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    RESULT:

PMID: 26824232
Subject&Disease: Osteoporosis (Prader-Willi Syndrome)
Sample: Bone tissue
Species: Mus musculus
ncRNA Category: snoRNA
ncRNA Symbols: Snord116
Accession number: null
chromosome Location: null
Expression pattern: Downregulation
High-throughput experiment methods: null
Low-throughput experiment methods: null
Targets of ncRNA: null
Detection methods for targets: null
Description the function of ncRNA: SnoRNA Snord116 as a critical contributor to the development of PWS exhibiting many of the classical symptoms of Prader-Willi Syndrome. PWCR which includes Snord116 in mice leads to a reduced bone mass phenotype, similar to that observed in humans.
Year: 2016
Title: Prader-Willi Critical Region, a Non-Translated, Imprinted Central Regulator of Bone Mass: Possible Role in Skeletal Abnormalities in Prader-Willi Syndrome.
External Link: Ensembl Link ; HGNC Link

 

 

ODNA
Harbin Medical University, China