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 |
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 |
Sec14l5 |
A |
T |
16: 4,998,570 (GRCm39) |
T537S |
probably damaging |
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 Dcc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00569:Dcc
|
APN |
18 |
71,517,296 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL00781:Dcc
|
APN |
18 |
71,942,266 (GRCm39) |
missense |
probably benign |
0.25 |
IGL00818:Dcc
|
APN |
18 |
72,088,083 (GRCm39) |
missense |
probably benign |
|
IGL00895:Dcc
|
APN |
18 |
71,943,871 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00969:Dcc
|
APN |
18 |
71,589,954 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01019:Dcc
|
APN |
18 |
71,942,161 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01132:Dcc
|
APN |
18 |
71,815,245 (GRCm39) |
nonsense |
probably null |
|
IGL01349:Dcc
|
APN |
18 |
71,503,808 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01355:Dcc
|
APN |
18 |
71,942,185 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01374:Dcc
|
APN |
18 |
71,507,624 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01947:Dcc
|
APN |
18 |
71,959,280 (GRCm39) |
missense |
probably benign |
|
IGL02470:Dcc
|
APN |
18 |
72,088,153 (GRCm39) |
splice site |
probably benign |
|
IGL02508:Dcc
|
APN |
18 |
71,503,773 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02999:Dcc
|
APN |
18 |
71,511,749 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL03034:Dcc
|
APN |
18 |
71,708,214 (GRCm39) |
nonsense |
probably null |
|
IGL03118:Dcc
|
APN |
18 |
71,553,344 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03133:Dcc
|
APN |
18 |
71,396,026 (GRCm39) |
splice site |
probably benign |
|
IGL03357:Dcc
|
APN |
18 |
71,460,625 (GRCm39) |
missense |
probably damaging |
1.00 |
Hyperrev
|
UTSW |
18 |
71,392,086 (GRCm39) |
missense |
probably damaging |
1.00 |
LCD18:Dcc
|
UTSW |
18 |
72,430,518 (GRCm39) |
intron |
probably benign |
|
P0031:Dcc
|
UTSW |
18 |
71,517,299 (GRCm39) |
splice site |
probably benign |
|
PIT4142001:Dcc
|
UTSW |
18 |
71,517,297 (GRCm39) |
splice site |
probably null |
|
R0076:Dcc
|
UTSW |
18 |
71,454,117 (GRCm39) |
nonsense |
probably null |
|
R0355:Dcc
|
UTSW |
18 |
71,708,279 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0383:Dcc
|
UTSW |
18 |
71,553,334 (GRCm39) |
missense |
probably damaging |
0.99 |
R0541:Dcc
|
UTSW |
18 |
71,392,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Dcc
|
UTSW |
18 |
71,942,275 (GRCm39) |
splice site |
probably benign |
|
R0762:Dcc
|
UTSW |
18 |
71,475,776 (GRCm39) |
splice site |
probably benign |
|
R0765:Dcc
|
UTSW |
18 |
71,496,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R0846:Dcc
|
UTSW |
18 |
71,959,283 (GRCm39) |
missense |
probably benign |
0.06 |
R1230:Dcc
|
UTSW |
18 |
71,815,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Dcc
|
UTSW |
18 |
71,553,409 (GRCm39) |
missense |
probably benign |
0.00 |
R1663:Dcc
|
UTSW |
18 |
71,959,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R1697:Dcc
|
UTSW |
18 |
71,503,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R1770:Dcc
|
UTSW |
18 |
71,579,470 (GRCm39) |
missense |
probably benign |
0.01 |
R1781:Dcc
|
UTSW |
18 |
71,511,788 (GRCm39) |
missense |
probably benign |
0.41 |
R1797:Dcc
|
UTSW |
18 |
71,500,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:Dcc
|
UTSW |
18 |
71,943,941 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2190:Dcc
|
UTSW |
18 |
71,680,491 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2248:Dcc
|
UTSW |
18 |
71,959,239 (GRCm39) |
missense |
probably benign |
0.00 |
R2262:Dcc
|
UTSW |
18 |
71,507,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R2442:Dcc
|
UTSW |
18 |
71,589,954 (GRCm39) |
missense |
probably damaging |
0.98 |
R3844:Dcc
|
UTSW |
18 |
71,959,257 (GRCm39) |
missense |
probably benign |
0.01 |
R4037:Dcc
|
UTSW |
18 |
72,483,468 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4085:Dcc
|
UTSW |
18 |
71,959,240 (GRCm39) |
missense |
probably benign |
0.00 |
R4344:Dcc
|
UTSW |
18 |
71,507,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R4499:Dcc
|
UTSW |
18 |
71,680,388 (GRCm39) |
missense |
probably benign |
0.07 |
R4611:Dcc
|
UTSW |
18 |
71,682,069 (GRCm39) |
splice site |
probably null |
|
R4811:Dcc
|
UTSW |
18 |
71,432,554 (GRCm39) |
missense |
probably benign |
0.31 |
R4937:Dcc
|
UTSW |
18 |
71,675,320 (GRCm39) |
nonsense |
probably null |
|
R5125:Dcc
|
UTSW |
18 |
71,589,948 (GRCm39) |
missense |
probably benign |
0.02 |
R5292:Dcc
|
UTSW |
18 |
71,439,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R5297:Dcc
|
UTSW |
18 |
71,511,809 (GRCm39) |
missense |
probably benign |
0.00 |
R5317:Dcc
|
UTSW |
18 |
71,517,226 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5691:Dcc
|
UTSW |
18 |
71,708,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R5693:Dcc
|
UTSW |
18 |
71,708,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Dcc
|
UTSW |
18 |
71,942,185 (GRCm39) |
missense |
probably benign |
0.00 |
R6291:Dcc
|
UTSW |
18 |
71,815,238 (GRCm39) |
missense |
probably benign |
0.06 |
R6307:Dcc
|
UTSW |
18 |
71,943,826 (GRCm39) |
missense |
probably benign |
0.15 |
R6343:Dcc
|
UTSW |
18 |
71,469,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R6508:Dcc
|
UTSW |
18 |
71,439,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R6701:Dcc
|
UTSW |
18 |
71,942,191 (GRCm39) |
missense |
probably benign |
0.02 |
R6810:Dcc
|
UTSW |
18 |
71,503,764 (GRCm39) |
missense |
probably damaging |
0.99 |
R7078:Dcc
|
UTSW |
18 |
71,680,469 (GRCm39) |
missense |
probably benign |
0.05 |
R7172:Dcc
|
UTSW |
18 |
71,511,755 (GRCm39) |
missense |
probably benign |
0.04 |
R7345:Dcc
|
UTSW |
18 |
71,511,895 (GRCm39) |
missense |
probably benign |
0.00 |
R7365:Dcc
|
UTSW |
18 |
71,959,194 (GRCm39) |
missense |
probably damaging |
0.98 |
R7395:Dcc
|
UTSW |
18 |
71,507,640 (GRCm39) |
nonsense |
probably null |
|
R7455:Dcc
|
UTSW |
18 |
71,553,394 (GRCm39) |
missense |
probably benign |
0.00 |
R7461:Dcc
|
UTSW |
18 |
71,439,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Dcc
|
UTSW |
18 |
71,553,317 (GRCm39) |
missense |
probably benign |
0.00 |
R7732:Dcc
|
UTSW |
18 |
71,579,506 (GRCm39) |
missense |
probably benign |
0.24 |
R7886:Dcc
|
UTSW |
18 |
72,087,939 (GRCm39) |
nonsense |
probably null |
|
R8097:Dcc
|
UTSW |
18 |
71,812,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R8137:Dcc
|
UTSW |
18 |
71,511,783 (GRCm39) |
missense |
probably benign |
0.00 |
R8188:Dcc
|
UTSW |
18 |
71,943,928 (GRCm39) |
missense |
probably benign |
|
R8236:Dcc
|
UTSW |
18 |
72,088,089 (GRCm39) |
missense |
probably benign |
|
R8802:Dcc
|
UTSW |
18 |
71,959,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R8869:Dcc
|
UTSW |
18 |
71,511,755 (GRCm39) |
missense |
probably benign |
0.04 |
R9221:Dcc
|
UTSW |
18 |
71,553,433 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9282:Dcc
|
UTSW |
18 |
71,815,249 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9366:Dcc
|
UTSW |
18 |
71,708,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R9566:Dcc
|
UTSW |
18 |
71,943,866 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9607:Dcc
|
UTSW |
18 |
71,721,072 (GRCm39) |
missense |
probably damaging |
1.00 |
W0251:Dcc
|
UTSW |
18 |
71,959,154 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Dcc
|
UTSW |
18 |
71,454,171 (GRCm39) |
missense |
probably damaging |
0.97 |
|