Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438H23Rik |
T |
C |
16: 90,852,995 (GRCm39) |
N47S |
probably benign |
Het |
AA986860 |
T |
C |
1: 130,665,430 (GRCm39) |
|
probably null |
Het |
Akap9 |
T |
A |
5: 4,096,492 (GRCm39) |
C2456S |
possibly damaging |
Het |
Anks3 |
C |
T |
16: 4,771,691 (GRCm39) |
R111H |
probably damaging |
Het |
Atp1a3 |
A |
T |
7: 24,687,401 (GRCm39) |
|
probably null |
Het |
Bahd1 |
T |
C |
2: 118,746,408 (GRCm39) |
L9P |
probably damaging |
Het |
Capn12 |
T |
C |
7: 28,587,123 (GRCm39) |
V364A |
possibly damaging |
Het |
Cds1 |
T |
A |
5: 101,944,891 (GRCm39) |
C122S |
probably damaging |
Het |
Cenpc1 |
T |
C |
5: 86,185,459 (GRCm39) |
T351A |
possibly damaging |
Het |
Cuzd1 |
T |
C |
7: 130,921,923 (GRCm39) |
|
probably benign |
Het |
Daxx |
T |
C |
17: 34,129,635 (GRCm39) |
L72P |
probably damaging |
Het |
Depdc1b |
A |
G |
13: 108,523,369 (GRCm39) |
I415V |
probably benign |
Het |
Dlg2 |
T |
C |
7: 92,024,845 (GRCm39) |
V675A |
probably damaging |
Het |
Dtx4 |
A |
G |
19: 12,469,515 (GRCm39) |
V204A |
probably benign |
Het |
Ganc |
T |
C |
2: 120,288,610 (GRCm39) |
V872A |
probably damaging |
Het |
Gm14403 |
A |
T |
2: 177,198,810 (GRCm39) |
R38W |
probably benign |
Het |
Gm4553 |
T |
C |
7: 141,719,423 (GRCm39) |
S2G |
unknown |
Het |
Gm8159 |
G |
A |
14: 4,635,226 (GRCm38) |
R148H |
possibly damaging |
Het |
Gsdmc3 |
T |
C |
15: 63,730,400 (GRCm39) |
|
probably null |
Het |
Ibtk |
C |
T |
9: 85,617,099 (GRCm39) |
G158R |
probably damaging |
Het |
Irx2 |
T |
A |
13: 72,779,675 (GRCm39) |
S320T |
possibly damaging |
Het |
Kctd7 |
A |
T |
5: 130,180,510 (GRCm39) |
|
probably null |
Het |
Kdr |
T |
C |
5: 76,129,465 (GRCm39) |
T141A |
probably benign |
Het |
Krt25 |
T |
A |
11: 99,212,109 (GRCm39) |
Q176L |
possibly damaging |
Het |
Krt71 |
T |
C |
15: 101,645,195 (GRCm39) |
N372S |
probably benign |
Het |
Mllt3 |
A |
G |
4: 87,707,621 (GRCm39) |
V446A |
probably damaging |
Het |
Or1j21 |
T |
A |
2: 36,683,903 (GRCm39) |
Y218* |
probably null |
Het |
Or4k38 |
A |
T |
2: 111,165,543 (GRCm39) |
D293E |
probably benign |
Het |
Or5p4 |
C |
T |
7: 107,680,727 (GRCm39) |
T242M |
probably damaging |
Het |
Or5p52 |
A |
C |
7: 107,502,397 (GRCm39) |
T158P |
possibly damaging |
Het |
Or9e1 |
T |
C |
11: 58,732,540 (GRCm39) |
V200A |
possibly damaging |
Het |
Poldip2 |
T |
C |
11: 78,403,294 (GRCm39) |
S18P |
possibly damaging |
Het |
Ptprd |
T |
G |
4: 76,055,122 (GRCm39) |
Q193P |
probably damaging |
Het |
Reck |
C |
T |
4: 43,922,838 (GRCm39) |
T371M |
possibly damaging |
Het |
Rnf144b |
G |
T |
13: 47,374,001 (GRCm39) |
R66L |
probably null |
Het |
Rpn2 |
T |
A |
2: 157,125,691 (GRCm39) |
D67E |
possibly damaging |
Het |
Scn11a |
A |
G |
9: 119,636,876 (GRCm39) |
F275S |
probably damaging |
Het |
Slc12a5 |
G |
A |
2: 164,838,805 (GRCm39) |
|
probably benign |
Het |
Snapc4 |
A |
G |
2: 26,264,658 (GRCm39) |
I253T |
probably damaging |
Het |
Usp9y |
A |
C |
Y: 1,315,930 (GRCm39) |
N2068K |
probably benign |
Het |
Vmn2r45 |
A |
G |
7: 8,478,380 (GRCm39) |
C536R |
probably damaging |
Het |
|
Other mutations in Tppp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0032:Tppp2
|
UTSW |
14 |
52,156,866 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0032:Tppp2
|
UTSW |
14 |
52,156,866 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0352:Tppp2
|
UTSW |
14 |
52,156,807 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1860:Tppp2
|
UTSW |
14 |
52,158,062 (GRCm39) |
missense |
probably benign |
0.00 |
R1861:Tppp2
|
UTSW |
14 |
52,158,062 (GRCm39) |
missense |
probably benign |
0.00 |
R4087:Tppp2
|
UTSW |
14 |
52,156,957 (GRCm39) |
splice site |
probably null |
|
R4484:Tppp2
|
UTSW |
14 |
52,156,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R4801:Tppp2
|
UTSW |
14 |
52,156,805 (GRCm39) |
missense |
probably benign |
0.00 |
R4802:Tppp2
|
UTSW |
14 |
52,156,805 (GRCm39) |
missense |
probably benign |
0.00 |
R5071:Tppp2
|
UTSW |
14 |
52,157,912 (GRCm39) |
missense |
probably benign |
0.01 |
R5073:Tppp2
|
UTSW |
14 |
52,157,912 (GRCm39) |
missense |
probably benign |
0.01 |
R5103:Tppp2
|
UTSW |
14 |
52,156,909 (GRCm39) |
missense |
probably benign |
0.05 |
R5407:Tppp2
|
UTSW |
14 |
52,156,955 (GRCm39) |
splice site |
probably null |
|
R5992:Tppp2
|
UTSW |
14 |
52,156,392 (GRCm39) |
missense |
probably benign |
0.08 |
R6124:Tppp2
|
UTSW |
14 |
52,156,937 (GRCm39) |
missense |
probably benign |
0.12 |
R7372:Tppp2
|
UTSW |
14 |
52,156,865 (GRCm39) |
missense |
probably benign |
0.08 |
R7506:Tppp2
|
UTSW |
14 |
52,158,058 (GRCm39) |
missense |
possibly damaging |
0.74 |
|