Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl6 |
A |
T |
11: 54,225,911 (GRCm39) |
N317I |
probably damaging |
Het |
Adam18 |
T |
A |
8: 25,118,147 (GRCm39) |
S590C |
possibly damaging |
Het |
Btrc |
G |
A |
19: 45,459,526 (GRCm39) |
E103K |
probably benign |
Het |
Cars1 |
A |
G |
7: 143,112,929 (GRCm39) |
M766T |
possibly damaging |
Het |
Cavin4 |
T |
C |
4: 48,671,999 (GRCm39) |
V148A |
probably benign |
Het |
Cdcp3 |
T |
C |
7: 130,830,643 (GRCm39) |
V359A |
probably damaging |
Het |
Cdkn2d |
T |
C |
9: 21,202,139 (GRCm39) |
D36G |
possibly damaging |
Het |
Cubn |
A |
T |
2: 13,292,510 (GRCm39) |
D3224E |
probably damaging |
Het |
Ebf1 |
A |
G |
11: 44,509,006 (GRCm39) |
M1V |
probably null |
Het |
Eif1ad7 |
T |
G |
12: 88,238,727 (GRCm39) |
N11T |
unknown |
Het |
Fcgbp |
A |
G |
7: 27,802,563 (GRCm39) |
D1497G |
probably damaging |
Het |
Fstl5 |
C |
T |
3: 76,496,260 (GRCm39) |
P341L |
probably damaging |
Het |
Fzd10 |
G |
A |
5: 128,678,771 (GRCm39) |
G164S |
probably benign |
Het |
Hrh3 |
C |
A |
2: 179,742,444 (GRCm39) |
E395* |
probably null |
Het |
Hsf4 |
G |
A |
8: 105,999,435 (GRCm39) |
V318M |
probably damaging |
Het |
Il21 |
T |
C |
3: 37,281,949 (GRCm39) |
E65G |
possibly damaging |
Het |
Kank1 |
A |
G |
19: 25,408,289 (GRCm39) |
D1256G |
possibly damaging |
Het |
Klhl22 |
A |
G |
16: 17,594,915 (GRCm39) |
N348S |
possibly damaging |
Het |
Krr1 |
T |
C |
10: 111,812,672 (GRCm39) |
I94T |
probably damaging |
Het |
Lpin2 |
A |
G |
17: 71,550,410 (GRCm39) |
D724G |
probably damaging |
Het |
Mn1 |
C |
A |
5: 111,566,393 (GRCm39) |
P121Q |
probably damaging |
Het |
Mphosph9 |
A |
T |
5: 124,463,015 (GRCm39) |
L10* |
probably null |
Het |
Mtus1 |
A |
T |
8: 41,536,795 (GRCm39) |
V307E |
probably benign |
Het |
Muc20 |
A |
G |
16: 32,615,155 (GRCm39) |
L74P |
probably damaging |
Het |
Nnat |
A |
G |
2: 157,403,701 (GRCm39) |
*113W |
probably null |
Het |
Or13a25 |
G |
T |
7: 140,247,794 (GRCm39) |
C191F |
probably damaging |
Het |
Or2f1b |
C |
T |
6: 42,739,672 (GRCm39) |
Q229* |
probably null |
Het |
Or4f14 |
A |
G |
2: 111,743,128 (GRCm39) |
V49A |
possibly damaging |
Het |
Or6b6 |
A |
T |
7: 106,571,103 (GRCm39) |
Y149* |
probably null |
Het |
Pkm |
T |
A |
9: 59,577,831 (GRCm39) |
V216E |
probably damaging |
Het |
Pla2g12a |
G |
A |
3: 129,674,900 (GRCm39) |
V19I |
unknown |
Het |
Pramel27 |
T |
C |
4: 143,578,267 (GRCm39) |
S176P |
|
Het |
Rai14 |
G |
A |
15: 10,595,116 (GRCm39) |
Q136* |
probably null |
Het |
Rnf150 |
T |
A |
8: 83,717,208 (GRCm39) |
N238K |
possibly damaging |
Het |
Rrp1 |
A |
G |
10: 78,240,757 (GRCm39) |
|
probably null |
Het |
Scaf8 |
T |
A |
17: 3,246,070 (GRCm39) |
L720M |
possibly damaging |
Het |
Slamf1 |
G |
T |
1: 171,625,771 (GRCm39) |
V316L |
probably damaging |
Het |
Slc14a1 |
C |
A |
18: 78,152,807 (GRCm39) |
A367S |
probably damaging |
Het |
Slc25a20 |
T |
C |
9: 108,549,675 (GRCm39) |
F86L |
probably benign |
Het |
Slc4a5 |
T |
G |
6: 83,217,714 (GRCm39) |
S131A |
probably benign |
Het |
Slitrk3 |
A |
G |
3: 72,958,649 (GRCm39) |
I41T |
probably benign |
Het |
Sntg1 |
A |
T |
1: 8,748,198 (GRCm39) |
L94Q |
probably damaging |
Het |
St18 |
T |
C |
1: 6,915,811 (GRCm39) |
C819R |
probably damaging |
Het |
St6galnac3 |
T |
A |
3: 153,117,177 (GRCm39) |
D182V |
probably benign |
Het |
Tubgcp2 |
T |
A |
7: 139,584,789 (GRCm39) |
T549S |
probably benign |
Het |
Vim |
A |
T |
2: 13,579,148 (GRCm39) |
|
probably benign |
Het |
Vmn2r118 |
C |
A |
17: 55,899,837 (GRCm39) |
R689I |
probably damaging |
Het |
Zbtb41 |
A |
T |
1: 139,375,255 (GRCm39) |
E905V |
probably damaging |
Het |
Zfyve9 |
A |
T |
4: 108,499,288 (GRCm39) |
D1284E |
possibly damaging |
Het |
|
Other mutations in Foxs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01641:Foxs1
|
APN |
2 |
152,774,232 (GRCm39) |
missense |
probably benign |
|
IGL02304:Foxs1
|
APN |
2 |
152,774,270 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02491:Foxs1
|
APN |
2 |
152,774,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03009:Foxs1
|
APN |
2 |
152,774,849 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03046:Foxs1
|
UTSW |
2 |
152,774,484 (GRCm39) |
missense |
probably benign |
0.00 |
R0158:Foxs1
|
UTSW |
2 |
152,774,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R0324:Foxs1
|
UTSW |
2 |
152,774,607 (GRCm39) |
missense |
probably benign |
0.02 |
R1616:Foxs1
|
UTSW |
2 |
152,774,559 (GRCm39) |
missense |
probably benign |
0.37 |
R1915:Foxs1
|
UTSW |
2 |
152,774,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R3113:Foxs1
|
UTSW |
2 |
152,774,156 (GRCm39) |
missense |
probably benign |
0.00 |
R4885:Foxs1
|
UTSW |
2 |
152,774,301 (GRCm39) |
missense |
probably benign |
0.00 |
R6084:Foxs1
|
UTSW |
2 |
152,774,762 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6265:Foxs1
|
UTSW |
2 |
152,774,098 (GRCm39) |
nonsense |
probably null |
|
R6720:Foxs1
|
UTSW |
2 |
152,774,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R6828:Foxs1
|
UTSW |
2 |
152,775,048 (GRCm39) |
nonsense |
probably null |
|
R6845:Foxs1
|
UTSW |
2 |
152,774,619 (GRCm39) |
missense |
probably benign |
|
R7456:Foxs1
|
UTSW |
2 |
152,775,045 (GRCm39) |
missense |
probably benign |
|
R7577:Foxs1
|
UTSW |
2 |
152,774,361 (GRCm39) |
missense |
probably benign |
0.01 |
R7746:Foxs1
|
UTSW |
2 |
152,775,028 (GRCm39) |
missense |
probably benign |
|
R7841:Foxs1
|
UTSW |
2 |
152,774,907 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8985:Foxs1
|
UTSW |
2 |
152,775,058 (GRCm39) |
start gained |
probably benign |
|
|