Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
G |
C |
3: 121,928,807 (GRCm39) |
G1340A |
probably benign |
Het |
Ambra1 |
T |
A |
2: 91,717,210 (GRCm39) |
Y836N |
probably damaging |
Het |
Arhgap26 |
A |
T |
18: 39,504,130 (GRCm39) |
H144L |
probably benign |
Het |
B3gnt5 |
A |
G |
16: 19,588,364 (GRCm39) |
I194M |
probably damaging |
Het |
Bltp1 |
G |
T |
3: 37,095,524 (GRCm39) |
G4509V |
probably damaging |
Het |
Bod1l |
A |
T |
5: 41,979,498 (GRCm39) |
C605* |
probably null |
Het |
C2cd3 |
G |
T |
7: 100,055,284 (GRCm39) |
K482N |
possibly damaging |
Het |
Cd300lg |
T |
A |
11: 101,934,047 (GRCm39) |
L98Q |
probably damaging |
Het |
Cerkl |
T |
A |
2: 79,171,701 (GRCm39) |
I386F |
possibly damaging |
Het |
Cfh |
T |
A |
1: 140,028,716 (GRCm39) |
D466V |
possibly damaging |
Het |
Crtc1 |
A |
T |
8: 70,850,949 (GRCm39) |
I221N |
probably damaging |
Het |
Ctnnbl1 |
T |
C |
2: 157,678,563 (GRCm39) |
S389P |
probably benign |
Het |
Ctsb |
A |
T |
14: 63,376,544 (GRCm39) |
D258V |
probably damaging |
Het |
Cuzd1 |
G |
T |
7: 130,913,432 (GRCm39) |
T395N |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,128,536 (GRCm39) |
T1240A |
probably benign |
Het |
Dok7 |
T |
A |
5: 35,221,671 (GRCm39) |
|
probably null |
Het |
Dscaml1 |
T |
C |
9: 45,361,882 (GRCm39) |
V214A |
probably damaging |
Het |
Enpp6 |
A |
T |
8: 47,518,469 (GRCm39) |
Y199F |
probably benign |
Het |
Entpd5 |
C |
A |
12: 84,441,434 (GRCm39) |
K111N |
probably damaging |
Het |
Fam98a |
A |
G |
17: 75,848,276 (GRCm39) |
L146S |
probably damaging |
Het |
Fhod3 |
A |
T |
18: 25,248,921 (GRCm39) |
I1367F |
probably damaging |
Het |
Fmnl2 |
A |
G |
2: 52,995,549 (GRCm39) |
E424G |
probably damaging |
Het |
Fpr3 |
T |
A |
17: 18,190,922 (GRCm39) |
Y64* |
probably null |
Het |
Fzd6 |
A |
T |
15: 38,895,019 (GRCm39) |
H395L |
probably damaging |
Het |
Gcsh |
T |
A |
8: 117,715,921 (GRCm39) |
H54L |
probably damaging |
Het |
Gsdma |
T |
A |
11: 98,567,210 (GRCm39) |
S437T |
unknown |
Het |
Gzmc |
A |
G |
14: 56,471,376 (GRCm39) |
V55A |
probably damaging |
Het |
Hecw2 |
T |
A |
1: 53,965,704 (GRCm39) |
|
probably null |
Het |
Ifi207 |
A |
G |
1: 173,555,306 (GRCm39) |
V792A |
probably benign |
Het |
Itpr3 |
C |
A |
17: 27,314,534 (GRCm39) |
N661K |
possibly damaging |
Het |
Jmy |
A |
T |
13: 93,577,819 (GRCm39) |
I783N |
probably benign |
Het |
Kcmf1 |
T |
C |
6: 72,820,003 (GRCm39) |
E281G |
possibly damaging |
Het |
Klra3 |
G |
C |
6: 130,310,107 (GRCm39) |
R138G |
probably benign |
Het |
Lgr6 |
T |
A |
1: 135,032,670 (GRCm39) |
Y70F |
possibly damaging |
Het |
Lnx1 |
T |
G |
5: 74,780,678 (GRCm39) |
D330A |
probably damaging |
Het |
Lrp5 |
T |
C |
19: 3,664,234 (GRCm39) |
N106S |
probably benign |
Het |
Mamdc4 |
C |
A |
2: 25,459,759 (GRCm39) |
R135L |
possibly damaging |
Het |
Mcm3ap |
A |
G |
10: 76,340,121 (GRCm39) |
E1464G |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,034,280 (GRCm39) |
V666A |
possibly damaging |
Het |
Mettl3 |
T |
A |
14: 52,534,385 (GRCm39) |
E331D |
probably benign |
Het |
Mphosph9 |
T |
C |
5: 124,405,204 (GRCm39) |
K789R |
probably damaging |
Het |
Mtf2 |
T |
C |
5: 108,239,995 (GRCm39) |
L234P |
probably damaging |
Het |
Ncdn |
C |
A |
4: 126,642,491 (GRCm39) |
E389* |
probably null |
Het |
Ndor1 |
A |
G |
2: 25,139,279 (GRCm39) |
S231P |
probably damaging |
Het |
Nelfa |
T |
G |
5: 34,056,215 (GRCm39) |
K483Q |
probably damaging |
Het |
Odad1 |
T |
A |
7: 45,592,282 (GRCm39) |
M354K |
probably benign |
Het |
Opn1sw |
C |
T |
6: 29,378,923 (GRCm39) |
R243Q |
probably benign |
Het |
Or13a24 |
T |
A |
7: 140,155,034 (GRCm39) |
|
probably null |
Het |
Or9e1 |
A |
G |
11: 58,732,792 (GRCm39) |
N284S |
probably damaging |
Het |
Pik3cd |
T |
C |
4: 149,739,653 (GRCm39) |
E584G |
probably damaging |
Het |
Plcb3 |
A |
T |
19: 6,935,041 (GRCm39) |
M870K |
possibly damaging |
Het |
Poc5 |
A |
G |
13: 96,528,152 (GRCm39) |
D16G |
probably damaging |
Het |
Prpf40a |
A |
G |
2: 53,035,852 (GRCm39) |
I633T |
probably damaging |
Het |
Ptpn13 |
G |
T |
5: 103,704,044 (GRCm39) |
E1359* |
probably null |
Het |
Ptprr |
C |
A |
10: 116,024,113 (GRCm39) |
Y4* |
probably null |
Het |
Rbm45 |
T |
C |
2: 76,202,503 (GRCm39) |
|
probably null |
Het |
Rfng |
C |
T |
11: 120,672,687 (GRCm39) |
W320* |
probably null |
Het |
Rgs6 |
G |
T |
12: 83,138,547 (GRCm39) |
V294L |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,169,002 (GRCm39) |
|
probably null |
Het |
Ruvbl2 |
T |
A |
7: 45,073,566 (GRCm39) |
N313I |
probably damaging |
Het |
Sema4g |
G |
A |
19: 44,981,256 (GRCm39) |
V70M |
probably damaging |
Het |
Siglec1 |
T |
C |
2: 130,918,078 (GRCm39) |
T969A |
probably benign |
Het |
Slc22a27 |
T |
A |
19: 7,844,348 (GRCm39) |
T431S |
possibly damaging |
Het |
Slc25a16 |
G |
A |
10: 62,756,643 (GRCm39) |
R38H |
probably damaging |
Het |
Slc38a6 |
T |
C |
12: 73,391,626 (GRCm39) |
V296A |
probably benign |
Het |
Sltm |
A |
G |
9: 70,493,948 (GRCm39) |
K782E |
probably damaging |
Het |
Styxl1 |
T |
A |
5: 135,799,175 (GRCm39) |
Y23F |
probably damaging |
Het |
Svs4 |
T |
C |
2: 164,120,148 (GRCm39) |
I20V |
unknown |
Het |
Syt14 |
G |
T |
1: 192,613,084 (GRCm39) |
T572K |
possibly damaging |
Het |
Tbc1d5 |
A |
T |
17: 51,227,603 (GRCm39) |
I214N |
possibly damaging |
Het |
Tm9sf3 |
A |
G |
19: 41,227,223 (GRCm39) |
S283P |
probably benign |
Het |
Tmtc1 |
C |
T |
6: 148,147,208 (GRCm39) |
|
probably null |
Het |
Ttll7 |
T |
A |
3: 146,602,422 (GRCm39) |
N73K |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,602,802 (GRCm39) |
K18473N |
probably damaging |
Het |
Ubr2 |
A |
C |
17: 47,278,173 (GRCm39) |
Y721* |
probably null |
Het |
Vmn1r14 |
T |
A |
6: 57,211,286 (GRCm39) |
I288N |
probably damaging |
Het |
Vmn2r103 |
T |
C |
17: 19,993,662 (GRCm39) |
I13T |
probably benign |
Het |
Vps13a |
A |
T |
19: 16,678,494 (GRCm39) |
Y1162* |
probably null |
Het |
Vps51 |
C |
A |
19: 6,121,497 (GRCm39) |
R175L |
probably benign |
Het |
Zfp523 |
C |
A |
17: 28,423,473 (GRCm39) |
S149R |
probably benign |
Het |
Zik1 |
A |
G |
7: 10,224,053 (GRCm39) |
I348T |
possibly damaging |
Het |
Znfx1 |
T |
A |
2: 166,898,708 (GRCm39) |
H72L |
probably benign |
Het |
|
Other mutations in Slc39a11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0011:Slc39a11
|
UTSW |
11 |
113,138,659 (GRCm39) |
missense |
probably benign |
0.00 |
R0614:Slc39a11
|
UTSW |
11 |
113,414,452 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0621:Slc39a11
|
UTSW |
11 |
113,354,905 (GRCm39) |
missense |
probably benign |
0.25 |
R0798:Slc39a11
|
UTSW |
11 |
113,414,330 (GRCm39) |
missense |
probably benign |
0.04 |
R0959:Slc39a11
|
UTSW |
11 |
113,354,899 (GRCm39) |
missense |
probably benign |
0.31 |
R1386:Slc39a11
|
UTSW |
11 |
113,138,550 (GRCm39) |
missense |
probably benign |
0.31 |
R1576:Slc39a11
|
UTSW |
11 |
113,450,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Slc39a11
|
UTSW |
11 |
113,354,800 (GRCm39) |
missense |
probably null |
0.98 |
R2127:Slc39a11
|
UTSW |
11 |
113,260,629 (GRCm39) |
missense |
probably benign |
|
R2218:Slc39a11
|
UTSW |
11 |
113,450,376 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6259:Slc39a11
|
UTSW |
11 |
113,354,780 (GRCm39) |
missense |
probably benign |
0.10 |
R7420:Slc39a11
|
UTSW |
11 |
113,138,648 (GRCm39) |
missense |
probably damaging |
0.99 |
R7440:Slc39a11
|
UTSW |
11 |
113,452,918 (GRCm39) |
missense |
probably damaging |
0.96 |
R7447:Slc39a11
|
UTSW |
11 |
113,452,849 (GRCm39) |
missense |
probably benign |
|
R7805:Slc39a11
|
UTSW |
11 |
113,482,781 (GRCm39) |
splice site |
probably null |
|
R8557:Slc39a11
|
UTSW |
11 |
113,141,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R9346:Slc39a11
|
UTSW |
11 |
113,414,449 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Slc39a11
|
UTSW |
11 |
113,141,372 (GRCm39) |
missense |
probably damaging |
1.00 |
|