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Gene: SNORD115-12 (small nucleolar RNA, C/D box 115-12) Homo sapiens
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Symbol: SNORD115-12
Name: small nucleolar RNA, C/D box 115-12
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia; INTERACTS WITH aflatoxin B1; cadmium atom; valproic acid
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-52-12
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381525,191,416 - 25,191,497 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,436,563 - 25,436,644 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,987,656 - 22,987,737 (+)NCBINCBI36hg18NCBI36
Celera153,598,575 - 3,598,656 (+)NCBI
Cytogenetic Map15q11.2NCBI
CHM1_11525,386,077 - 25,386,158 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - curated
References - uncurated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD115-12
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1604081
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2019-10-16
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.