Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: ESS2 ENSDARG00000060922

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Description

ess-2 splicing factor homolog [Source:ZFIN;Acc:ZDB-GENE-030131-2843]

Gene Synonyms

dgcr14, fc19d10, wu:fc19d10, zgc:162979

Location

Chromosome 10: 42,089,267-42,108,137 reverse strand.

GRCz11:CM002894.2

About this gene

This gene has 1 transcript (splice variant) and 200 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000132976.3	ESS2-201	2510	469aa	ENSDARP00000116212.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QAX0	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,

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Summary

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