Summary
- Splice variants
- Transcript comparison
- Gene alleles
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Gene: insv FBgn0031434

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Description

insensitive

Gene Synonyms

insv

Location

Primary_assembly 2L: 2,575,280-2,576,997 reverse strand.

BDGP6.46:AE014134.6

About this gene

This gene has 2 transcripts (splice variants) and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0077746	insv-RA	1654	376aa	FBpp0077426	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8SYK5	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,
FBtr0344854	insv-RB	1335	376aa	FBpp0311169	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8SYK5	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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