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Gene: SNORD115-22 (small nucleolar RNA, C/D box 115-22) Homo sapiens
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Symbol: SNORD115-22
Name: small nucleolar RNA, C/D box 115-22
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia; INTERACTS WITH valproic acid
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-52-22
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1525,209,918 - 25,209,999 (+)Ensembl
GRCh381525,209,918 - 25,209,999 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,455,065 - 25,455,146 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361523,006,158 - 23,006,239 (+)NCBINCBI36hg18NCBI36
Celera153,617,089 - 3,617,170 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,579,549 - 3,579,630 (+)NCBIHuRef
CHM1_11525,404,579 - 25,404,660 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD115-22
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1606846
Created: 2007-04-29
Species: Homo sapiens
Last Modified: 2019-12-25
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.