Gene: Hspb8 ENSMUSG00000041548

Description

heat shock protein 8 [Source:MGI Symbol;Acc:MGI:2135756]

Gene Synonyms

Cryac, D5Ucla4, E2IG1, H11, H11K, HSP20-like, HSP22

Location

Chromosome 5: 116,546,550-116,560,923 reverse strand.

GRCm39:CM000998.3

About this gene

This gene has 2 transcripts (splice variants), 215 orthologues, 8 paralogues and is associated with 34 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000036991.5	Hspb8-201	1816	196aa	ENSMUSP00000037007.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS19600	Q9JK92	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000133335.2	Hspb8-202	749	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:2,

Gene: Hspb8 ENSMUSG00000041548

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Gene: Hspb8 ENSMUSG00000041548

Summary

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