Incidental Mutation 'R4657:Cfap65'
ID |
352479 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cfap65
|
Ensembl Gene |
ENSMUSG00000047021 |
Gene Name |
cilia and flagella associated protein 65 |
Synonyms |
Ccdc108, B230363K08Rik |
MMRRC Submission |
041917-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.677)
|
Stock # |
R4657 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
74941230-74974758 bp(-) (GRCm39) |
Type of Mutation |
intron |
DNA Base Change (assembly) |
T to A
at 74964513 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000092440
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094844]
|
AlphaFold |
Q3V0B4 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000094844
|
SMART Domains |
Protein: ENSMUSP00000092440 Gene: ENSMUSG00000047021
Domain | Start | End | E-Value | Type |
transmembrane domain
|
111 |
133 |
N/A |
INTRINSIC |
low complexity region
|
212 |
223 |
N/A |
INTRINSIC |
internal_repeat_1
|
745 |
890 |
9.31e-5 |
PROSPERO |
internal_repeat_1
|
1167 |
1322 |
9.31e-5 |
PROSPERO |
low complexity region
|
1350 |
1361 |
N/A |
INTRINSIC |
low complexity region
|
1574 |
1592 |
N/A |
INTRINSIC |
coiled coil region
|
1687 |
1724 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000130489
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139950
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.4%
- 20x: 95.6%
|
Validation Efficiency |
98% (105/107) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. The chicken ortholog of this gene is involved in the Rose-comb mutation, which is a large chromosome inversion, resulting in altered comb morphology and defects in sperm motility. [provided by RefSeq, Aug 2016]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
A |
T |
11: 119,904,304 (GRCm39) |
V264E |
possibly damaging |
Het |
Abcg1 |
T |
A |
17: 31,327,408 (GRCm39) |
W368R |
probably benign |
Het |
Acin1 |
A |
G |
14: 54,880,504 (GRCm39) |
I476T |
possibly damaging |
Het |
Acsm1 |
T |
A |
7: 119,239,917 (GRCm39) |
I287N |
possibly damaging |
Het |
Adgrv1 |
C |
T |
13: 81,553,483 (GRCm39) |
V5464I |
probably benign |
Het |
AI429214 |
T |
A |
8: 37,461,545 (GRCm39) |
L231Q |
probably damaging |
Het |
Akp3 |
A |
G |
1: 87,053,556 (GRCm39) |
|
probably benign |
Het |
Amy2b |
C |
T |
3: 113,060,793 (GRCm39) |
|
noncoding transcript |
Het |
Apoa5 |
A |
G |
9: 46,181,170 (GRCm39) |
Q82R |
probably benign |
Het |
Arhgap44 |
A |
G |
11: 64,896,278 (GRCm39) |
|
probably null |
Het |
Arhgef38 |
C |
A |
3: 132,940,442 (GRCm39) |
G48V |
probably damaging |
Het |
Bltp3a |
T |
A |
17: 28,109,079 (GRCm39) |
F1099L |
probably benign |
Het |
Bod1l |
G |
T |
5: 41,975,955 (GRCm39) |
N1786K |
probably benign |
Het |
Cav2 |
A |
T |
6: 17,281,409 (GRCm39) |
D17V |
probably null |
Het |
Ccdc148 |
G |
T |
2: 58,891,900 (GRCm39) |
N238K |
probably benign |
Het |
Ccin |
A |
T |
4: 43,984,981 (GRCm39) |
I463F |
probably damaging |
Het |
Cd8b1 |
C |
T |
6: 71,306,758 (GRCm39) |
H162Y |
possibly damaging |
Het |
Cdh16 |
T |
A |
8: 105,341,858 (GRCm39) |
|
probably null |
Het |
Clec4n |
T |
C |
6: 123,209,155 (GRCm39) |
|
probably null |
Het |
Cpne7 |
T |
A |
8: 123,861,314 (GRCm39) |
*558R |
probably null |
Het |
Cs |
A |
G |
10: 128,189,006 (GRCm39) |
I172V |
probably benign |
Het |
Cyp2ab1 |
A |
T |
16: 20,131,822 (GRCm39) |
L306Q |
probably damaging |
Het |
D16Ertd472e |
A |
T |
16: 78,344,814 (GRCm39) |
V98E |
probably damaging |
Het |
Dcaf15 |
A |
C |
8: 84,829,467 (GRCm39) |
S92A |
probably damaging |
Het |
Dkk3 |
T |
C |
7: 111,748,253 (GRCm39) |
|
probably null |
Het |
Dnah11 |
A |
T |
12: 118,156,162 (GRCm39) |
C163S |
probably benign |
Het |
Eda2r |
T |
A |
X: 96,385,239 (GRCm39) |
Q171L |
probably damaging |
Het |
Eml4 |
A |
T |
17: 83,758,377 (GRCm39) |
K397* |
probably null |
Het |
Eml6 |
A |
T |
11: 29,755,108 (GRCm39) |
I889N |
possibly damaging |
Het |
Etaa1 |
A |
T |
11: 17,896,964 (GRCm39) |
D384E |
possibly damaging |
Het |
Fzr1 |
T |
A |
10: 81,203,386 (GRCm39) |
|
probably null |
Het |
Gm13889 |
G |
T |
2: 93,786,921 (GRCm39) |
F61L |
probably damaging |
Het |
Gm14149 |
A |
T |
2: 151,072,684 (GRCm39) |
|
noncoding transcript |
Het |
Gm5828 |
T |
A |
1: 16,839,642 (GRCm39) |
|
noncoding transcript |
Het |
Gm5866 |
G |
A |
5: 52,740,262 (GRCm39) |
|
noncoding transcript |
Het |
Gp2 |
T |
C |
7: 119,056,391 (GRCm39) |
I27M |
probably benign |
Het |
Gpr83 |
G |
A |
9: 14,778,279 (GRCm39) |
|
probably null |
Het |
Gucd1 |
T |
C |
10: 75,346,959 (GRCm39) |
N97S |
probably benign |
Het |
H2bc27 |
C |
T |
11: 58,839,797 (GRCm39) |
P11L |
probably benign |
Het |
H2-Q7 |
T |
A |
17: 35,661,735 (GRCm39) |
V326E |
possibly damaging |
Het |
Haao |
A |
T |
17: 84,139,774 (GRCm39) |
D227E |
possibly damaging |
Het |
Hipk3 |
C |
T |
2: 104,264,104 (GRCm39) |
S819N |
probably benign |
Het |
Hlcs |
A |
G |
16: 94,063,557 (GRCm39) |
V501A |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,500,301 (GRCm39) |
Y3964H |
probably damaging |
Het |
Ifi204 |
C |
A |
1: 173,587,927 (GRCm39) |
|
probably benign |
Het |
Ifi211 |
A |
G |
1: 173,735,226 (GRCm39) |
F68L |
probably benign |
Het |
Ift57 |
A |
G |
16: 49,582,957 (GRCm39) |
|
probably null |
Het |
Ighv5-12-4 |
A |
T |
12: 113,725,887 (GRCm39) |
L112* |
probably null |
Het |
Il1rl2 |
CTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATT |
CTTTATTTTATTTTATTTTATTTTATTTTATTTTATT |
1: 40,366,470 (GRCm39) |
|
probably benign |
Het |
Il36a |
T |
A |
2: 24,114,416 (GRCm39) |
M97K |
possibly damaging |
Het |
Itsn2 |
A |
G |
12: 4,763,197 (GRCm39) |
*1686W |
probably null |
Het |
Jkamp |
G |
T |
12: 72,140,823 (GRCm39) |
V123F |
probably damaging |
Het |
Kat7 |
C |
A |
11: 95,168,424 (GRCm39) |
V411L |
probably damaging |
Het |
Kcnj5 |
A |
G |
9: 32,233,973 (GRCm39) |
V114A |
probably benign |
Het |
Krtap5-4 |
T |
A |
7: 141,857,491 (GRCm39) |
C54S |
unknown |
Het |
Lats1 |
T |
A |
10: 7,581,448 (GRCm39) |
N744K |
possibly damaging |
Het |
Lpo |
T |
C |
11: 87,705,173 (GRCm39) |
E387G |
probably damaging |
Het |
Lrba |
T |
G |
3: 86,644,471 (GRCm39) |
M388R |
probably damaging |
Het |
Lrp2 |
C |
A |
2: 69,297,337 (GRCm39) |
R3208L |
probably damaging |
Het |
Mterf1b |
T |
A |
5: 4,247,176 (GRCm39) |
C272* |
probably null |
Het |
Myh15 |
A |
T |
16: 48,992,421 (GRCm39) |
R1632* |
probably null |
Het |
Myo3b |
T |
C |
2: 70,069,243 (GRCm39) |
V494A |
possibly damaging |
Het |
Myo9a |
T |
C |
9: 59,782,699 (GRCm39) |
|
probably null |
Het |
Nelfa |
T |
G |
5: 34,059,157 (GRCm39) |
S233R |
probably benign |
Het |
Nr4a3 |
A |
T |
4: 48,051,522 (GRCm39) |
E121V |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,933,116 (GRCm39) |
E5406D |
probably damaging |
Het |
Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
Or1j18 |
T |
A |
2: 36,624,415 (GRCm39) |
Y27* |
probably null |
Het |
Or7e177 |
A |
C |
9: 20,211,919 (GRCm39) |
H142P |
probably damaging |
Het |
Oxct2b |
T |
C |
4: 123,010,926 (GRCm39) |
L282P |
probably damaging |
Het |
Pappa |
G |
A |
4: 65,233,033 (GRCm39) |
|
probably null |
Het |
Pcdhb14 |
A |
G |
18: 37,581,900 (GRCm39) |
I335M |
possibly damaging |
Het |
Pcsk1 |
T |
A |
13: 75,280,354 (GRCm39) |
D726E |
probably damaging |
Het |
Pkhd1 |
T |
A |
1: 20,434,391 (GRCm39) |
Q2349L |
possibly damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,410,743 (GRCm39) |
C2750Y |
probably damaging |
Het |
Ppp2r3d |
A |
G |
9: 124,476,821 (GRCm38) |
C26R |
unknown |
Het |
Prex2 |
T |
A |
1: 11,136,049 (GRCm39) |
I74N |
probably benign |
Het |
Ptgir |
A |
G |
7: 16,641,071 (GRCm39) |
D121G |
probably benign |
Het |
Pwwp3a |
T |
A |
10: 80,068,848 (GRCm39) |
C331S |
probably benign |
Het |
Ralbp1 |
T |
C |
17: 66,159,686 (GRCm39) |
S526G |
probably null |
Het |
Ric8b |
T |
C |
10: 84,828,001 (GRCm39) |
Y442H |
probably damaging |
Het |
Rpap1 |
C |
T |
2: 119,605,487 (GRCm39) |
D385N |
probably benign |
Het |
Sash1 |
T |
C |
10: 8,601,424 (GRCm39) |
Y1177C |
probably damaging |
Het |
Shroom1 |
T |
C |
11: 53,356,415 (GRCm39) |
I363T |
possibly damaging |
Het |
Slc26a9 |
T |
C |
1: 131,680,876 (GRCm39) |
L95P |
probably damaging |
Het |
Slc44a5 |
A |
G |
3: 153,962,221 (GRCm39) |
T385A |
possibly damaging |
Het |
Slc5a9 |
C |
A |
4: 111,748,941 (GRCm39) |
|
probably null |
Het |
Slc7a1 |
T |
A |
5: 148,289,209 (GRCm39) |
M13L |
probably benign |
Het |
Snrpb2 |
A |
G |
2: 142,912,893 (GRCm39) |
N172S |
possibly damaging |
Het |
Spns1 |
G |
T |
7: 125,973,474 (GRCm39) |
|
probably benign |
Het |
Srsf6 |
T |
A |
2: 162,775,347 (GRCm39) |
S86R |
probably benign |
Het |
Stk25 |
A |
T |
1: 93,553,378 (GRCm39) |
|
probably benign |
Het |
Szt2 |
A |
T |
4: 118,254,866 (GRCm39) |
C275S |
probably benign |
Het |
Tcp10b |
T |
A |
17: 13,292,504 (GRCm39) |
|
probably null |
Het |
Tmem248 |
T |
A |
5: 130,260,615 (GRCm39) |
L60H |
probably damaging |
Het |
Trim27 |
T |
C |
13: 21,367,930 (GRCm39) |
I182T |
probably damaging |
Het |
Tspan10 |
A |
G |
11: 120,335,324 (GRCm39) |
N145D |
probably damaging |
Het |
Vps13d |
A |
G |
4: 144,801,412 (GRCm39) |
F487S |
probably damaging |
Het |
Wdr86 |
A |
T |
5: 24,923,229 (GRCm39) |
D154E |
probably benign |
Het |
Wfdc18 |
C |
A |
11: 83,600,695 (GRCm39) |
A32D |
possibly damaging |
Het |
Wrn |
A |
T |
8: 33,826,019 (GRCm39) |
|
probably null |
Het |
Zfp811 |
C |
A |
17: 33,019,897 (GRCm39) |
E7* |
probably null |
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 |
|
IGL01526:Cfap65
|
APN |
1 |
74,950,237 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
74,944,872 (GRCm39) |
missense |
probably damaging |
0.99 |
R1079:Cfap65
|
UTSW |
1 |
74,941,606 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
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 |
|
Predicted Primers |
PCR Primer
(F):5'- GGACAGGGTTCAAATGTCATTC -3'
(R):5'- ACCCACTGTTTCTGGACCTG -3'
Sequencing Primer
(F):5'- AGGGTTCAAATGTCATTCTTCTTGC -3'
(R):5'- TGATTGGGACCTGCCATTCAGAC -3'
|
Posted On |
2015-10-08 |