Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Rps26-ps13 ENSRNOG00000052877

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Description

ribosomal protein S26, pseudo 13 [Source:RGD Symbol;Acc:1562415]

Gene Synonyms

LOC303862, RGD1562415, Rps26l1, Rps26l2

Location

Primary_assembly 11: 83,864,291-83,864,680 forward strand.

GRCr8:CM070401.1

About this gene

This gene has 1 transcript (splice variant), 116 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000087747.3	Rps26-ps13-201	390	105aa	ENSRNOP00000074056.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K743	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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