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: meis2b ENSDARG00000077840

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Description

Meis homeobox 2b [Source:NCBI gene (formerly Entrezgene);Acc:30066]

Location

Chromosome 20: 10,098,590-10,120,442 reverse strand.

GRCz11:CM002904.2

About this gene

This gene has 3 transcripts (splice variants), 79 orthologues, 15 paralogues and is associated with 17 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000033976.7	meis2b-201	3446	393aa	ENSDARP00000034815.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9DDE0	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,
ENSDART00000144970.3	meis2b-203	3104	393aa	ENSDARP00000121019.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9DDE0	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,
ENSDART00000143510.2	meis2b-202	843	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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