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Gene: SNORD115-18 (small nucleolar RNA, C/D box 115-18) Homo sapiens
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Symbol: SNORD115-18
Name: small nucleolar RNA, C/D box 115-18
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-52-18
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1525,203,227 - 25,203,308 (+)Ensembl
GRCh381525,203,227 - 25,203,308 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,448,374 - 25,448,455 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,999,467 - 22,999,548 (+)NCBINCBI36hg18NCBI36
Celera153,610,386 - 3,610,467 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,572,850 - 3,572,931 (+)NCBIHuRef
CHM1_11525,397,888 - 25,397,969 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD115-18
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1604075
Created: 2007-04-28
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.