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Gene: RNU105B (RNA, U105B small nucleolar) Homo sapiens
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Symbol: RNU105B
Name: RNA, U105B small nucleolar
Description: ASSOCIATED WITH early infantile epileptic encephalopathy 12
Type: snorna
RefSeq Status: VALIDATED
Also known as: 105B; E1-2
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl208,831,186 - 8,831,393 (+)EnsemblGRCh38hg38GRCh38
GRCh38208,831,185 - 8,831,393 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37208,811,832 - 8,812,040 (+)NCBIGRCh37GRCh37hg19GRCh37
Celera208,881,370 - 8,881,578 (+)NCBI
Cytogenetic Map20p12.3NCBI
HuRef208,763,481 - 8,763,689 (+)NCBIHuRef
CHM1_1208,812,795 - 8,813,003 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on RNU105B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1352899
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2020-03-31
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.