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Gene: EPN2-IT1 (EPN2 intronic transcript 1) Homo sapiens
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Symbol: EPN2-IT1
Name: EPN2 intronic transcript 1
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH 2-hydroxypropanoic acid; rac-lactic acid
Type: ncrna
RefSeq Status: PREDICTED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381719,271,393 - 19,274,388 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371719,174,706 - 19,177,701 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map17p11.2NCBI
HuRef1718,554,476 - 18,557,471 (+)NCBIHuRef
CHM1_11719,183,455 - 19,186,450 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations

Genomics


Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on EPN2-IT1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 6481022
Created: 2012-04-10
Species: Homo sapiens
Last Modified: 2020-09-08
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.