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

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Gene: Hmgb1l5 ENSRNOG00000051482

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Description

high mobility group box 1 like 5 [Source:RGD Symbol;Acc:1563668]

Gene Synonyms

AABR07006627.1, LOC108348989, LOC497907, RGD1563668

Location

Primary_assembly 19: 71,943,082-71,944,278 reverse strand.

GRCr8:CM070409.1

About this gene

This gene has 1 transcript (splice variant), 291 orthologues and 52 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000086591.3	Hmgb1l5-201	1197	214aa	ENSRNOP00000073890.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K6P4 A6KJ57	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,

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Summary

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