Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgra3 |
G |
T |
5: 50,136,484 (GRCm39) |
T667N |
probably benign |
Het |
Aff4 |
T |
C |
11: 53,290,633 (GRCm39) |
I531T |
probably benign |
Het |
Akap9 |
C |
T |
5: 4,082,728 (GRCm39) |
Q1951* |
probably null |
Het |
Arhgef10 |
C |
T |
8: 14,978,889 (GRCm39) |
T52M |
possibly damaging |
Het |
Atg2a |
A |
G |
19: 6,305,787 (GRCm39) |
E1132G |
possibly damaging |
Het |
AW551984 |
A |
C |
9: 39,504,241 (GRCm39) |
I575S |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,543,031 (GRCm39) |
E460G |
probably damaging |
Het |
Ctse |
A |
G |
1: 131,600,273 (GRCm39) |
I341V |
probably benign |
Het |
Dcpp1 |
A |
T |
17: 24,101,568 (GRCm39) |
I106L |
possibly damaging |
Het |
Dcxr |
T |
A |
11: 120,616,809 (GRCm39) |
M158L |
probably benign |
Het |
Dnah11 |
A |
T |
12: 118,023,623 (GRCm39) |
|
probably benign |
Het |
Dnah7a |
T |
A |
1: 53,512,023 (GRCm39) |
I3013F |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,867,391 (GRCm39) |
D281G |
possibly damaging |
Het |
Dpysl3 |
G |
A |
18: 43,491,365 (GRCm39) |
H136Y |
probably damaging |
Het |
Eaf1 |
C |
T |
14: 31,219,744 (GRCm39) |
T61M |
probably damaging |
Het |
Fmnl1 |
A |
G |
11: 103,083,598 (GRCm39) |
T441A |
probably benign |
Het |
Hmgcll1 |
C |
T |
9: 75,988,720 (GRCm39) |
P197L |
probably benign |
Het |
Kdm4b |
T |
C |
17: 56,703,234 (GRCm39) |
V643A |
probably benign |
Het |
Lrch2 |
A |
G |
X: 146,336,716 (GRCm39) |
F111L |
possibly damaging |
Het |
Macf1 |
A |
T |
4: 123,265,559 (GRCm39) |
|
probably benign |
Het |
Mfsd4b2 |
T |
C |
10: 39,797,687 (GRCm39) |
N223D |
probably damaging |
Het |
Mug1 |
G |
A |
6: 121,861,649 (GRCm39) |
|
probably null |
Het |
Nek7 |
A |
T |
1: 138,414,838 (GRCm39) |
L270Q |
probably damaging |
Het |
Nexn |
T |
A |
3: 151,953,881 (GRCm39) |
D127V |
probably damaging |
Het |
Nxf3 |
A |
G |
X: 134,980,322 (GRCm39) |
F130S |
probably damaging |
Het |
Or11a4 |
T |
A |
17: 37,536,057 (GRCm39) |
F14I |
probably damaging |
Het |
Or52ac1 |
A |
G |
7: 104,245,741 (GRCm39) |
S216P |
probably damaging |
Het |
Pcdhb16 |
G |
A |
18: 37,611,411 (GRCm39) |
V124I |
possibly damaging |
Het |
Podxl |
T |
C |
6: 31,501,394 (GRCm39) |
D387G |
possibly damaging |
Het |
Prp2rt |
T |
A |
13: 97,235,682 (GRCm39) |
T22S |
probably null |
Het |
Rab3d |
C |
A |
9: 21,827,020 (GRCm39) |
R70M |
probably damaging |
Het |
Ripk2 |
A |
T |
4: 16,139,240 (GRCm39) |
M219K |
possibly damaging |
Het |
Rnf146 |
A |
G |
10: 29,223,349 (GRCm39) |
V179A |
probably damaging |
Het |
Robo1 |
G |
T |
16: 72,786,504 (GRCm39) |
V839L |
probably benign |
Het |
Rttn |
T |
A |
18: 89,038,329 (GRCm39) |
N808K |
probably damaging |
Het |
Slc12a3 |
T |
G |
8: 95,075,220 (GRCm39) |
V738G |
probably benign |
Het |
Slc26a3 |
T |
C |
12: 31,497,830 (GRCm39) |
V78A |
probably damaging |
Het |
Slc26a9 |
G |
A |
1: 131,691,781 (GRCm39) |
V675M |
probably damaging |
Het |
Sncb |
T |
A |
13: 54,910,509 (GRCm39) |
I76F |
probably benign |
Het |
Stat4 |
G |
A |
1: 52,053,029 (GRCm39) |
R70H |
probably damaging |
Het |
Tle6 |
T |
C |
10: 81,434,474 (GRCm39) |
M42V |
probably benign |
Het |
Tmem67 |
T |
C |
4: 12,068,882 (GRCm39) |
T439A |
probably benign |
Het |
Ugt2b35 |
C |
A |
5: 87,151,141 (GRCm39) |
T249K |
possibly damaging |
Het |
Vmn1r231 |
C |
T |
17: 21,109,997 (GRCm39) |
R306K |
probably benign |
Het |
Vmn1r42 |
A |
T |
6: 89,822,023 (GRCm39) |
I182N |
possibly damaging |
Het |
Zfhx3 |
T |
C |
8: 109,520,515 (GRCm39) |
S546P |
probably damaging |
Het |
Zic3 |
G |
T |
X: 57,076,899 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Cfap299 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00775:Cfap299
|
APN |
5 |
98,932,369 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01133:Cfap299
|
APN |
5 |
98,646,240 (GRCm39) |
critical splice donor site |
probably null |
|
LCD18:Cfap299
|
UTSW |
5 |
98,855,367 (GRCm39) |
intron |
probably benign |
|
PIT4514001:Cfap299
|
UTSW |
5 |
98,949,730 (GRCm39) |
missense |
probably benign |
0.00 |
R0962:Cfap299
|
UTSW |
5 |
98,714,420 (GRCm39) |
intron |
probably benign |
|
R1545:Cfap299
|
UTSW |
5 |
98,477,291 (GRCm39) |
missense |
probably benign |
0.25 |
R1886:Cfap299
|
UTSW |
5 |
98,949,690 (GRCm39) |
missense |
probably benign |
0.41 |
R1954:Cfap299
|
UTSW |
5 |
98,714,612 (GRCm39) |
intron |
probably benign |
|
R1965:Cfap299
|
UTSW |
5 |
98,494,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R2008:Cfap299
|
UTSW |
5 |
98,885,561 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3873:Cfap299
|
UTSW |
5 |
98,885,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R4940:Cfap299
|
UTSW |
5 |
98,885,495 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5708:Cfap299
|
UTSW |
5 |
98,885,566 (GRCm39) |
missense |
probably benign |
|
R6509:Cfap299
|
UTSW |
5 |
98,477,256 (GRCm39) |
missense |
probably benign |
0.16 |
R6595:Cfap299
|
UTSW |
5 |
98,949,717 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7009:Cfap299
|
UTSW |
5 |
98,932,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R7911:Cfap299
|
UTSW |
5 |
98,885,567 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8211:Cfap299
|
UTSW |
5 |
98,477,294 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8317:Cfap299
|
UTSW |
5 |
98,885,459 (GRCm39) |
missense |
probably benign |
0.21 |
R9058:Cfap299
|
UTSW |
5 |
98,932,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R9293:Cfap299
|
UTSW |
5 |
98,646,162 (GRCm39) |
missense |
probably benign |
0.13 |
R9505:Cfap299
|
UTSW |
5 |
98,477,213 (GRCm39) |
start codon destroyed |
probably null |
0.21 |
R9681:Cfap299
|
UTSW |
5 |
98,477,214 (GRCm39) |
start codon destroyed |
probably null |
0.65 |
Z1177:Cfap299
|
UTSW |
5 |
98,949,693 (GRCm39) |
missense |
probably damaging |
1.00 |
|