Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,242,134 (GRCm39) |
E1332D |
probably benign |
Het |
Abca5 |
C |
A |
11: 110,220,043 (GRCm39) |
V8L |
probably benign |
Het |
Abcc8 |
C |
T |
7: 45,773,339 (GRCm39) |
E797K |
probably benign |
Het |
Acd |
C |
A |
8: 106,425,039 (GRCm39) |
|
probably null |
Het |
Adam34l |
A |
T |
8: 44,078,132 (GRCm39) |
Y697* |
probably null |
Het |
Adamts12 |
T |
C |
15: 11,311,240 (GRCm39) |
S1166P |
probably benign |
Het |
Alox12b |
T |
C |
11: 69,049,199 (GRCm39) |
Y83H |
possibly damaging |
Het |
Antxr2 |
A |
T |
5: 98,178,297 (GRCm39) |
S38T |
probably damaging |
Het |
Aox1 |
A |
G |
1: 58,115,262 (GRCm39) |
E749G |
probably damaging |
Het |
Arpc1a |
T |
A |
5: 145,043,901 (GRCm39) |
C344S |
possibly damaging |
Het |
Bcan |
T |
C |
3: 87,902,908 (GRCm39) |
Y290C |
probably damaging |
Het |
Bod1l |
G |
A |
5: 41,991,018 (GRCm39) |
S179F |
possibly damaging |
Het |
Catsper3 |
A |
C |
13: 55,953,561 (GRCm39) |
D224A |
probably damaging |
Het |
Ccar2 |
A |
G |
14: 70,377,946 (GRCm39) |
S680P |
probably damaging |
Het |
Ccdc18 |
A |
G |
5: 108,368,703 (GRCm39) |
H1275R |
possibly damaging |
Het |
Ccdc40 |
T |
C |
11: 119,150,730 (GRCm39) |
M1011T |
possibly damaging |
Het |
Cfap46 |
T |
A |
7: 139,263,386 (GRCm39) |
D17V |
probably damaging |
Het |
Csn1s2a |
T |
C |
5: 87,926,058 (GRCm39) |
F45L |
probably benign |
Het |
Cwf19l2 |
T |
G |
9: 3,458,802 (GRCm39) |
N750K |
possibly damaging |
Het |
Cyb5r4 |
A |
G |
9: 86,922,462 (GRCm39) |
D157G |
probably benign |
Het |
D130040H23Rik |
T |
A |
8: 69,755,354 (GRCm39) |
I253N |
probably benign |
Het |
Dennd4a |
C |
T |
9: 64,804,516 (GRCm39) |
A1285V |
probably benign |
Het |
Dlat |
A |
G |
9: 50,548,874 (GRCm39) |
S561P |
probably damaging |
Het |
Dlgap2 |
T |
A |
8: 14,823,347 (GRCm39) |
V522E |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,331,859 (GRCm39) |
Y2148* |
probably null |
Het |
Dnase2a |
T |
C |
8: 85,635,392 (GRCm39) |
|
probably benign |
Het |
Elapor2 |
A |
G |
5: 9,468,007 (GRCm39) |
E225G |
probably damaging |
Het |
Fam83f |
T |
C |
15: 80,574,113 (GRCm39) |
|
probably benign |
Het |
Firrm |
G |
A |
1: 163,792,363 (GRCm39) |
L545F |
probably damaging |
Het |
Foxi1 |
A |
T |
11: 34,157,937 (GRCm39) |
N29K |
possibly damaging |
Het |
Galk2 |
T |
C |
2: 125,817,183 (GRCm39) |
L324P |
probably benign |
Het |
Gdpd4 |
G |
A |
7: 97,622,162 (GRCm39) |
V214I |
probably benign |
Het |
Gfra3 |
C |
T |
18: 34,844,373 (GRCm39) |
A56T |
probably damaging |
Het |
Glyctk |
A |
G |
9: 106,032,547 (GRCm39) |
S489P |
probably damaging |
Het |
Izumo4 |
A |
T |
10: 80,539,569 (GRCm39) |
I135F |
probably damaging |
Het |
Krt87 |
T |
A |
15: 101,385,071 (GRCm39) |
T342S |
probably benign |
Het |
L1td1 |
T |
A |
4: 98,625,714 (GRCm39) |
D636E |
possibly damaging |
Het |
Letm2 |
A |
G |
8: 26,086,460 (GRCm39) |
|
probably benign |
Het |
Lpin1 |
A |
G |
12: 16,591,744 (GRCm39) |
F828L |
probably damaging |
Het |
Lrrc37 |
T |
C |
11: 103,511,431 (GRCm39) |
D179G |
unknown |
Het |
Mdn1 |
T |
A |
4: 32,763,339 (GRCm39) |
D5146E |
probably damaging |
Het |
Megf10 |
T |
A |
18: 57,324,257 (GRCm39) |
Y99* |
probably null |
Het |
Men1 |
A |
G |
19: 6,387,660 (GRCm39) |
D285G |
probably damaging |
Het |
Mertk |
T |
G |
2: 128,643,116 (GRCm39) |
D838E |
probably benign |
Het |
Mta1 |
T |
C |
12: 113,091,694 (GRCm39) |
S266P |
possibly damaging |
Het |
Mta3 |
G |
A |
17: 84,089,397 (GRCm39) |
V320M |
probably damaging |
Het |
Nlrp9c |
G |
A |
7: 26,084,245 (GRCm39) |
Q445* |
probably null |
Het |
Or2m12 |
A |
T |
16: 19,105,357 (GRCm39) |
N45K |
probably damaging |
Het |
Or51e1 |
T |
C |
7: 102,358,961 (GRCm39) |
I165T |
possibly damaging |
Het |
Or8b38 |
A |
T |
9: 37,972,646 (GRCm39) |
K10I |
probably benign |
Het |
Or8d6 |
T |
G |
9: 39,854,117 (GRCm39) |
I187R |
probably damaging |
Het |
Pbrm1 |
T |
A |
14: 30,828,132 (GRCm39) |
L1320I |
probably damaging |
Het |
Pdzd2 |
G |
T |
15: 12,457,972 (GRCm39) |
T297K |
probably damaging |
Het |
Pfas |
T |
C |
11: 68,882,795 (GRCm39) |
D782G |
probably damaging |
Het |
Pik3c3 |
T |
C |
18: 30,426,185 (GRCm39) |
|
probably null |
Het |
Pira2 |
T |
C |
7: 3,847,452 (GRCm39) |
N79S |
probably damaging |
Het |
Pkdrej |
G |
T |
15: 85,700,632 (GRCm39) |
T1768K |
probably damaging |
Het |
Plcb3 |
T |
C |
19: 6,940,353 (GRCm39) |
I439V |
probably benign |
Het |
Pold4 |
T |
A |
19: 4,282,593 (GRCm39) |
Y58* |
probably null |
Het |
Ppef2 |
T |
G |
5: 92,398,371 (GRCm39) |
Q49P |
probably damaging |
Het |
Ralgapa1 |
T |
A |
12: 55,723,817 (GRCm39) |
I2026F |
possibly damaging |
Het |
Rest |
T |
A |
5: 77,416,209 (GRCm39) |
V141E |
possibly damaging |
Het |
Rnf139 |
T |
C |
15: 58,771,202 (GRCm39) |
V409A |
probably benign |
Het |
Rnpc3 |
T |
C |
3: 113,404,704 (GRCm39) |
|
probably benign |
Het |
S100a10 |
A |
T |
3: 93,468,377 (GRCm39) |
E36V |
probably benign |
Het |
S1pr3 |
A |
C |
13: 51,573,952 (GRCm39) |
K378Q |
probably benign |
Het |
Scaper |
T |
A |
9: 55,593,222 (GRCm39) |
I472F |
probably damaging |
Het |
Sgcg |
G |
A |
14: 61,477,896 (GRCm39) |
|
probably benign |
Het |
Shank1 |
A |
T |
7: 43,991,539 (GRCm39) |
R69* |
probably null |
Het |
Shoc1 |
G |
A |
4: 59,054,142 (GRCm39) |
|
probably benign |
Het |
Siglecf |
A |
G |
7: 43,004,967 (GRCm39) |
N399S |
probably benign |
Het |
Slc25a54 |
T |
A |
3: 108,987,932 (GRCm39) |
Y24* |
probably null |
Het |
Slc29a4 |
T |
C |
5: 142,707,243 (GRCm39) |
*529R |
probably null |
Het |
Slc41a2 |
G |
A |
10: 83,137,029 (GRCm39) |
Q293* |
probably null |
Het |
Slc4a7 |
T |
C |
14: 14,737,509 (GRCm38) |
|
probably null |
Het |
Slfn9 |
G |
T |
11: 82,872,402 (GRCm39) |
T778N |
probably benign |
Het |
Ssr2 |
T |
C |
3: 88,483,949 (GRCm39) |
|
probably benign |
Het |
Tecrl |
T |
A |
5: 83,502,706 (GRCm39) |
T33S |
probably benign |
Het |
Tnfrsf9 |
T |
A |
4: 151,018,804 (GRCm39) |
C158* |
probably null |
Het |
Tradd |
T |
C |
8: 105,985,792 (GRCm39) |
E253G |
possibly damaging |
Het |
Usp34 |
A |
G |
11: 23,314,479 (GRCm39) |
H807R |
probably benign |
Het |
Vmn2r129 |
G |
T |
4: 156,686,692 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r27 |
T |
C |
6: 124,201,170 (GRCm39) |
I262M |
probably benign |
Het |
Vps13a |
A |
G |
19: 16,737,316 (GRCm39) |
V91A |
probably damaging |
Het |
Vwf |
C |
T |
6: 125,619,902 (GRCm39) |
R1527C |
probably damaging |
Het |
Zfp526 |
T |
G |
7: 24,924,594 (GRCm39) |
D284E |
possibly damaging |
Het |
Zfp646 |
T |
C |
7: 127,483,021 (GRCm39) |
F1733L |
possibly damaging |
Het |
Zfp90 |
A |
G |
8: 107,145,755 (GRCm39) |
H29R |
probably benign |
Het |
Zkscan4 |
A |
G |
13: 21,668,104 (GRCm39) |
E185G |
probably benign |
Het |
|
Other mutations in Wwc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00432:Wwc1
|
APN |
11 |
35,735,029 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01161:Wwc1
|
APN |
11 |
35,758,103 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01401:Wwc1
|
APN |
11 |
35,789,445 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01771:Wwc1
|
APN |
11 |
35,744,185 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01804:Wwc1
|
APN |
11 |
35,732,751 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02079:Wwc1
|
APN |
11 |
35,766,885 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02201:Wwc1
|
APN |
11 |
35,734,978 (GRCm39) |
splice site |
probably benign |
|
IGL03376:Wwc1
|
APN |
11 |
35,743,121 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03403:Wwc1
|
APN |
11 |
35,806,111 (GRCm39) |
missense |
possibly damaging |
0.94 |
BB002:Wwc1
|
UTSW |
11 |
35,734,990 (GRCm39) |
missense |
probably benign |
0.00 |
BB012:Wwc1
|
UTSW |
11 |
35,734,990 (GRCm39) |
missense |
probably benign |
0.00 |
P0008:Wwc1
|
UTSW |
11 |
35,744,178 (GRCm39) |
splice site |
probably benign |
|
R0277:Wwc1
|
UTSW |
11 |
35,743,175 (GRCm39) |
missense |
probably damaging |
0.99 |
R0321:Wwc1
|
UTSW |
11 |
35,732,637 (GRCm39) |
nonsense |
probably null |
|
R0323:Wwc1
|
UTSW |
11 |
35,743,175 (GRCm39) |
missense |
probably damaging |
0.99 |
R0629:Wwc1
|
UTSW |
11 |
35,744,299 (GRCm39) |
missense |
probably benign |
0.18 |
R1302:Wwc1
|
UTSW |
11 |
35,734,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R1769:Wwc1
|
UTSW |
11 |
35,752,671 (GRCm39) |
missense |
probably benign |
|
R2000:Wwc1
|
UTSW |
11 |
35,767,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Wwc1
|
UTSW |
11 |
35,780,180 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2138:Wwc1
|
UTSW |
11 |
35,732,714 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2140:Wwc1
|
UTSW |
11 |
35,761,355 (GRCm39) |
missense |
probably benign |
0.01 |
R2680:Wwc1
|
UTSW |
11 |
35,766,756 (GRCm39) |
missense |
probably benign |
0.23 |
R3864:Wwc1
|
UTSW |
11 |
35,801,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R4773:Wwc1
|
UTSW |
11 |
35,758,123 (GRCm39) |
missense |
probably benign |
|
R4926:Wwc1
|
UTSW |
11 |
35,780,227 (GRCm39) |
missense |
probably benign |
0.17 |
R4980:Wwc1
|
UTSW |
11 |
35,778,930 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4990:Wwc1
|
UTSW |
11 |
35,767,393 (GRCm39) |
missense |
probably benign |
0.00 |
R5044:Wwc1
|
UTSW |
11 |
35,774,172 (GRCm39) |
missense |
probably benign |
0.45 |
R5238:Wwc1
|
UTSW |
11 |
35,766,723 (GRCm39) |
missense |
probably benign |
0.02 |
R5421:Wwc1
|
UTSW |
11 |
35,801,123 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5421:Wwc1
|
UTSW |
11 |
35,766,890 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5461:Wwc1
|
UTSW |
11 |
35,758,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R5705:Wwc1
|
UTSW |
11 |
35,767,423 (GRCm39) |
missense |
probably damaging |
0.99 |
R5847:Wwc1
|
UTSW |
11 |
35,758,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R5993:Wwc1
|
UTSW |
11 |
35,743,163 (GRCm39) |
missense |
probably benign |
0.17 |
R6006:Wwc1
|
UTSW |
11 |
35,780,100 (GRCm39) |
missense |
probably damaging |
0.98 |
R6006:Wwc1
|
UTSW |
11 |
35,761,809 (GRCm39) |
missense |
probably null |
1.00 |
R6516:Wwc1
|
UTSW |
11 |
35,758,129 (GRCm39) |
missense |
probably benign |
0.05 |
R6519:Wwc1
|
UTSW |
11 |
35,744,264 (GRCm39) |
missense |
probably benign |
0.04 |
R6520:Wwc1
|
UTSW |
11 |
35,744,264 (GRCm39) |
missense |
probably benign |
0.04 |
R6525:Wwc1
|
UTSW |
11 |
35,744,264 (GRCm39) |
missense |
probably benign |
0.04 |
R6526:Wwc1
|
UTSW |
11 |
35,744,264 (GRCm39) |
missense |
probably benign |
0.04 |
R6527:Wwc1
|
UTSW |
11 |
35,744,264 (GRCm39) |
missense |
probably benign |
0.04 |
R6528:Wwc1
|
UTSW |
11 |
35,744,264 (GRCm39) |
missense |
probably benign |
0.04 |
R7060:Wwc1
|
UTSW |
11 |
35,806,003 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7156:Wwc1
|
UTSW |
11 |
35,788,201 (GRCm39) |
critical splice donor site |
probably null |
|
R7448:Wwc1
|
UTSW |
11 |
35,766,533 (GRCm39) |
missense |
probably benign |
|
R7586:Wwc1
|
UTSW |
11 |
35,735,022 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7793:Wwc1
|
UTSW |
11 |
35,759,936 (GRCm39) |
missense |
probably benign |
0.21 |
R7925:Wwc1
|
UTSW |
11 |
35,734,990 (GRCm39) |
missense |
probably benign |
0.00 |
R8296:Wwc1
|
UTSW |
11 |
35,761,384 (GRCm39) |
splice site |
probably benign |
|
R8369:Wwc1
|
UTSW |
11 |
35,758,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R8735:Wwc1
|
UTSW |
11 |
35,774,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R8804:Wwc1
|
UTSW |
11 |
35,774,144 (GRCm39) |
missense |
probably benign |
0.30 |
R9081:Wwc1
|
UTSW |
11 |
35,782,331 (GRCm39) |
missense |
probably benign |
0.12 |
R9281:Wwc1
|
UTSW |
11 |
35,780,211 (GRCm39) |
missense |
probably benign |
0.03 |
R9561:Wwc1
|
UTSW |
11 |
35,870,796 (GRCm39) |
critical splice donor site |
probably null |
|
R9619:Wwc1
|
UTSW |
11 |
35,766,779 (GRCm39) |
missense |
probably damaging |
0.98 |
R9713:Wwc1
|
UTSW |
11 |
35,766,576 (GRCm39) |
missense |
probably benign |
0.33 |
X0025:Wwc1
|
UTSW |
11 |
35,766,867 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1088:Wwc1
|
UTSW |
11 |
35,774,309 (GRCm39) |
missense |
possibly damaging |
0.62 |
|