Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
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: CG9123 FBgn0030629

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Gene Synonyms

CG9123

Location

Primary_assembly X: 15,340,373-15,342,117 reverse strand.

BDGP6.54:AE014298.5

About this gene

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

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0074019	CG9123-RA	1592	434aa	FBpp0073836	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B3DN58 C5I7A9 C5I7D3 C5I7I9 C5I7J7 C5I7K5 C5I7L3 C5I7R1 C5I7R9 Q9VXW4	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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