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: EHF ENSSSCG00000013300

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Description

ETS homologous factor [Source:VGNC Symbol;Acc:VGNC:87599]

Location

Primary_assembly 2: 26,291,480-26,340,245 reverse strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 2 transcripts (splice variants), 204 orthologues and 27 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000078467.1	EHF-201	8385	300aa	ENSSSCP00000069624.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1SQF9 A0A8D0Z6P9	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,
ENSSSCT00000083760.1	EHF-202	8316	277aa	ENSSSCP00000072217.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1SRX3 A0A8D1U8H1	-

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Summary

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