Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
A |
T |
11: 110,216,548 (GRCm38) |
I747N |
probably benign |
Het |
Adamtsl2 |
A |
G |
2: 27,083,256 (GRCm38) |
Y97C |
probably damaging |
Het |
Alox12e |
A |
G |
11: 70,321,181 (GRCm38) |
|
probably benign |
Het |
Alpk2 |
A |
T |
18: 65,281,004 (GRCm38) |
S2014T |
probably damaging |
Het |
Ankrd36 |
A |
T |
11: 5,689,340 (GRCm38) |
|
probably null |
Het |
Apobec1 |
T |
C |
6: 122,581,397 (GRCm38) |
D133G |
probably damaging |
Het |
Arfgef1 |
A |
T |
1: 10,213,141 (GRCm38) |
I181N |
probably damaging |
Het |
Cilp2 |
A |
G |
8: 69,882,410 (GRCm38) |
V646A |
probably damaging |
Het |
Clasrp |
A |
G |
7: 19,584,464 (GRCm38) |
|
probably null |
Het |
Cnot2 |
T |
C |
10: 116,494,846 (GRCm38) |
T423A |
probably benign |
Het |
Crtap |
T |
C |
9: 114,384,806 (GRCm38) |
D227G |
probably benign |
Het |
Cyp17a1 |
A |
G |
19: 46,670,551 (GRCm38) |
F217S |
probably damaging |
Het |
Ddx60 |
A |
G |
8: 61,987,421 (GRCm38) |
M1036V |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 118,010,125 (GRCm38) |
I2818N |
probably benign |
Het |
Dok6 |
T |
A |
18: 89,473,947 (GRCm38) |
I169F |
possibly damaging |
Het |
Duox2 |
T |
A |
2: 122,281,726 (GRCm38) |
R1326S |
probably benign |
Het |
Epha10 |
A |
G |
4: 124,902,568 (GRCm38) |
T357A |
unknown |
Het |
Ephb2 |
A |
C |
4: 136,655,940 (GRCm38) |
F942C |
probably damaging |
Het |
Gabrb2 |
A |
G |
11: 42,593,917 (GRCm38) |
N267S |
possibly damaging |
Het |
Gabrr3 |
A |
T |
16: 59,461,638 (GRCm38) |
Y452F |
probably benign |
Het |
Gen1 |
A |
G |
12: 11,242,418 (GRCm38) |
S457P |
probably damaging |
Het |
Gm1993 |
C |
T |
X: 25,560,356 (GRCm38) |
R77H |
probably damaging |
Het |
Gm5592 |
G |
A |
7: 41,216,159 (GRCm38) |
|
probably benign |
Het |
Hmbox1 |
A |
G |
14: 64,903,233 (GRCm38) |
|
probably null |
Het |
Hus1 |
A |
T |
11: 9,007,617 (GRCm38) |
|
probably null |
Het |
Ino80 |
G |
A |
2: 119,402,358 (GRCm38) |
R1160W |
probably damaging |
Het |
Kalrn |
A |
T |
16: 34,392,042 (GRCm38) |
F27L |
probably damaging |
Het |
Kri1 |
A |
T |
9: 21,280,384 (GRCm38) |
F187L |
probably damaging |
Het |
Lekr1 |
A |
T |
3: 65,783,915 (GRCm38) |
|
noncoding transcript |
Het |
Mapk15 |
T |
C |
15: 75,998,750 (GRCm38) |
|
probably benign |
Het |
Mrgpre |
G |
A |
7: 143,781,104 (GRCm38) |
L221F |
probably damaging |
Het |
Mrpl50 |
A |
T |
4: 49,514,399 (GRCm38) |
S91T |
possibly damaging |
Het |
Muc4 |
T |
C |
16: 32,753,802 (GRCm38) |
I1226T |
probably benign |
Het |
Mup15 |
A |
G |
4: 61,438,217 (GRCm38) |
|
probably null |
Het |
Ncapd3 |
A |
G |
9: 27,094,615 (GRCm38) |
D1469G |
probably damaging |
Het |
Nlrp9b |
G |
A |
7: 20,026,681 (GRCm38) |
|
probably null |
Het |
Npy6r |
A |
T |
18: 44,275,917 (GRCm38) |
Y135F |
probably benign |
Het |
Or7e170 |
A |
C |
9: 19,883,979 (GRCm38) |
C109G |
probably benign |
Het |
Phf14 |
G |
A |
6: 12,006,824 (GRCm38) |
R825Q |
probably damaging |
Het |
Pigg |
A |
G |
5: 108,332,885 (GRCm38) |
M379V |
probably benign |
Het |
Plppr3 |
T |
A |
10: 79,866,063 (GRCm38) |
Q315L |
probably benign |
Het |
Plxnd1 |
C |
A |
6: 115,955,756 (GRCm38) |
C1921F |
probably damaging |
Het |
Ptger4 |
A |
C |
15: 5,243,133 (GRCm38) |
S2A |
probably benign |
Het |
Qrfprl |
A |
T |
6: 65,454,991 (GRCm38) |
M293L |
probably benign |
Het |
Rab4a |
A |
T |
8: 123,834,060 (GRCm38) |
D196V |
probably benign |
Het |
Rbck1 |
G |
A |
2: 152,318,733 (GRCm38) |
Q428* |
probably null |
Het |
Rgs14 |
A |
T |
13: 55,380,062 (GRCm38) |
N266I |
probably damaging |
Het |
Serpina1c |
A |
T |
12: 103,898,708 (GRCm38) |
|
probably benign |
Het |
Sesn3 |
G |
A |
9: 14,321,220 (GRCm38) |
R263H |
probably benign |
Het |
Slfn1 |
A |
T |
11: 83,121,463 (GRCm38) |
D135V |
probably benign |
Het |
Spata17 |
T |
C |
1: 187,193,996 (GRCm38) |
K46E |
possibly damaging |
Het |
Srcin1 |
A |
C |
11: 97,534,934 (GRCm38) |
D432E |
probably damaging |
Het |
Stxbp5 |
T |
C |
10: 9,838,144 (GRCm38) |
E217G |
probably damaging |
Het |
Terf2ip |
A |
G |
8: 112,012,017 (GRCm38) |
D179G |
probably damaging |
Het |
Tll1 |
A |
G |
8: 64,056,309 (GRCm38) |
F556L |
possibly damaging |
Het |
Tmed4 |
CTCTTTCT |
CTCT |
11: 6,274,461 (GRCm38) |
|
probably null |
Het |
Trappc9 |
G |
T |
15: 72,937,067 (GRCm38) |
Q537K |
possibly damaging |
Het |
Trim30a |
G |
T |
7: 104,411,188 (GRCm38) |
C460* |
probably null |
Het |
Trim35 |
T |
C |
14: 66,307,873 (GRCm38) |
Y298H |
probably damaging |
Het |
Ugt3a1 |
T |
A |
15: 9,306,393 (GRCm38) |
H209Q |
probably benign |
Het |
Ulk4 |
T |
C |
9: 121,192,764 (GRCm38) |
K627R |
probably damaging |
Het |
Wnk1 |
T |
C |
6: 119,951,911 (GRCm38) |
T1319A |
possibly damaging |
Het |
Wnt9b |
G |
A |
11: 103,732,155 (GRCm38) |
R141C |
probably damaging |
Het |
Zfp735 |
A |
G |
11: 73,689,785 (GRCm38) |
M37V |
probably benign |
Het |
Zmym1 |
A |
T |
4: 127,050,835 (GRCm38) |
N186K |
probably benign |
Het |
|
Other mutations in Fscn3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01290:Fscn3
|
APN |
6 |
28,430,506 (GRCm38) |
missense |
probably benign |
0.43 |
IGL01312:Fscn3
|
APN |
6 |
28,434,470 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01634:Fscn3
|
APN |
6 |
28,430,538 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01899:Fscn3
|
APN |
6 |
28,436,079 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01928:Fscn3
|
APN |
6 |
28,430,182 (GRCm38) |
missense |
possibly damaging |
0.65 |
IGL02334:Fscn3
|
APN |
6 |
28,428,154 (GRCm38) |
splice site |
probably null |
|
IGL02959:Fscn3
|
APN |
6 |
28,435,998 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL03201:Fscn3
|
APN |
6 |
28,430,605 (GRCm38) |
missense |
probably benign |
0.07 |
IGL03202:Fscn3
|
APN |
6 |
28,434,452 (GRCm38) |
missense |
probably benign |
0.10 |
IGL03227:Fscn3
|
APN |
6 |
28,434,430 (GRCm38) |
missense |
probably benign |
0.00 |
0152:Fscn3
|
UTSW |
6 |
28,429,967 (GRCm38) |
unclassified |
probably benign |
|
R1478:Fscn3
|
UTSW |
6 |
28,430,568 (GRCm38) |
missense |
probably benign |
|
R1502:Fscn3
|
UTSW |
6 |
28,435,623 (GRCm38) |
missense |
probably benign |
0.05 |
R1955:Fscn3
|
UTSW |
6 |
28,430,236 (GRCm38) |
missense |
possibly damaging |
0.82 |
R2122:Fscn3
|
UTSW |
6 |
28,430,389 (GRCm38) |
missense |
probably benign |
0.18 |
R2135:Fscn3
|
UTSW |
6 |
28,431,584 (GRCm38) |
missense |
probably benign |
0.02 |
R3713:Fscn3
|
UTSW |
6 |
28,428,092 (GRCm38) |
missense |
possibly damaging |
0.89 |
R3715:Fscn3
|
UTSW |
6 |
28,428,092 (GRCm38) |
missense |
possibly damaging |
0.89 |
R3778:Fscn3
|
UTSW |
6 |
28,430,032 (GRCm38) |
missense |
possibly damaging |
0.72 |
R4745:Fscn3
|
UTSW |
6 |
28,435,628 (GRCm38) |
missense |
probably damaging |
0.98 |
R4764:Fscn3
|
UTSW |
6 |
28,436,201 (GRCm38) |
makesense |
probably null |
|
R4794:Fscn3
|
UTSW |
6 |
28,430,596 (GRCm38) |
missense |
probably damaging |
1.00 |
R5738:Fscn3
|
UTSW |
6 |
28,430,031 (GRCm38) |
missense |
possibly damaging |
0.56 |
R5951:Fscn3
|
UTSW |
6 |
28,436,174 (GRCm38) |
missense |
possibly damaging |
0.88 |
R5994:Fscn3
|
UTSW |
6 |
28,430,295 (GRCm38) |
missense |
probably benign |
|
R6595:Fscn3
|
UTSW |
6 |
28,430,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R7323:Fscn3
|
UTSW |
6 |
28,431,545 (GRCm38) |
missense |
possibly damaging |
0.53 |
R7738:Fscn3
|
UTSW |
6 |
28,434,446 (GRCm38) |
missense |
probably benign |
0.01 |
R7840:Fscn3
|
UTSW |
6 |
28,430,176 (GRCm38) |
missense |
probably damaging |
1.00 |
R8169:Fscn3
|
UTSW |
6 |
28,430,329 (GRCm38) |
missense |
possibly damaging |
0.79 |
R8991:Fscn3
|
UTSW |
6 |
28,434,473 (GRCm38) |
missense |
probably benign |
|
R9111:Fscn3
|
UTSW |
6 |
28,430,311 (GRCm38) |
missense |
probably damaging |
0.98 |
R9350:Fscn3
|
UTSW |
6 |
28,430,433 (GRCm38) |
nonsense |
probably null |
|
R9370:Fscn3
|
UTSW |
6 |
28,434,536 (GRCm38) |
missense |
probably benign |
|
R9410:Fscn3
|
UTSW |
6 |
28,430,433 (GRCm38) |
nonsense |
probably null |
|
|