Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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Ontologies
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Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
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ID History
- Gene history

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Gene: insb FBgn0034224

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Description

insensible

Gene Synonyms

insb

Location

Primary_assembly 2R: 17,475,214-17,476,272 reverse strand.

BDGP6.46:AE013599.5

About this gene

This gene has 2 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0345651	insb-RB	1059	176aa	FBpp0311712	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q7JZ51	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,
FBtr0086953	insb-RA	854	176aa	FBpp0086109	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q7JZ51	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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