Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A1bg |
T |
G |
15: 60,791,482 (GRCm39) |
|
probably benign |
Het |
Abcg4 |
T |
G |
9: 44,188,946 (GRCm39) |
|
probably benign |
Het |
Afm |
C |
A |
5: 90,693,243 (GRCm39) |
|
probably benign |
Het |
Ahrr |
G |
A |
13: 74,431,143 (GRCm39) |
|
probably benign |
Het |
Aplnr |
T |
A |
2: 84,967,620 (GRCm39) |
|
probably null |
Het |
Arih2 |
T |
A |
9: 108,488,926 (GRCm39) |
H264L |
probably damaging |
Het |
Atp1a1 |
A |
T |
3: 101,487,151 (GRCm39) |
I886N |
possibly damaging |
Het |
Bmf |
A |
T |
2: 118,380,103 (GRCm39) |
V14E |
probably damaging |
Het |
Ccdc116 |
T |
C |
16: 16,961,903 (GRCm39) |
E15G |
probably damaging |
Het |
Ccdc175 |
T |
C |
12: 72,182,739 (GRCm39) |
N427D |
possibly damaging |
Het |
Chd3 |
A |
G |
11: 69,240,732 (GRCm39) |
L1569P |
probably damaging |
Het |
Cntn2 |
G |
A |
1: 132,443,918 (GRCm39) |
Q457* |
probably null |
Het |
Coro1a |
A |
T |
7: 126,300,585 (GRCm39) |
|
probably benign |
Het |
Cracr2b |
T |
A |
7: 141,043,672 (GRCm39) |
L91Q |
probably damaging |
Het |
Ctdspl |
T |
C |
9: 118,849,114 (GRCm39) |
|
probably null |
Het |
Dip2b |
T |
A |
15: 100,067,193 (GRCm39) |
L565Q |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,671,939 (GRCm39) |
C1004S |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 118,009,257 (GRCm39) |
I2135N |
possibly damaging |
Het |
Dnah14 |
A |
G |
1: 181,596,972 (GRCm39) |
|
probably benign |
Het |
Dnase1 |
T |
C |
16: 3,856,810 (GRCm39) |
V147A |
probably damaging |
Het |
Dusp8 |
T |
C |
7: 141,635,791 (GRCm39) |
|
probably benign |
Het |
Fer1l6 |
T |
C |
15: 58,534,636 (GRCm39) |
Y1828H |
probably damaging |
Het |
Flvcr1 |
A |
G |
1: 190,740,388 (GRCm39) |
V544A |
probably benign |
Het |
Fsd1l |
T |
C |
4: 53,687,209 (GRCm39) |
V311A |
probably benign |
Het |
Glud1 |
G |
A |
14: 34,056,225 (GRCm39) |
G300S |
probably benign |
Het |
Gm4847 |
C |
T |
1: 166,458,055 (GRCm39) |
V433I |
probably benign |
Het |
Gstm3 |
T |
G |
3: 107,875,156 (GRCm39) |
Y62S |
probably damaging |
Het |
Gtse1 |
C |
T |
15: 85,746,636 (GRCm39) |
P151S |
probably benign |
Het |
Herc2 |
T |
C |
7: 55,857,560 (GRCm39) |
S4048P |
probably benign |
Het |
Hp1bp3 |
T |
A |
4: 137,948,994 (GRCm39) |
I19K |
probably benign |
Het |
Htr7 |
C |
A |
19: 36,018,940 (GRCm39) |
|
probably benign |
Het |
Il1a |
C |
T |
2: 129,150,994 (GRCm39) |
D10N |
probably damaging |
Het |
Il22ra2 |
A |
T |
10: 19,500,206 (GRCm39) |
N39I |
probably damaging |
Het |
Kcnn4 |
T |
C |
7: 24,078,680 (GRCm39) |
C267R |
possibly damaging |
Het |
Larp1 |
A |
G |
11: 57,946,299 (GRCm39) |
K879R |
possibly damaging |
Het |
Lcn5 |
T |
A |
2: 25,551,417 (GRCm39) |
|
probably benign |
Het |
Lep |
T |
A |
6: 29,068,971 (GRCm39) |
C7* |
probably null |
Het |
Magi2 |
A |
T |
5: 20,816,053 (GRCm39) |
Y747F |
probably benign |
Het |
Mast4 |
T |
C |
13: 102,878,566 (GRCm39) |
T1223A |
probably damaging |
Het |
Mcc |
C |
T |
18: 44,579,000 (GRCm39) |
E803K |
probably damaging |
Het |
Mtmr4 |
T |
C |
11: 87,502,334 (GRCm39) |
I796T |
probably benign |
Het |
Myef2 |
A |
T |
2: 124,950,898 (GRCm39) |
D312E |
probably benign |
Het |
Myl3 |
A |
C |
9: 110,596,997 (GRCm39) |
D119A |
probably damaging |
Het |
Myo19 |
T |
A |
11: 84,778,995 (GRCm39) |
|
probably null |
Het |
Naa15 |
T |
G |
3: 51,377,640 (GRCm39) |
H763Q |
probably damaging |
Het |
Pde5a |
C |
T |
3: 122,618,551 (GRCm39) |
|
probably benign |
Het |
Plpp2 |
C |
T |
10: 79,363,078 (GRCm39) |
R184H |
probably benign |
Het |
Rab19 |
T |
G |
6: 39,366,621 (GRCm39) |
L179V |
probably damaging |
Het |
Rims2 |
T |
A |
15: 39,398,362 (GRCm39) |
M1087K |
probably damaging |
Het |
Riox2 |
C |
A |
16: 59,309,730 (GRCm39) |
D361E |
probably benign |
Het |
Sh3rf1 |
T |
A |
8: 61,679,327 (GRCm39) |
V123E |
probably damaging |
Het |
Slc35e1 |
A |
T |
8: 73,238,553 (GRCm39) |
N318K |
probably damaging |
Het |
Slc9a2 |
A |
T |
1: 40,802,762 (GRCm39) |
E604V |
probably benign |
Het |
Srp72 |
T |
C |
5: 77,135,732 (GRCm39) |
S221P |
probably damaging |
Het |
Tbx19 |
A |
T |
1: 164,988,089 (GRCm39) |
S15T |
possibly damaging |
Het |
Tcea2 |
A |
G |
2: 181,327,610 (GRCm39) |
T112A |
probably benign |
Het |
Tesk1 |
T |
A |
4: 43,445,368 (GRCm39) |
D230E |
probably damaging |
Het |
Tm4sf5 |
C |
T |
11: 70,401,538 (GRCm39) |
A179V |
probably damaging |
Het |
Tnr |
G |
T |
1: 159,679,986 (GRCm39) |
G320V |
probably damaging |
Het |
Trappc11 |
A |
T |
8: 47,956,355 (GRCm39) |
C874S |
possibly damaging |
Het |
Trpm3 |
T |
A |
19: 22,891,810 (GRCm39) |
Y885N |
probably damaging |
Het |
Unc5a |
T |
A |
13: 55,150,692 (GRCm39) |
C505S |
probably damaging |
Het |
Vmn1r28 |
G |
A |
6: 58,242,702 (GRCm39) |
A182T |
probably benign |
Het |
Xpo5 |
T |
C |
17: 46,515,712 (GRCm39) |
|
probably benign |
Het |
Zfp637 |
C |
A |
6: 117,822,629 (GRCm39) |
H252Q |
probably damaging |
Het |
Zfp646 |
T |
A |
7: 127,479,903 (GRCm39) |
D693E |
probably damaging |
Het |
|
Other mutations in Cfap53 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00579:Cfap53
|
APN |
18 |
74,438,611 (GRCm39) |
nonsense |
probably null |
|
IGL00667:Cfap53
|
APN |
18 |
74,433,263 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00917:Cfap53
|
APN |
18 |
74,432,367 (GRCm39) |
missense |
probably benign |
0.08 |
R0009:Cfap53
|
UTSW |
18 |
74,432,247 (GRCm39) |
missense |
probably benign |
0.00 |
R0035:Cfap53
|
UTSW |
18 |
74,433,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R0035:Cfap53
|
UTSW |
18 |
74,433,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Cfap53
|
UTSW |
18 |
74,432,244 (GRCm39) |
missense |
probably benign |
0.09 |
R0601:Cfap53
|
UTSW |
18 |
74,433,221 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0939:Cfap53
|
UTSW |
18 |
74,438,801 (GRCm39) |
missense |
probably null |
0.72 |
R1166:Cfap53
|
UTSW |
18 |
74,433,251 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1588:Cfap53
|
UTSW |
18 |
74,440,444 (GRCm39) |
missense |
probably benign |
|
R2105:Cfap53
|
UTSW |
18 |
74,416,294 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2186:Cfap53
|
UTSW |
18 |
74,462,576 (GRCm39) |
splice site |
probably null |
|
R3723:Cfap53
|
UTSW |
18 |
74,492,640 (GRCm39) |
missense |
probably benign |
0.13 |
R3724:Cfap53
|
UTSW |
18 |
74,492,640 (GRCm39) |
missense |
probably benign |
0.13 |
R3904:Cfap53
|
UTSW |
18 |
74,440,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R5156:Cfap53
|
UTSW |
18 |
74,492,838 (GRCm39) |
utr 3 prime |
probably benign |
|
R5262:Cfap53
|
UTSW |
18 |
74,462,530 (GRCm39) |
missense |
probably benign |
0.39 |
R5928:Cfap53
|
UTSW |
18 |
74,492,811 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6405:Cfap53
|
UTSW |
18 |
74,492,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R6653:Cfap53
|
UTSW |
18 |
74,433,280 (GRCm39) |
missense |
probably damaging |
0.97 |
R6675:Cfap53
|
UTSW |
18 |
74,440,447 (GRCm39) |
critical splice donor site |
probably null |
|
R7011:Cfap53
|
UTSW |
18 |
74,462,564 (GRCm39) |
missense |
probably benign |
0.13 |
R7397:Cfap53
|
UTSW |
18 |
74,416,294 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8943:Cfap53
|
UTSW |
18 |
74,432,253 (GRCm39) |
missense |
probably damaging |
0.97 |
R9132:Cfap53
|
UTSW |
18 |
74,416,272 (GRCm39) |
missense |
probably damaging |
0.98 |
R9159:Cfap53
|
UTSW |
18 |
74,416,272 (GRCm39) |
missense |
probably damaging |
0.98 |
R9389:Cfap53
|
UTSW |
18 |
74,432,414 (GRCm39) |
critical splice donor site |
probably null |
|
R9548:Cfap53
|
UTSW |
18 |
74,438,040 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9679:Cfap53
|
UTSW |
18 |
74,492,656 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9792:Cfap53
|
UTSW |
18 |
74,438,741 (GRCm39) |
missense |
probably benign |
0.44 |
R9793:Cfap53
|
UTSW |
18 |
74,438,741 (GRCm39) |
missense |
probably benign |
0.44 |
R9795:Cfap53
|
UTSW |
18 |
74,438,741 (GRCm39) |
missense |
probably benign |
0.44 |
Z1177:Cfap53
|
UTSW |
18 |
74,438,623 (GRCm39) |
nonsense |
probably null |
|
|