Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: CG12239 FBgn0029810

Gene Synonyms

CG12239

Location

BDGP6.46:AE014298.5

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0070814	CG12239-RA	2343	650aa	FBpp0070780	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A9YIW8 A9YIW9 A9YIX3 A9YIY2 A9YIY4 A9YIY7 A9YIY8 A9YIZ2 F6J3Q6 F6J3R4 F6J3R9 F6J3S0 F6J3S4 F6JAV0 F6JAV1 F6JAV7 F6JAW4 F6JAW6 Q9W472	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,

Summary