Entry Detail



General Information

Database ID:SKCM05253
Cancer Type:melanoma
Dataset:GSE38495
CTCs/CTM Isolation Method:immunomagnetic purification



Gene Information

ncRNA Symbol:HR
Full Name:HR, lysine demethylase and nuclear receptor corepressor
Category:mRNA
Synonyms:ALUNC|AU|HSA277165|HYPT4|MUHH|MUHH1
Chromosome:chr8
Strand:-
Coordinate:
Start Site(bp):22114415End Site(bp):22133384
Gene Summary:This gene encodes a protein that is involved in hair growth. This protein functions as a transcriptional corepressor of multiple nuclear receptors, including thyroid hormone receptor, the retinoic acid receptor-related orphan receptors and the vitamin D receptors, and it interacts with histone deacetylases. The translation of this protein is modulated by a regulatory open reading frame (ORF) that exists upstream of the primary ORF. Mutations in this upstream ORF cause Marie Unna hereditary hypotrichosis (MUHH), an autosomal dominant form of genetic hair loss. Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions, other diseases resulting in hair loss. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2014]
External Links:
Ensembl ID:ENSG00000168453
HGNC ID:HGNC:5172
Entrez Gene:55806



Expression Profile of HR Gene

 







Regulatory Relationship

mRNA targets:NA
miRNA targets:
miRNA NamePITAmiRandaRNAhybrid
hsa-miR-122-5p
YES
YES
NO
hsa-miR-136-5p
YES
YES
NO
hsa-miR-140-3p
YES
NO
YES
hsa-miR-214-3p
YES
YES
NO
hsa-miR-374a-5p
YES
YES
YES
hsa-miR-374b-5p
YES
YES
YES
hsa-miR-491-5p
YES
YES
NO
hsa-miR-873-5p
YES
YES
YES
Display: