,195 |
E29D |
probably benign |
Het |
Zfp599 |
T |
A |
9: 22,249,745 |
K375* |
probably null |
Het |
|