Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700102P08Rik |
T |
A |
9: 108,270,439 (GRCm39) |
M1K |
probably null |
Het |
2810021J22Rik |
T |
C |
11: 58,771,166 (GRCm39) |
L216S |
possibly damaging |
Het |
4933405O20Rik |
G |
A |
7: 50,249,220 (GRCm39) |
E85K |
possibly damaging |
Het |
Agrn |
A |
G |
4: 156,257,492 (GRCm39) |
F1153L |
probably damaging |
Het |
Cbx8 |
A |
G |
11: 118,929,742 (GRCm39) |
S284P |
probably damaging |
Het |
Cep128 |
A |
G |
12: 91,305,893 (GRCm39) |
L170P |
probably damaging |
Het |
Cyp4f14 |
T |
A |
17: 33,126,959 (GRCm39) |
T324S |
probably damaging |
Het |
Daw1 |
G |
T |
1: 83,170,419 (GRCm39) |
V244L |
probably benign |
Het |
Eef2kmt |
A |
G |
16: 5,063,222 (GRCm39) |
V306A |
probably benign |
Het |
Enah |
A |
T |
1: 181,763,293 (GRCm39) |
|
probably null |
Het |
Fam171b |
T |
C |
2: 83,683,949 (GRCm39) |
|
probably null |
Het |
Fsip2 |
C |
T |
2: 82,808,925 (GRCm39) |
T1748I |
possibly damaging |
Het |
Gabrg2 |
C |
T |
11: 41,862,559 (GRCm39) |
G175D |
probably damaging |
Het |
Gtf2h3 |
C |
T |
5: 124,722,360 (GRCm39) |
T121I |
probably benign |
Het |
Hmcn1 |
G |
T |
1: 150,458,047 (GRCm39) |
N33K |
probably damaging |
Het |
Incenp |
T |
A |
19: 9,855,770 (GRCm39) |
E514V |
unknown |
Het |
Kank3 |
T |
C |
17: 34,036,917 (GRCm39) |
S74P |
probably benign |
Het |
Lrriq1 |
G |
T |
10: 103,051,206 (GRCm39) |
N515K |
probably benign |
Het |
Mfsd13b |
G |
A |
7: 120,591,056 (GRCm39) |
D266N |
probably damaging |
Het |
Neto1 |
T |
C |
18: 86,422,998 (GRCm39) |
Y152H |
probably damaging |
Het |
Nub1 |
C |
A |
5: 24,900,533 (GRCm39) |
F145L |
probably benign |
Het |
Nufip1 |
T |
C |
14: 76,351,715 (GRCm39) |
|
probably null |
Het |
Pard6g |
T |
A |
18: 80,123,116 (GRCm39) |
V50E |
probably benign |
Het |
Polr3a |
T |
C |
14: 24,505,009 (GRCm39) |
I1084V |
possibly damaging |
Het |
Rapgef5 |
A |
C |
12: 117,703,379 (GRCm39) |
N431T |
probably damaging |
Het |
Rassf9 |
A |
T |
10: 102,381,205 (GRCm39) |
T196S |
probably damaging |
Het |
Rrp12 |
T |
C |
19: 41,865,029 (GRCm39) |
Y764C |
probably benign |
Het |
Slfn8 |
T |
C |
11: 82,908,550 (GRCm39) |
|
probably null |
Het |
Smox |
T |
A |
2: 131,363,026 (GRCm39) |
V265D |
probably damaging |
Het |
Sult1b1 |
T |
C |
5: 87,678,510 (GRCm39) |
I105V |
probably benign |
Het |
Sycp2 |
T |
C |
2: 178,045,554 (GRCm39) |
D22G |
probably damaging |
Het |
Tbck |
G |
A |
3: 132,456,977 (GRCm39) |
M630I |
possibly damaging |
Het |
Tenm4 |
G |
C |
7: 96,486,538 (GRCm39) |
G965R |
possibly damaging |
Het |
Trappc10 |
G |
A |
10: 78,023,694 (GRCm39) |
T1258I |
probably damaging |
Het |
Tssk1 |
G |
A |
16: 17,713,123 (GRCm39) |
G303S |
probably benign |
Het |
Tstd2 |
T |
C |
4: 46,120,461 (GRCm39) |
Y313C |
probably damaging |
Het |
Usp42 |
G |
A |
5: 143,707,401 (GRCm39) |
T260M |
probably damaging |
Het |
Xpo7 |
G |
A |
14: 70,921,171 (GRCm39) |
T599I |
probably damaging |
Het |
Zfp553 |
A |
G |
7: 126,836,013 (GRCm39) |
K523E |
probably benign |
Het |
|
Other mutations in Wdr43 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Wdr43
|
APN |
17 |
71,959,809 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02077:Wdr43
|
APN |
17 |
71,947,286 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02114:Wdr43
|
APN |
17 |
71,959,843 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02252:Wdr43
|
APN |
17 |
71,933,845 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02352:Wdr43
|
APN |
17 |
71,939,043 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02359:Wdr43
|
APN |
17 |
71,939,043 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03082:Wdr43
|
APN |
17 |
71,945,336 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03095:Wdr43
|
APN |
17 |
71,948,282 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02837:Wdr43
|
UTSW |
17 |
71,949,731 (GRCm39) |
missense |
probably benign |
0.00 |
R0039:Wdr43
|
UTSW |
17 |
71,960,487 (GRCm39) |
nonsense |
probably null |
|
R0164:Wdr43
|
UTSW |
17 |
71,938,992 (GRCm39) |
splice site |
probably benign |
|
R0271:Wdr43
|
UTSW |
17 |
71,933,820 (GRCm39) |
missense |
probably benign |
0.00 |
R1117:Wdr43
|
UTSW |
17 |
71,923,382 (GRCm39) |
missense |
probably benign |
0.35 |
R1873:Wdr43
|
UTSW |
17 |
71,940,647 (GRCm39) |
missense |
probably benign |
0.05 |
R1973:Wdr43
|
UTSW |
17 |
71,947,235 (GRCm39) |
missense |
probably benign |
0.00 |
R3620:Wdr43
|
UTSW |
17 |
71,957,601 (GRCm39) |
missense |
probably benign |
0.13 |
R3922:Wdr43
|
UTSW |
17 |
71,945,296 (GRCm39) |
splice site |
probably benign |
|
R4097:Wdr43
|
UTSW |
17 |
71,964,532 (GRCm39) |
missense |
probably benign |
|
R5067:Wdr43
|
UTSW |
17 |
71,933,849 (GRCm39) |
missense |
probably benign |
|
R6251:Wdr43
|
UTSW |
17 |
71,957,048 (GRCm39) |
splice site |
probably null |
|
R6364:Wdr43
|
UTSW |
17 |
71,964,649 (GRCm39) |
missense |
probably damaging |
0.96 |
R7086:Wdr43
|
UTSW |
17 |
71,923,434 (GRCm39) |
missense |
probably benign |
0.02 |
R7725:Wdr43
|
UTSW |
17 |
71,923,338 (GRCm39) |
missense |
probably benign |
0.27 |
R8104:Wdr43
|
UTSW |
17 |
71,923,350 (GRCm39) |
missense |
probably benign |
0.01 |
R8901:Wdr43
|
UTSW |
17 |
71,932,461 (GRCm39) |
missense |
probably benign |
0.00 |
R9648:Wdr43
|
UTSW |
17 |
71,960,494 (GRCm39) |
missense |
probably benign |
0.04 |
|