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InnateDB Gene
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IDBG-109205.5
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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SNORD115-1
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Gene Name
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small nucleolar RNA, C/D box 115-1
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Synonyms
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Species
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Homo sapiens
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Ensembl Gene
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ENSG00000201831
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Encoded Proteins
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Protein Structure
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Useful resources
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Stemformatics
EHFPI
ImmGen
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| Summary |
This gene encodes a small nucleolar RNA (snoRNA) that is found clustered with dozens of other similar snoRNAs on chromosome 15. These genes are found mostly within introns of the IC-SNURF-SNRPN transcript, which is paternally imprinted and from the Prader-Willi/Angelman syndrome (PWS) region. This gene has been designated as copy 1 of the cluster and may be involved in the regulation of RNA editing and/or alternative splicing of the serotonin receptor 2C (HTR2C) transcript. This gene is not thought to play a major role in PWS. [provided by RefSeq, Jul 2008]
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| Type |
snoRNA
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Genomic Location
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Chromosome 15:25170723-25170804
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Strand
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Forward strand
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Band
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q11.2
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Transcripts
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Number of Interactions
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This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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No orthologs found for this gene |
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SwissProt
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TrEMBL
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UniProt Splice Variant
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Entrez Gene
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338433
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UniGene
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RefSeq
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NR_001291
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HUGO
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HGNC:33020
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OMIM
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609837
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CCDS
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| HPRD |
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IMGT
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EMBL
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GenPept
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RNA Seq Atlas
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338433
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Version 5.4