Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: EPN1 ENSPTRG00000011524

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Description

epsin 1 [Source:VGNC Symbol;Acc:VGNC:2389]

Location

Chromosome 19: 58,117,410-58,136,248 forward strand.

Pan_tro_3.0:CM000333.3

About this gene

This gene has 2 transcripts (splice variants), 255 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000021474.6	EPN1-201	1989	662aa	ENSPTRP00000019816.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XY70 H2QH77	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,
ENSPTRT00000080795.1	EPN1-202	1731	576aa	ENSPTRP00000082408.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2Y4D3 K7BRI5	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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