Entry Detail



General Information

Database ID:SKCM05703
Cancer Type:melanoma
Dataset:GSE38495
CTCs/CTM Isolation Method:immunomagnetic purification



Gene Information

ncRNA Symbol:RTTN
Full Name:rotatin
Category:mRNA
Synonyms:MSSP
Chromosome:chr18
Strand:-
Coordinate:
Start Site(bp):70003031End Site(bp):70205945
Gene Summary:This gene encodes a large protein whose specific function is unknown. Absence of the orthologous protein in mouse results in embryonic lethality with deficient axial rotation, abnormal differentiation of the neural tube, and randomized looping of the heart tube during development. In human, mutations in this gene are associated with polymicrogyria with seizures. In human fibroblasts this protein localizes at the ciliary basal bodies. Given the intracellular localization of this protein and the phenotypic effects of mutations, this gene is suspected of playing a role in the maintenance of normal ciliary structure which in turn effects the developmental process of left-right organ specification, axial rotation, and perhaps notochord development. [provided by RefSeq, Jan 2013]
External Links:
Ensembl ID:ENSG00000176225
HGNC ID:HGNC:18654
Entrez Gene:25914



Expression Profile of RTTN Gene

 







Regulatory Relationship

mRNA targets:NA
miRNA targets:
miRNA NamePITAmiRandaRNAhybrid
hsa-let-7a-5p
YES
YES
NO
hsa-let-7b-5p
YES
YES
NO
hsa-let-7c-5p
YES
YES
NO
hsa-let-7d-5p
YES
YES
NO
hsa-let-7e-5p
YES
YES
NO
hsa-let-7f-5p
YES
YES
NO
hsa-let-7g-5p
YES
YES
NO
hsa-let-7i-5p
YES
YES
NO
hsa-miR-124-3p
YES
YES
NO
hsa-miR-183-5p
YES
YES
NO
hsa-miR-194-5p
YES
YES
NO
hsa-miR-22-3p
YES
YES
NO
hsa-miR-382-5p
YES
YES
NO
hsa-miR-421
YES
YES
NO
hsa-miR-506-3p
YES
YES
NO
hsa-miR-98-5p
YES
YES
NO
Display: