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
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: HOXB8 ENSSSCG00000017537

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Description

homeobox B8 [Source:VGNC Symbol;Acc:VGNC:88948]

Location

Primary_assembly 12: 24,865,984-24,868,930 reverse strand.

Sscrofa11.1:CM000823.5

About this gene

This gene has 1 transcript (splice variant), 201 orthologues and 41 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000019091.5	HOXB8-201	1867	243aa	ENSSSCP00000018585.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UQX1 F1RWG3	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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