Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1300017J02Rik |
A |
C |
9: 103,263,057 |
Y488D |
possibly damaging |
Het |
Arhgap5 |
T |
C |
12: 52,519,623 |
F1126L |
probably benign |
Het |
Arhgef11 |
G |
T |
3: 87,735,896 |
A1472S |
probably benign |
Het |
Armc9 |
G |
A |
1: 86,257,270 |
R681K |
probably benign |
Het |
Atxn2 |
T |
A |
5: 121,747,421 |
|
probably null |
Het |
B3gnt6 |
C |
A |
7: 98,194,743 |
L3F |
probably benign |
Het |
Cand2 |
A |
G |
6: 115,792,391 |
T721A |
probably damaging |
Het |
Cntn2 |
A |
T |
1: 132,522,386 |
M590K |
probably benign |
Het |
Cntn4 |
A |
T |
6: 106,667,457 |
D622V |
probably damaging |
Het |
Des |
T |
G |
1: 75,360,628 |
S71A |
probably benign |
Het |
Dnah5 |
C |
A |
15: 28,263,599 |
R827S |
probably damaging |
Het |
Dstn |
G |
A |
2: 143,938,535 |
G52S |
probably benign |
Het |
Eln |
T |
A |
5: 134,707,981 |
R704* |
probably null |
Het |
Fezf2 |
T |
A |
14: 12,342,607 |
K419N |
probably damaging |
Het |
Gm9268 |
A |
G |
7: 43,024,718 |
Y400C |
probably damaging |
Het |
Grin3a |
G |
A |
4: 49,665,501 |
R1045* |
probably null |
Het |
Herc2 |
T |
A |
7: 56,206,578 |
H3921Q |
probably damaging |
Het |
Hs3st2 |
A |
G |
7: 121,501,032 |
E367G |
possibly damaging |
Het |
Hydin |
G |
A |
8: 110,598,984 |
R4675H |
probably damaging |
Het |
Irf2bp1 |
T |
C |
7: 19,004,734 |
S100P |
possibly damaging |
Het |
Itga10 |
A |
G |
3: 96,652,530 |
I500M |
possibly damaging |
Het |
Kcnt2 |
T |
C |
1: 140,507,762 |
V496A |
probably damaging |
Het |
Mansc1 |
T |
C |
6: 134,610,707 |
D169G |
probably benign |
Het |
Mdn1 |
T |
A |
4: 32,741,835 |
S3869T |
probably damaging |
Het |
Mrgprb4 |
G |
A |
7: 48,199,120 |
T20I |
probably benign |
Het |
Nek4 |
A |
G |
14: 30,957,296 |
E198G |
probably damaging |
Het |
Olfr1120 |
G |
T |
2: 87,358,265 |
V274L |
probably benign |
Het |
Olfr1131 |
C |
A |
2: 87,629,282 |
T273K |
possibly damaging |
Het |
Olfr1380 |
G |
A |
11: 49,564,302 |
C127Y |
probably damaging |
Het |
Ppfia4 |
A |
T |
1: 134,319,372 |
F537I |
probably benign |
Het |
Rarb |
A |
G |
14: 16,434,293 |
V295A |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 29,040,679 |
S3941P |
probably damaging |
Het |
Scnn1b |
A |
G |
7: 121,912,475 |
N370S |
probably damaging |
Het |
Stard9 |
C |
A |
2: 120,673,636 |
S221R |
probably damaging |
Het |
Sv2c |
C |
T |
13: 95,989,811 |
G311D |
probably damaging |
Het |
Tas2r109 |
T |
C |
6: 132,980,893 |
I25V |
probably benign |
Het |
Tbcel |
A |
C |
9: 42,437,157 |
I305S |
probably damaging |
Het |
Tmem35b |
A |
G |
4: 127,126,197 |
|
probably null |
Het |
Tmem38b |
T |
C |
4: 53,840,765 |
L60S |
probably damaging |
Het |
Tmtc4 |
A |
G |
14: 122,945,554 |
I244T |
possibly damaging |
Het |
Usp9y |
C |
A |
Y: 1,394,002 |
C576F |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,704,953 |
N629K |
possibly damaging |
Het |
Vmn2r22 |
T |
C |
6: 123,637,404 |
Y409C |
probably damaging |
Het |
|