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: FoxP FBgn0262477

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Description

Forkhead box P

Gene Synonyms

FoxP

Location

Primary_assembly 3R: 9,726,020-9,730,872 reverse strand.

BDGP6.54:AE014297.3

About this gene

This gene has 3 transcripts (splice variants), 4 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0304869	FoxP-RC	3552	520aa	FBpp0293409	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0B4K6N2 E0WMM3 K4EN08 U3MV10 U3MV70 U3MWN6 U3MWP4 U3MX98 U3MXA6 U3N1V8	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,
FBtr0433516	FoxP-RE	2800	393aa	FBpp0390648	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A126GUS5 K4ENJ1	-
FBtr0329937	FoxP-RD	2428	442aa	FBpp0302969	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E0WMM2 K4EQ40 Q9VH87	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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