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

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Gene: hpxb ENSDARG00000051912

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Description

hemopexin b [Source:ZFIN;Acc:ZDB-GENE-060929-800]

Gene Synonyms

hbxb, smarca2, zgc:152945

Location

Chromosome 16: 2,394,193-2,414,063 reverse strand.

GRCz11:CM002900.2

About this gene

This gene has 1 transcript (splice variant), 175 orthologues and 28 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000073621.6	hpxb-201	1397	168aa	ENSDARP00000068111.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FFU0	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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