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: Molecular function
- GO: Biological process
- GO: Cellular component
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: CG7461 FBgn0034432

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Location

Primary_assembly 2R: 19,305,172-19,307,445 forward strand.

BDGP6.32:AE013599.5

About this gene

This gene has 2 transcripts (splice variants), 189 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
CG7461-RC	FBtr0345425	2274	627aa	FBpp0311550	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1ZBJ2	NM_001299682 NM_001299682.1 NM_137565.3 NP_001286611 NP_001286611.1 NP_611409.2	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,
CG7461-RB	FBtr0300283	2013	627aa	FBpp0289511	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1ZBJ2 C9QPI7	NM_001299682.1 NM_137565 NM_137565.3 NP_001286611.1 NP_611409 NP_611409.2	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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Gene-based displays