Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: HMGN2 ENSSSCG00070025139

Description

Sus scrofa high mobility group nucleosomal binding domain 2 (HMGN2), transcript variant 1, mRNA. [Source:RefSeq mRNA;Acc:NM_001244112]

Gene Synonyms

HMG17

Location

USMARCv1.0:CM009091.1

About this gene

This gene has 2 transcripts (splice variants).

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00070050262.1	HMGN2-201	1330	90aa	ENSSSCP00070042470.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P80272	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,
ENSSSCT00070050288.1	HMGN2-202	258	85aa	ENSSSCP00070042493.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1VNB4	-

Summary