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: CG18266 FBgn0031724

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Gene Synonyms

CG18266

Location

Primary_assembly 2L: 5,596,833-5,598,636 forward strand.

BDGP6.46:AE014134.6

About this gene

This gene has 1 transcript (splice variant), 171 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0079109	CG18266-RA	1804	486aa	FBpp0078741	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AMX1 A0AMX2 A0AMX3 C0MIG7 C0MIG8 C0MIG9 C0MIH5 C0MIH6 C0MIH7 Q9VMP0	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,

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Summary

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