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: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Hbp1 ENSRNOG00000008927

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Description

HMG-box transcription factor 1 [Source:RGD Symbol;Acc:620444]

Gene Synonyms

Hmgb1

Location

Primary_assembly 6: 54,256,864-54,283,366 reverse strand.

GRCr8:CM070396.1

About this gene

This gene has 2 transcripts (splice variants), 266 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000094150.2	Hbp1-202	3118	532aa	ENSRNOP00000077814.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y7X5	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,
ENSRNOT00000012004.6	Hbp1-201	3013	523aa	ENSRNOP00000012004.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HB56 Z4YNI2	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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