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

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Gene: Hmgxb3 ENSRNOG00000018132

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Description

HMG-box containing 3 [Source:RGD Symbol;Acc:1560009]

Gene Synonyms

LOC361335

Location

Primary_assembly 18: 56,860,947-56,908,419 reverse strand.

GRCr8:CM070408.1

About this gene

This gene has 2 transcripts (splice variants), 200 orthologues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000164101.1	Hmgxb3-202	5012	1309aa	ENSRNOP00000103890.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000024704.10	Hmgxb3-201	5174	1286aa	ENSRNOP00000024704.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IXF9 F1MAL8	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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