Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy3 |
A |
G |
12: 4,250,906 (GRCm39) |
D555G |
probably benign |
Het |
Anks1b |
T |
A |
10: 89,999,127 (GRCm39) |
C411* |
probably null |
Het |
Atp5pf |
A |
T |
16: 84,625,358 (GRCm39) |
Y82N |
probably damaging |
Het |
Cd19 |
A |
T |
7: 126,012,730 (GRCm39) |
V221D |
possibly damaging |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cyp4f13 |
A |
T |
17: 33,148,110 (GRCm39) |
|
probably null |
Het |
Ddrgk1 |
T |
C |
2: 130,496,629 (GRCm39) |
D245G |
probably damaging |
Het |
Eya2 |
A |
G |
2: 165,557,872 (GRCm39) |
D156G |
possibly damaging |
Het |
Gm42763 |
T |
C |
9: 110,374,365 (GRCm39) |
|
probably benign |
Het |
Gtdc1 |
T |
C |
2: 44,460,435 (GRCm39) |
Y417C |
probably damaging |
Het |
Map1b |
T |
C |
13: 99,569,914 (GRCm39) |
T936A |
unknown |
Het |
Med23 |
G |
A |
10: 24,779,641 (GRCm39) |
R906K |
probably damaging |
Het |
Mill2 |
G |
A |
7: 18,592,168 (GRCm39) |
W263* |
probably null |
Het |
Mup20 |
T |
C |
4: 61,970,237 (GRCm39) |
N107D |
possibly damaging |
Het |
Neb |
A |
G |
2: 52,083,177 (GRCm39) |
|
probably benign |
Het |
Ntrk2 |
A |
G |
13: 59,208,194 (GRCm39) |
N680S |
probably damaging |
Het |
Or12d2 |
A |
C |
17: 37,624,802 (GRCm39) |
S158A |
probably damaging |
Het |
Or9a2 |
C |
T |
6: 41,748,490 (GRCm39) |
V248I |
probably damaging |
Het |
Pik3c3 |
T |
C |
18: 30,477,113 (GRCm39) |
I878T |
probably damaging |
Het |
Plxnd1 |
A |
G |
6: 115,932,703 (GRCm39) |
*1926R |
probably null |
Het |
Prl8a9 |
T |
A |
13: 27,743,432 (GRCm39) |
L124F |
probably damaging |
Het |
Proser3 |
A |
T |
7: 30,242,958 (GRCm39) |
N206K |
possibly damaging |
Het |
Rasef |
G |
T |
4: 73,652,725 (GRCm39) |
T439N |
probably damaging |
Het |
Slc6a18 |
T |
C |
13: 73,825,904 (GRCm39) |
T49A |
probably benign |
Het |
Spag17 |
A |
C |
3: 99,983,187 (GRCm39) |
T1496P |
probably damaging |
Het |
Vmn1r63 |
A |
C |
7: 5,806,038 (GRCm39) |
V198G |
probably damaging |
Het |
Vmn2r112 |
T |
C |
17: 22,833,975 (GRCm39) |
S548P |
probably damaging |
Het |
Vps13a |
T |
C |
19: 16,688,305 (GRCm39) |
D834G |
probably benign |
Het |
Vps8 |
A |
T |
16: 21,340,653 (GRCm39) |
N799I |
probably damaging |
Het |
Zfhx4 |
A |
G |
3: 5,464,663 (GRCm39) |
H1632R |
possibly damaging |
Het |
Zp1 |
T |
A |
19: 10,897,851 (GRCm39) |
E30V |
probably benign |
Het |
|
Other mutations in Pde3a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01388:Pde3a
|
APN |
6 |
141,405,464 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01400:Pde3a
|
APN |
6 |
141,404,954 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01752:Pde3a
|
APN |
6 |
141,433,339 (GRCm39) |
splice site |
probably benign |
|
IGL01819:Pde3a
|
APN |
6 |
141,433,263 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02014:Pde3a
|
APN |
6 |
141,404,870 (GRCm39) |
missense |
probably null |
1.00 |
IGL02119:Pde3a
|
APN |
6 |
141,405,529 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02677:Pde3a
|
APN |
6 |
141,350,898 (GRCm39) |
splice site |
probably benign |
|
IGL02961:Pde3a
|
APN |
6 |
141,405,426 (GRCm39) |
nonsense |
probably null |
|
IGL03034:Pde3a
|
APN |
6 |
141,438,126 (GRCm39) |
splice site |
probably benign |
|
IGL03142:Pde3a
|
APN |
6 |
141,438,025 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4305001:Pde3a
|
UTSW |
6 |
141,438,036 (GRCm39) |
missense |
probably benign |
0.04 |
R0412:Pde3a
|
UTSW |
6 |
141,444,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R0517:Pde3a
|
UTSW |
6 |
141,444,383 (GRCm39) |
nonsense |
probably null |
|
R0573:Pde3a
|
UTSW |
6 |
141,437,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R0621:Pde3a
|
UTSW |
6 |
141,195,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Pde3a
|
UTSW |
6 |
141,405,042 (GRCm39) |
splice site |
probably benign |
|
R1065:Pde3a
|
UTSW |
6 |
141,422,458 (GRCm39) |
splice site |
probably benign |
|
R1110:Pde3a
|
UTSW |
6 |
141,405,042 (GRCm39) |
splice site |
probably benign |
|
R1462:Pde3a
|
UTSW |
6 |
141,405,560 (GRCm39) |
missense |
probably benign |
0.05 |
R1462:Pde3a
|
UTSW |
6 |
141,405,560 (GRCm39) |
missense |
probably benign |
0.05 |
R1470:Pde3a
|
UTSW |
6 |
141,411,932 (GRCm39) |
missense |
probably benign |
0.41 |
R1470:Pde3a
|
UTSW |
6 |
141,411,932 (GRCm39) |
missense |
probably benign |
0.41 |
R1480:Pde3a
|
UTSW |
6 |
141,433,300 (GRCm39) |
missense |
probably benign |
0.17 |
R1559:Pde3a
|
UTSW |
6 |
141,404,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R1862:Pde3a
|
UTSW |
6 |
141,433,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R1862:Pde3a
|
UTSW |
6 |
141,196,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R1902:Pde3a
|
UTSW |
6 |
141,444,496 (GRCm39) |
missense |
probably benign |
|
R1909:Pde3a
|
UTSW |
6 |
141,195,965 (GRCm39) |
missense |
probably benign |
0.00 |
R2048:Pde3a
|
UTSW |
6 |
141,434,732 (GRCm39) |
splice site |
probably benign |
|
R2144:Pde3a
|
UTSW |
6 |
141,435,837 (GRCm39) |
missense |
probably benign |
0.40 |
R2155:Pde3a
|
UTSW |
6 |
141,429,640 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2208:Pde3a
|
UTSW |
6 |
141,196,073 (GRCm39) |
missense |
probably damaging |
0.97 |
R2405:Pde3a
|
UTSW |
6 |
141,426,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R4592:Pde3a
|
UTSW |
6 |
141,404,942 (GRCm39) |
missense |
probably benign |
0.13 |
R4677:Pde3a
|
UTSW |
6 |
141,411,865 (GRCm39) |
missense |
probably benign |
0.02 |
R4803:Pde3a
|
UTSW |
6 |
141,404,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R4887:Pde3a
|
UTSW |
6 |
141,416,668 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4999:Pde3a
|
UTSW |
6 |
141,195,751 (GRCm39) |
missense |
probably benign |
0.00 |
R5055:Pde3a
|
UTSW |
6 |
141,433,682 (GRCm39) |
nonsense |
probably null |
|
R5181:Pde3a
|
UTSW |
6 |
141,426,981 (GRCm39) |
critical splice donor site |
probably null |
|
R5640:Pde3a
|
UTSW |
6 |
141,429,641 (GRCm39) |
missense |
probably damaging |
0.99 |
R5694:Pde3a
|
UTSW |
6 |
141,196,228 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6176:Pde3a
|
UTSW |
6 |
141,444,615 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6394:Pde3a
|
UTSW |
6 |
141,433,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R6692:Pde3a
|
UTSW |
6 |
141,425,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Pde3a
|
UTSW |
6 |
141,433,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R7137:Pde3a
|
UTSW |
6 |
141,444,472 (GRCm39) |
missense |
probably benign |
0.26 |
R7163:Pde3a
|
UTSW |
6 |
141,433,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R7677:Pde3a
|
UTSW |
6 |
141,195,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7754:Pde3a
|
UTSW |
6 |
141,404,975 (GRCm39) |
missense |
probably benign |
0.32 |
R8037:Pde3a
|
UTSW |
6 |
141,429,650 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8123:Pde3a
|
UTSW |
6 |
141,411,917 (GRCm39) |
missense |
probably benign |
0.00 |
R8206:Pde3a
|
UTSW |
6 |
141,433,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R8262:Pde3a
|
UTSW |
6 |
141,433,527 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8376:Pde3a
|
UTSW |
6 |
141,426,947 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8893:Pde3a
|
UTSW |
6 |
141,405,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R9037:Pde3a
|
UTSW |
6 |
141,416,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R9158:Pde3a
|
UTSW |
6 |
141,195,614 (GRCm39) |
missense |
probably benign |
|
R9222:Pde3a
|
UTSW |
6 |
141,437,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Pde3a
|
UTSW |
6 |
141,425,202 (GRCm39) |
missense |
probably benign |
0.01 |
R9385:Pde3a
|
UTSW |
6 |
141,437,982 (GRCm39) |
missense |
probably benign |
0.30 |
X0053:Pde3a
|
UTSW |
6 |
141,429,695 (GRCm39) |
splice site |
probably null |
|
X0062:Pde3a
|
UTSW |
6 |
141,195,710 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Pde3a
|
UTSW |
6 |
141,196,195 (GRCm39) |
missense |
probably benign |
0.39 |
|