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: Epn2 ENSRNOG00000060550

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Description

epsin 2 [Source:RGD Symbol;Acc:619773]

Location

Primary_assembly 10: 46,697,238-46,759,092 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 4 transcripts (splice variants), 206 orthologues, 5 paralogues and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000091963.3	Epn2-203	4450	652aa	ENSRNOP00000073697.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LQ45	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000085703.3	Epn2-201	4414	640aa	ENSRNOP00000074461.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q505I9	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000155858.1	Epn2-204	4089	595aa	ENSRNOP00000106806.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000087102.3	Epn2-202	1978	604aa	ENSRNOP00000070453.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JXY9	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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