Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: HMGXB4 ENSPTRG00000014296

.

Description

HMG-box containing 4 [Source:VGNC Symbol;Acc:VGNC:5269]

Location

Chromosome 22: 21,851,888-21,890,216 forward strand.

Pan_tro_3.0:CM000335.3

About this gene

This gene has 2 transcripts (splice variants), 229 orthologues and 32 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000026708.4	HMGXB4-202	4134	601aa	ENSPTRP00000024618.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XW59 H2QLJ9	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,
ENSPTRT00000105960.1	HMGXB4-201	4249	492aa	ENSPTRP00000066818.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RR71	-

.

Summary

.

.