Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
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: Bspry ENSRNOG00000015105

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Description

B-box and SPRY domain containing [Source:RGD Symbol;Acc:708400]

Gene Synonyms

LOC64027

Location

Primary_assembly 5: 80,942,979-80,988,154 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 4 transcripts (splice variants), 119 orthologues and 62 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000126839.1	Bspry-203	1472	478aa	ENSRNOP00000106074.1	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,
ENSRNOT00000020366.7	Bspry-201	2183	448aa	ENSRNOP00000020366.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6P6S3	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000164064.1	Bspry-204	2136	434aa	ENSRNOP00000103067.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000112332.2	Bspry-202	1931	452aa	ENSRNOP00000080296.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZPH1	-

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Summary

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