Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: ephb2a ENSDARG00000037373

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Description

EPH receptor B2 [Source:HGNC Symbol;Acc:HGNC:3393]

Location

Chromosome 23: 21,803,410-21,946,659 reverse strand.

GRCz11:CM002907.2

About this gene

This gene has 3 transcripts (splice variants), 208 orthologues and 76 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSDART00000148120.4	ephb2a-201	6435	1015aa	ENSDARP00000112928.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000184524.1	ephb2a-202	2929	291aa	ENSDARP00000147857.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-
ENSDART00000190409.1	ephb2a-203	1444	394aa	ENSDARP00000153304.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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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