Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ace |
C |
T |
11: 105,867,449 (GRCm39) |
Q484* |
probably null |
Het |
Ackr3 |
T |
C |
1: 90,141,703 (GRCm39) |
I54T |
probably damaging |
Het |
Aco1 |
G |
A |
4: 40,183,605 (GRCm39) |
G508S |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
Ankef1 |
T |
C |
2: 136,387,658 (GRCm39) |
S192P |
possibly damaging |
Het |
Ankrd16 |
T |
G |
2: 11,794,559 (GRCm39) |
C315G |
possibly damaging |
Het |
Ankzf1 |
T |
C |
1: 75,172,887 (GRCm39) |
S328P |
probably damaging |
Het |
Aqp2 |
A |
G |
15: 99,480,981 (GRCm39) |
I176V |
probably benign |
Het |
Arhgap45 |
A |
G |
10: 79,863,014 (GRCm39) |
Y730C |
probably damaging |
Het |
Armh3 |
A |
T |
19: 45,953,820 (GRCm39) |
I188K |
probably damaging |
Het |
Asxl2 |
A |
G |
12: 3,543,779 (GRCm39) |
E316G |
probably damaging |
Het |
Btbd17 |
A |
T |
11: 114,682,778 (GRCm39) |
|
probably null |
Het |
Calu |
A |
G |
6: 29,372,614 (GRCm39) |
Y263C |
probably damaging |
Het |
Ccdc122 |
T |
C |
14: 77,306,391 (GRCm39) |
|
probably null |
Het |
Cenpf |
T |
C |
1: 189,389,098 (GRCm39) |
K1578R |
probably damaging |
Het |
Cep120 |
A |
G |
18: 53,852,384 (GRCm39) |
V498A |
possibly damaging |
Het |
Ces1a |
T |
A |
8: 93,774,703 (GRCm39) |
N12Y |
probably benign |
Het |
Chmp1a |
A |
T |
8: 123,934,761 (GRCm39) |
M65K |
probably damaging |
Het |
Cnot1 |
G |
T |
8: 96,466,461 (GRCm39) |
T1592K |
possibly damaging |
Het |
Cps1 |
T |
A |
1: 67,243,797 (GRCm39) |
I1091N |
probably benign |
Het |
Dhx32 |
T |
C |
7: 133,323,021 (GRCm39) |
N731S |
probably benign |
Het |
Dhx33 |
G |
A |
11: 70,890,669 (GRCm39) |
R177W |
probably damaging |
Het |
Dmd |
G |
C |
X: 83,356,089 (GRCm39) |
A2257P |
probably benign |
Het |
Dnah10 |
T |
C |
5: 124,891,738 (GRCm39) |
S3259P |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,496,855 (GRCm39) |
I3134V |
probably benign |
Het |
Dock3 |
A |
G |
9: 106,870,662 (GRCm39) |
F584S |
possibly damaging |
Het |
Dtnb |
A |
G |
12: 3,831,273 (GRCm39) |
T658A |
probably benign |
Het |
Duox2 |
T |
A |
2: 122,125,639 (GRCm39) |
S323C |
probably damaging |
Het |
Elovl3 |
A |
T |
19: 46,120,606 (GRCm39) |
E33V |
probably damaging |
Het |
Enpp5 |
T |
C |
17: 44,396,264 (GRCm39) |
F392S |
probably benign |
Het |
Eogt |
T |
C |
6: 97,108,337 (GRCm39) |
T235A |
probably benign |
Het |
Etv3 |
T |
C |
3: 87,443,526 (GRCm39) |
V370A |
probably benign |
Het |
Ewsr1 |
C |
T |
11: 5,021,555 (GRCm39) |
R466H |
unknown |
Het |
Fcgbp |
G |
A |
7: 27,819,814 (GRCm39) |
G2514S |
probably damaging |
Het |
Flt1 |
A |
T |
5: 147,536,416 (GRCm39) |
D808E |
possibly damaging |
Het |
Glg1 |
C |
T |
8: 111,895,303 (GRCm39) |
G836E |
probably damaging |
Het |
Gm17334 |
A |
G |
11: 53,663,654 (GRCm39) |
|
probably benign |
Het |
Gpbp1 |
A |
T |
13: 111,589,941 (GRCm39) |
D51E |
probably benign |
Het |
Il12rb2 |
C |
G |
6: 67,337,536 (GRCm39) |
C115S |
probably damaging |
Het |
Il1rl1 |
T |
C |
1: 40,501,204 (GRCm39) |
S527P |
probably damaging |
Het |
Ireb2 |
A |
G |
9: 54,788,733 (GRCm39) |
D69G |
probably benign |
Het |
Kif5a |
T |
C |
10: 127,081,238 (GRCm39) |
D232G |
probably damaging |
Het |
M1ap |
A |
G |
6: 82,958,863 (GRCm39) |
I165V |
probably benign |
Het |
Mff |
T |
A |
1: 82,729,421 (GRCm39) |
L287H |
probably damaging |
Het |
Mmp27 |
A |
G |
9: 7,577,740 (GRCm39) |
M311V |
possibly damaging |
Het |
Mpped2 |
T |
A |
2: 106,575,147 (GRCm39) |
Y77* |
probably null |
Het |
Mybbp1a |
G |
A |
11: 72,332,271 (GRCm39) |
S21N |
probably benign |
Het |
Obscn |
G |
C |
11: 58,960,107 (GRCm39) |
I3253M |
probably damaging |
Het |
Obscn |
T |
C |
11: 59,023,478 (GRCm39) |
D633G |
probably damaging |
Het |
Olr1 |
C |
T |
6: 129,479,057 (GRCm39) |
V54I |
probably benign |
Het |
Or10j3b |
A |
T |
1: 173,043,377 (GRCm39) |
D53V |
probably damaging |
Het |
Or4a74 |
A |
G |
2: 89,439,822 (GRCm39) |
V208A |
probably benign |
Het |
Phlpp2 |
T |
C |
8: 110,655,124 (GRCm39) |
S605P |
possibly damaging |
Het |
Plekhg4 |
TAGTCGATGCCCGAGTC |
TAGTC |
8: 106,103,084 (GRCm39) |
|
probably benign |
Het |
Potefam1 |
T |
C |
2: 111,030,763 (GRCm39) |
E382G |
probably damaging |
Het |
Prss8 |
C |
A |
7: 127,526,266 (GRCm39) |
R148L |
possibly damaging |
Het |
Psg27 |
T |
C |
7: 18,294,342 (GRCm39) |
D355G |
probably damaging |
Het |
Rabgef1 |
C |
A |
5: 130,216,402 (GRCm39) |
Q52K |
probably benign |
Het |
Rnf6 |
C |
T |
5: 146,147,716 (GRCm39) |
R434H |
probably damaging |
Het |
Rpl26 |
A |
G |
11: 68,794,099 (GRCm39) |
E88G |
probably benign |
Het |
Rpn1 |
T |
A |
6: 88,077,944 (GRCm39) |
L460Q |
probably damaging |
Het |
Sap130 |
T |
A |
18: 31,781,332 (GRCm39) |
I165N |
probably damaging |
Het |
Sash1 |
A |
G |
10: 8,632,461 (GRCm39) |
V258A |
probably damaging |
Het |
Scarb1 |
G |
T |
5: 125,371,207 (GRCm39) |
N288K |
probably benign |
Het |
Sec16a |
A |
G |
2: 26,330,251 (GRCm39) |
I588T |
probably damaging |
Het |
Shank2 |
C |
A |
7: 143,963,277 (GRCm39) |
S295Y |
probably damaging |
Het |
Slc15a3 |
T |
C |
19: 10,834,663 (GRCm39) |
S515P |
probably damaging |
Het |
Slc25a13 |
A |
T |
6: 6,114,017 (GRCm39) |
M285K |
probably benign |
Het |
Slc39a11 |
A |
G |
11: 113,354,800 (GRCm39) |
I143T |
probably null |
Het |
Smarcd2 |
A |
T |
11: 106,156,133 (GRCm39) |
L42* |
probably null |
Het |
Smc3 |
A |
G |
19: 53,619,964 (GRCm39) |
D620G |
probably benign |
Het |
Spata31g1 |
A |
T |
4: 42,974,171 (GRCm39) |
D1168V |
probably benign |
Het |
Syt10 |
C |
T |
15: 89,674,979 (GRCm39) |
D456N |
probably damaging |
Het |
Taar4 |
A |
C |
10: 23,837,071 (GRCm39) |
Q227P |
probably benign |
Het |
Tasor |
T |
A |
14: 27,183,170 (GRCm39) |
I543K |
probably benign |
Het |
Tecta |
G |
T |
9: 42,248,575 (GRCm39) |
Y1937* |
probably null |
Het |
Tex10 |
C |
T |
4: 48,456,800 (GRCm39) |
R637Q |
probably benign |
Het |
Tmem130 |
T |
A |
5: 144,692,084 (GRCm39) |
T107S |
possibly damaging |
Het |
Tmem132d |
T |
C |
5: 128,346,195 (GRCm39) |
D109G |
probably damaging |
Het |
Tmem81 |
A |
G |
1: 132,435,644 (GRCm39) |
Y150C |
probably damaging |
Het |
Tnrc18 |
C |
T |
5: 142,745,461 (GRCm39) |
|
probably null |
Het |
Trim43a |
A |
G |
9: 88,468,147 (GRCm39) |
K256R |
possibly damaging |
Het |
Trpm6 |
A |
G |
19: 18,855,103 (GRCm39) |
T1921A |
probably damaging |
Het |
Tubb3 |
C |
T |
8: 124,148,009 (GRCm39) |
A314V |
probably damaging |
Het |
Ube3b |
A |
C |
5: 114,553,316 (GRCm39) |
N896T |
probably benign |
Het |
Unc80 |
G |
A |
1: 66,718,903 (GRCm39) |
|
probably null |
Het |
Upb1 |
A |
G |
10: 75,260,347 (GRCm39) |
T134A |
probably damaging |
Het |
Vmn2r15 |
A |
T |
5: 109,434,619 (GRCm39) |
M695K |
possibly damaging |
Het |
Zfp619 |
T |
A |
7: 39,184,185 (GRCm39) |
Y72N |
probably benign |
Het |
Zfp672 |
G |
T |
11: 58,207,462 (GRCm39) |
H286Q |
possibly damaging |
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 |
|
R1870:Wwc1
|
UTSW |
11 |
35,752,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R2000:Wwc1
|
UTSW |
11 |
35,767,374 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|