Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg8 |
C |
A |
17: 84,995,957 (GRCm39) |
|
probably null |
Het |
Alms1 |
A |
G |
6: 85,654,946 (GRCm39) |
E2695G |
probably damaging |
Het |
B3galnt2 |
A |
G |
13: 14,162,016 (GRCm39) |
N246D |
probably benign |
Het |
Ces1h |
A |
T |
8: 94,079,098 (GRCm39) |
M495K |
unknown |
Het |
Chga |
A |
G |
12: 102,529,058 (GRCm39) |
E345G |
probably damaging |
Het |
Chrnb3 |
T |
C |
8: 27,875,129 (GRCm39) |
F43L |
probably benign |
Het |
Cwf19l2 |
C |
A |
9: 3,409,990 (GRCm39) |
Q40K |
probably benign |
Het |
Dlg2 |
T |
C |
7: 91,614,853 (GRCm39) |
I264T |
probably damaging |
Het |
Dnah1 |
C |
T |
14: 31,008,853 (GRCm39) |
V1974M |
probably damaging |
Het |
Foxf2 |
C |
A |
13: 31,810,172 (GRCm39) |
P37Q |
unknown |
Het |
Gtf2e2 |
T |
C |
8: 34,266,473 (GRCm39) |
|
probably benign |
Het |
Hectd3 |
C |
A |
4: 116,857,785 (GRCm39) |
|
probably benign |
Het |
Hectd3 |
T |
C |
4: 116,857,786 (GRCm39) |
|
probably benign |
Het |
Hectd3 |
T |
C |
4: 116,857,784 (GRCm39) |
|
probably benign |
Het |
Ift122 |
A |
T |
6: 115,894,018 (GRCm39) |
H901L |
probably benign |
Het |
Itih1 |
C |
T |
14: 30,664,846 (GRCm39) |
|
probably null |
Het |
Krt84 |
C |
A |
15: 101,436,208 (GRCm39) |
M460I |
probably benign |
Het |
Moxd1 |
C |
T |
10: 24,158,491 (GRCm39) |
H382Y |
probably damaging |
Het |
Npy6r |
A |
T |
18: 44,409,511 (GRCm39) |
T311S |
probably damaging |
Het |
Or1p1 |
C |
T |
11: 74,179,952 (GRCm39) |
T160I |
probably damaging |
Het |
Or52n3 |
C |
T |
7: 104,530,724 (GRCm39) |
T270I |
probably benign |
Het |
Pbk |
T |
C |
14: 66,051,340 (GRCm39) |
I126T |
probably damaging |
Het |
Pde1b |
C |
T |
15: 103,435,107 (GRCm39) |
S400F |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,326,965 (GRCm39) |
C300S |
probably damaging |
Het |
Pnpla6 |
C |
T |
8: 3,573,808 (GRCm39) |
R419W |
probably damaging |
Het |
Ppp4r3a |
A |
G |
12: 101,016,053 (GRCm39) |
L33P |
probably damaging |
Het |
Ralb |
T |
A |
1: 119,403,770 (GRCm39) |
D119V |
probably benign |
Het |
Relb |
A |
C |
7: 19,356,849 (GRCm39) |
|
probably null |
Het |
Rims1 |
T |
A |
1: 22,507,323 (GRCm39) |
D609V |
probably damaging |
Het |
Scnn1a |
A |
G |
6: 125,315,342 (GRCm39) |
T377A |
probably benign |
Het |
Slc13a2 |
T |
C |
11: 78,291,374 (GRCm39) |
T367A |
probably damaging |
Het |
Sort1 |
T |
C |
3: 108,263,623 (GRCm39) |
L807P |
probably damaging |
Het |
Sptbn1 |
C |
A |
11: 30,060,818 (GRCm39) |
E2051* |
probably null |
Het |
St6galnac1 |
T |
C |
11: 116,658,532 (GRCm39) |
I311V |
probably damaging |
Het |
|
Other mutations in Ctu1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
waverer
|
UTSW |
7 |
43,326,046 (GRCm39) |
missense |
probably damaging |
0.96 |
R0557:Ctu1
|
UTSW |
7 |
43,326,583 (GRCm39) |
missense |
unknown |
|
R2974:Ctu1
|
UTSW |
7 |
43,325,074 (GRCm39) |
splice site |
probably benign |
|
R3805:Ctu1
|
UTSW |
7 |
43,326,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Ctu1
|
UTSW |
7 |
43,326,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6863:Ctu1
|
UTSW |
7 |
43,326,046 (GRCm39) |
missense |
probably damaging |
0.96 |
R6999:Ctu1
|
UTSW |
7 |
43,324,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R7379:Ctu1
|
UTSW |
7 |
43,326,490 (GRCm39) |
small deletion |
probably benign |
|
R7395:Ctu1
|
UTSW |
7 |
43,326,019 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8870:Ctu1
|
UTSW |
7 |
43,324,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R9066:Ctu1
|
UTSW |
7 |
43,326,019 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9430:Ctu1
|
UTSW |
7 |
43,326,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R9522:Ctu1
|
UTSW |
7 |
43,324,900 (GRCm39) |
missense |
probably benign |
0.19 |
|