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

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Gene: HOXB13 ENSBTAG00000014663

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Description

homeobox B13 [Source:VGNC Symbol;Acc:VGNC:29917]

Location

Primary_assembly 19: 37,792,257-37,794,223 forward strand.

ARS-UCD2.0:CM008186.2

About this gene

This gene has 1 transcript (splice variant), 193 orthologues and 42 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000019523.7	HOXB13-201	1090	285aa	ENSBTAP00000019523.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BPB2	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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