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Gene: SNORD116-12 (small nucleolar RNA, C/D box 116-12) Homo sapiens
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Symbol: SNORD116-12
Name: small nucleolar RNA, C/D box 116-12
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-85-12
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381525,077,050 - 25,077,143 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,322,197 - 25,322,290 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,873,290 - 22,873,383 (+)NCBINCBI36hg18NCBI36
Celera153,484,168 - 3,484,261 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,458,055 - 3,458,148 (+)NCBIHuRef
CHM1_11525,271,717 - 25,271,810 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated
References - uncurated

Genomics

miRNA Target Status

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD116-12
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1604106
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.