Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
A |
T |
9: 44,277,489 |
L469* |
probably null |
Het |
Calr3 |
T |
A |
8: 72,434,821 |
Y46F |
probably damaging |
Het |
Clcn4 |
A |
G |
7: 7,290,465 |
C491R |
probably damaging |
Het |
Col6a5 |
G |
T |
9: 105,934,321 |
D666E |
unknown |
Het |
D130052B06Rik |
G |
A |
11: 33,623,780 |
V126M |
probably damaging |
Het |
Ddx27 |
A |
G |
2: 167,027,913 |
I389M |
possibly damaging |
Het |
Dgka |
T |
C |
10: 128,733,384 |
I160V |
possibly damaging |
Het |
E430018J23Rik |
A |
G |
7: 127,392,252 |
Y188H |
probably damaging |
Het |
Enpp6 |
T |
C |
8: 47,030,532 |
S120P |
probably damaging |
Het |
Ezh1 |
A |
G |
11: 101,203,289 |
I459T |
probably benign |
Het |
Fam91a1 |
A |
G |
15: 58,453,061 |
|
probably benign |
Het |
Foxn2 |
T |
C |
17: 88,462,947 |
L74P |
probably damaging |
Het |
Fscn2 |
T |
C |
11: 120,362,499 |
V264A |
probably benign |
Het |
Gmeb2 |
G |
A |
2: 181,265,883 |
T54I |
probably damaging |
Het |
Hmcn2 |
A |
T |
2: 31,413,367 |
K3007* |
probably null |
Het |
Lgi1 |
A |
G |
19: 38,284,005 |
D84G |
probably benign |
Het |
Mier2 |
T |
C |
10: 79,547,721 |
I196V |
probably damaging |
Het |
Nipal2 |
T |
C |
15: 34,600,077 |
Y198C |
probably damaging |
Het |
Npas2 |
A |
C |
1: 39,312,996 |
S176R |
probably benign |
Het |
Olfr914 |
A |
T |
9: 38,606,938 |
I158F |
probably benign |
Het |
Pam |
A |
C |
1: 97,840,367 |
C713G |
probably damaging |
Het |
Pcdh17 |
C |
A |
14: 84,446,661 |
D189E |
probably damaging |
Het |
Pcdhb8 |
T |
A |
18: 37,356,223 |
I318N |
possibly damaging |
Het |
Pcyt2 |
A |
G |
11: 120,611,407 |
S300P |
possibly damaging |
Het |
Pkdrej |
A |
G |
15: 85,817,296 |
S1480P |
probably damaging |
Het |
Plekhd1 |
G |
A |
12: 80,719,007 |
|
probably null |
Het |
Plxna2 |
A |
T |
1: 194,762,570 |
S757C |
probably damaging |
Het |
Prkdc |
A |
T |
16: 15,651,519 |
K163* |
probably null |
Het |
Serpina3f |
A |
T |
12: 104,217,004 |
T42S |
probably damaging |
Het |
Sesn2 |
T |
C |
4: 132,493,793 |
N456D |
probably benign |
Het |
Tas2r105 |
A |
T |
6: 131,687,180 |
L95Q |
possibly damaging |
Het |
Tln1 |
A |
G |
4: 43,539,522 |
V1600A |
probably benign |
Het |
Zfp808 |
A |
G |
13: 62,173,180 |
K741R |
probably benign |
Het |
|