Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afg3l1 |
T |
C |
8: 124,228,293 (GRCm39) |
S666P |
probably damaging |
Het |
B3gntl1 |
A |
T |
11: 121,514,980 (GRCm39) |
W263R |
probably damaging |
Het |
Carmil3 |
A |
G |
14: 55,732,899 (GRCm39) |
N270S |
possibly damaging |
Het |
Ctdp1 |
T |
C |
18: 80,492,569 (GRCm39) |
E642G |
probably damaging |
Het |
Cyp2b9 |
A |
T |
7: 25,909,531 (GRCm39) |
K433M |
probably damaging |
Het |
Dcc |
A |
G |
18: 71,721,056 (GRCm39) |
V435A |
possibly damaging |
Het |
Defa26 |
A |
T |
8: 22,108,875 (GRCm39) |
M87L |
probably benign |
Het |
Dnah11 |
T |
A |
12: 117,958,962 (GRCm39) |
I2974L |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,685,943 (GRCm39) |
D131G |
possibly damaging |
Het |
Dock6 |
A |
T |
9: 21,725,861 (GRCm39) |
S1447R |
probably benign |
Het |
Dtl |
G |
T |
1: 191,307,462 (GRCm39) |
N17K |
probably benign |
Het |
Grid2 |
A |
G |
6: 64,322,718 (GRCm39) |
I573V |
possibly damaging |
Het |
Hoxa9 |
T |
C |
6: 52,202,684 (GRCm39) |
E134G |
possibly damaging |
Het |
Kcnn3 |
A |
T |
3: 89,574,399 (GRCm39) |
N637I |
probably damaging |
Het |
Ktn1 |
T |
C |
14: 47,901,532 (GRCm39) |
F97L |
probably benign |
Het |
Lmbrd2 |
T |
C |
15: 9,165,939 (GRCm39) |
I271T |
probably damaging |
Het |
Lrp6 |
A |
C |
6: 134,456,729 (GRCm39) |
I845S |
probably damaging |
Het |
Med13l |
T |
A |
5: 118,879,891 (GRCm39) |
N994K |
probably benign |
Het |
Mrrf |
A |
T |
2: 36,067,125 (GRCm39) |
|
probably null |
Het |
Mtmr1 |
G |
A |
X: 70,431,837 (GRCm39) |
V125I |
probably damaging |
Het |
Nol8 |
C |
T |
13: 49,815,923 (GRCm39) |
A677V |
possibly damaging |
Het |
Or13g1 |
T |
A |
7: 85,956,057 (GRCm39) |
N88I |
probably benign |
Het |
Or51k1 |
T |
G |
7: 103,661,266 (GRCm39) |
L214F |
probably damaging |
Het |
Or8k3 |
A |
T |
2: 86,059,057 (GRCm39) |
V86D |
probably damaging |
Het |
Paxip1 |
C |
A |
5: 27,965,084 (GRCm39) |
V659F |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,571,104 (GRCm39) |
V163A |
probably damaging |
Het |
Pkn3 |
T |
A |
2: 29,977,184 (GRCm39) |
H641Q |
probably damaging |
Het |
Plekhg6 |
G |
A |
6: 125,347,623 (GRCm39) |
R444C |
probably damaging |
Het |
Rfx2 |
T |
C |
17: 57,106,308 (GRCm39) |
E175G |
probably benign |
Het |
Samd9l |
A |
C |
6: 3,377,264 (GRCm39) |
|
probably benign |
Het |
Serpinb9d |
A |
G |
13: 33,379,949 (GRCm39) |
E96G |
probably damaging |
Het |
Setd4 |
T |
C |
16: 93,388,006 (GRCm39) |
E160G |
probably damaging |
Het |
Sf3b2 |
C |
T |
19: 5,324,852 (GRCm39) |
D845N |
probably damaging |
Het |
Slc16a4 |
A |
G |
3: 107,208,413 (GRCm39) |
I308V |
possibly damaging |
Het |
Slco2b1 |
T |
A |
7: 99,339,644 (GRCm39) |
N100Y |
probably damaging |
Het |
Sptbn1 |
A |
T |
11: 30,071,545 (GRCm39) |
S1475R |
probably benign |
Het |
Tecta |
T |
C |
9: 42,278,100 (GRCm39) |
D1136G |
probably benign |
Het |
Tmem94 |
G |
C |
11: 115,679,543 (GRCm39) |
R273S |
probably damaging |
Het |
Tns3 |
A |
G |
11: 8,395,730 (GRCm39) |
S1225P |
possibly damaging |
Het |
Ugt2b36 |
A |
G |
5: 87,239,834 (GRCm39) |
Y184H |
probably benign |
Het |
Vmn2r59 |
A |
T |
7: 41,662,150 (GRCm39) |
M555K |
probably benign |
Het |
|
Other mutations in Sec14l5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01771:Sec14l5
|
APN |
16 |
4,996,494 (GRCm39) |
critical splice donor site |
probably null |
|
R0226:Sec14l5
|
UTSW |
16 |
4,998,167 (GRCm39) |
missense |
probably benign |
0.18 |
R0333:Sec14l5
|
UTSW |
16 |
4,984,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R0581:Sec14l5
|
UTSW |
16 |
4,996,349 (GRCm39) |
splice site |
probably null |
|
R2109:Sec14l5
|
UTSW |
16 |
4,984,968 (GRCm39) |
nonsense |
probably null |
|
R2230:Sec14l5
|
UTSW |
16 |
4,994,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R2944:Sec14l5
|
UTSW |
16 |
4,998,697 (GRCm39) |
missense |
probably benign |
0.05 |
R3001:Sec14l5
|
UTSW |
16 |
4,989,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R3002:Sec14l5
|
UTSW |
16 |
4,989,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R3409:Sec14l5
|
UTSW |
16 |
4,983,518 (GRCm39) |
splice site |
probably null |
|
R3432:Sec14l5
|
UTSW |
16 |
4,996,463 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3913:Sec14l5
|
UTSW |
16 |
4,965,720 (GRCm39) |
splice site |
probably benign |
|
R4941:Sec14l5
|
UTSW |
16 |
4,994,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R5468:Sec14l5
|
UTSW |
16 |
4,985,004 (GRCm39) |
splice site |
probably null |
|
R5474:Sec14l5
|
UTSW |
16 |
4,996,382 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5871:Sec14l5
|
UTSW |
16 |
4,986,717 (GRCm39) |
missense |
probably benign |
0.00 |
R6226:Sec14l5
|
UTSW |
16 |
4,994,429 (GRCm39) |
missense |
probably damaging |
0.99 |
R6315:Sec14l5
|
UTSW |
16 |
4,998,141 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6333:Sec14l5
|
UTSW |
16 |
4,984,908 (GRCm39) |
missense |
probably benign |
0.00 |
R6360:Sec14l5
|
UTSW |
16 |
4,990,859 (GRCm39) |
missense |
probably damaging |
0.99 |
R7426:Sec14l5
|
UTSW |
16 |
4,998,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:Sec14l5
|
UTSW |
16 |
4,994,364 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Sec14l5
|
UTSW |
16 |
4,993,966 (GRCm39) |
missense |
probably benign |
0.00 |
|