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: CG8671 FBgn0032938

Gene Synonyms

CG8671

Location

BDGP6.46:AE014134.6

About this gene

This gene has 7 transcripts (splice variants) and 535 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0346464	CG8671-RG	4975	1039aa	FBpp0312114	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9VID5	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,
FBtr0081483	CG8671-RA	4222	1039aa	FBpp0081012	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9VID5	-
FBtr0330679	CG8671-RE	4183	867aa	FBpp0303529	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M9PDX3	-
FBtr0330680	CG8671-RF	3739	878aa	FBpp0303530	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M9PDK6	-
FBtr0114602	CG8671-RC	3658	851aa	FBpp0113094	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A2VEG3	-
FBtr0330678	CG8671-RD	3603	655aa	FBpp0303528	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M9PDD2	-
FBtr0081484	CG8671-RB	2431	467aa	FBpp0081013	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8SZ43	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