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: meox2a ENSDARG00000040911

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Description

mesenchyme homeobox 2 [Source:HGNC Symbol;Acc:HGNC:7014]

Location

Chromosome 15: 34,428,308-34,468,599 reverse strand.

GRCz11:CM002899.2

About this gene

This gene has 2 transcripts (splice variants), 192 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000059954.4	meox2a-201	2006	302aa	ENSDARP00000059953.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FEH1	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,
ENSDART00000192984.1	meox2a-202	1848	302aa	ENSDARP00000148505.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FEH1	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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