Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd12 |
A |
T |
2: 150,834,377 |
S353R |
probably damaging |
Het |
Ap1ar |
T |
C |
3: 127,812,779 |
|
probably null |
Het |
Asxl1 |
C |
A |
2: 153,393,425 |
N213K |
probably benign |
Het |
Cacna1e |
A |
G |
1: 154,398,568 |
V2197A |
probably damaging |
Het |
Cacna2d2 |
G |
A |
9: 107,524,135 |
E706K |
possibly damaging |
Het |
Cfap46 |
C |
T |
7: 139,653,498 |
V296I |
probably benign |
Het |
Cldn5 |
A |
G |
16: 18,777,293 |
T100A |
probably benign |
Het |
Ctnna1 |
C |
A |
18: 35,252,723 |
N802K |
possibly damaging |
Het |
Dip2c |
A |
G |
13: 9,621,882 |
T968A |
probably benign |
Het |
Dnaaf5 |
ACCCAGCACCTGGAGATCGTCC |
ACC |
5: 139,161,859 |
|
probably null |
Het |
Dnajc13 |
A |
G |
9: 104,217,728 |
M585T |
probably damaging |
Het |
Donson |
G |
T |
16: 91,683,797 |
T262K |
possibly damaging |
Het |
E2f3 |
T |
A |
13: 29,985,804 |
|
probably benign |
Het |
Fam110c |
A |
G |
12: 31,075,179 |
E380G |
possibly damaging |
Het |
Gbp9 |
T |
G |
5: 105,094,161 |
T177P |
probably damaging |
Het |
Gins3 |
C |
T |
8: 95,638,018 |
A132V |
probably benign |
Het |
Glra3 |
T |
A |
8: 56,125,310 |
Y467* |
probably null |
Het |
Gm12394 |
T |
A |
4: 42,793,223 |
H303L |
probably benign |
Het |
Gm7138 |
A |
G |
10: 77,776,610 |
|
probably benign |
Het |
Golim4 |
T |
C |
3: 75,895,001 |
E328G |
probably damaging |
Het |
Habp2 |
T |
A |
19: 56,312,956 |
C270* |
probably null |
Het |
Hecw2 |
A |
G |
1: 53,925,308 |
|
probably null |
Het |
Hmcn1 |
A |
T |
1: 150,758,391 |
Y815N |
possibly damaging |
Het |
Igfn1 |
A |
T |
1: 135,959,881 |
C2482S |
possibly damaging |
Het |
Igkv4-71 |
A |
G |
6: 69,243,276 |
V57A |
probably damaging |
Het |
Itpkb |
G |
A |
1: 180,333,343 |
E345K |
possibly damaging |
Het |
Itpr3 |
G |
A |
17: 27,115,919 |
V2136M |
possibly damaging |
Het |
Kcnh3 |
A |
G |
15: 99,229,330 |
T336A |
probably damaging |
Het |
Kdm4d |
T |
C |
9: 14,463,939 |
T208A |
possibly damaging |
Het |
Kntc1 |
T |
C |
5: 123,778,267 |
F721S |
probably damaging |
Het |
Krt10 |
A |
G |
11: 99,389,260 |
|
probably benign |
Het |
Lgals3bp |
T |
A |
11: 118,398,541 |
N28I |
probably damaging |
Het |
Matn2 |
T |
C |
15: 34,378,697 |
L293P |
probably damaging |
Het |
Mical3 |
T |
C |
6: 120,973,420 |
E1010G |
probably damaging |
Het |
Mpp4 |
C |
A |
1: 59,130,065 |
R380L |
probably damaging |
Het |
Msh5 |
A |
G |
17: 35,031,766 |
F469L |
possibly damaging |
Het |
Ncam2 |
A |
G |
16: 81,512,959 |
T446A |
probably benign |
Het |
Neurl4 |
A |
G |
11: 69,909,236 |
D1050G |
probably damaging |
Het |
Olfml2b |
T |
C |
1: 170,682,224 |
Y714H |
possibly damaging |
Het |
Olfr1173 |
T |
C |
2: 88,274,692 |
D119G |
probably damaging |
Het |
Olfr895 |
T |
C |
9: 38,269,217 |
S235P |
probably benign |
Het |
Pcnx2 |
T |
C |
8: 125,761,618 |
E1729G |
probably damaging |
Het |
Peg10 |
GCACATCAGGATCC |
GCACATCAGGATCCCCATCAGGATCCTCCACATCAGGATCC |
6: 4,756,452 |
|
probably benign |
Het |
Pex1 |
T |
A |
5: 3,631,707 |
L1051Q |
probably damaging |
Het |
Prkag2 |
T |
A |
5: 24,869,139 |
R283* |
probably null |
Het |
Prrc1 |
T |
A |
18: 57,371,431 |
M238K |
probably damaging |
Het |
Ptprj |
T |
C |
2: 90,469,717 |
T247A |
probably benign |
Het |
Ptprz1 |
A |
G |
6: 22,999,615 |
Y568C |
probably damaging |
Het |
Rab36 |
G |
A |
10: 75,048,459 |
A114T |
probably damaging |
Het |
Rfx7 |
T |
C |
9: 72,619,449 |
V1307A |
probably benign |
Het |
Scaf1 |
A |
C |
7: 45,007,827 |
|
probably benign |
Het |
Sema4g |
A |
T |
19: 44,998,427 |
T440S |
probably benign |
Het |
Setbp1 |
A |
T |
18: 78,857,383 |
V1023E |
probably damaging |
Het |
Slc46a2 |
T |
C |
4: 59,913,931 |
I331V |
possibly damaging |
Het |
Slc4a7 |
C |
T |
14: 14,786,313 |
R1000C |
probably damaging |
Het |
Sorcs2 |
T |
C |
5: 36,065,409 |
H162R |
probably benign |
Het |
St5 |
G |
A |
7: 109,525,548 |
R675* |
probably null |
Het |
Strip2 |
G |
A |
6: 29,920,532 |
|
probably null |
Het |
Stx2 |
T |
A |
5: 128,994,868 |
I42L |
probably benign |
Het |
Tas2r124 |
A |
T |
6: 132,755,447 |
T240S |
probably benign |
Het |
Tgfbrap1 |
A |
T |
1: 43,075,910 |
V10D |
probably damaging |
Het |
Tmem41a |
T |
A |
16: 21,947,431 |
Y19F |
probably benign |
Het |
Tmprss5 |
A |
G |
9: 49,107,139 |
T74A |
possibly damaging |
Het |
Trim16 |
G |
T |
11: 62,836,761 |
R216L |
probably benign |
Het |
Trmt10c |
T |
C |
16: 56,034,507 |
K255R |
probably benign |
Het |
Trpm2 |
A |
T |
10: 77,933,649 |
V747E |
probably damaging |
Het |
Ube2v2 |
T |
C |
16: 15,581,141 |
D28G |
possibly damaging |
Het |
Uty |
G |
A |
Y: 1,157,928 |
T705I |
possibly damaging |
Het |
Vmn2r80 |
A |
T |
10: 79,148,876 |
I21F |
probably benign |
Het |
Wdr11 |
T |
C |
7: 129,602,999 |
L176S |
probably damaging |
Het |
Zfp992 |
A |
G |
4: 146,466,862 |
T347A |
probably benign |
Het |
|