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Gene: SNORA22B (small nucleolar RNA, H/ACA box 22B) Homo sapiens
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Symbol: SNORA22B
Name: small nucleolar RNA, H/ACA box 22B
Description: ASSOCIATED WITH autistic disorder
Type: snorna
RefSeq Status: PROVISIONAL
Orthologs:
No known orthologs. homologs ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38756,055,365 - 56,055,502 (+)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic Map7p11.2NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORA22B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 12738275
Created: 2017-01-31
Species: Homo sapiens
Last Modified: 2019-11-26
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.