Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
A |
11: 110,069,655 (GRCm39) |
K1554* |
probably null |
Het |
Car12 |
C |
T |
9: 66,661,008 (GRCm39) |
T124I |
probably damaging |
Het |
Ccdc180 |
T |
A |
4: 45,900,470 (GRCm39) |
I278K |
possibly damaging |
Het |
Disp1 |
A |
T |
1: 182,869,087 (GRCm39) |
M1111K |
probably damaging |
Het |
Fpr1 |
A |
T |
17: 18,096,897 (GRCm39) |
M364K |
probably benign |
Het |
Gad1-ps |
A |
G |
10: 99,280,383 (GRCm39) |
|
noncoding transcript |
Het |
Grn |
A |
G |
11: 102,324,069 (GRCm39) |
T53A |
probably benign |
Het |
Hmgxb3 |
T |
C |
18: 61,280,454 (GRCm39) |
N683S |
probably damaging |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Mfap3 |
T |
C |
11: 57,420,406 (GRCm39) |
V129A |
probably damaging |
Het |
Mip |
T |
A |
10: 128,061,875 (GRCm39) |
L42* |
probably null |
Het |
Myh4 |
T |
A |
11: 67,137,276 (GRCm39) |
L499Q |
possibly damaging |
Het |
Ncln |
C |
T |
10: 81,323,519 (GRCm39) |
V51I |
probably benign |
Het |
Nmnat3 |
T |
A |
9: 98,281,533 (GRCm39) |
I45N |
probably damaging |
Het |
Or1e32 |
T |
C |
11: 73,705,012 (GRCm39) |
R299G |
probably benign |
Het |
Osbpl9 |
T |
C |
4: 108,940,290 (GRCm39) |
I232V |
probably benign |
Het |
Pcdha12 |
A |
T |
18: 37,155,243 (GRCm39) |
H654L |
probably damaging |
Het |
Pcmtd2 |
A |
T |
2: 181,496,922 (GRCm39) |
I300F |
probably damaging |
Het |
Pgm1 |
C |
T |
4: 99,813,222 (GRCm39) |
T11I |
probably benign |
Het |
Phf24 |
G |
A |
4: 42,938,316 (GRCm39) |
V226I |
probably benign |
Het |
Pigo |
T |
C |
4: 43,021,083 (GRCm39) |
T612A |
probably benign |
Het |
Plekhh3 |
T |
C |
11: 101,054,973 (GRCm39) |
|
probably benign |
Het |
Ptprf |
T |
C |
4: 118,068,629 (GRCm39) |
D1713G |
probably damaging |
Het |
Rbp3 |
G |
T |
14: 33,676,069 (GRCm39) |
V6F |
probably benign |
Het |
Sac3d1 |
T |
C |
19: 6,168,387 (GRCm39) |
K77R |
probably benign |
Het |
Slc1a6 |
T |
A |
10: 78,624,915 (GRCm39) |
S107T |
probably damaging |
Het |
Syce1l |
A |
G |
8: 114,381,579 (GRCm39) |
Q164R |
probably benign |
Het |
Tgfbi |
T |
C |
13: 56,757,547 (GRCm39) |
Y30H |
probably damaging |
Het |
Tmem217 |
A |
T |
17: 29,745,532 (GRCm39) |
V66D |
probably damaging |
Het |
Tnn |
C |
A |
1: 159,934,625 (GRCm39) |
D1263Y |
probably damaging |
Het |
Ylpm1 |
T |
C |
12: 85,076,145 (GRCm39) |
F499L |
probably damaging |
Het |
|
Other mutations in Pds5b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00719:Pds5b
|
APN |
5 |
150,646,007 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01530:Pds5b
|
APN |
5 |
150,715,640 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01812:Pds5b
|
APN |
5 |
150,704,154 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02163:Pds5b
|
APN |
5 |
150,679,871 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02730:Pds5b
|
APN |
5 |
150,704,217 (GRCm39) |
splice site |
probably benign |
|
IGL02825:Pds5b
|
APN |
5 |
150,652,435 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03143:Pds5b
|
APN |
5 |
150,702,722 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03379:Pds5b
|
APN |
5 |
150,711,796 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4283001:Pds5b
|
UTSW |
5 |
150,701,774 (GRCm39) |
missense |
probably damaging |
0.99 |
R0026:Pds5b
|
UTSW |
5 |
150,673,295 (GRCm39) |
splice site |
probably benign |
|
R0197:Pds5b
|
UTSW |
5 |
150,677,896 (GRCm39) |
missense |
probably benign |
0.28 |
R0347:Pds5b
|
UTSW |
5 |
150,659,892 (GRCm39) |
splice site |
probably benign |
|
R0396:Pds5b
|
UTSW |
5 |
150,702,740 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0400:Pds5b
|
UTSW |
5 |
150,646,818 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0442:Pds5b
|
UTSW |
5 |
150,640,009 (GRCm39) |
splice site |
probably benign |
|
R0745:Pds5b
|
UTSW |
5 |
150,729,136 (GRCm39) |
missense |
probably benign |
|
R0839:Pds5b
|
UTSW |
5 |
150,688,427 (GRCm39) |
missense |
probably benign |
0.23 |
R0866:Pds5b
|
UTSW |
5 |
150,662,656 (GRCm39) |
splice site |
probably benign |
|
R1247:Pds5b
|
UTSW |
5 |
150,698,819 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R1330:Pds5b
|
UTSW |
5 |
150,684,542 (GRCm39) |
missense |
probably damaging |
0.97 |
R1440:Pds5b
|
UTSW |
5 |
150,677,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R1526:Pds5b
|
UTSW |
5 |
150,639,865 (GRCm39) |
splice site |
probably null |
|
R2010:Pds5b
|
UTSW |
5 |
150,698,819 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2051:Pds5b
|
UTSW |
5 |
150,671,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R2507:Pds5b
|
UTSW |
5 |
150,679,893 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3820:Pds5b
|
UTSW |
5 |
150,659,802 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3911:Pds5b
|
UTSW |
5 |
150,670,171 (GRCm39) |
missense |
probably benign |
0.41 |
R4077:Pds5b
|
UTSW |
5 |
150,717,824 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4118:Pds5b
|
UTSW |
5 |
150,698,819 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4342:Pds5b
|
UTSW |
5 |
150,724,319 (GRCm39) |
missense |
probably benign |
0.17 |
R4416:Pds5b
|
UTSW |
5 |
150,659,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R4503:Pds5b
|
UTSW |
5 |
150,652,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R4524:Pds5b
|
UTSW |
5 |
150,711,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4579:Pds5b
|
UTSW |
5 |
150,670,197 (GRCm39) |
missense |
probably damaging |
0.98 |
R4623:Pds5b
|
UTSW |
5 |
150,724,066 (GRCm39) |
missense |
probably benign |
0.37 |
R4847:Pds5b
|
UTSW |
5 |
150,671,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Pds5b
|
UTSW |
5 |
150,639,927 (GRCm39) |
missense |
probably benign |
0.21 |
R5271:Pds5b
|
UTSW |
5 |
150,646,818 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5281:Pds5b
|
UTSW |
5 |
150,670,073 (GRCm39) |
missense |
probably benign |
0.26 |
R5337:Pds5b
|
UTSW |
5 |
150,717,062 (GRCm39) |
missense |
probably benign |
0.03 |
R5635:Pds5b
|
UTSW |
5 |
150,701,686 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5677:Pds5b
|
UTSW |
5 |
150,639,926 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6005:Pds5b
|
UTSW |
5 |
150,693,241 (GRCm39) |
splice site |
probably null |
|
R6139:Pds5b
|
UTSW |
5 |
150,724,242 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6225:Pds5b
|
UTSW |
5 |
150,670,083 (GRCm39) |
missense |
probably damaging |
0.98 |
R6279:Pds5b
|
UTSW |
5 |
150,646,713 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6300:Pds5b
|
UTSW |
5 |
150,646,713 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6666:Pds5b
|
UTSW |
5 |
150,701,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Pds5b
|
UTSW |
5 |
150,729,026 (GRCm39) |
splice site |
probably null |
|
R7038:Pds5b
|
UTSW |
5 |
150,724,225 (GRCm39) |
missense |
probably benign |
0.02 |
R7046:Pds5b
|
UTSW |
5 |
150,673,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Pds5b
|
UTSW |
5 |
150,717,747 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7138:Pds5b
|
UTSW |
5 |
150,724,142 (GRCm39) |
nonsense |
probably null |
|
R7255:Pds5b
|
UTSW |
5 |
150,720,132 (GRCm39) |
missense |
probably benign |
0.33 |
R7467:Pds5b
|
UTSW |
5 |
150,659,792 (GRCm39) |
missense |
probably damaging |
0.99 |
R7488:Pds5b
|
UTSW |
5 |
150,646,802 (GRCm39) |
missense |
probably damaging |
0.97 |
R7512:Pds5b
|
UTSW |
5 |
150,711,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R7561:Pds5b
|
UTSW |
5 |
150,662,783 (GRCm39) |
critical splice donor site |
probably null |
|
R7576:Pds5b
|
UTSW |
5 |
150,701,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R7889:Pds5b
|
UTSW |
5 |
150,715,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R7982:Pds5b
|
UTSW |
5 |
150,693,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R8059:Pds5b
|
UTSW |
5 |
150,731,300 (GRCm39) |
missense |
unknown |
|
R8211:Pds5b
|
UTSW |
5 |
150,652,407 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8412:Pds5b
|
UTSW |
5 |
150,643,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R8503:Pds5b
|
UTSW |
5 |
150,639,972 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8556:Pds5b
|
UTSW |
5 |
150,716,073 (GRCm39) |
missense |
probably benign |
|
R8786:Pds5b
|
UTSW |
5 |
150,704,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R8929:Pds5b
|
UTSW |
5 |
150,643,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R8985:Pds5b
|
UTSW |
5 |
150,724,239 (GRCm39) |
missense |
probably benign |
0.38 |
R9184:Pds5b
|
UTSW |
5 |
150,724,249 (GRCm39) |
missense |
probably benign |
0.04 |
R9343:Pds5b
|
UTSW |
5 |
150,704,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R9432:Pds5b
|
UTSW |
5 |
150,693,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R9571:Pds5b
|
UTSW |
5 |
150,645,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R9712:Pds5b
|
UTSW |
5 |
150,729,128 (GRCm39) |
missense |
possibly damaging |
0.87 |
|