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

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Gene: epn1b ENSDARG00000079847

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Description

epsin 1b [Source:NCBI gene (formerly Entrezgene);Acc:792915]

Location

Chromosome 19: 10,375,782-10,395,683 reverse strand.

GRCz11:CM002903.2

About this gene

This gene has 2 transcripts (splice variants), 183 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000109488.3	epn1b-201	2531	504aa	ENSDARP00000101039.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B3DIW6	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, 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,
ENSDART00000191549.1	epn1b-202	5851	504aa	ENSDARP00000155809.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B3DIW6	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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