Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700025F22Rik |
T |
A |
19: 11,163,447 |
M3L |
probably benign |
Het |
Arhgef4 |
G |
A |
1: 34,723,477 |
A605T |
unknown |
Het |
Atp13a3 |
A |
G |
16: 30,332,285 |
V1069A |
possibly damaging |
Het |
Atp1a2 |
C |
G |
1: 172,289,336 |
R238P |
probably damaging |
Het |
Baz2b |
A |
G |
2: 59,906,948 |
S1877P |
probably damaging |
Het |
Ccdc114 |
A |
G |
7: 45,941,710 |
E203G |
probably damaging |
Het |
Ccdc27 |
A |
T |
4: 154,036,191 |
S383T |
probably benign |
Het |
Cr1l |
A |
G |
1: 195,111,122 |
V377A |
probably benign |
Het |
Dazap1 |
A |
G |
10: 80,277,660 |
E130G |
probably benign |
Het |
Dchs1 |
G |
T |
7: 105,764,938 |
A890E |
probably benign |
Het |
Dock10 |
G |
A |
1: 80,505,176 |
T2143I |
probably benign |
Het |
Eif3j1 |
A |
G |
2: 122,041,178 |
D60G |
probably benign |
Het |
Enah |
A |
G |
1: 181,918,571 |
S382P |
probably damaging |
Het |
Fam171b |
A |
T |
2: 83,879,264 |
K427* |
probably null |
Het |
Fmn2 |
A |
T |
1: 174,612,553 |
I1179L |
possibly damaging |
Het |
Focad |
C |
T |
4: 88,401,068 |
R1505* |
probably null |
Het |
Frem1 |
T |
C |
4: 82,983,337 |
T985A |
probably benign |
Het |
Gm3404 |
A |
T |
5: 146,528,107 |
Q219L |
possibly damaging |
Het |
Gm5592 |
A |
C |
7: 41,286,535 |
S154R |
probably damaging |
Het |
Gpn3 |
C |
T |
5: 122,372,575 |
|
probably benign |
Het |
Gpr158 |
A |
G |
2: 21,810,554 |
E586G |
probably damaging |
Het |
Gstp2 |
A |
T |
19: 4,040,499 |
I162N |
probably benign |
Het |
Lin7a |
T |
A |
10: 107,380,215 |
|
probably null |
Het |
Loxl4 |
G |
A |
19: 42,595,378 |
L745F |
probably benign |
Het |
Mybpc1 |
A |
G |
10: 88,568,619 |
I172T |
possibly damaging |
Het |
Nalcn |
A |
G |
14: 123,409,749 |
W571R |
possibly damaging |
Het |
Nkx2-5 |
G |
C |
17: 26,841,121 |
P79A |
probably benign |
Het |
Nufip2 |
A |
G |
11: 77,691,661 |
T134A |
probably benign |
Het |
Olfr1042 |
C |
T |
2: 86,159,456 |
V305I |
probably benign |
Het |
Olfr1463 |
A |
G |
19: 13,235,104 |
M285V |
possibly damaging |
Het |
Phkb |
A |
G |
8: 86,018,542 |
D616G |
probably benign |
Het |
Plch1 |
C |
T |
3: 63,781,390 |
W131* |
probably null |
Het |
Prl7b1 |
A |
T |
13: 27,602,895 |
|
probably null |
Het |
Prop1 |
G |
A |
11: 50,952,199 |
P54S |
probably benign |
Het |
Ptcd3 |
C |
T |
6: 71,885,327 |
V509I |
probably benign |
Het |
Ptprg |
T |
A |
14: 12,226,314 |
D527E |
probably damaging |
Het |
Rapgef2 |
C |
T |
3: 79,079,132 |
V1182I |
probably benign |
Het |
Rfx7 |
C |
A |
9: 72,618,414 |
P962Q |
probably damaging |
Het |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,579,908 |
|
probably benign |
Homo |
Slc38a9 |
A |
G |
13: 112,726,100 |
I444M |
probably benign |
Het |
Sorbs1 |
T |
C |
19: 40,321,819 |
T492A |
probably damaging |
Het |
Synj1 |
A |
T |
16: 90,938,630 |
S1478R |
probably benign |
Het |
Tnn |
T |
A |
1: 160,145,204 |
N276I |
probably damaging |
Het |
Trbv19 |
G |
A |
6: 41,178,758 |
G21D |
probably damaging |
Het |
Ube2o |
A |
T |
11: 116,539,359 |
D1184E |
probably benign |
Het |
Vmn1r181 |
G |
A |
7: 23,984,758 |
R216Q |
probably benign |
Het |
Vmn2r108 |
A |
T |
17: 20,471,715 |
L182* |
probably null |
Het |
Vmn2r15 |
A |
G |
5: 109,286,271 |
*856R |
probably null |
Het |
Vmn2r70 |
G |
A |
7: 85,558,879 |
H797Y |
probably benign |
Het |
Zfp11 |
C |
T |
5: 129,656,523 |
A625T |
possibly damaging |
Het |
|