Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
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: Spn28B FBgn0083141

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Description

Serpin 28B

Gene Synonyms

Spn28B

Location

Primary_assembly 2L: 7,581,924-7,583,333 forward strand.

BDGP6.46:AE014134.6

About this gene

This gene has 2 transcripts (splice variants) and 23 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0079470	Spn28B-RA	1248	378aa	FBpp0079094	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9VLZ8	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,
FBtr0335485	Spn28B-RB	1186	378aa	FBpp0307458	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H8F4V2 Q4V4T7 Q4V6K6 Q9VLZ8	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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