Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Asb13 |
A |
C |
13: 3,692,092 (GRCm39) |
H24P |
probably damaging |
Het |
Avpr1b |
T |
A |
1: 131,527,480 (GRCm39) |
M1K |
probably null |
Het |
Baz1a |
T |
C |
12: 54,958,182 (GRCm39) |
E1023G |
probably benign |
Het |
Bpifb5 |
A |
G |
2: 154,070,820 (GRCm39) |
T204A |
probably benign |
Het |
Cfap157 |
C |
T |
2: 32,669,954 (GRCm39) |
V210M |
probably damaging |
Het |
Clock |
A |
G |
5: 76,374,976 (GRCm39) |
V731A |
possibly damaging |
Het |
Cntn6 |
C |
T |
6: 104,753,389 (GRCm39) |
T447I |
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,421,556 (GRCm39) |
I288T |
probably damaging |
Het |
Far2 |
T |
C |
6: 148,076,639 (GRCm39) |
F494S |
possibly damaging |
Het |
Fnd3c2 |
G |
A |
X: 105,290,760 (GRCm39) |
T302I |
possibly damaging |
Het |
Foxp3 |
A |
G |
X: 7,457,639 (GRCm39) |
I281V |
probably benign |
Het |
Fryl |
A |
G |
5: 73,240,715 (GRCm39) |
I1295T |
probably benign |
Het |
Gpr82 |
T |
C |
X: 13,531,829 (GRCm39) |
S126P |
probably benign |
Het |
Gria4 |
T |
A |
9: 4,464,372 (GRCm39) |
Q530L |
probably benign |
Het |
Hivep1 |
A |
C |
13: 42,313,232 (GRCm39) |
D1824A |
probably benign |
Het |
Kif13a |
A |
G |
13: 46,966,218 (GRCm39) |
V400A |
possibly damaging |
Het |
Map3k21 |
C |
A |
8: 126,668,759 (GRCm39) |
L782I |
probably benign |
Het |
Nphs2 |
A |
C |
1: 156,146,317 (GRCm39) |
T98P |
probably damaging |
Het |
Pdss2 |
CGGAG |
CG |
10: 43,097,927 (GRCm39) |
|
probably benign |
Het |
Pkd2l1 |
A |
G |
19: 44,146,070 (GRCm39) |
|
probably null |
Het |
Rbm28 |
A |
T |
6: 29,128,577 (GRCm39) |
S48R |
probably damaging |
Het |
Rimkla |
C |
T |
4: 119,335,177 (GRCm39) |
V69M |
probably damaging |
Het |
Scg3 |
T |
A |
9: 75,573,017 (GRCm39) |
I305F |
probably damaging |
Het |
Slc22a1 |
T |
A |
17: 12,881,679 (GRCm39) |
N310I |
probably damaging |
Het |
Slc26a9 |
T |
C |
1: 131,692,768 (GRCm39) |
V700A |
probably benign |
Het |
Snx15 |
T |
C |
19: 6,171,915 (GRCm39) |
I140V |
probably benign |
Het |
Spryd3 |
C |
T |
15: 102,036,969 (GRCm39) |
|
probably null |
Het |
Srebf1 |
T |
C |
11: 60,094,942 (GRCm39) |
T486A |
probably benign |
Het |
Syne2 |
AGAGTGAG |
AGAGTGAGTGAG |
12: 76,144,734 (GRCm39) |
|
probably null |
Het |
Tbl1xr1 |
T |
A |
3: 22,258,158 (GRCm39) |
|
probably null |
Het |
Tmcc1 |
A |
T |
6: 116,019,951 (GRCm39) |
H281Q |
probably benign |
Het |
Ttc39b |
T |
A |
4: 83,159,938 (GRCm39) |
M413L |
probably benign |
Het |
Vmn2r101 |
C |
A |
17: 19,810,373 (GRCm39) |
H386Q |
probably benign |
Het |
Zbtb47 |
T |
C |
9: 121,592,327 (GRCm39) |
F251L |
probably benign |
Het |
|
Other mutations in Fibin |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02676:Fibin
|
APN |
2 |
110,192,929 (GRCm39) |
missense |
probably benign |
0.36 |
R0478:Fibin
|
UTSW |
2 |
110,193,079 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1135:Fibin
|
UTSW |
2 |
110,192,567 (GRCm39) |
missense |
probably benign |
0.00 |
R2437:Fibin
|
UTSW |
2 |
110,192,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R2857:Fibin
|
UTSW |
2 |
110,192,542 (GRCm39) |
missense |
probably damaging |
0.99 |
R2859:Fibin
|
UTSW |
2 |
110,192,542 (GRCm39) |
missense |
probably damaging |
0.99 |
R2887:Fibin
|
UTSW |
2 |
110,193,122 (GRCm39) |
missense |
probably benign |
|
R4119:Fibin
|
UTSW |
2 |
110,193,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R4979:Fibin
|
UTSW |
2 |
110,192,963 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6232:Fibin
|
UTSW |
2 |
110,193,041 (GRCm39) |
missense |
probably damaging |
0.99 |
R7137:Fibin
|
UTSW |
2 |
110,193,001 (GRCm39) |
missense |
probably damaging |
0.99 |
R7849:Fibin
|
UTSW |
2 |
110,192,825 (GRCm39) |
missense |
probably damaging |
0.99 |
R9675:Fibin
|
UTSW |
2 |
110,192,495 (GRCm39) |
missense |
probably benign |
0.06 |
|