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

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Gene: hoxb13a ENSDARG00000056015

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Description

homeobox B13a [Source:ZFIN;Acc:ZDB-GENE-050812-1]

Gene Synonyms

zgc:136601

Location

Chromosome 3: 23,654,233-23,655,834 forward strand.

GRCz11:CM002887.2

About this gene

This gene has 1 transcript (splice variant), 192 orthologues, 53 paralogues and is associated with 23 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000078428.5	hoxb13a-201	1170	303aa	ENSDARP00000072890.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q1ECY2	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,

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Summary

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