Entry Detail



General Information

Database ID:SKCM07523
Cancer Type:melanoma
Dataset:GSE38495
CTCs/CTM Isolation Method:immunomagnetic purification



Gene Information

ncRNA Symbol:TTC8
Full Name:tetratricopeptide repeat domain 8
Category:mRNA
Synonyms:BBS8|RP51
Chromosome:chr14
Strand:+
Coordinate:
Start Site(bp):88824153End Site(bp):88881078
Gene Summary:This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. A mutation in this gene has also been implicated in nonsyndromic retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
External Links:
Ensembl ID:ENSG00000165533
HGNC ID:HGNC:20087
Entrez Gene:123016



Expression Profile of TTC8 Gene

 







Regulatory Relationship

mRNA targets:NA
miRNA targets:
miRNA NamePITAmiRandaRNAhybrid
hsa-miR-155-5p
YES
YES
NO
hsa-miR-183-5p
YES
YES
NO
hsa-miR-18a-5p
YES
YES
NO
hsa-miR-18b-5p
YES
YES
NO
hsa-miR-197-3p
YES
YES
NO
hsa-miR-221-3p
YES
YES
NO
hsa-miR-222-3p
YES
YES
NO
hsa-miR-30a-5p
YES
YES
NO
hsa-miR-30b-5p
YES
YES
NO
hsa-miR-30c-5p
YES
YES
NO
hsa-miR-30d-5p
YES
YES
NO
hsa-miR-30e-5p
YES
YES
NO
hsa-miR-340-5p
YES
YES
NO
hsa-miR-374a-5p
YES
YES
NO
hsa-miR-374b-5p
YES
YES
NO
hsa-miR-486-5p
YES
YES
NO
hsa-miR-495-3p
YES
YES
NO
hsa-miR-543
YES
YES
NO
Display: