Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: ESS2 ENSPTRG00000014055

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Description

ess-2 splicing factor homolog [Source:VGNC Symbol;Acc:VGNC:14855]

Location

Chromosome 22: 5,667,726-5,678,396 reverse strand.

Pan_tro_3.0:CM000335.3

About this gene

This gene has 2 transcripts (splice variants) and 198 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000026248.7	ESS2-201	1778	476aa	ENSPTRP00000024204.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XUT4 H2QL81	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,
ENSPTRT00000090217.1	ESS2-202	882	293aa	ENSPTRP00000069587.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RZ37 A0A6D2Y7X5	-

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Summary

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