Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700062C07Rik |
A |
G |
18: 24,606,013 (GRCm39) |
N36S |
possibly damaging |
Het |
Ankrd39 |
A |
G |
1: 36,586,236 (GRCm39) |
S11P |
probably benign |
Het |
Aox1 |
A |
G |
1: 58,338,978 (GRCm39) |
S324G |
probably benign |
Het |
Atl3 |
T |
C |
19: 7,509,703 (GRCm39) |
V477A |
probably benign |
Het |
Bcar1 |
T |
C |
8: 112,447,525 (GRCm39) |
T151A |
probably benign |
Het |
Cdc42bpg |
A |
G |
19: 6,365,296 (GRCm39) |
T718A |
possibly damaging |
Het |
Col9a1 |
C |
T |
1: 24,283,462 (GRCm39) |
R843C |
probably damaging |
Het |
Dnah12 |
T |
A |
14: 26,430,341 (GRCm39) |
D316E |
possibly damaging |
Het |
Fat2 |
A |
G |
11: 55,175,127 (GRCm39) |
V1862A |
probably damaging |
Het |
Fbxw5 |
C |
A |
2: 25,393,472 (GRCm39) |
N233K |
probably damaging |
Het |
Fcer2a |
A |
G |
8: 3,738,831 (GRCm39) |
F75L |
probably benign |
Het |
Fhod3 |
A |
G |
18: 25,123,123 (GRCm39) |
K271R |
probably null |
Het |
Gimd1 |
T |
C |
3: 132,350,169 (GRCm39) |
V144A |
possibly damaging |
Het |
Glt1d1 |
T |
C |
5: 127,768,176 (GRCm39) |
|
probably null |
Het |
Hecw2 |
C |
T |
1: 53,871,804 (GRCm39) |
V1381M |
probably damaging |
Het |
Kansl1l |
C |
T |
1: 66,812,637 (GRCm39) |
D459N |
probably damaging |
Het |
Lmtk3 |
G |
A |
7: 45,443,486 (GRCm39) |
C723Y |
possibly damaging |
Het |
Muc4 |
T |
C |
16: 32,576,200 (GRCm39) |
|
probably benign |
Het |
Myom1 |
T |
A |
17: 71,399,135 (GRCm39) |
V999E |
probably damaging |
Het |
Nckap5 |
A |
G |
1: 125,955,376 (GRCm39) |
L460P |
probably benign |
Het |
Or12d17 |
T |
C |
17: 37,777,715 (GRCm39) |
M206T |
probably damaging |
Het |
Phf13 |
A |
T |
4: 152,076,552 (GRCm39) |
N213K |
probably damaging |
Het |
Phldb3 |
T |
C |
7: 24,326,745 (GRCm39) |
I591T |
probably damaging |
Het |
Pik3cb |
T |
C |
9: 98,983,229 (GRCm39) |
|
probably null |
Het |
Pkd1l1 |
C |
T |
11: 8,815,543 (GRCm39) |
R1456K |
possibly damaging |
Het |
Plekhh2 |
A |
G |
17: 84,893,765 (GRCm39) |
E860G |
possibly damaging |
Het |
Resf1 |
T |
A |
6: 149,227,041 (GRCm39) |
M29K |
possibly damaging |
Het |
Rest |
A |
G |
5: 77,429,959 (GRCm39) |
T793A |
probably benign |
Het |
Ropn1 |
C |
T |
16: 34,498,826 (GRCm39) |
Q205* |
probably null |
Het |
Sacs |
A |
C |
14: 61,440,906 (GRCm39) |
K984T |
probably benign |
Het |
Samd11 |
G |
A |
4: 156,334,943 (GRCm39) |
R102C |
probably damaging |
Het |
Shank1 |
C |
A |
7: 43,969,160 (GRCm39) |
H352N |
unknown |
Het |
Slc22a27 |
A |
T |
19: 7,903,244 (GRCm39) |
I162K |
possibly damaging |
Het |
Snx8 |
A |
G |
5: 140,341,800 (GRCm39) |
L121P |
probably damaging |
Het |
Sumf1 |
A |
C |
6: 108,131,974 (GRCm39) |
V156G |
probably damaging |
Het |
Tln1 |
A |
T |
4: 43,536,104 (GRCm39) |
V2027E |
probably damaging |
Het |
Trdn |
A |
G |
10: 33,326,994 (GRCm39) |
I594M |
probably benign |
Het |
Trim5 |
C |
G |
7: 103,926,022 (GRCm39) |
E180Q |
possibly damaging |
Het |
Tsen2 |
A |
G |
6: 115,524,785 (GRCm39) |
|
probably benign |
Het |
Tubb1 |
A |
T |
2: 174,297,526 (GRCm39) |
E45V |
probably null |
Het |
Vmn2r67 |
T |
A |
7: 84,799,722 (GRCm39) |
|
probably null |
Het |
Zcchc14 |
CTGATGGTGGTGGTGATGGTGGTGG |
CTGATGGTGGTGG |
8: 122,331,031 (GRCm39) |
|
probably benign |
Het |
Zfp160 |
T |
A |
17: 21,246,000 (GRCm39) |
F183L |
probably benign |
Het |
|
Other mutations in Satl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00766:Satl1
|
APN |
X |
111,315,466 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4246:Satl1
|
UTSW |
X |
111,316,033 (GRCm39) |
missense |
probably benign |
|
R4247:Satl1
|
UTSW |
X |
111,316,033 (GRCm39) |
missense |
probably benign |
|
R4248:Satl1
|
UTSW |
X |
111,316,033 (GRCm39) |
missense |
probably benign |
|
R4250:Satl1
|
UTSW |
X |
111,316,033 (GRCm39) |
missense |
probably benign |
|
R6067:Satl1
|
UTSW |
X |
111,315,613 (GRCm39) |
missense |
probably benign |
|
R6079:Satl1
|
UTSW |
X |
111,315,613 (GRCm39) |
missense |
probably benign |
|
R6138:Satl1
|
UTSW |
X |
111,315,613 (GRCm39) |
missense |
probably benign |
|
U15987:Satl1
|
UTSW |
X |
111,315,613 (GRCm39) |
missense |
probably benign |
|
Z1176:Satl1
|
UTSW |
X |
111,314,689 (GRCm39) |
missense |
probably benign |
0.08 |
|