Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
T |
C |
6: 86,936,071 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
G |
A |
13: 81,627,861 (GRCm39) |
R3667* |
probably null |
Het |
Adh5 |
T |
G |
3: 138,156,835 (GRCm39) |
C174G |
probably damaging |
Het |
Cap1 |
A |
C |
4: 122,756,692 (GRCm39) |
|
probably null |
Het |
Caps2 |
G |
A |
10: 112,051,490 (GRCm39) |
R587H |
probably damaging |
Het |
Ccn1 |
T |
A |
3: 145,353,525 (GRCm39) |
M346L |
possibly damaging |
Het |
Cdo1 |
A |
G |
18: 46,848,812 (GRCm39) |
V142A |
probably damaging |
Het |
Chuk |
T |
C |
19: 44,079,467 (GRCm39) |
T345A |
probably damaging |
Het |
Cobll1 |
T |
C |
2: 64,932,409 (GRCm39) |
|
probably null |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Cop1 |
T |
C |
1: 159,147,386 (GRCm39) |
Y571H |
probably benign |
Het |
Cstpp1 |
T |
A |
2: 91,214,182 (GRCm39) |
T58S |
probably damaging |
Het |
Dnah11 |
G |
T |
12: 117,897,585 (GRCm39) |
N3548K |
probably damaging |
Het |
Ehhadh |
G |
T |
16: 21,592,247 (GRCm39) |
S152* |
probably null |
Het |
Fitm2 |
T |
C |
2: 163,311,734 (GRCm39) |
T160A |
probably benign |
Het |
Fos |
C |
T |
12: 85,522,457 (GRCm39) |
T162I |
probably damaging |
Het |
Fsd2 |
T |
C |
7: 81,190,145 (GRCm39) |
I546V |
probably benign |
Het |
Gal3st2c |
T |
C |
1: 93,934,669 (GRCm39) |
V19A |
possibly damaging |
Het |
Gorasp2 |
T |
A |
2: 70,521,298 (GRCm39) |
S443T |
probably benign |
Het |
Klf4 |
G |
A |
4: 55,530,191 (GRCm39) |
H307Y |
probably damaging |
Het |
Ldc1 |
A |
C |
4: 130,115,417 (GRCm39) |
S44A |
probably benign |
Het |
Mark3 |
A |
G |
12: 111,593,658 (GRCm39) |
D230G |
possibly damaging |
Het |
Mnat1 |
T |
G |
12: 73,170,706 (GRCm39) |
|
probably null |
Het |
Or5m9b |
T |
C |
2: 85,905,510 (GRCm39) |
L142P |
possibly damaging |
Het |
Otogl |
T |
G |
10: 107,608,157 (GRCm39) |
T2073P |
probably benign |
Het |
Pdxdc1 |
A |
C |
16: 13,672,257 (GRCm39) |
|
probably null |
Het |
Pkhd1l1 |
T |
C |
15: 44,358,993 (GRCm39) |
S401P |
probably damaging |
Het |
Polr1a |
T |
C |
6: 71,901,627 (GRCm39) |
Y262H |
probably damaging |
Het |
Pramel19 |
A |
T |
4: 101,798,447 (GRCm39) |
K139N |
probably benign |
Het |
Scamp4 |
T |
C |
10: 80,450,537 (GRCm39) |
F205L |
probably benign |
Het |
Scn1a |
C |
T |
2: 66,155,099 (GRCm39) |
S620N |
probably benign |
Het |
Scn7a |
C |
T |
2: 66,527,944 (GRCm39) |
D849N |
possibly damaging |
Het |
Slc17a8 |
T |
C |
10: 89,442,596 (GRCm39) |
D79G |
possibly damaging |
Het |
Sync |
A |
G |
4: 129,187,897 (GRCm39) |
S310G |
probably benign |
Het |
Tbc1d9b |
A |
C |
11: 50,062,148 (GRCm39) |
I1219L |
probably benign |
Het |
Vmn1r47 |
T |
A |
6: 89,999,657 (GRCm39) |
M263K |
probably benign |
Het |
Zfp773 |
A |
T |
7: 7,135,691 (GRCm39) |
C302S |
probably damaging |
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 |
R0370:Dcc
|
UTSW |
18 |
71,721,056 (GRCm39) |
missense |
possibly damaging |
0.92 |
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 |
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 |
|