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Gene: SNORD116-17 (small nucleolar RNA, C/D box 116-17) Homo sapiens
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Symbol: SNORD116-17
Name: small nucleolar RNA, C/D box 116-17
CRRD ID: 1604101
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-85-17
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1525,083,588 - 25,083,679 (+)EnsemblGRCh38hg38GRCh38
GRCh381525,083,587 - 25,083,680 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,328,734 - 25,328,827 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,879,827 - 22,879,920 (+)NCBINCBI36hg18NCBI36
Celera153,490,705 - 3,490,798 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,464,592 - 3,464,685 (+)NCBIHuRef
CHM1_11525,278,254 - 25,278,347 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD116-17
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1604101
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2020-09-16
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.