Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
G |
A |
5: 113,332,001 (GRCm39) |
R738C |
possibly damaging |
Het |
Acot12 |
G |
A |
13: 91,919,844 (GRCm39) |
V260M |
probably benign |
Het |
Alkbh8 |
A |
T |
9: 3,359,503 (GRCm39) |
H264L |
probably damaging |
Het |
Arfgef2 |
C |
T |
2: 166,715,623 (GRCm39) |
T1356I |
probably damaging |
Het |
Arhgap27 |
A |
T |
11: 103,251,130 (GRCm39) |
N199K |
probably damaging |
Het |
Asic2 |
T |
C |
11: 81,858,824 (GRCm39) |
R63G |
probably damaging |
Het |
Aspa |
T |
A |
11: 73,204,378 (GRCm39) |
M197L |
probably benign |
Het |
BC005537 |
C |
T |
13: 24,987,382 (GRCm39) |
R7W |
possibly damaging |
Het |
Brdt |
A |
T |
5: 107,518,045 (GRCm39) |
I723L |
probably benign |
Het |
C2cd3 |
T |
A |
7: 100,118,698 (GRCm39) |
F2312Y |
probably damaging |
Het |
Cd19 |
T |
C |
7: 126,009,698 (GRCm39) |
N456S |
probably damaging |
Het |
Ceacam1 |
G |
T |
7: 25,175,954 (GRCm39) |
A80E |
probably damaging |
Het |
Cep135 |
T |
C |
5: 76,788,803 (GRCm39) |
V1132A |
probably benign |
Het |
Cep85 |
A |
G |
4: 133,859,609 (GRCm39) |
C687R |
probably damaging |
Het |
Cln5 |
A |
G |
14: 103,313,501 (GRCm39) |
Y251C |
probably damaging |
Het |
Crygc |
A |
G |
1: 65,111,014 (GRCm39) |
M91T |
possibly damaging |
Het |
Ddt |
T |
C |
10: 75,609,060 (GRCm39) |
K33R |
probably damaging |
Het |
Dhfr |
G |
A |
13: 92,494,471 (GRCm39) |
W58* |
probably null |
Het |
Dhx40 |
T |
C |
11: 86,688,532 (GRCm39) |
E297G |
probably benign |
Het |
Dner |
T |
C |
1: 84,361,602 (GRCm39) |
Y669C |
probably benign |
Het |
Dpys |
G |
T |
15: 39,656,782 (GRCm39) |
F428L |
probably damaging |
Het |
Dspp |
A |
C |
5: 104,323,531 (GRCm39) |
T225P |
probably damaging |
Het |
Elac2 |
A |
G |
11: 64,890,213 (GRCm39) |
K656E |
probably damaging |
Het |
Ern1 |
T |
A |
11: 106,349,845 (GRCm39) |
R24* |
probably null |
Het |
F2rl2 |
T |
C |
13: 95,837,519 (GRCm39) |
I188T |
probably damaging |
Het |
Fam83b |
C |
T |
9: 76,399,426 (GRCm39) |
C559Y |
possibly damaging |
Het |
Fat1 |
T |
G |
8: 45,504,259 (GRCm39) |
F4584C |
probably benign |
Het |
Gabra6 |
G |
A |
11: 42,207,322 (GRCm39) |
T254I |
possibly damaging |
Het |
Garem1 |
T |
C |
18: 21,432,757 (GRCm39) |
D24G |
probably damaging |
Het |
Gas2l2 |
A |
T |
11: 83,312,816 (GRCm39) |
L832* |
probably null |
Het |
Gpr68 |
C |
T |
12: 100,845,497 (GRCm39) |
D16N |
probably benign |
Het |
Il17b |
T |
C |
18: 61,825,480 (GRCm39) |
I172T |
probably damaging |
Het |
Ildr2 |
T |
G |
1: 166,136,861 (GRCm39) |
S567A |
probably benign |
Het |
Kalrn |
A |
G |
16: 33,809,217 (GRCm39) |
V2557A |
probably damaging |
Het |
Kif1b |
A |
G |
4: 149,268,833 (GRCm39) |
S1627P |
probably benign |
Het |
Kif5a |
G |
A |
10: 127,079,343 (GRCm39) |
T285M |
probably damaging |
Het |
Lrif1 |
G |
A |
3: 106,640,459 (GRCm39) |
|
probably null |
Het |
Lrrn2 |
C |
T |
1: 132,867,116 (GRCm39) |
T727I |
unknown |
Het |
Lsg1 |
T |
C |
16: 30,383,540 (GRCm39) |
E560G |
probably benign |
Het |
Map4k4 |
C |
A |
1: 40,013,204 (GRCm39) |
Q100K |
unknown |
Het |
Mipep |
A |
T |
14: 61,040,385 (GRCm39) |
R302W |
probably damaging |
Het |
Morf4l1 |
G |
T |
9: 89,975,844 (GRCm39) |
T316K |
probably damaging |
Het |
Mov10 |
A |
T |
3: 104,711,994 (GRCm39) |
V126E |
probably damaging |
Het |
Muc2 |
T |
A |
7: 141,303,471 (GRCm39) |
C559S |
|
Het |
Myh7 |
A |
G |
14: 55,226,530 (GRCm39) |
Y410H |
probably damaging |
Het |
Nf1 |
T |
A |
11: 79,309,414 (GRCm39) |
Y433N |
probably damaging |
Het |
Nmd3 |
T |
C |
3: 69,633,750 (GRCm39) |
L79P |
probably damaging |
Het |
Nol10 |
G |
T |
12: 17,408,239 (GRCm39) |
S155I |
probably null |
Het |
Or2n1 |
T |
C |
17: 38,486,830 (GRCm39) |
L285P |
possibly damaging |
Het |
Or4p8 |
T |
C |
2: 88,727,408 (GRCm39) |
I178V |
probably benign |
Het |
Or52n2c |
T |
A |
7: 104,574,311 (GRCm39) |
Y220F |
probably damaging |
Het |
Or5b12 |
A |
G |
19: 12,896,911 (GRCm39) |
I254T |
probably benign |
Het |
Polr1c |
C |
T |
17: 46,555,817 (GRCm39) |
G188D |
probably benign |
Het |
Prpf31 |
A |
G |
7: 3,633,859 (GRCm39) |
M65V |
probably benign |
Het |
Pum2 |
A |
G |
12: 8,763,595 (GRCm39) |
T251A |
probably benign |
Het |
Rabgap1 |
G |
A |
2: 37,377,142 (GRCm39) |
V325I |
probably benign |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Rpl15 |
G |
T |
14: 18,269,017 (GRCm38) |
Y203* |
probably null |
Het |
Sac3d1 |
G |
A |
19: 6,168,456 (GRCm39) |
P54L |
possibly damaging |
Het |
Serpina3g |
A |
G |
12: 104,206,510 (GRCm39) |
I104V |
probably benign |
Het |
Setd2 |
C |
T |
9: 110,379,082 (GRCm39) |
Q966* |
probably null |
Het |
Simc1 |
G |
T |
13: 54,651,713 (GRCm39) |
D9Y |
unknown |
Het |
Slc5a8 |
T |
C |
10: 88,757,567 (GRCm39) |
L519S |
probably benign |
Het |
Srcap |
C |
A |
7: 127,138,366 (GRCm39) |
Q1179K |
possibly damaging |
Het |
Srd5a3 |
T |
C |
5: 76,295,583 (GRCm39) |
L91P |
probably damaging |
Het |
Stab1 |
T |
C |
14: 30,876,429 (GRCm39) |
T887A |
probably benign |
Het |
Sult2a6 |
A |
G |
7: 13,988,737 (GRCm39) |
F8L |
not run |
Het |
Thsd7a |
A |
T |
6: 12,471,123 (GRCm39) |
C498* |
probably null |
Het |
Timp4 |
T |
C |
6: 115,227,355 (GRCm39) |
I75V |
probably benign |
Het |
Tspyl4 |
T |
A |
10: 34,174,096 (GRCm39) |
M196K |
probably damaging |
Het |
Ubr2 |
T |
C |
17: 47,301,934 (GRCm39) |
E172G |
probably benign |
Het |
Ubr5 |
G |
A |
15: 37,980,076 (GRCm39) |
A2434V |
probably null |
Het |
Unc13c |
T |
G |
9: 73,602,159 (GRCm39) |
L1362F |
probably damaging |
Het |
Vmn2r11 |
A |
G |
5: 109,199,986 (GRCm39) |
V489A |
probably damaging |
Het |
Vps39 |
T |
C |
2: 120,169,875 (GRCm39) |
T226A |
possibly damaging |
Het |
Zan |
C |
T |
5: 137,471,863 (GRCm39) |
E185K |
probably damaging |
Het |
|
Other mutations in Pde3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01509:Pde3b
|
APN |
7 |
114,117,645 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01637:Pde3b
|
APN |
7 |
114,126,136 (GRCm39) |
nonsense |
probably null |
|
IGL02004:Pde3b
|
APN |
7 |
114,118,852 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02113:Pde3b
|
APN |
7 |
114,126,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02201:Pde3b
|
APN |
7 |
114,133,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02266:Pde3b
|
APN |
7 |
114,126,201 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02601:Pde3b
|
APN |
7 |
114,122,577 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02641:Pde3b
|
APN |
7 |
114,130,052 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02671:Pde3b
|
APN |
7 |
114,122,580 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02691:Pde3b
|
APN |
7 |
114,107,320 (GRCm39) |
splice site |
probably benign |
|
IGL02719:Pde3b
|
APN |
7 |
114,105,483 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03092:Pde3b
|
APN |
7 |
114,122,583 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4342:Pde3b
|
UTSW |
7 |
114,134,010 (GRCm39) |
small insertion |
probably benign |
|
R0208:Pde3b
|
UTSW |
7 |
114,097,216 (GRCm39) |
missense |
probably benign |
0.00 |
R1191:Pde3b
|
UTSW |
7 |
114,118,810 (GRCm39) |
missense |
probably benign |
0.01 |
R1514:Pde3b
|
UTSW |
7 |
114,130,001 (GRCm39) |
missense |
probably damaging |
0.98 |
R1612:Pde3b
|
UTSW |
7 |
114,118,791 (GRCm39) |
nonsense |
probably null |
|
R2081:Pde3b
|
UTSW |
7 |
114,122,657 (GRCm39) |
missense |
probably benign |
|
R2433:Pde3b
|
UTSW |
7 |
114,126,072 (GRCm39) |
missense |
probably benign |
0.30 |
R2508:Pde3b
|
UTSW |
7 |
114,126,092 (GRCm39) |
nonsense |
probably null |
|
R3842:Pde3b
|
UTSW |
7 |
114,126,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R4082:Pde3b
|
UTSW |
7 |
114,093,823 (GRCm39) |
missense |
probably benign |
0.04 |
R4115:Pde3b
|
UTSW |
7 |
114,120,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R4197:Pde3b
|
UTSW |
7 |
114,130,107 (GRCm39) |
splice site |
probably benign |
|
R4236:Pde3b
|
UTSW |
7 |
114,120,923 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4355:Pde3b
|
UTSW |
7 |
114,015,522 (GRCm39) |
missense |
probably benign |
|
R4411:Pde3b
|
UTSW |
7 |
114,133,984 (GRCm39) |
small deletion |
probably benign |
|
R4430:Pde3b
|
UTSW |
7 |
114,133,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R4901:Pde3b
|
UTSW |
7 |
114,107,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R4969:Pde3b
|
UTSW |
7 |
114,118,847 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5314:Pde3b
|
UTSW |
7 |
114,093,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R5346:Pde3b
|
UTSW |
7 |
114,105,425 (GRCm39) |
missense |
probably benign |
0.00 |
R5706:Pde3b
|
UTSW |
7 |
114,120,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R5844:Pde3b
|
UTSW |
7 |
114,108,106 (GRCm39) |
missense |
probably benign |
0.01 |
R6014:Pde3b
|
UTSW |
7 |
114,015,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Pde3b
|
UTSW |
7 |
114,107,502 (GRCm39) |
missense |
probably benign |
0.00 |
R6190:Pde3b
|
UTSW |
7 |
114,122,267 (GRCm39) |
splice site |
probably null |
|
R7220:Pde3b
|
UTSW |
7 |
114,135,297 (GRCm39) |
missense |
probably damaging |
0.97 |
R7239:Pde3b
|
UTSW |
7 |
114,015,384 (GRCm39) |
missense |
probably damaging |
0.99 |
R7818:Pde3b
|
UTSW |
7 |
114,090,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R8443:Pde3b
|
UTSW |
7 |
114,126,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R8483:Pde3b
|
UTSW |
7 |
114,118,803 (GRCm39) |
missense |
probably benign |
0.15 |
R8516:Pde3b
|
UTSW |
7 |
114,126,084 (GRCm39) |
missense |
probably benign |
0.01 |
R8754:Pde3b
|
UTSW |
7 |
114,015,278 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9017:Pde3b
|
UTSW |
7 |
114,015,695 (GRCm39) |
nonsense |
probably null |
|
R9221:Pde3b
|
UTSW |
7 |
114,014,697 (GRCm39) |
start gained |
probably benign |
|
R9302:Pde3b
|
UTSW |
7 |
114,122,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R9799:Pde3b
|
UTSW |
7 |
114,122,613 (GRCm39) |
missense |
probably damaging |
1.00 |
RF051:Pde3b
|
UTSW |
7 |
114,134,010 (GRCm39) |
small insertion |
probably benign |
|
|