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: Pex7 FBgn0035922

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Description

Peroxin 7

Gene Synonyms

Pex7

Location

Primary_assembly 3L: 8,647,145-8,651,011 forward strand.

BDGP6.54:AE014296.5

About this gene

This gene has 2 transcripts (splice variants), 200 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0076568	Pex7-RA	1443	339aa	FBpp0076295	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9VSN7	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,
FBtr0273328	Pex7-RB	1391	339aa	FBpp0271836	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H0RNM0 Q4V4T3 Q4V6K2 Q4V6Q4 Q9VSN7	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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