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Gene: SNORD3B-1 (small nucleolar RNA, C/D box 3B-1) Homo sapiens
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Symbol: SNORD3B-1
Name: small nucleolar RNA, C/D box 3B-1
RGD ID: 1351412
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH 2-hydroxypropanoic acid; butanal; dexamethasone
Type: snorna
RefSeq Status: VALIDATED
Also known as: RNU3A1; U3a; U3b1; U3b2
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1719,061,912 - 19,062,669 (+)EnsemblGRCh38hg38GRCh38
GRCh381719,061,912 - 19,062,128 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371718,965,225 - 18,965,441 (+)NCBIGRCh37GRCh37hg19GRCh37
Celera1937,418,900 - 37,418,971 (-)NCBI
Cytogenetic Map17p11.2NCBI
HuRef1937,056,189 - 37,056,260 (-)NCBIHuRef
CHM1_11718,974,076 - 18,974,292 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction 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 SNORD3B-1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1351412
Created: 2005-03-08
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.