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

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DB built by FlyBase

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Gene: CG10932 FBgn0029969

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Location

Primary_assembly X: 7,887,130-7,888,785 reverse strand.

BDGP6.32:AE014298.5

About this gene

This gene has 2 transcripts (splice variants), 161 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
CG10932-RB	FBtr0345982	1656	410aa	FBpp0311869	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9W3N9	NM_001298058 NM_001298058.1 NM_132186.2 NP_001284987 NP_001284987.1 NP_572414.1	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,
CG10932-RA	FBtr0071143	1517	410aa	FBpp0071095	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9W3N9	NM_001298058.1 NM_132186 NM_132186.2 NP_001284987.1 NP_572414 NP_572414.1	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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