Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
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Ontologies
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
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External references
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ID History
- Gene history

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Gene: CG11034 FBgn0031741

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Gene Synonyms

CG11034

Location

Primary_assembly 2L: 5,805,395-5,809,063 forward strand.

BDGP6.46:AE014134.6

About this gene

This gene has 3 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0342609	CG11034-RC	2545	751aa	FBpp0309549	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9VMM2	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,
FBtr0344769	CG11034-RD	2414	85aa	FBpp0311098	Gene/transcipt that contains an open reading frame (ORF).Protein coding	X2J9G3	-
FBtr0306841	CG11034-RB	2409	751aa	FBpp0297739	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9VMM2	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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