Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: SNORA11D (small nucleolar RNA, H/ACA box 11D) Homo sapiens
Analyze
Symbol: SNORA11D
Name: small nucleolar RNA, H/ACA box 11D
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH valproic acid
Type: snorna
RefSeq Status: VALIDATED
Also known as: FLJ39060
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X52,190,622 - 52,190,748 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X51,933,718 - 51,933,844 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X51,933,718 - 51,933,844 (+)NCBINCBI36hg18NCBI36
CeleraX55,921,742 - 55,921,868 (+)NCBI
Cytogenetic MapXp11.22NCBI
HuRefX49,241,810 - 49,241,936 (-)NCBIHuRef
CHM1_1X51,945,901 - 51,946,027 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

miRNA Target Status

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORA11D
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1642096
Created: 2007-08-31
Species: Homo sapiens
Last Modified: 2019-10-16
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.