Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
T |
17: 24,334,271 (GRCm38) |
F155L |
possibly damaging |
Het |
Adcy6 |
A |
G |
15: 98,598,659 (GRCm38) |
I545T |
probably damaging |
Het |
Akip1 |
C |
A |
7: 109,704,986 (GRCm38) |
S90* |
probably null |
Het |
Anln |
T |
C |
9: 22,362,888 (GRCm38) |
D551G |
possibly damaging |
Het |
Arhgef17 |
T |
C |
7: 100,931,129 (GRCm38) |
Q204R |
possibly damaging |
Het |
Arl6ip1 |
AAAATAAATAAATAAATAAATAAATA |
AAAATAAATAAATAAATAAATAAATAAATA |
7: 118,121,899 (GRCm38) |
|
probably benign |
Het |
Bcl2l11 |
A |
G |
2: 128,129,646 (GRCm38) |
E75G |
probably benign |
Het |
Cfap45 |
A |
G |
1: 172,545,108 (GRCm38) |
I457V |
probably benign |
Het |
Cntln |
C |
A |
4: 85,096,842 (GRCm38) |
H1123Q |
probably benign |
Het |
Cops3 |
C |
T |
11: 59,827,845 (GRCm38) |
|
probably null |
Het |
Dis3l2 |
A |
T |
1: 87,049,671 (GRCm38) |
T861S |
probably benign |
Het |
Dnajc11 |
A |
G |
4: 151,973,617 (GRCm38) |
N281S |
possibly damaging |
Het |
Fabp3 |
C |
T |
4: 130,312,452 (GRCm38) |
|
probably null |
Het |
Fras1 |
A |
G |
5: 96,709,895 (GRCm38) |
D2016G |
probably benign |
Het |
Gpr39 |
G |
A |
1: 125,677,991 (GRCm38) |
V219I |
probably benign |
Het |
Greb1 |
T |
C |
12: 16,699,675 (GRCm38) |
D1050G |
probably damaging |
Het |
Kcnh6 |
T |
C |
11: 106,009,049 (GRCm38) |
F48S |
probably damaging |
Het |
Kdm1b |
C |
T |
13: 47,063,077 (GRCm38) |
R308W |
probably damaging |
Het |
Mrm2 |
T |
C |
5: 140,328,496 (GRCm38) |
T195A |
probably benign |
Het |
Myzap |
T |
C |
9: 71,550,246 (GRCm38) |
E289G |
possibly damaging |
Het |
Nemp1 |
A |
G |
10: 127,696,344 (GRCm38) |
E373G |
probably benign |
Het |
Olfr1100 |
T |
C |
2: 86,978,670 (GRCm38) |
N42S |
probably damaging |
Het |
Olfr155 |
T |
A |
4: 43,854,834 (GRCm38) |
I175N |
probably damaging |
Het |
Polr1c |
A |
T |
17: 46,247,809 (GRCm38) |
|
probably null |
Het |
Rev1 |
A |
G |
1: 38,059,194 (GRCm38) |
M756T |
possibly damaging |
Het |
Sacs |
A |
G |
14: 61,191,938 (GRCm38) |
D482G |
probably damaging |
Het |
Sfrp4 |
A |
G |
13: 19,623,766 (GRCm38) |
M112V |
possibly damaging |
Het |
Slc7a4 |
T |
C |
16: 17,575,345 (GRCm38) |
T197A |
probably benign |
Het |
Snx27 |
C |
T |
3: 94,526,439 (GRCm38) |
|
probably benign |
Het |
Spata5 |
T |
A |
3: 37,432,027 (GRCm38) |
N299K |
probably benign |
Het |
Speer2 |
T |
C |
16: 69,858,849 (GRCm38) |
K30E |
probably damaging |
Het |
Ssh2 |
G |
A |
11: 77,450,184 (GRCm38) |
A721T |
probably benign |
Het |
Trappc3 |
A |
G |
4: 126,272,751 (GRCm38) |
D39G |
possibly damaging |
Het |
Ttc28 |
G |
A |
5: 111,271,224 (GRCm38) |
S1362N |
possibly damaging |
Het |
Ugt2b35 |
A |
T |
5: 87,008,275 (GRCm38) |
K409* |
probably null |
Het |
Vmn2r92 |
A |
T |
17: 18,171,316 (GRCm38) |
M527L |
probably benign |
Het |
Zbed5 |
T |
A |
5: 129,902,851 (GRCm38) |
L547* |
probably null |
Het |
|
Other mutations in Cfap65 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01107:Cfap65
|
APN |
1 |
74,919,183 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01526:Cfap65
|
APN |
1 |
74,911,078 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01716:Cfap65
|
APN |
1 |
74,927,194 (GRCm38) |
missense |
probably benign |
|
IGL01780:Cfap65
|
APN |
1 |
74,928,348 (GRCm38) |
nonsense |
probably null |
|
IGL01993:Cfap65
|
APN |
1 |
74,920,543 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02164:Cfap65
|
APN |
1 |
74,928,145 (GRCm38) |
missense |
possibly damaging |
0.87 |
IGL02350:Cfap65
|
APN |
1 |
74,928,348 (GRCm38) |
nonsense |
probably null |
|
IGL02357:Cfap65
|
APN |
1 |
74,928,348 (GRCm38) |
nonsense |
probably null |
|
IGL02576:Cfap65
|
APN |
1 |
74,903,458 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02756:Cfap65
|
APN |
1 |
74,905,080 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02792:Cfap65
|
APN |
1 |
74,927,178 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02874:Cfap65
|
APN |
1 |
74,911,108 (GRCm38) |
nonsense |
probably null |
|
IGL03101:Cfap65
|
APN |
1 |
74,928,433 (GRCm38) |
missense |
possibly damaging |
0.61 |
IGL03348:Cfap65
|
APN |
1 |
74,927,619 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03396:Cfap65
|
APN |
1 |
74,904,642 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4131001:Cfap65
|
UTSW |
1 |
74,928,342 (GRCm38) |
missense |
probably benign |
0.05 |
R0077:Cfap65
|
UTSW |
1 |
74,931,918 (GRCm38) |
missense |
probably damaging |
1.00 |
R0227:Cfap65
|
UTSW |
1 |
74,931,958 (GRCm38) |
nonsense |
probably null |
|
R0281:Cfap65
|
UTSW |
1 |
74,927,071 (GRCm38) |
missense |
probably damaging |
1.00 |
R0312:Cfap65
|
UTSW |
1 |
74,904,067 (GRCm38) |
missense |
probably damaging |
1.00 |
R0331:Cfap65
|
UTSW |
1 |
74,929,302 (GRCm38) |
missense |
probably damaging |
1.00 |
R0331:Cfap65
|
UTSW |
1 |
74,929,301 (GRCm38) |
missense |
probably damaging |
1.00 |
R0347:Cfap65
|
UTSW |
1 |
74,926,444 (GRCm38) |
missense |
probably damaging |
1.00 |
R0359:Cfap65
|
UTSW |
1 |
74,920,601 (GRCm38) |
missense |
probably benign |
0.00 |
R0361:Cfap65
|
UTSW |
1 |
74,925,440 (GRCm38) |
missense |
probably damaging |
1.00 |
R0465:Cfap65
|
UTSW |
1 |
74,916,884 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0549:Cfap65
|
UTSW |
1 |
74,918,444 (GRCm38) |
missense |
probably benign |
0.01 |
R0646:Cfap65
|
UTSW |
1 |
74,902,169 (GRCm38) |
missense |
probably benign |
0.09 |
R0734:Cfap65
|
UTSW |
1 |
74,918,887 (GRCm38) |
missense |
probably damaging |
1.00 |
R0763:Cfap65
|
UTSW |
1 |
74,904,682 (GRCm38) |
missense |
probably damaging |
0.99 |
R0990:Cfap65
|
UTSW |
1 |
74,921,519 (GRCm38) |
missense |
possibly damaging |
0.60 |
R1079:Cfap65
|
UTSW |
1 |
74,905,713 (GRCm38) |
missense |
probably damaging |
0.99 |
R1079:Cfap65
|
UTSW |
1 |
74,902,447 (GRCm38) |
missense |
probably damaging |
0.98 |
R1083:Cfap65
|
UTSW |
1 |
74,918,504 (GRCm38) |
splice site |
probably benign |
|
R1159:Cfap65
|
UTSW |
1 |
74,929,340 (GRCm38) |
missense |
probably damaging |
1.00 |
R1282:Cfap65
|
UTSW |
1 |
74,925,104 (GRCm38) |
missense |
probably benign |
0.03 |
R1644:Cfap65
|
UTSW |
1 |
74,917,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R1796:Cfap65
|
UTSW |
1 |
74,918,948 (GRCm38) |
missense |
probably damaging |
1.00 |
R1950:Cfap65
|
UTSW |
1 |
74,907,660 (GRCm38) |
missense |
probably damaging |
1.00 |
R2079:Cfap65
|
UTSW |
1 |
74,917,199 (GRCm38) |
missense |
probably benign |
0.30 |
R2132:Cfap65
|
UTSW |
1 |
74,907,691 (GRCm38) |
missense |
probably damaging |
1.00 |
R2136:Cfap65
|
UTSW |
1 |
74,917,273 (GRCm38) |
frame shift |
probably null |
|
R2219:Cfap65
|
UTSW |
1 |
74,904,025 (GRCm38) |
missense |
probably damaging |
1.00 |
R2220:Cfap65
|
UTSW |
1 |
74,904,025 (GRCm38) |
missense |
probably damaging |
1.00 |
R2291:Cfap65
|
UTSW |
1 |
74,926,475 (GRCm38) |
missense |
probably damaging |
1.00 |
R2417:Cfap65
|
UTSW |
1 |
74,927,186 (GRCm38) |
small insertion |
probably benign |
|
R3114:Cfap65
|
UTSW |
1 |
74,927,132 (GRCm38) |
missense |
probably damaging |
1.00 |
R4202:Cfap65
|
UTSW |
1 |
74,920,542 (GRCm38) |
missense |
probably damaging |
1.00 |
R4214:Cfap65
|
UTSW |
1 |
74,927,681 (GRCm38) |
missense |
possibly damaging |
0.93 |
R4254:Cfap65
|
UTSW |
1 |
74,903,358 (GRCm38) |
missense |
probably benign |
0.17 |
R4547:Cfap65
|
UTSW |
1 |
74,907,612 (GRCm38) |
missense |
probably damaging |
1.00 |
R4588:Cfap65
|
UTSW |
1 |
74,904,056 (GRCm38) |
missense |
possibly damaging |
0.92 |
R4657:Cfap65
|
UTSW |
1 |
74,925,354 (GRCm38) |
intron |
probably benign |
|
R4701:Cfap65
|
UTSW |
1 |
74,918,908 (GRCm38) |
missense |
probably damaging |
0.96 |
R4755:Cfap65
|
UTSW |
1 |
74,928,361 (GRCm38) |
missense |
probably damaging |
1.00 |
R4820:Cfap65
|
UTSW |
1 |
74,927,632 (GRCm38) |
missense |
probably benign |
0.06 |
R4831:Cfap65
|
UTSW |
1 |
74,917,295 (GRCm38) |
missense |
possibly damaging |
0.93 |
R4866:Cfap65
|
UTSW |
1 |
74,925,557 (GRCm38) |
missense |
probably damaging |
1.00 |
R4869:Cfap65
|
UTSW |
1 |
74,919,261 (GRCm38) |
missense |
probably benign |
0.00 |
R4881:Cfap65
|
UTSW |
1 |
74,907,613 (GRCm38) |
missense |
probably damaging |
1.00 |
R4884:Cfap65
|
UTSW |
1 |
74,903,124 (GRCm38) |
missense |
possibly damaging |
0.47 |
R4950:Cfap65
|
UTSW |
1 |
74,906,336 (GRCm38) |
nonsense |
probably null |
|
R5074:Cfap65
|
UTSW |
1 |
74,922,978 (GRCm38) |
missense |
probably benign |
0.04 |
R5083:Cfap65
|
UTSW |
1 |
74,906,441 (GRCm38) |
missense |
probably damaging |
1.00 |
R5164:Cfap65
|
UTSW |
1 |
74,926,516 (GRCm38) |
missense |
probably damaging |
1.00 |
R5268:Cfap65
|
UTSW |
1 |
74,924,902 (GRCm38) |
missense |
probably benign |
0.07 |
R5333:Cfap65
|
UTSW |
1 |
74,903,175 (GRCm38) |
missense |
probably benign |
0.03 |
R5417:Cfap65
|
UTSW |
1 |
74,925,100 (GRCm38) |
missense |
probably damaging |
1.00 |
R5582:Cfap65
|
UTSW |
1 |
74,907,518 (GRCm38) |
intron |
probably benign |
|
R5669:Cfap65
|
UTSW |
1 |
74,924,968 (GRCm38) |
missense |
probably damaging |
0.99 |
R6010:Cfap65
|
UTSW |
1 |
74,923,031 (GRCm38) |
missense |
probably damaging |
1.00 |
R6084:Cfap65
|
UTSW |
1 |
74,920,405 (GRCm38) |
missense |
probably damaging |
1.00 |
R6112:Cfap65
|
UTSW |
1 |
74,903,139 (GRCm38) |
missense |
probably benign |
0.14 |
R6425:Cfap65
|
UTSW |
1 |
74,927,709 (GRCm38) |
missense |
probably benign |
0.00 |
R6677:Cfap65
|
UTSW |
1 |
74,904,685 (GRCm38) |
missense |
probably damaging |
1.00 |
R6693:Cfap65
|
UTSW |
1 |
74,917,286 (GRCm38) |
missense |
probably benign |
0.00 |
R6838:Cfap65
|
UTSW |
1 |
74,932,021 (GRCm38) |
missense |
probably benign |
0.06 |
R6861:Cfap65
|
UTSW |
1 |
74,925,115 (GRCm38) |
missense |
probably damaging |
1.00 |
R6958:Cfap65
|
UTSW |
1 |
74,931,899 (GRCm38) |
missense |
possibly damaging |
0.58 |
R7134:Cfap65
|
UTSW |
1 |
74,926,633 (GRCm38) |
missense |
probably benign |
0.01 |
R7320:Cfap65
|
UTSW |
1 |
74,926,604 (GRCm38) |
missense |
probably damaging |
0.99 |
R7340:Cfap65
|
UTSW |
1 |
74,921,583 (GRCm38) |
missense |
probably benign |
0.07 |
R7426:Cfap65
|
UTSW |
1 |
74,920,426 (GRCm38) |
missense |
possibly damaging |
0.92 |
R7529:Cfap65
|
UTSW |
1 |
74,926,610 (GRCm38) |
missense |
probably damaging |
1.00 |
R7634:Cfap65
|
UTSW |
1 |
74,902,434 (GRCm38) |
missense |
probably damaging |
1.00 |
R7654:Cfap65
|
UTSW |
1 |
74,933,144 (GRCm38) |
missense |
probably benign |
0.44 |
R7704:Cfap65
|
UTSW |
1 |
74,928,368 (GRCm38) |
missense |
probably benign |
0.19 |
R7727:Cfap65
|
UTSW |
1 |
74,926,625 (GRCm38) |
missense |
probably benign |
0.00 |
R7895:Cfap65
|
UTSW |
1 |
74,933,162 (GRCm38) |
missense |
probably benign |
0.05 |
R8215:Cfap65
|
UTSW |
1 |
74,910,743 (GRCm38) |
missense |
probably damaging |
1.00 |
R8344:Cfap65
|
UTSW |
1 |
74,928,044 (GRCm38) |
missense |
probably benign |
0.01 |
R8345:Cfap65
|
UTSW |
1 |
74,928,044 (GRCm38) |
missense |
probably benign |
0.01 |
R8413:Cfap65
|
UTSW |
1 |
74,917,169 (GRCm38) |
nonsense |
probably null |
|
R8431:Cfap65
|
UTSW |
1 |
74,928,044 (GRCm38) |
missense |
probably benign |
0.01 |
R8432:Cfap65
|
UTSW |
1 |
74,928,044 (GRCm38) |
missense |
probably benign |
0.01 |
R8528:Cfap65
|
UTSW |
1 |
74,905,937 (GRCm38) |
missense |
possibly damaging |
0.88 |
R8809:Cfap65
|
UTSW |
1 |
74,903,223 (GRCm38) |
missense |
probably benign |
0.43 |
R8996:Cfap65
|
UTSW |
1 |
74,902,188 (GRCm38) |
missense |
probably benign |
0.11 |
R9020:Cfap65
|
UTSW |
1 |
74,920,393 (GRCm38) |
missense |
probably damaging |
1.00 |
R9043:Cfap65
|
UTSW |
1 |
74,904,688 (GRCm38) |
missense |
possibly damaging |
0.88 |
R9127:Cfap65
|
UTSW |
1 |
74,919,351 (GRCm38) |
splice site |
probably benign |
|
R9187:Cfap65
|
UTSW |
1 |
74,917,358 (GRCm38) |
missense |
probably benign |
0.00 |
R9210:Cfap65
|
UTSW |
1 |
74,920,408 (GRCm38) |
missense |
probably benign |
|
R9212:Cfap65
|
UTSW |
1 |
74,920,408 (GRCm38) |
missense |
probably benign |
|
R9273:Cfap65
|
UTSW |
1 |
74,921,610 (GRCm38) |
missense |
probably benign |
0.00 |
R9454:Cfap65
|
UTSW |
1 |
74,905,051 (GRCm38) |
missense |
probably damaging |
1.00 |
R9514:Cfap65
|
UTSW |
1 |
74,906,309 (GRCm38) |
critical splice donor site |
probably null |
|
R9595:Cfap65
|
UTSW |
1 |
74,907,378 (GRCm38) |
missense |
probably damaging |
1.00 |
R9721:Cfap65
|
UTSW |
1 |
74,919,342 (GRCm38) |
missense |
probably benign |
0.16 |
R9742:Cfap65
|
UTSW |
1 |
74,904,681 (GRCm38) |
missense |
probably benign |
0.08 |
RF009:Cfap65
|
UTSW |
1 |
74,905,647 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Cfap65
|
UTSW |
1 |
74,910,747 (GRCm38) |
missense |
probably damaging |
1.00 |
|