Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: MESP2 ENSPTRG00000007440

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Description

mesoderm posterior bHLH transcription factor 2 [Source:VGNC Symbol;Acc:VGNC:1920]

Location

Chromosome 15: 70,539,411-70,553,789 forward strand.

Pan_tro_3.0:CM000329.3

About this gene

This gene has 2 transcripts (splice variants), 278 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000013727.3	MESP2-202	1886	389aa	ENSPTRP00000012724.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2X8X2 H2QA25	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,
ENSPTRT00000109142.1	MESP2-201	300	99aa	ENSPTRP00000085971.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3T9Q8	-

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Summary

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