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Gene: SNORD108 (small nucleolar RNA, C/D box 108) Homo sapiens
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Symbol: SNORD108
Name: small nucleolar RNA, C/D box 108
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia; INTERACTS WITH aflatoxin B1
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-437
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1524,986,925 - 24,986,995 (+)Ensembl
GRCh381524,986,925 - 24,986,993 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,232,072 - 25,232,140 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,783,165 - 22,783,233 (+)NCBINCBI36hg18NCBI36
Celera153,394,065 - 3,394,133 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,367,992 - 3,368,060 (+)NCBIHuRef
CHM1_11525,181,614 - 25,181,682 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD108
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1605817
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.