Gene Information
|
Gene Name
|
CFAP418 |
|
Gene ID
|
157657
|
|
Gene Full Name
|
cilia and flagella associated protein 418 |
|
Gene Alias
|
BBS21|C8orf37|CORD16|FAP418|MOT25|RP64|smalltalk |
|
Transcripts
|
ENSG00000156172
|
|
Virus
|
HTLV1 |
|
Gene Type
|
protein-coding |
|
HPA Location Info
|
Plasma membrane, Primary cilium;Vesicles, Cell Junctions, Centrosome;
|
|
Membrane Info
|
Disease related genes, Human disease related genes, Predicted intracellular proteins |
|
Uniport_ID
|
Q96NL8
|
|
HGNC ID
|
HGNC:27232
|
|
OMIM ID
|
614477 |
|
Summary
|
This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012] |
Target gene [CFAP418] related to VISs
Integration Table: if previous studies reported that target gene was altered by virus integration events, the overlap between VISs in this literature and Cistrome factors was listed in this section
| DVID |
Chromosome |
HM |
TFBS |
CA |
Sum of Overlapped Records |
Detail |
| 6027177 |
chr8 |
0 |
0 |
2 |
2 |
View |
Target gene [CFAP418] related to Omics data
| Data ID |
Experiment type |
Sample number |
Platform |
|
GSE52244
|
Expression array |
15 |
[HuEx-1_0-st] Affymetrix Human Exon 1.0 ST Array [probe set (exon) version] |
|
GSE224047
|
RNA-seq |
10 |
Illumina NextSeq 500 (Homo sapiens) |
|
C GSE94732
|
Chip-seq |
24 |
Illumina NextSeq 500 (Homo sapiens);illumina Genome Analyzer IIx (Homo sapiens) |
When the gene can detect a peak in the dataset, a peak plot will be displayed.
> Dataset: GSE94732 - CFAP418 peak across samples
|
Peak Plot
|
|
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