Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
C |
A |
16: 14,445,449 |
R758S |
probably benign |
Het |
Acnat1 |
A |
T |
4: 49,447,716 |
H288Q |
possibly damaging |
Het |
Adamts1 |
T |
C |
16: 85,802,226 |
E162G |
possibly damaging |
Het |
Akap11 |
A |
G |
14: 78,513,661 |
S429P |
probably benign |
Het |
Alg14 |
T |
C |
3: 121,361,766 |
Y212H |
probably damaging |
Het |
Cacna1g |
T |
C |
11: 94,466,181 |
T97A |
probably damaging |
Het |
Ccdc112 |
T |
A |
18: 46,287,754 |
N310Y |
possibly damaging |
Het |
Cenpl |
A |
T |
1: 161,086,004 |
Y328F |
probably damaging |
Het |
Cep162 |
G |
A |
9: 87,204,080 |
H1064Y |
probably benign |
Het |
Cnksr3 |
T |
A |
10: 7,154,324 |
E126D |
probably benign |
Het |
Ctsh |
T |
A |
9: 90,061,565 |
M81K |
probably benign |
Het |
D6Wsu163e |
A |
G |
6: 126,955,149 |
T284A |
probably damaging |
Het |
Dab1 |
C |
T |
4: 104,731,751 |
A524V |
probably benign |
Het |
Dnaaf1 |
T |
A |
8: 119,582,877 |
M196K |
probably benign |
Het |
Dnah9 |
C |
A |
11: 65,834,386 |
G4314C |
probably damaging |
Het |
Dph1 |
A |
G |
11: 75,179,731 |
Y361H |
probably damaging |
Het |
Ect2 |
C |
T |
3: 27,150,072 |
M29I |
probably benign |
Het |
Eif3h |
T |
C |
15: 51,797,670 |
Y167C |
probably damaging |
Het |
Epc2 |
C |
T |
2: 49,532,089 |
R332C |
probably damaging |
Het |
Gfm2 |
A |
G |
13: 97,162,934 |
I386V |
probably benign |
Het |
Gpd1l |
G |
A |
9: 114,914,331 |
T167I |
probably damaging |
Het |
Hsph1 |
T |
A |
5: 149,623,485 |
K567* |
probably null |
Het |
Igfn1 |
T |
G |
1: 135,969,388 |
S1147R |
probably benign |
Het |
Itgb4 |
T |
C |
11: 115,983,764 |
V406A |
probably benign |
Het |
Kcna2 |
A |
G |
3: 107,105,113 |
I337V |
possibly damaging |
Het |
Kcnab1 |
T |
C |
3: 65,302,194 |
|
probably null |
Het |
Kri1 |
G |
T |
9: 21,280,492 |
|
probably benign |
Het |
Lrguk |
T |
A |
6: 34,133,387 |
I801K |
possibly damaging |
Het |
Magi2 |
A |
T |
5: 20,602,460 |
N871Y |
probably damaging |
Het |
Map3k10 |
G |
T |
7: 27,661,556 |
|
probably null |
Het |
Mrps25 |
T |
C |
6: 92,178,740 |
T71A |
probably damaging |
Het |
Myo15 |
G |
A |
11: 60,499,495 |
W945* |
probably null |
Het |
Ncan |
A |
T |
8: 70,102,454 |
I1021N |
probably damaging |
Het |
Ncf4 |
C |
A |
15: 78,250,382 |
S11R |
probably benign |
Het |
Neb |
A |
C |
2: 52,196,295 |
S5255R |
possibly damaging |
Het |
Nop2 |
TGATGAAGATGAAGATGA |
TGATGAAGATGA |
6: 125,137,079 |
|
probably benign |
Het |
Olfr1155 |
T |
C |
2: 87,942,721 |
|
probably null |
Het |
Olfr1189 |
G |
A |
2: 88,592,172 |
A123T |
probably damaging |
Het |
Olfr992 |
A |
T |
2: 85,400,441 |
F31I |
probably damaging |
Het |
Pacs1 |
T |
C |
19: 5,153,714 |
I328V |
probably damaging |
Het |
Pafah2 |
GCCCC |
GCCCCC |
4: 134,425,541 |
|
probably null |
Het |
Pan2 |
A |
G |
10: 128,304,378 |
H56R |
possibly damaging |
Het |
Pigo |
G |
A |
4: 43,024,710 |
R124* |
probably null |
Het |
Ppfia2 |
A |
G |
10: 106,927,710 |
D1188G |
probably benign |
Het |
Ppp1r16b |
A |
G |
2: 158,761,435 |
N327D |
probably damaging |
Het |
Psd3 |
A |
G |
8: 67,720,004 |
C223R |
possibly damaging |
Het |
Rad50 |
A |
G |
11: 53,702,107 |
V72A |
possibly damaging |
Het |
Rcor3 |
T |
A |
1: 192,100,833 |
D445V |
possibly damaging |
Het |
Rundc1 |
T |
A |
11: 101,433,681 |
H404Q |
probably benign |
Het |
Ryr1 |
T |
C |
7: 29,079,811 |
K2083E |
probably benign |
Het |
Scd3 |
C |
A |
19: 44,235,842 |
H171Q |
probably damaging |
Het |
Scrn2 |
T |
C |
11: 97,032,195 |
F155L |
probably benign |
Het |
Serpina12 |
A |
T |
12: 104,032,510 |
L323Q |
probably damaging |
Het |
Sptlc3 |
T |
A |
2: 139,625,923 |
M467K |
probably benign |
Het |
Stard9 |
G |
T |
2: 120,698,489 |
R1742S |
possibly damaging |
Het |
Thbd |
A |
T |
2: 148,407,684 |
L88* |
probably null |
Het |
Tln2 |
G |
A |
9: 67,362,687 |
Q477* |
probably null |
Het |
Tnn |
T |
A |
1: 160,116,182 |
E1020D |
possibly damaging |
Het |
Trip12 |
A |
T |
1: 84,749,269 |
H3Q |
probably damaging |
Het |
Vmn2r115 |
ATCTTCT |
ATCT |
17: 23,359,988 |
|
probably benign |
Het |
Vmp1 |
G |
A |
11: 86,643,587 |
Q165* |
probably null |
Het |
Zfp758 |
T |
A |
17: 22,375,223 |
M230K |
probably benign |
Het |
|