Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg3 |
A |
G |
5: 105,087,027 (GRCm39) |
I565T |
probably damaging |
Het |
Adamts8 |
G |
A |
9: 30,864,778 (GRCm39) |
C423Y |
probably damaging |
Het |
Adamts8 |
G |
A |
9: 30,870,209 (GRCm39) |
|
probably null |
Het |
Ahctf1 |
A |
C |
1: 179,613,660 (GRCm39) |
V490G |
possibly damaging |
Het |
Akap13 |
A |
G |
7: 75,261,218 (GRCm39) |
T478A |
possibly damaging |
Het |
Ampd2 |
C |
A |
3: 107,987,432 (GRCm39) |
V134L |
probably benign |
Het |
Ano9 |
T |
C |
7: 140,683,989 (GRCm39) |
S559G |
probably damaging |
Het |
Aox1 |
A |
G |
1: 58,376,590 (GRCm39) |
T924A |
probably damaging |
Het |
Atp13a1 |
A |
G |
8: 70,259,870 (GRCm39) |
E1126G |
probably damaging |
Het |
Bcan |
A |
G |
3: 87,900,382 (GRCm39) |
V617A |
probably benign |
Het |
Cfap57 |
C |
T |
4: 118,472,128 (GRCm39) |
V84I |
probably benign |
Het |
Cldnd1 |
A |
T |
16: 58,550,078 (GRCm39) |
N87I |
possibly damaging |
Het |
Enpp2 |
A |
T |
15: 54,709,275 (GRCm39) |
V784E |
probably damaging |
Het |
Eps8 |
T |
A |
6: 137,507,575 (GRCm39) |
Y51F |
possibly damaging |
Het |
Fam184b |
T |
C |
5: 45,741,595 (GRCm39) |
K212R |
probably benign |
Het |
Fbn1 |
A |
C |
2: 125,254,706 (GRCm39) |
C186G |
possibly damaging |
Het |
Glyr1 |
T |
C |
16: 4,836,785 (GRCm39) |
T460A |
probably benign |
Het |
Gm19410 |
G |
A |
8: 36,238,940 (GRCm39) |
G70R |
probably damaging |
Het |
Gna15 |
G |
A |
10: 81,359,745 (GRCm39) |
T15I |
probably damaging |
Het |
Heg1 |
T |
C |
16: 33,571,570 (GRCm39) |
C1198R |
probably damaging |
Het |
Hoxd1 |
A |
G |
2: 74,594,504 (GRCm39) |
Y253C |
probably damaging |
Het |
Il17re |
G |
T |
6: 113,443,111 (GRCm39) |
Q316H |
probably damaging |
Het |
Jakmip1 |
C |
A |
5: 37,331,182 (GRCm39) |
P621T |
probably benign |
Het |
Krt71 |
T |
C |
15: 101,643,894 (GRCm39) |
Y448C |
probably damaging |
Het |
Lgals8 |
A |
G |
13: 12,468,137 (GRCm39) |
|
probably null |
Het |
Marchf11 |
A |
G |
15: 26,409,505 (GRCm39) |
*401W |
probably null |
Het |
Mctp1 |
A |
T |
13: 76,789,829 (GRCm39) |
|
probably null |
Het |
Mms19 |
C |
A |
19: 41,944,400 (GRCm39) |
V310F |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,392,674 (GRCm39) |
F3296I |
probably damaging |
Het |
Myo7b |
A |
T |
18: 32,146,422 (GRCm39) |
I121N |
probably damaging |
Het |
Nr0b2 |
T |
C |
4: 133,280,847 (GRCm39) |
S38P |
probably benign |
Het |
Nudt16l1 |
T |
A |
16: 4,757,243 (GRCm39) |
M52K |
probably benign |
Het |
Or3a4 |
A |
G |
11: 73,945,054 (GRCm39) |
I177T |
probably damaging |
Het |
Or8k32 |
T |
C |
2: 86,368,566 (GRCm39) |
N229S |
probably benign |
Het |
Polr3gl |
A |
T |
3: 96,489,552 (GRCm39) |
|
probably null |
Het |
Ptch2 |
T |
A |
4: 116,963,198 (GRCm39) |
F228L |
probably benign |
Het |
Slc35d1 |
A |
G |
4: 103,070,360 (GRCm39) |
|
probably null |
Het |
Slc41a1 |
G |
A |
1: 131,768,635 (GRCm39) |
V198I |
probably damaging |
Het |
Slc5a7 |
T |
C |
17: 54,583,709 (GRCm39) |
D527G |
possibly damaging |
Het |
Spaca7b |
A |
G |
8: 11,705,615 (GRCm39) |
I164T |
unknown |
Het |
Spag16 |
G |
T |
1: 69,866,247 (GRCm39) |
A29S |
probably benign |
Het |
Speer4f2 |
T |
A |
5: 17,582,630 (GRCm39) |
D284E |
unknown |
Het |
Sspo |
A |
G |
6: 48,465,434 (GRCm39) |
|
probably null |
Het |
Tdpoz1 |
T |
C |
3: 93,578,517 (GRCm39) |
K89R |
possibly damaging |
Het |
Tek |
C |
T |
4: 94,740,111 (GRCm39) |
|
probably null |
Het |
Tet3 |
C |
T |
6: 83,353,956 (GRCm39) |
V902M |
probably damaging |
Het |
Tpcn2 |
C |
T |
7: 144,810,928 (GRCm39) |
V590M |
probably damaging |
Het |
Trcg1 |
T |
C |
9: 57,149,499 (GRCm39) |
V357A |
probably benign |
Het |
Tspan18 |
A |
G |
2: 93,041,203 (GRCm39) |
V133A |
probably benign |
Het |
Unc5b |
A |
T |
10: 60,613,322 (GRCm39) |
W305R |
probably damaging |
Het |
Vmn2r95 |
T |
A |
17: 18,660,529 (GRCm39) |
L314I |
possibly damaging |
Het |
Wdsub1 |
G |
A |
2: 59,707,061 (GRCm39) |
A178V |
probably damaging |
Het |
Zfp407 |
A |
G |
18: 84,577,754 (GRCm39) |
S1120P |
probably benign |
Het |
Zfp57 |
T |
C |
17: 37,320,566 (GRCm39) |
F140S |
probably damaging |
Het |
|
Other mutations in Fsip1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00819:Fsip1
|
APN |
2 |
118,080,393 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01676:Fsip1
|
APN |
2 |
118,070,865 (GRCm39) |
splice site |
probably benign |
|
IGL02039:Fsip1
|
APN |
2 |
118,070,895 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02337:Fsip1
|
APN |
2 |
118,082,195 (GRCm39) |
nonsense |
probably null |
|
IGL02668:Fsip1
|
APN |
2 |
118,082,206 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03101:Fsip1
|
APN |
2 |
118,072,144 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03155:Fsip1
|
APN |
2 |
118,082,220 (GRCm39) |
missense |
probably benign |
0.06 |
R0045:Fsip1
|
UTSW |
2 |
118,078,773 (GRCm39) |
splice site |
probably null |
|
R0045:Fsip1
|
UTSW |
2 |
118,078,773 (GRCm39) |
splice site |
probably null |
|
R1225:Fsip1
|
UTSW |
2 |
118,078,831 (GRCm39) |
missense |
probably damaging |
0.98 |
R1824:Fsip1
|
UTSW |
2 |
118,063,389 (GRCm39) |
missense |
probably damaging |
0.98 |
R2048:Fsip1
|
UTSW |
2 |
118,072,197 (GRCm39) |
missense |
probably damaging |
0.97 |
R2229:Fsip1
|
UTSW |
2 |
118,052,925 (GRCm39) |
missense |
probably benign |
0.00 |
R3026:Fsip1
|
UTSW |
2 |
118,080,384 (GRCm39) |
missense |
probably benign |
0.06 |
R3746:Fsip1
|
UTSW |
2 |
118,063,531 (GRCm39) |
missense |
probably damaging |
0.98 |
R6275:Fsip1
|
UTSW |
2 |
118,035,583 (GRCm39) |
missense |
probably benign |
0.06 |
R6395:Fsip1
|
UTSW |
2 |
118,067,406 (GRCm39) |
missense |
probably damaging |
0.99 |
R6923:Fsip1
|
UTSW |
2 |
118,080,394 (GRCm39) |
missense |
probably benign |
0.01 |
R7868:Fsip1
|
UTSW |
2 |
117,966,967 (GRCm39) |
nonsense |
probably null |
|
R8237:Fsip1
|
UTSW |
2 |
118,063,483 (GRCm39) |
missense |
probably damaging |
0.99 |
R8245:Fsip1
|
UTSW |
2 |
118,075,359 (GRCm39) |
missense |
unknown |
|
R8345:Fsip1
|
UTSW |
2 |
118,070,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8376:Fsip1
|
UTSW |
2 |
118,063,519 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8765:Fsip1
|
UTSW |
2 |
118,082,154 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9734:Fsip1
|
UTSW |
2 |
118,070,916 (GRCm39) |
missense |
probably benign |
|
Z1176:Fsip1
|
UTSW |
2 |
117,966,964 (GRCm39) |
missense |
possibly damaging |
0.89 |
|