Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: eslec ENSDARG00000079043

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Description

eosinophil lineage-specific marker [Source:ZFIN;Acc:ZDB-GENE-090313-394]

Location

Chromosome 1: 9,994,811-10,000,376 forward strand.

GRCz11:CM002885.2

About this gene

This gene has 2 transcripts (splice variants), 179 orthologues and 68 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000110749.4	eslec-201	770	161aa	ENSDARP00000102128.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B8A5M2	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,
ENSDART00000143719.3	eslec-202	680	161aa	ENSDARP00000122934.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B8A5M2	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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