Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1500002C15Rik |
G |
T |
4: 155,818,628 (GRCm39) |
|
probably benign |
Het |
4933430I17Rik |
G |
T |
4: 62,450,858 (GRCm39) |
R107L |
possibly damaging |
Het |
Acvr1 |
A |
T |
2: 58,348,997 (GRCm39) |
D388E |
probably benign |
Het |
Art3 |
T |
C |
5: 92,562,199 (GRCm39) |
S354P |
probably damaging |
Het |
Bpnt1 |
C |
A |
1: 185,077,591 (GRCm39) |
S102* |
probably null |
Het |
Ces1a |
G |
T |
8: 93,771,726 (GRCm39) |
P24T |
probably damaging |
Het |
Cracd |
T |
A |
5: 77,005,478 (GRCm39) |
M613K |
unknown |
Het |
Csn2 |
T |
C |
5: 87,842,838 (GRCm39) |
H47R |
possibly damaging |
Het |
Gm14496 |
T |
A |
2: 181,637,458 (GRCm39) |
D177E |
probably benign |
Het |
Hmbs |
A |
G |
9: 44,250,845 (GRCm39) |
V126A |
possibly damaging |
Het |
Ica1l |
A |
G |
1: 60,054,916 (GRCm39) |
M105T |
probably damaging |
Het |
Morc2a |
G |
A |
11: 3,600,428 (GRCm39) |
E17K |
probably benign |
Het |
Mroh8 |
T |
C |
2: 157,080,232 (GRCm39) |
|
probably benign |
Het |
Mroh9 |
G |
T |
1: 162,883,172 (GRCm39) |
L436I |
probably damaging |
Het |
Nup54 |
T |
C |
5: 92,565,334 (GRCm39) |
D461G |
probably benign |
Het |
Or10ag2 |
A |
T |
2: 87,249,319 (GRCm39) |
D309V |
probably damaging |
Het |
Or2t45 |
A |
G |
11: 58,669,123 (GRCm39) |
T57A |
probably benign |
Het |
Pcid2 |
G |
A |
8: 13,135,319 (GRCm39) |
|
probably benign |
Het |
Ppp1r3b |
G |
T |
8: 35,851,872 (GRCm39) |
R237L |
probably benign |
Het |
Prdm11 |
A |
G |
2: 92,843,102 (GRCm39) |
V119A |
probably damaging |
Het |
S100a7l2 |
T |
A |
3: 90,995,612 (GRCm39) |
|
probably benign |
Het |
Serpina5 |
T |
A |
12: 104,068,149 (GRCm39) |
V70E |
probably damaging |
Het |
Skap2 |
C |
T |
6: 51,884,894 (GRCm39) |
D249N |
probably benign |
Het |
Slc22a29 |
A |
T |
19: 8,184,542 (GRCm39) |
|
probably benign |
Het |
Slc4a1ap |
C |
A |
5: 31,685,571 (GRCm39) |
T283K |
possibly damaging |
Het |
Slc6a21 |
T |
G |
7: 44,937,220 (GRCm39) |
I575S |
probably damaging |
Het |
Smpd1 |
T |
G |
7: 105,203,982 (GRCm39) |
W82G |
probably benign |
Het |
Snx14 |
T |
A |
9: 88,263,553 (GRCm39) |
M897L |
probably damaging |
Het |
Tjp1 |
A |
G |
7: 64,972,406 (GRCm39) |
V586A |
probably damaging |
Het |
Tmc8 |
T |
C |
11: 117,682,910 (GRCm39) |
|
probably benign |
Het |
Trim34a |
A |
G |
7: 103,909,706 (GRCm39) |
Y298C |
probably damaging |
Het |
Ube3c |
T |
C |
5: 29,872,960 (GRCm39) |
V1000A |
probably damaging |
Het |
|
Other mutations in Cfap65 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01107:Cfap65
|
APN |
1 |
74,958,342 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01716:Cfap65
|
APN |
1 |
74,966,353 (GRCm39) |
missense |
probably benign |
|
IGL01780:Cfap65
|
APN |
1 |
74,967,507 (GRCm39) |
nonsense |
probably null |
|
IGL01993:Cfap65
|
APN |
1 |
74,959,702 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02164:Cfap65
|
APN |
1 |
74,967,304 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02350:Cfap65
|
APN |
1 |
74,967,507 (GRCm39) |
nonsense |
probably null |
|
IGL02357:Cfap65
|
APN |
1 |
74,967,507 (GRCm39) |
nonsense |
probably null |
|
IGL02576:Cfap65
|
APN |
1 |
74,942,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02756:Cfap65
|
APN |
1 |
74,944,239 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02792:Cfap65
|
APN |
1 |
74,966,337 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02874:Cfap65
|
APN |
1 |
74,950,267 (GRCm39) |
nonsense |
probably null |
|
IGL03101:Cfap65
|
APN |
1 |
74,967,592 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03348:Cfap65
|
APN |
1 |
74,966,778 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03396:Cfap65
|
APN |
1 |
74,943,801 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4131001:Cfap65
|
UTSW |
1 |
74,967,501 (GRCm39) |
missense |
probably benign |
0.05 |
R0077:Cfap65
|
UTSW |
1 |
74,971,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R0227:Cfap65
|
UTSW |
1 |
74,971,117 (GRCm39) |
nonsense |
probably null |
|
R0281:Cfap65
|
UTSW |
1 |
74,966,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Cfap65
|
UTSW |
1 |
74,943,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R0331:Cfap65
|
UTSW |
1 |
74,968,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R0331:Cfap65
|
UTSW |
1 |
74,968,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R0347:Cfap65
|
UTSW |
1 |
74,965,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R0359:Cfap65
|
UTSW |
1 |
74,959,760 (GRCm39) |
missense |
probably benign |
0.00 |
R0361:Cfap65
|
UTSW |
1 |
74,964,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R0465:Cfap65
|
UTSW |
1 |
74,956,043 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0549:Cfap65
|
UTSW |
1 |
74,957,603 (GRCm39) |
missense |
probably benign |
0.01 |
R0646:Cfap65
|
UTSW |
1 |
74,941,328 (GRCm39) |
missense |
probably benign |
0.09 |
R0734:Cfap65
|
UTSW |
1 |
74,958,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R0763:Cfap65
|
UTSW |
1 |
74,943,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R0990:Cfap65
|
UTSW |
1 |
74,960,678 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1079:Cfap65
|
UTSW |
1 |
74,941,606 (GRCm39) |
missense |
probably damaging |
0.98 |
R1079:Cfap65
|
UTSW |
1 |
74,944,872 (GRCm39) |
missense |
probably damaging |
0.99 |
R1083:Cfap65
|
UTSW |
1 |
74,957,663 (GRCm39) |
splice site |
probably benign |
|
R1159:Cfap65
|
UTSW |
1 |
74,968,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R1282:Cfap65
|
UTSW |
1 |
74,964,263 (GRCm39) |
missense |
probably benign |
0.03 |
R1644:Cfap65
|
UTSW |
1 |
74,956,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R1796:Cfap65
|
UTSW |
1 |
74,958,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R1950:Cfap65
|
UTSW |
1 |
74,946,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R2079:Cfap65
|
UTSW |
1 |
74,956,358 (GRCm39) |
missense |
probably benign |
0.30 |
R2132:Cfap65
|
UTSW |
1 |
74,946,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R2136:Cfap65
|
UTSW |
1 |
74,956,432 (GRCm39) |
frame shift |
probably null |
|
R2219:Cfap65
|
UTSW |
1 |
74,943,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R2220:Cfap65
|
UTSW |
1 |
74,943,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R2291:Cfap65
|
UTSW |
1 |
74,965,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R2417:Cfap65
|
UTSW |
1 |
74,966,345 (GRCm39) |
small insertion |
probably benign |
|
R3114:Cfap65
|
UTSW |
1 |
74,966,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R4202:Cfap65
|
UTSW |
1 |
74,959,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R4214:Cfap65
|
UTSW |
1 |
74,966,840 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4254:Cfap65
|
UTSW |
1 |
74,942,517 (GRCm39) |
missense |
probably benign |
0.17 |
R4547:Cfap65
|
UTSW |
1 |
74,946,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R4548:Cfap65
|
UTSW |
1 |
74,946,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R4588:Cfap65
|
UTSW |
1 |
74,943,215 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4657:Cfap65
|
UTSW |
1 |
74,964,513 (GRCm39) |
intron |
probably benign |
|
R4701:Cfap65
|
UTSW |
1 |
74,958,067 (GRCm39) |
missense |
probably damaging |
0.96 |
R4755:Cfap65
|
UTSW |
1 |
74,967,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Cfap65
|
UTSW |
1 |
74,966,791 (GRCm39) |
missense |
probably benign |
0.06 |
R4831:Cfap65
|
UTSW |
1 |
74,956,454 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4866:Cfap65
|
UTSW |
1 |
74,964,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R4869:Cfap65
|
UTSW |
1 |
74,958,420 (GRCm39) |
missense |
probably benign |
0.00 |
R4881:Cfap65
|
UTSW |
1 |
74,946,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R4884:Cfap65
|
UTSW |
1 |
74,942,283 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4950:Cfap65
|
UTSW |
1 |
74,945,495 (GRCm39) |
nonsense |
probably null |
|
R5074:Cfap65
|
UTSW |
1 |
74,962,137 (GRCm39) |
missense |
probably benign |
0.04 |
R5083:Cfap65
|
UTSW |
1 |
74,945,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R5164:Cfap65
|
UTSW |
1 |
74,965,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R5268:Cfap65
|
UTSW |
1 |
74,964,061 (GRCm39) |
missense |
probably benign |
0.07 |
R5333:Cfap65
|
UTSW |
1 |
74,942,334 (GRCm39) |
missense |
probably benign |
0.03 |
R5417:Cfap65
|
UTSW |
1 |
74,964,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R5582:Cfap65
|
UTSW |
1 |
74,946,677 (GRCm39) |
intron |
probably benign |
|
R5669:Cfap65
|
UTSW |
1 |
74,964,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R6010:Cfap65
|
UTSW |
1 |
74,962,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R6084:Cfap65
|
UTSW |
1 |
74,959,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R6112:Cfap65
|
UTSW |
1 |
74,942,298 (GRCm39) |
missense |
probably benign |
0.14 |
R6425:Cfap65
|
UTSW |
1 |
74,966,868 (GRCm39) |
missense |
probably benign |
0.00 |
R6677:Cfap65
|
UTSW |
1 |
74,943,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R6693:Cfap65
|
UTSW |
1 |
74,956,445 (GRCm39) |
missense |
probably benign |
0.00 |
R6838:Cfap65
|
UTSW |
1 |
74,971,180 (GRCm39) |
missense |
probably benign |
0.06 |
R6861:Cfap65
|
UTSW |
1 |
74,964,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R6958:Cfap65
|
UTSW |
1 |
74,971,058 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7134:Cfap65
|
UTSW |
1 |
74,965,792 (GRCm39) |
missense |
probably benign |
0.01 |
R7320:Cfap65
|
UTSW |
1 |
74,965,763 (GRCm39) |
missense |
probably damaging |
0.99 |
R7340:Cfap65
|
UTSW |
1 |
74,960,742 (GRCm39) |
missense |
probably benign |
0.07 |
R7426:Cfap65
|
UTSW |
1 |
74,959,585 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7529:Cfap65
|
UTSW |
1 |
74,965,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R7634:Cfap65
|
UTSW |
1 |
74,941,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R7654:Cfap65
|
UTSW |
1 |
74,972,303 (GRCm39) |
missense |
probably benign |
0.44 |
R7704:Cfap65
|
UTSW |
1 |
74,967,527 (GRCm39) |
missense |
probably benign |
0.19 |
R7727:Cfap65
|
UTSW |
1 |
74,965,784 (GRCm39) |
missense |
probably benign |
0.00 |
R7895:Cfap65
|
UTSW |
1 |
74,972,321 (GRCm39) |
missense |
probably benign |
0.05 |
R8215:Cfap65
|
UTSW |
1 |
74,949,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R8344:Cfap65
|
UTSW |
1 |
74,967,203 (GRCm39) |
missense |
probably benign |
0.01 |
R8345:Cfap65
|
UTSW |
1 |
74,967,203 (GRCm39) |
missense |
probably benign |
0.01 |
R8413:Cfap65
|
UTSW |
1 |
74,956,328 (GRCm39) |
nonsense |
probably null |
|
R8431:Cfap65
|
UTSW |
1 |
74,967,203 (GRCm39) |
missense |
probably benign |
0.01 |
R8432:Cfap65
|
UTSW |
1 |
74,967,203 (GRCm39) |
missense |
probably benign |
0.01 |
R8528:Cfap65
|
UTSW |
1 |
74,945,096 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8809:Cfap65
|
UTSW |
1 |
74,942,382 (GRCm39) |
missense |
probably benign |
0.43 |
R8996:Cfap65
|
UTSW |
1 |
74,941,347 (GRCm39) |
missense |
probably benign |
0.11 |
R9020:Cfap65
|
UTSW |
1 |
74,959,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R9043:Cfap65
|
UTSW |
1 |
74,943,847 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9127:Cfap65
|
UTSW |
1 |
74,958,510 (GRCm39) |
splice site |
probably benign |
|
R9187:Cfap65
|
UTSW |
1 |
74,956,517 (GRCm39) |
missense |
probably benign |
0.00 |
R9210:Cfap65
|
UTSW |
1 |
74,959,567 (GRCm39) |
missense |
probably benign |
|
R9212:Cfap65
|
UTSW |
1 |
74,959,567 (GRCm39) |
missense |
probably benign |
|
R9273:Cfap65
|
UTSW |
1 |
74,960,769 (GRCm39) |
missense |
probably benign |
0.00 |
R9454:Cfap65
|
UTSW |
1 |
74,944,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R9514:Cfap65
|
UTSW |
1 |
74,945,468 (GRCm39) |
critical splice donor site |
probably null |
|
R9595:Cfap65
|
UTSW |
1 |
74,946,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R9721:Cfap65
|
UTSW |
1 |
74,958,501 (GRCm39) |
missense |
probably benign |
0.16 |
R9742:Cfap65
|
UTSW |
1 |
74,943,840 (GRCm39) |
missense |
probably benign |
0.08 |
RF009:Cfap65
|
UTSW |
1 |
74,944,806 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cfap65
|
UTSW |
1 |
74,949,906 (GRCm39) |
missense |
probably damaging |
1.00 |
|