Entry Detail



General Information

Database ID:SKCM04818
Cancer Type:melanoma
Dataset:GSE38495
CTCs/CTM Isolation Method:immunomagnetic purification



Gene Information

ncRNA Symbol:OPN1SW
Full Name:opsin 1, short wave sensitive
Category:mRNA
Synonyms:BCP|BOP|CBT
Chromosome:chr7
Strand:-
Coordinate:
Start Site(bp):128772491End Site(bp):128775790
Gene Summary:This gene belongs to the G-protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic. [provided by RefSeq, Jul 2008]
External Links:
Ensembl ID:ENSG00000128617
HGNC ID:HGNC:1012
Entrez Gene:611



Expression Profile of OPN1SW Gene

 







Regulatory Relationship

mRNA targets:NA
miRNA targets:NA
Display:N/A