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Gene: SNORD66 (small nucleolar RNA, C/D box 66) Homo sapiens
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Symbol: SNORD66
Name: small nucleolar RNA, C/D box 66
Description: ASSOCIATED WITH Currarino syndrome; INTERACTS WITH 2-hydroxypropanoic acid; aflatoxin B1; rac-lactic acid
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-142
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl3184,325,696 - 184,325,771 (+)Ensembl
GRCh383184,325,696 - 184,325,771 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh373184,043,484 - 184,043,559 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 363185,526,178 - 185,526,253 (+)NCBINCBI36hg18NCBI36
Celera3182,484,380 - 182,484,455 (+)NCBI
Cytogenetic Map3q27.1NCBI
HuRef3181,450,110 - 181,450,185 (+)NCBIHuRef
CHM1_13184,007,940 - 184,008,015 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD66
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1602543
Created: 2007-04-27
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.