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Gene: EGOT (eosinophil granule ontogeny transcript) Homo sapiens
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Symbol: EGOT
Name: eosinophil granule ontogeny transcript
Description: ASSOCIATED WITH Neurodevelopmental Disorders; spinocerebellar ataxia type 15; INTERACTS WITH 2-hydroxypropanoic acid; aflatoxin B2; benzo[a]pyrene
Type: ncrna
RefSeq Status: VALIDATED
Also known as: EGO; eosinophil granule ontogeny transcript (non-protein coding); NCRNA00190
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl34,749,192 - 4,751,590 (-)Ensembl
GRCh3834,749,192 - 4,751,590 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh3734,790,876 - 4,793,274 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3634,790,876 - 4,793,274 (-)NCBINCBI36hg18NCBI36
Celera34,728,876 - 4,731,274 (-)NCBI
Cytogenetic Map3p26.1NCBI
HuRef34,724,364 - 4,726,762 (-)NCBIHuRef
CHM1_134,741,108 - 4,743,506 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Promoters
Clinical Variants

Additional Information

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

CRRD Object Information
CRRD ID: 2312701
Created: 2009-08-28
Species: Homo sapiens
Last Modified: 2019-12-31
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.