Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
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: HMGN5 ENSBTAG00000001877

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Description

high mobility group nucleosome binding domain 5 [Source:VGNC Symbol;Acc:VGNC:56709]

Location

Primary_assembly X: 71,422,826-71,433,953 forward strand.

ARS-UCD2.0:CM008197.2

About this gene

This gene has 2 transcripts (splice variants) and 60 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000082587.3	HMGN5-201	2837	299aa	ENSBTAP00000061898.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LWS9	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,
ENSBTAT00000053474.3	HMGN5-202	474	158aa	ENSBTAP00000051689.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BA81	-

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Summary

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