Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alpk2 |
A |
C |
18: 65,440,367 (GRCm39) |
V809G |
possibly damaging |
Het |
Bank1 |
T |
A |
3: 135,772,151 (GRCm39) |
D493V |
probably damaging |
Het |
Camk2d |
T |
C |
3: 126,604,273 (GRCm39) |
|
probably benign |
Het |
Ccdc17 |
T |
A |
4: 116,455,745 (GRCm39) |
L292H |
probably damaging |
Het |
Ccdc7b |
A |
G |
8: 129,837,498 (GRCm39) |
|
probably benign |
Het |
Cd34 |
C |
A |
1: 194,641,525 (GRCm39) |
T317K |
probably damaging |
Het |
Col6a5 |
C |
G |
9: 105,789,649 (GRCm39) |
|
probably null |
Het |
Colgalt2 |
G |
T |
1: 152,384,312 (GRCm39) |
A551S |
possibly damaging |
Het |
Copa |
T |
C |
1: 171,918,592 (GRCm39) |
|
probably benign |
Het |
Coq7 |
T |
C |
7: 118,128,867 (GRCm39) |
D56G |
probably damaging |
Het |
Dlg4 |
C |
T |
11: 69,922,610 (GRCm39) |
T201I |
probably damaging |
Het |
Dnah7a |
T |
A |
1: 53,536,264 (GRCm39) |
D2593V |
probably benign |
Het |
Ect2l |
T |
A |
10: 18,018,788 (GRCm39) |
E536V |
probably damaging |
Het |
Emilin3 |
A |
G |
2: 160,752,799 (GRCm39) |
|
probably benign |
Het |
Eml2 |
T |
C |
7: 18,935,479 (GRCm39) |
|
probably benign |
Het |
Fam135b |
C |
T |
15: 71,320,505 (GRCm39) |
|
probably benign |
Het |
Gart |
C |
T |
16: 91,430,790 (GRCm39) |
R424H |
probably benign |
Het |
Gramd1a |
A |
G |
7: 30,842,049 (GRCm39) |
L80P |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,358,163 (GRCm39) |
K2415E |
probably benign |
Het |
Ica1 |
C |
T |
6: 8,644,256 (GRCm39) |
|
probably benign |
Het |
Idi2l |
T |
A |
13: 8,990,958 (GRCm39) |
|
probably benign |
Het |
Iyd |
A |
T |
10: 3,497,127 (GRCm39) |
M161L |
probably damaging |
Het |
Kdm5a |
T |
C |
6: 120,392,200 (GRCm39) |
L974S |
probably damaging |
Het |
Kif1a |
T |
C |
1: 92,947,605 (GRCm39) |
D1619G |
probably damaging |
Het |
Lypd8 |
C |
T |
11: 58,275,499 (GRCm39) |
T78M |
probably damaging |
Het |
Marchf10 |
T |
A |
11: 105,280,986 (GRCm39) |
H433L |
probably benign |
Het |
Mbp |
A |
G |
18: 82,572,742 (GRCm39) |
Y13C |
probably damaging |
Het |
Mertk |
A |
T |
2: 128,580,233 (GRCm39) |
N229I |
probably damaging |
Het |
Msrb2 |
T |
A |
2: 19,398,091 (GRCm39) |
D116E |
probably damaging |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Otoa |
G |
A |
7: 120,744,873 (GRCm39) |
|
probably benign |
Het |
Pclo |
A |
G |
5: 14,719,552 (GRCm39) |
T1230A |
unknown |
Het |
Polrmt |
T |
C |
10: 79,574,979 (GRCm39) |
T851A |
possibly damaging |
Het |
Prpf6 |
C |
T |
2: 181,277,841 (GRCm39) |
P401L |
probably damaging |
Het |
Rasgrp4 |
A |
G |
7: 28,839,635 (GRCm39) |
|
probably benign |
Het |
Rc3h2 |
A |
T |
2: 37,272,064 (GRCm39) |
|
probably benign |
Het |
Reps1 |
A |
G |
10: 17,996,841 (GRCm39) |
T588A |
probably damaging |
Het |
Rtel1 |
A |
C |
2: 180,993,674 (GRCm39) |
S782R |
probably benign |
Het |
Sacm1l |
A |
G |
9: 123,378,060 (GRCm39) |
|
probably benign |
Het |
Skic3 |
G |
C |
13: 76,298,848 (GRCm39) |
V1185L |
possibly damaging |
Het |
Skint5 |
A |
T |
4: 113,588,266 (GRCm39) |
L728* |
probably null |
Het |
Slc9b2 |
T |
A |
3: 135,029,536 (GRCm39) |
|
probably benign |
Het |
Snapc3 |
A |
T |
4: 83,368,397 (GRCm39) |
H298L |
probably benign |
Het |
Tex9 |
A |
T |
9: 72,399,233 (GRCm39) |
M1K |
probably null |
Het |
Trappc13 |
C |
T |
13: 104,291,424 (GRCm39) |
|
probably benign |
Het |
Usp3 |
C |
T |
9: 66,425,726 (GRCm39) |
R467H |
probably benign |
Het |
Vmn2r11 |
T |
A |
5: 109,195,597 (GRCm39) |
L576F |
possibly damaging |
Het |
Wnk4 |
T |
C |
11: 101,165,849 (GRCm39) |
F792S |
probably benign |
Het |
Zfp1007 |
T |
C |
5: 109,826,442 (GRCm39) |
|
probably null |
Het |
Zfp280d |
T |
C |
9: 72,269,230 (GRCm39) |
V764A |
probably benign |
Het |
Zfp69 |
G |
A |
4: 120,806,622 (GRCm39) |
Q4* |
probably null |
Het |
Zfp692 |
T |
G |
11: 58,200,449 (GRCm39) |
L206R |
probably damaging |
Het |
Zic2 |
CCCACCACCACCATCACCACCACCACC |
CCCACCATCACCACCACCACC |
14: 122,713,776 (GRCm39) |
|
probably benign |
Het |
Zic4 |
T |
A |
9: 91,266,170 (GRCm39) |
Y264* |
probably null |
Het |
Zic4 |
T |
A |
9: 91,266,172 (GRCm39) |
M272K |
probably benign |
Het |
Zscan4b |
A |
T |
7: 10,635,390 (GRCm39) |
N284K |
probably damaging |
Het |
|
Other mutations in Fhip2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01366:Fhip2b
|
APN |
14 |
70,822,813 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01862:Fhip2b
|
APN |
14 |
70,825,130 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02306:Fhip2b
|
APN |
14 |
70,826,437 (GRCm39) |
missense |
probably benign |
|
IGL02534:Fhip2b
|
APN |
14 |
70,823,630 (GRCm39) |
missense |
probably benign |
|
IGL02534:Fhip2b
|
APN |
14 |
70,823,128 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03071:Fhip2b
|
APN |
14 |
70,823,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03162:Fhip2b
|
APN |
14 |
70,824,994 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03166:Fhip2b
|
APN |
14 |
70,827,616 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03134:Fhip2b
|
UTSW |
14 |
70,826,149 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0043:Fhip2b
|
UTSW |
14 |
70,826,101 (GRCm39) |
missense |
probably benign |
0.45 |
R0691:Fhip2b
|
UTSW |
14 |
70,825,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R1680:Fhip2b
|
UTSW |
14 |
70,824,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R1727:Fhip2b
|
UTSW |
14 |
70,831,438 (GRCm39) |
missense |
probably damaging |
0.98 |
R2059:Fhip2b
|
UTSW |
14 |
70,822,489 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2362:Fhip2b
|
UTSW |
14 |
70,823,805 (GRCm39) |
missense |
probably benign |
0.18 |
R3423:Fhip2b
|
UTSW |
14 |
70,824,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R4233:Fhip2b
|
UTSW |
14 |
70,824,318 (GRCm39) |
missense |
probably damaging |
0.99 |
R4770:Fhip2b
|
UTSW |
14 |
70,825,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R5903:Fhip2b
|
UTSW |
14 |
70,829,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R6217:Fhip2b
|
UTSW |
14 |
70,829,198 (GRCm39) |
splice site |
probably null |
|
R6665:Fhip2b
|
UTSW |
14 |
70,823,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R7424:Fhip2b
|
UTSW |
14 |
70,831,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R9176:Fhip2b
|
UTSW |
14 |
70,826,540 (GRCm39) |
missense |
probably benign |
0.40 |
R9393:Fhip2b
|
UTSW |
14 |
70,831,463 (GRCm39) |
nonsense |
probably null |
|
R9486:Fhip2b
|
UTSW |
14 |
70,826,479 (GRCm39) |
missense |
probably benign |
0.00 |
R9529:Fhip2b
|
UTSW |
14 |
70,822,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R9610:Fhip2b
|
UTSW |
14 |
70,824,258 (GRCm39) |
missense |
probably benign |
0.44 |
R9611:Fhip2b
|
UTSW |
14 |
70,824,258 (GRCm39) |
missense |
probably benign |
0.44 |
R9646:Fhip2b
|
UTSW |
14 |
70,827,808 (GRCm39) |
missense |
probably damaging |
0.99 |
R9699:Fhip2b
|
UTSW |
14 |
70,825,179 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9760:Fhip2b
|
UTSW |
14 |
70,827,621 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Fhip2b
|
UTSW |
14 |
70,823,644 (GRCm39) |
missense |
not run |
|
Z1177:Fhip2b
|
UTSW |
14 |
70,823,644 (GRCm39) |
missense |
not run |
|
|