Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl3 |
T |
C |
4: 144,182,953 (GRCm39) |
T172A |
probably benign |
Het |
Atp6v1c1 |
T |
C |
15: 38,674,210 (GRCm39) |
|
probably null |
Het |
Bpifc |
G |
A |
10: 85,836,496 (GRCm39) |
T3I |
possibly damaging |
Het |
Car12 |
A |
G |
9: 66,624,840 (GRCm39) |
|
probably null |
Het |
Ccrl2 |
A |
G |
9: 110,884,938 (GRCm39) |
F187L |
possibly damaging |
Het |
Col4a3 |
T |
G |
1: 82,695,732 (GRCm39) |
|
probably benign |
Het |
Cyb5r2 |
T |
C |
7: 107,356,114 (GRCm39) |
|
probably null |
Het |
Elfn2 |
A |
G |
15: 78,556,096 (GRCm39) |
V817A |
probably damaging |
Het |
Eln |
C |
T |
5: 134,738,960 (GRCm39) |
|
probably null |
Het |
Eml5 |
T |
C |
12: 98,757,645 (GRCm39) |
E1896G |
possibly damaging |
Het |
G530012D18Rik |
CACAGA |
CA |
1: 85,504,875 (GRCm39) |
|
probably null |
Het |
Galnt11 |
C |
T |
5: 25,452,536 (GRCm39) |
T16I |
probably damaging |
Het |
Gars1 |
C |
T |
6: 55,054,708 (GRCm39) |
H672Y |
probably benign |
Het |
Gpr155 |
T |
A |
2: 73,178,526 (GRCm39) |
H726L |
probably benign |
Het |
Inpp1 |
T |
A |
1: 52,829,332 (GRCm39) |
N229I |
possibly damaging |
Het |
Isg20 |
A |
C |
7: 78,566,281 (GRCm39) |
I77L |
probably damaging |
Het |
Kit |
G |
C |
5: 75,797,977 (GRCm39) |
D422H |
possibly damaging |
Het |
Lonp2 |
A |
G |
8: 87,435,570 (GRCm39) |
E602G |
possibly damaging |
Het |
Mink1 |
T |
C |
11: 70,503,334 (GRCm39) |
V1143A |
probably damaging |
Het |
Myh6 |
A |
C |
14: 55,201,102 (GRCm39) |
L120R |
probably benign |
Het |
Myo18a |
T |
A |
11: 77,733,925 (GRCm39) |
|
probably null |
Het |
Nphs2 |
T |
C |
1: 156,151,308 (GRCm39) |
V249A |
probably damaging |
Het |
Npsr1 |
A |
G |
9: 24,224,648 (GRCm39) |
K342E |
probably benign |
Het |
Nrros |
C |
T |
16: 31,962,975 (GRCm39) |
W311* |
probably null |
Het |
Nudt18 |
G |
T |
14: 70,817,056 (GRCm39) |
G162V |
possibly damaging |
Het |
Odam |
A |
G |
5: 88,040,278 (GRCm39) |
D248G |
probably benign |
Het |
Or1e30 |
T |
C |
11: 73,678,264 (GRCm39) |
S167P |
probably benign |
Het |
Or4c119 |
A |
G |
2: 88,987,498 (GRCm39) |
V7A |
probably damaging |
Het |
Or51d1 |
A |
G |
7: 102,348,369 (GRCm39) |
E308G |
probably benign |
Het |
Or51h5 |
T |
C |
7: 102,577,615 (GRCm39) |
V260A |
probably benign |
Het |
Or8b3 |
G |
T |
9: 38,314,669 (GRCm39) |
M166I |
probably damaging |
Het |
Pde4b |
G |
T |
4: 102,462,492 (GRCm39) |
D723Y |
probably benign |
Het |
Pdzrn3 |
T |
C |
6: 101,127,915 (GRCm39) |
E917G |
probably damaging |
Het |
Ppip5k1 |
C |
T |
2: 121,168,108 (GRCm39) |
R715H |
probably damaging |
Het |
Prkdc |
T |
A |
16: 15,505,216 (GRCm39) |
|
probably benign |
Het |
Ptp4a3 |
A |
G |
15: 73,625,618 (GRCm39) |
Y21C |
probably damaging |
Het |
Ptprk |
C |
A |
10: 28,468,763 (GRCm39) |
|
probably benign |
Het |
Rfesd |
C |
A |
13: 76,150,991 (GRCm39) |
|
probably null |
Het |
Rtel1 |
A |
T |
2: 180,993,656 (GRCm39) |
K592* |
probably null |
Het |
Siah1a |
T |
A |
8: 87,451,898 (GRCm39) |
K195N |
probably damaging |
Het |
Slc5a5 |
G |
T |
8: 71,341,231 (GRCm39) |
D369E |
probably damaging |
Het |
Slc6a6 |
A |
T |
6: 91,701,891 (GRCm39) |
I100F |
probably benign |
Het |
Smtn |
T |
C |
11: 3,467,781 (GRCm39) |
I913V |
probably benign |
Het |
Stk17b |
A |
G |
1: 53,800,235 (GRCm39) |
S248P |
probably damaging |
Het |
Sun1 |
C |
T |
5: 139,211,193 (GRCm39) |
H149Y |
probably damaging |
Het |
Taar5 |
T |
C |
10: 23,846,992 (GRCm39) |
I130T |
possibly damaging |
Het |
Tmem132b |
G |
T |
5: 125,826,353 (GRCm39) |
V448F |
probably damaging |
Het |
Tmem94 |
C |
A |
11: 115,685,154 (GRCm39) |
N888K |
possibly damaging |
Het |
Trpc1 |
T |
C |
9: 95,588,896 (GRCm39) |
N742S |
probably damaging |
Het |
Ttbk2 |
T |
C |
2: 120,637,330 (GRCm39) |
T112A |
probably damaging |
Het |
Tubb2a |
A |
T |
13: 34,259,439 (GRCm39) |
L117Q |
probably damaging |
Het |
Vmn1r60 |
T |
A |
7: 5,547,819 (GRCm39) |
M94L |
probably benign |
Het |
Vmn2r83 |
A |
G |
10: 79,327,653 (GRCm39) |
T754A |
probably benign |
Het |
|
Other mutations in Cep250 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00484:Cep250
|
APN |
2 |
155,833,249 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01077:Cep250
|
APN |
2 |
155,804,054 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01084:Cep250
|
APN |
2 |
155,840,313 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01400:Cep250
|
APN |
2 |
155,840,211 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01570:Cep250
|
APN |
2 |
155,809,583 (GRCm39) |
splice site |
probably benign |
|
IGL01583:Cep250
|
APN |
2 |
155,818,069 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01590:Cep250
|
APN |
2 |
155,834,237 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01647:Cep250
|
APN |
2 |
155,825,296 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01959:Cep250
|
APN |
2 |
155,825,279 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02066:Cep250
|
APN |
2 |
155,818,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02219:Cep250
|
APN |
2 |
155,833,514 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02322:Cep250
|
APN |
2 |
155,832,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02728:Cep250
|
APN |
2 |
155,825,198 (GRCm39) |
unclassified |
probably benign |
|
IGL02955:Cep250
|
APN |
2 |
155,817,676 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03369:Cep250
|
APN |
2 |
155,832,191 (GRCm39) |
missense |
probably benign |
0.00 |
R0366:Cep250
|
UTSW |
2 |
155,830,321 (GRCm39) |
missense |
probably benign |
0.00 |
R0403:Cep250
|
UTSW |
2 |
155,834,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R0441:Cep250
|
UTSW |
2 |
155,813,924 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0482:Cep250
|
UTSW |
2 |
155,806,894 (GRCm39) |
splice site |
probably benign |
|
R0507:Cep250
|
UTSW |
2 |
155,834,452 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0614:Cep250
|
UTSW |
2 |
155,812,017 (GRCm39) |
nonsense |
probably null |
|
R0855:Cep250
|
UTSW |
2 |
155,806,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Cep250
|
UTSW |
2 |
155,806,209 (GRCm39) |
splice site |
probably benign |
|
R1137:Cep250
|
UTSW |
2 |
155,832,760 (GRCm39) |
missense |
probably benign |
0.05 |
R1270:Cep250
|
UTSW |
2 |
155,832,601 (GRCm39) |
missense |
probably benign |
0.01 |
R1313:Cep250
|
UTSW |
2 |
155,813,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R1313:Cep250
|
UTSW |
2 |
155,813,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R1470:Cep250
|
UTSW |
2 |
155,832,995 (GRCm39) |
missense |
probably damaging |
0.99 |
R1470:Cep250
|
UTSW |
2 |
155,832,995 (GRCm39) |
missense |
probably damaging |
0.99 |
R1703:Cep250
|
UTSW |
2 |
155,807,466 (GRCm39) |
missense |
probably benign |
0.23 |
R1705:Cep250
|
UTSW |
2 |
155,805,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R1740:Cep250
|
UTSW |
2 |
155,815,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R1796:Cep250
|
UTSW |
2 |
155,834,107 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1897:Cep250
|
UTSW |
2 |
155,818,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R1900:Cep250
|
UTSW |
2 |
155,827,294 (GRCm39) |
critical splice donor site |
probably null |
|
R1958:Cep250
|
UTSW |
2 |
155,818,301 (GRCm39) |
splice site |
probably null |
|
R1974:Cep250
|
UTSW |
2 |
155,831,424 (GRCm39) |
missense |
probably damaging |
0.96 |
R2015:Cep250
|
UTSW |
2 |
155,823,373 (GRCm39) |
missense |
probably damaging |
0.96 |
R2224:Cep250
|
UTSW |
2 |
155,833,737 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2266:Cep250
|
UTSW |
2 |
155,818,090 (GRCm39) |
missense |
probably benign |
0.13 |
R2278:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2332:Cep250
|
UTSW |
2 |
155,832,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R2364:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2366:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2367:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2385:Cep250
|
UTSW |
2 |
155,816,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R2830:Cep250
|
UTSW |
2 |
155,825,236 (GRCm39) |
missense |
probably benign |
0.00 |
R2895:Cep250
|
UTSW |
2 |
155,834,042 (GRCm39) |
missense |
probably benign |
0.00 |
R2965:Cep250
|
UTSW |
2 |
155,836,798 (GRCm39) |
missense |
probably benign |
0.44 |
R2966:Cep250
|
UTSW |
2 |
155,836,798 (GRCm39) |
missense |
probably benign |
0.44 |
R3016:Cep250
|
UTSW |
2 |
155,833,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R3052:Cep250
|
UTSW |
2 |
155,832,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R3424:Cep250
|
UTSW |
2 |
155,823,381 (GRCm39) |
missense |
probably benign |
0.02 |
R3930:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4085:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4087:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4090:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4110:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4355:Cep250
|
UTSW |
2 |
155,833,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4601:Cep250
|
UTSW |
2 |
155,803,973 (GRCm39) |
missense |
probably benign |
0.10 |
R4721:Cep250
|
UTSW |
2 |
155,812,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Cep250
|
UTSW |
2 |
155,830,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5053:Cep250
|
UTSW |
2 |
155,804,848 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5090:Cep250
|
UTSW |
2 |
155,818,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R5744:Cep250
|
UTSW |
2 |
155,823,394 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5775:Cep250
|
UTSW |
2 |
155,811,294 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5986:Cep250
|
UTSW |
2 |
155,821,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R6112:Cep250
|
UTSW |
2 |
155,836,503 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6152:Cep250
|
UTSW |
2 |
155,823,358 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6823:Cep250
|
UTSW |
2 |
155,823,379 (GRCm39) |
missense |
probably benign |
0.02 |
R6859:Cep250
|
UTSW |
2 |
155,834,446 (GRCm39) |
missense |
probably benign |
0.24 |
R6900:Cep250
|
UTSW |
2 |
155,838,190 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7107:Cep250
|
UTSW |
2 |
155,837,314 (GRCm39) |
missense |
probably benign |
0.00 |
R7131:Cep250
|
UTSW |
2 |
155,806,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R7178:Cep250
|
UTSW |
2 |
155,815,375 (GRCm39) |
nonsense |
probably null |
|
R7241:Cep250
|
UTSW |
2 |
155,833,472 (GRCm39) |
missense |
probably benign |
0.20 |
R7264:Cep250
|
UTSW |
2 |
155,821,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R7290:Cep250
|
UTSW |
2 |
155,834,682 (GRCm39) |
missense |
probably benign |
0.03 |
R7367:Cep250
|
UTSW |
2 |
155,811,227 (GRCm39) |
missense |
probably benign |
0.00 |
R7397:Cep250
|
UTSW |
2 |
155,823,331 (GRCm39) |
missense |
probably damaging |
0.99 |
R7768:Cep250
|
UTSW |
2 |
155,827,929 (GRCm39) |
missense |
|
|
R7823:Cep250
|
UTSW |
2 |
155,807,336 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8152:Cep250
|
UTSW |
2 |
155,811,227 (GRCm39) |
missense |
probably benign |
0.00 |
R8331:Cep250
|
UTSW |
2 |
155,832,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R8559:Cep250
|
UTSW |
2 |
155,834,656 (GRCm39) |
missense |
probably damaging |
0.99 |
R8972:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8973:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8974:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8975:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8976:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9072:Cep250
|
UTSW |
2 |
155,834,035 (GRCm39) |
missense |
probably benign |
0.01 |
R9123:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9127:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9128:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9167:Cep250
|
UTSW |
2 |
155,828,920 (GRCm39) |
missense |
|
|
R9189:Cep250
|
UTSW |
2 |
155,818,350 (GRCm39) |
missense |
probably benign |
0.00 |
R9198:Cep250
|
UTSW |
2 |
155,830,354 (GRCm39) |
critical splice donor site |
probably null |
|
R9227:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9228:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9292:Cep250
|
UTSW |
2 |
155,832,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R9516:Cep250
|
UTSW |
2 |
155,833,459 (GRCm39) |
missense |
probably benign |
0.00 |
R9723:Cep250
|
UTSW |
2 |
155,823,337 (GRCm39) |
missense |
probably benign |
0.00 |
R9760:Cep250
|
UTSW |
2 |
155,818,473 (GRCm39) |
missense |
probably benign |
0.02 |
X0061:Cep250
|
UTSW |
2 |
155,803,905 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Cep250
|
UTSW |
2 |
155,818,387 (GRCm39) |
missense |
probably benign |
0.03 |
|