Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
G |
5: 8,986,873 (GRCm39) |
F764C |
probably damaging |
Het |
Aff1 |
A |
G |
5: 103,982,078 (GRCm39) |
D739G |
possibly damaging |
Het |
Atosb |
A |
G |
4: 43,034,531 (GRCm39) |
S355P |
probably damaging |
Het |
Atp1a3 |
T |
C |
7: 24,677,980 (GRCm39) |
Y1012C |
probably damaging |
Het |
Btbd10 |
T |
C |
7: 112,929,133 (GRCm39) |
T206A |
probably benign |
Het |
Capn8 |
G |
T |
1: 182,456,199 (GRCm39) |
A650S |
possibly damaging |
Het |
Catsper1 |
A |
C |
19: 5,386,070 (GRCm39) |
N101T |
probably damaging |
Het |
Cdh23 |
A |
C |
10: 60,160,755 (GRCm39) |
S2070R |
probably benign |
Het |
Cep350 |
A |
G |
1: 155,737,518 (GRCm39) |
V2775A |
probably benign |
Het |
Clybl |
G |
A |
14: 122,419,194 (GRCm39) |
|
probably null |
Het |
Cog4 |
T |
A |
8: 111,579,004 (GRCm39) |
N148K |
probably benign |
Het |
Dbnl |
G |
A |
11: 5,741,839 (GRCm39) |
G44D |
possibly damaging |
Het |
Dgcr2 |
A |
T |
16: 17,667,630 (GRCm39) |
N276K |
possibly damaging |
Het |
Dnah9 |
T |
A |
11: 65,746,060 (GRCm39) |
T4018S |
possibly damaging |
Het |
Dock3 |
A |
G |
9: 106,774,539 (GRCm39) |
L72P |
probably benign |
Het |
Dync2i2 |
T |
C |
2: 29,928,374 (GRCm39) |
D84G |
probably benign |
Het |
Fabp4 |
T |
C |
3: 10,271,105 (GRCm39) |
T51A |
probably benign |
Het |
Fars2 |
T |
A |
13: 36,430,409 (GRCm39) |
I279N |
probably damaging |
Het |
Fas |
A |
T |
19: 34,296,049 (GRCm39) |
Q164L |
probably benign |
Het |
Focad |
A |
G |
4: 88,072,905 (GRCm39) |
K107E |
probably damaging |
Het |
Gga3 |
G |
A |
11: 115,479,305 (GRCm39) |
S338L |
probably benign |
Het |
Grip1 |
A |
G |
10: 119,765,940 (GRCm39) |
R91G |
probably damaging |
Het |
Igkv3-7 |
A |
G |
6: 70,584,942 (GRCm39) |
D94G |
possibly damaging |
Het |
Kank3 |
G |
C |
17: 34,036,627 (GRCm39) |
R165P |
probably damaging |
Het |
Kmt2d |
A |
T |
15: 98,762,048 (GRCm39) |
L434Q |
unknown |
Het |
Krt18 |
A |
G |
15: 101,938,265 (GRCm39) |
T163A |
possibly damaging |
Het |
Lcn10 |
T |
A |
2: 25,575,298 (GRCm39) |
|
probably benign |
Het |
Lrrc37a |
G |
T |
11: 103,394,795 (GRCm39) |
P210Q |
probably benign |
Het |
Lyst |
T |
A |
13: 13,852,548 (GRCm39) |
S2183T |
probably benign |
Het |
Mga |
G |
A |
2: 119,769,272 (GRCm39) |
|
probably benign |
Het |
Myh9 |
G |
A |
15: 77,661,137 (GRCm39) |
A818V |
possibly damaging |
Het |
Or1j15 |
T |
C |
2: 36,458,703 (GRCm39) |
I31T |
probably benign |
Het |
Or1o3 |
G |
T |
17: 37,573,807 (GRCm39) |
Y249* |
probably null |
Het |
Or8b1 |
A |
T |
9: 38,399,597 (GRCm39) |
I91F |
probably benign |
Het |
Pik3cb |
A |
T |
9: 98,936,117 (GRCm39) |
Y772N |
possibly damaging |
Het |
Ppl |
C |
G |
16: 4,906,854 (GRCm39) |
R1147P |
probably damaging |
Het |
Prl3d2 |
A |
T |
13: 27,307,926 (GRCm39) |
D69V |
probably benign |
Het |
Psd3 |
A |
G |
8: 68,172,596 (GRCm39) |
F871L |
probably damaging |
Het |
Rlf |
G |
A |
4: 121,045,432 (GRCm39) |
P152S |
probably benign |
Het |
Rpa1 |
T |
C |
11: 75,204,167 (GRCm39) |
E270G |
possibly damaging |
Het |
Scfd2 |
T |
C |
5: 74,691,656 (GRCm39) |
T209A |
probably benign |
Het |
Scn11a |
A |
G |
9: 119,621,410 (GRCm39) |
L669P |
probably damaging |
Het |
Sec31b |
A |
T |
19: 44,506,106 (GRCm39) |
C933* |
probably null |
Het |
Serpina3k |
G |
T |
12: 104,309,292 (GRCm39) |
M245I |
probably benign |
Het |
Slc9a3 |
T |
A |
13: 74,305,823 (GRCm39) |
I280N |
probably damaging |
Het |
Soat1 |
A |
G |
1: 156,261,772 (GRCm39) |
V412A |
probably damaging |
Het |
Spata31d1a |
A |
T |
13: 59,850,596 (GRCm39) |
S511T |
possibly damaging |
Het |
Sphkap |
A |
T |
1: 83,253,384 (GRCm39) |
V1455E |
possibly damaging |
Het |
Spns1 |
G |
A |
7: 125,971,593 (GRCm39) |
S319F |
possibly damaging |
Het |
Tbxas1 |
G |
T |
6: 39,048,364 (GRCm39) |
M403I |
|
Het |
Tln2 |
A |
T |
9: 67,157,866 (GRCm39) |
C1158S |
probably damaging |
Het |
Tnrc18 |
T |
C |
5: 142,778,811 (GRCm39) |
T98A |
possibly damaging |
Het |
Ttc23 |
T |
C |
7: 67,319,494 (GRCm39) |
L118P |
probably damaging |
Het |
Tyr |
T |
A |
7: 87,087,223 (GRCm39) |
I430L |
probably damaging |
Het |
Uck2 |
A |
G |
1: 167,070,715 (GRCm39) |
F5L |
probably benign |
Het |
Ush2a |
G |
A |
1: 188,485,847 (GRCm39) |
V2986I |
probably benign |
Het |
Vmn2r96 |
A |
G |
17: 18,802,888 (GRCm39) |
D266G |
probably benign |
Het |
Yrdc |
A |
G |
4: 124,747,677 (GRCm39) |
D213G |
probably benign |
Het |
Zfp612 |
C |
A |
8: 110,815,603 (GRCm39) |
T270K |
probably damaging |
Het |
|
Other mutations in Pde7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00901:Pde7b
|
APN |
10 |
20,494,875 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01312:Pde7b
|
APN |
10 |
20,311,940 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01728:Pde7b
|
APN |
10 |
20,310,210 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01868:Pde7b
|
APN |
10 |
20,282,911 (GRCm39) |
nonsense |
probably null |
|
PIT4431001:Pde7b
|
UTSW |
10 |
20,276,291 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0241:Pde7b
|
UTSW |
10 |
20,311,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Pde7b
|
UTSW |
10 |
20,311,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0505:Pde7b
|
UTSW |
10 |
20,314,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R1386:Pde7b
|
UTSW |
10 |
20,294,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R1518:Pde7b
|
UTSW |
10 |
20,423,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R1539:Pde7b
|
UTSW |
10 |
20,355,432 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1547:Pde7b
|
UTSW |
10 |
20,310,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R1571:Pde7b
|
UTSW |
10 |
20,288,836 (GRCm39) |
missense |
probably benign |
0.05 |
R1611:Pde7b
|
UTSW |
10 |
20,310,236 (GRCm39) |
missense |
probably benign |
0.14 |
R1722:Pde7b
|
UTSW |
10 |
20,311,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R2275:Pde7b
|
UTSW |
10 |
20,276,165 (GRCm39) |
makesense |
probably null |
|
R4622:Pde7b
|
UTSW |
10 |
20,294,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Pde7b
|
UTSW |
10 |
20,314,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4757:Pde7b
|
UTSW |
10 |
20,423,688 (GRCm39) |
missense |
probably benign |
0.01 |
R4823:Pde7b
|
UTSW |
10 |
20,314,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R4889:Pde7b
|
UTSW |
10 |
20,423,823 (GRCm39) |
missense |
probably benign |
0.16 |
R4910:Pde7b
|
UTSW |
10 |
20,600,480 (GRCm39) |
unclassified |
probably benign |
|
R4923:Pde7b
|
UTSW |
10 |
20,288,873 (GRCm39) |
missense |
probably damaging |
0.98 |
R5349:Pde7b
|
UTSW |
10 |
20,494,932 (GRCm39) |
missense |
probably damaging |
0.99 |
R6258:Pde7b
|
UTSW |
10 |
20,316,546 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6645:Pde7b
|
UTSW |
10 |
20,486,312 (GRCm39) |
critical splice donor site |
probably null |
|
R7000:Pde7b
|
UTSW |
10 |
20,319,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R7510:Pde7b
|
UTSW |
10 |
20,288,761 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7717:Pde7b
|
UTSW |
10 |
20,282,937 (GRCm39) |
missense |
probably benign |
0.05 |
R7817:Pde7b
|
UTSW |
10 |
20,319,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R8692:Pde7b
|
UTSW |
10 |
20,423,639 (GRCm39) |
missense |
probably benign |
0.10 |
|