Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: MEOX2 ENSGGOG00000006252

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Description

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

Location

Chromosome 7: 15,551,124-15,623,464 reverse strand.

gorGor4:FR853100.2

About this gene

This gene has 1 transcript (splice variant), 125 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGGOT00000006278.3	MEOX2-201	2359	303aa	ENSGGOP00000006114.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3QTT1	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,

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Summary

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