Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts7 |
A |
G |
9: 90,062,761 (GRCm39) |
Y405C |
probably damaging |
Het |
Ago3 |
A |
T |
4: 126,239,356 (GRCm39) |
S832T |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,093,948 (GRCm39) |
F2157I |
probably damaging |
Het |
Anapc5 |
T |
C |
5: 122,929,798 (GRCm39) |
E561G |
possibly damaging |
Het |
Art5 |
T |
C |
7: 101,747,545 (GRCm39) |
H78R |
probably benign |
Het |
Blvra |
T |
A |
2: 126,932,304 (GRCm39) |
|
probably null |
Het |
Ccdc171 |
A |
G |
4: 83,575,579 (GRCm39) |
T488A |
possibly damaging |
Het |
Crtc3 |
A |
T |
7: 80,239,543 (GRCm39) |
M603K |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 15,981,037 (GRCm39) |
|
probably null |
Het |
Dbh |
C |
A |
2: 27,067,343 (GRCm39) |
H409Q |
possibly damaging |
Het |
Gm12185 |
T |
C |
11: 48,798,747 (GRCm39) |
Y582C |
probably damaging |
Het |
Gm12185 |
T |
C |
11: 48,798,921 (GRCm39) |
N524S |
possibly damaging |
Het |
Gm7356 |
A |
C |
17: 14,221,672 (GRCm39) |
I119R |
probably damaging |
Het |
Heatr1 |
T |
A |
13: 12,449,392 (GRCm39) |
D1963E |
probably benign |
Het |
Ighv1-37 |
A |
T |
12: 114,860,147 (GRCm39) |
V21D |
probably damaging |
Het |
Itga3 |
T |
G |
11: 94,948,119 (GRCm39) |
Q602P |
probably benign |
Het |
Kcmf1 |
G |
A |
6: 72,826,574 (GRCm39) |
R152C |
probably damaging |
Het |
Lin54 |
T |
C |
5: 100,633,262 (GRCm39) |
I141V |
possibly damaging |
Het |
Mast1 |
T |
A |
8: 85,647,990 (GRCm39) |
H497L |
probably damaging |
Het |
Mrpl44 |
T |
C |
1: 79,753,971 (GRCm39) |
F41S |
possibly damaging |
Het |
Myo18b |
T |
C |
5: 112,840,891 (GRCm39) |
R2301G |
probably damaging |
Het |
Nek1 |
A |
T |
8: 61,460,247 (GRCm39) |
M58L |
possibly damaging |
Het |
Or4k15c |
T |
C |
14: 50,321,156 (GRCm39) |
|
probably null |
Het |
Orc4 |
G |
A |
2: 48,827,501 (GRCm39) |
P31S |
probably benign |
Het |
P3h3 |
A |
G |
6: 124,831,371 (GRCm39) |
V338A |
possibly damaging |
Het |
Pabir3 |
G |
A |
X: 52,382,376 (GRCm39) |
R94H |
possibly damaging |
Het |
Pcdha7 |
T |
C |
18: 37,108,460 (GRCm39) |
V495A |
possibly damaging |
Het |
Plcb3 |
T |
C |
19: 6,933,640 (GRCm39) |
E895G |
probably benign |
Het |
Plekha5 |
A |
G |
6: 140,516,057 (GRCm39) |
E770G |
probably damaging |
Het |
Ptchd3 |
C |
T |
11: 121,727,257 (GRCm39) |
S377F |
probably damaging |
Het |
Ptprj |
C |
T |
2: 90,270,299 (GRCm39) |
D1266N |
probably damaging |
Het |
Raly |
A |
T |
2: 154,707,853 (GRCm39) |
E291V |
probably damaging |
Het |
Rnf217 |
C |
A |
10: 31,484,759 (GRCm39) |
C141F |
possibly damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Slc12a3 |
A |
G |
8: 95,083,714 (GRCm39) |
M914V |
probably null |
Het |
Tbc1d9 |
A |
G |
8: 83,997,547 (GRCm39) |
T1035A |
probably damaging |
Het |
Tex14 |
C |
T |
11: 87,427,655 (GRCm39) |
R36* |
probably null |
Het |
Tiparp |
A |
G |
3: 65,453,768 (GRCm39) |
D172G |
probably benign |
Het |
Ttc3 |
T |
A |
16: 94,267,736 (GRCm39) |
|
probably benign |
Het |
Ubr1 |
T |
C |
2: 120,772,963 (GRCm39) |
T426A |
possibly damaging |
Het |
Vmn1r77 |
T |
A |
7: 11,775,756 (GRCm39) |
H177Q |
probably benign |
Het |
Vmn2r72 |
T |
A |
7: 85,401,134 (GRCm39) |
H95L |
probably benign |
Het |
Vwc2l |
G |
A |
1: 70,921,298 (GRCm39) |
C151Y |
probably damaging |
Het |
Wdr12 |
T |
C |
1: 60,117,354 (GRCm39) |
Y414C |
probably benign |
Het |
Zfp609 |
A |
C |
9: 65,610,890 (GRCm39) |
V691G |
probably benign |
Het |
Zmiz1 |
T |
C |
14: 25,646,084 (GRCm39) |
Y254H |
probably damaging |
Het |
|
Other mutations in Uap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02170:Uap1
|
APN |
1 |
169,994,281 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02330:Uap1
|
APN |
1 |
169,977,896 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03383:Uap1
|
APN |
1 |
169,986,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R0382:Uap1
|
UTSW |
1 |
169,989,051 (GRCm39) |
missense |
probably benign |
0.00 |
R0696:Uap1
|
UTSW |
1 |
169,976,843 (GRCm39) |
missense |
probably benign |
0.23 |
R1055:Uap1
|
UTSW |
1 |
169,984,480 (GRCm39) |
splice site |
probably benign |
|
R1463:Uap1
|
UTSW |
1 |
169,977,952 (GRCm39) |
missense |
probably benign |
|
R1522:Uap1
|
UTSW |
1 |
169,978,510 (GRCm39) |
critical splice donor site |
probably null |
|
R2257:Uap1
|
UTSW |
1 |
169,986,312 (GRCm39) |
splice site |
probably benign |
|
R4061:Uap1
|
UTSW |
1 |
169,986,415 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5068:Uap1
|
UTSW |
1 |
169,989,032 (GRCm39) |
missense |
probably damaging |
0.98 |
R5341:Uap1
|
UTSW |
1 |
169,971,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R5712:Uap1
|
UTSW |
1 |
169,994,414 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5772:Uap1
|
UTSW |
1 |
169,988,949 (GRCm39) |
missense |
probably benign |
0.20 |
R5869:Uap1
|
UTSW |
1 |
169,978,707 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6229:Uap1
|
UTSW |
1 |
169,994,302 (GRCm39) |
missense |
probably benign |
|
R7216:Uap1
|
UTSW |
1 |
169,986,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R8079:Uap1
|
UTSW |
1 |
169,986,332 (GRCm39) |
missense |
probably damaging |
0.97 |
R8323:Uap1
|
UTSW |
1 |
169,978,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R8854:Uap1
|
UTSW |
1 |
169,976,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Uap1
|
UTSW |
1 |
169,977,013 (GRCm39) |
nonsense |
probably null |
|
|