Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aamp |
T |
A |
1: 74,320,683 (GRCm39) |
|
probably benign |
Het |
Birc6 |
A |
G |
17: 75,003,386 (GRCm39) |
E4752G |
possibly damaging |
Het |
Chd1 |
C |
T |
17: 15,954,535 (GRCm39) |
P468S |
probably damaging |
Het |
Cnot3 |
A |
G |
7: 3,661,067 (GRCm39) |
D556G |
probably benign |
Het |
Csnk1d |
A |
G |
11: 120,863,338 (GRCm39) |
Y201H |
probably damaging |
Het |
Dhtkd1 |
A |
G |
2: 5,935,717 (GRCm39) |
S132P |
possibly damaging |
Het |
Dhx58 |
G |
T |
11: 100,593,090 (GRCm39) |
Q206K |
probably benign |
Het |
Dio1 |
C |
A |
4: 107,149,574 (GRCm39) |
V195F |
probably damaging |
Het |
Dio3 |
T |
C |
12: 110,245,916 (GRCm39) |
V84A |
probably benign |
Het |
Dnai4 |
T |
A |
4: 102,944,545 (GRCm39) |
I3L |
possibly damaging |
Het |
Extl3 |
T |
C |
14: 65,314,693 (GRCm39) |
K163R |
probably benign |
Het |
Fat2 |
A |
T |
11: 55,201,950 (GRCm39) |
S375T |
probably damaging |
Het |
Fbrs |
A |
G |
7: 127,086,841 (GRCm39) |
D73G |
probably damaging |
Het |
Fnip1 |
A |
G |
11: 54,390,393 (GRCm39) |
|
probably benign |
Het |
Frmpd4 |
A |
G |
X: 166,280,851 (GRCm39) |
V343A |
probably damaging |
Het |
Gcc1 |
T |
C |
6: 28,420,468 (GRCm39) |
D283G |
probably benign |
Het |
Ghr |
T |
C |
15: 3,349,528 (GRCm39) |
D550G |
probably damaging |
Het |
Glycam1 |
G |
A |
15: 103,471,307 (GRCm39) |
|
probably benign |
Het |
Gpatch8 |
A |
G |
11: 102,369,417 (GRCm39) |
S1374P |
probably damaging |
Het |
Grm1 |
A |
T |
10: 10,565,197 (GRCm39) |
M1037K |
probably benign |
Het |
Gtpbp3 |
T |
C |
8: 71,945,242 (GRCm39) |
L438P |
probably damaging |
Het |
Ifi205 |
G |
T |
1: 173,842,627 (GRCm39) |
N356K |
probably damaging |
Het |
Ifi206 |
A |
G |
1: 173,309,132 (GRCm39) |
L288P |
probably benign |
Het |
Ift57 |
T |
C |
16: 49,584,252 (GRCm39) |
V291A |
probably benign |
Het |
Kif13a |
A |
C |
13: 46,938,772 (GRCm39) |
C166G |
probably damaging |
Het |
Lypd6 |
A |
G |
2: 50,080,740 (GRCm39) |
T143A |
possibly damaging |
Het |
Mtus2 |
G |
A |
5: 148,014,748 (GRCm39) |
A514T |
probably benign |
Het |
Neu2 |
T |
C |
1: 87,524,674 (GRCm39) |
W220R |
probably damaging |
Het |
Notch3 |
T |
C |
17: 32,377,612 (GRCm39) |
S155G |
possibly damaging |
Het |
Nrxn2 |
A |
G |
19: 6,505,015 (GRCm39) |
E286G |
probably damaging |
Het |
Oog2 |
T |
A |
4: 143,921,799 (GRCm39) |
D236E |
probably benign |
Het |
Pck1 |
A |
G |
2: 173,000,075 (GRCm39) |
H502R |
probably benign |
Het |
Pld1 |
A |
G |
3: 28,102,188 (GRCm39) |
Y313C |
probably damaging |
Het |
Rhox3f |
A |
T |
X: 36,763,192 (GRCm39) |
|
probably benign |
Het |
Rpl34 |
A |
G |
3: 130,520,613 (GRCm39) |
|
probably benign |
Het |
Sema4c |
T |
C |
1: 36,595,031 (GRCm39) |
K31E |
probably damaging |
Het |
Septin11 |
T |
C |
5: 93,296,443 (GRCm39) |
|
probably null |
Het |
Slc4a9 |
T |
A |
18: 36,668,498 (GRCm39) |
|
probably null |
Het |
Snrnp200 |
T |
A |
2: 127,059,408 (GRCm39) |
S434T |
probably benign |
Het |
Snx13 |
A |
T |
12: 35,136,940 (GRCm39) |
I134F |
probably damaging |
Het |
Syt2 |
T |
C |
1: 134,675,369 (GRCm39) |
S407P |
probably benign |
Het |
Tbc1d19 |
T |
C |
5: 54,046,755 (GRCm39) |
|
probably null |
Het |
Tbc1d32 |
G |
T |
10: 56,074,638 (GRCm39) |
Q192K |
possibly damaging |
Het |
Ubr4 |
T |
A |
4: 139,148,560 (GRCm39) |
C1681* |
probably null |
Het |
Vmn1r43 |
T |
A |
6: 89,847,043 (GRCm39) |
I148F |
possibly damaging |
Het |
Vwa8 |
T |
C |
14: 79,162,781 (GRCm39) |
V187A |
possibly damaging |
Het |
|
Other mutations in Onecut3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
|
R5479:Onecut3
|
UTSW |
10 |
80,349,856 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|