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: CG3795 FBgn0025378

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Location

Primary_assembly X: 1,708,806-1,710,182 reverse strand.

BDGP6.32:AE014298.5

About this gene

This gene has 2 transcripts (splice variants), 102 orthologues and 19 paralogues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
CG3795-RB	FBtr0344154	1247	305aa	FBpp0310567	Gene/transcipt that contains an open reading frame (ORF).Protein coding	O76920 Q8MRL2	NM_001297861 NM_001297861.1 NM_130583.3 NP_001284790 NP_001284790.1 NP_569939.2	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,
CG3795-RA	FBtr0070278	1115	305aa	FBpp0070268	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8MRL2	NM_001297861.1 NM_130583 NM_130583.3 NP_001284790.1 NP_569939 NP_569939.2	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