Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl5 |
G |
T |
19: 55,268,894 (GRCm39) |
C185F |
probably damaging |
Het |
Adad2 |
C |
A |
8: 120,341,654 (GRCm39) |
T185N |
possibly damaging |
Het |
Apbb1 |
A |
T |
7: 105,214,232 (GRCm39) |
V315E |
probably damaging |
Het |
Arfrp1 |
T |
C |
2: 181,006,191 (GRCm39) |
T32A |
probably damaging |
Het |
B020004C17Rik |
T |
C |
14: 57,253,999 (GRCm39) |
S41P |
probably benign |
Het |
Celsr3 |
T |
C |
9: 108,721,743 (GRCm39) |
|
probably null |
Het |
Chd8 |
C |
T |
14: 52,452,652 (GRCm39) |
G1289D |
probably benign |
Het |
Ctrl |
A |
G |
8: 106,659,672 (GRCm39) |
F59S |
probably damaging |
Het |
Cyp4v3 |
T |
A |
8: 45,763,243 (GRCm39) |
D356V |
probably benign |
Het |
Dgka |
T |
A |
10: 128,565,541 (GRCm39) |
|
probably null |
Het |
Dnah7b |
T |
C |
1: 46,262,265 (GRCm39) |
Y2043H |
probably damaging |
Het |
Eya3 |
A |
G |
4: 132,400,244 (GRCm39) |
T88A |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,489,912 (GRCm39) |
D3608G |
possibly damaging |
Het |
Fmo1 |
T |
C |
1: 162,677,793 (GRCm39) |
T108A |
probably damaging |
Het |
Frs3 |
A |
G |
17: 48,012,635 (GRCm39) |
E114G |
probably damaging |
Het |
Ftcd |
A |
T |
10: 76,413,850 (GRCm39) |
M85L |
probably benign |
Het |
Ggnbp2 |
T |
C |
11: 84,745,169 (GRCm39) |
S189G |
probably benign |
Het |
Gm3629 |
C |
T |
14: 17,875,765 (GRCm39) |
R35H |
unknown |
Het |
Gnai2 |
T |
G |
9: 107,512,365 (GRCm39) |
M18L |
probably benign |
Het |
Gpx5 |
T |
C |
13: 21,476,805 (GRCm39) |
Y9C |
probably benign |
Het |
Grik1 |
C |
A |
16: 87,732,914 (GRCm39) |
A668S |
probably damaging |
Het |
Hectd4 |
A |
T |
5: 121,445,011 (GRCm39) |
M83L |
probably benign |
Het |
Klra9 |
T |
C |
6: 130,156,075 (GRCm39) |
R227G |
probably benign |
Het |
Maz |
A |
T |
7: 126,624,860 (GRCm39) |
V197D |
possibly damaging |
Het |
Mbd5 |
T |
C |
2: 49,162,917 (GRCm39) |
V241A |
probably damaging |
Het |
Mdga2 |
C |
T |
12: 66,701,950 (GRCm39) |
C417Y |
probably damaging |
Het |
Mios |
C |
T |
6: 8,215,314 (GRCm39) |
T170I |
probably benign |
Het |
Myh13 |
G |
A |
11: 67,239,648 (GRCm39) |
A733T |
probably damaging |
Het |
Ncam2 |
C |
T |
16: 81,231,766 (GRCm39) |
R77* |
probably null |
Het |
Nfs1 |
G |
A |
2: 155,970,422 (GRCm39) |
T297I |
probably damaging |
Het |
Nrbf2 |
A |
G |
10: 67,120,870 (GRCm39) |
|
probably null |
Het |
Nrg1 |
T |
C |
8: 32,308,405 (GRCm39) |
Y537C |
probably damaging |
Het |
Or4p8 |
T |
C |
2: 88,727,035 (GRCm39) |
D302G |
probably benign |
Het |
Pard3 |
G |
A |
8: 128,096,836 (GRCm39) |
R333Q |
probably damaging |
Het |
Parp4 |
T |
C |
14: 56,861,552 (GRCm39) |
F962L |
probably benign |
Het |
Pilra |
A |
G |
5: 137,834,318 (GRCm39) |
S22P |
possibly damaging |
Het |
Piwil4 |
T |
C |
9: 14,616,337 (GRCm39) |
Y673C |
probably damaging |
Het |
Plxna2 |
G |
A |
1: 194,476,181 (GRCm39) |
D1134N |
probably benign |
Het |
Pnpla7 |
T |
C |
2: 24,909,453 (GRCm39) |
V681A |
possibly damaging |
Het |
Ppfibp1 |
T |
A |
6: 146,931,648 (GRCm39) |
|
probably null |
Het |
Ptprz1 |
C |
T |
6: 23,001,665 (GRCm39) |
L1252F |
probably benign |
Het |
Sptb |
T |
C |
12: 76,646,625 (GRCm39) |
E1999G |
probably benign |
Het |
Stat3 |
T |
C |
11: 100,780,714 (GRCm39) |
|
probably benign |
Het |
Usp25 |
T |
C |
16: 76,904,801 (GRCm39) |
V789A |
possibly damaging |
Het |
Zfp148 |
C |
A |
16: 33,317,589 (GRCm39) |
Q712K |
probably damaging |
Het |
|
Other mutations in Onecut3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02476:Onecut3
|
APN |
10 |
80,349,724 (GRCm39) |
missense |
probably benign |
0.33 |
R2072:Onecut3
|
UTSW |
10 |
80,330,848 (GRCm39) |
missense |
unknown |
|
R4230:Onecut3
|
UTSW |
10 |
80,349,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R4248:Onecut3
|
UTSW |
10 |
80,349,963 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4764:Onecut3
|
UTSW |
10 |
80,331,541 (GRCm39) |
missense |
unknown |
|
R5001:Onecut3
|
UTSW |
10 |
80,331,154 (GRCm39) |
missense |
unknown |
|
R6394:Onecut3
|
UTSW |
10 |
80,331,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R6450:Onecut3
|
UTSW |
10 |
80,331,922 (GRCm39) |
missense |
probably damaging |
0.96 |
R7483:Onecut3
|
UTSW |
10 |
80,331,310 (GRCm39) |
missense |
unknown |
|
R8317:Onecut3
|
UTSW |
10 |
80,331,161 (GRCm39) |
missense |
unknown |
|
R8756:Onecut3
|
UTSW |
10 |
80,349,750 (GRCm39) |
missense |
probably damaging |
0.98 |
R9515:Onecut3
|
UTSW |
10 |
80,331,887 (GRCm39) |
nonsense |
probably null |
|
|