Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
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: Rpn13R FBgn0029745

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Description

Regulatory particle non-ATPase 13-related

Gene Synonyms

Rpn13R

Location

Primary_assembly X: 5,131,898-5,132,985 forward strand.

BDGP6.46:AE014298.5

About this gene

This gene has 1 transcript (splice variant), 258 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0070741	Rpn13R-RA	1088	324aa	FBpp0070709	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B4F540 B4F541 B4F542 B4F543 B4F544 B4F551 C0ML33 C0ML36 C0ML40 Q9W4E6	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,

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Summary

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