Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Rps10-ps22 ENSRNOG00000049099

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Description

ribosomal protein S10, pseudo 22 [Source:RGD Symbol;Acc:1561871]

Gene Synonyms

AABR07057264.1, LOC299823, LOC497882, RGD1561871, RGD1564698, Rps10-ps20, Rps10l2, Rps10l3, Rps10l5

Location

Primary_assembly 15: 20,787,968-20,788,849 forward strand.

GRCr8:CM070405.1

About this gene

This gene has 1 transcript (splice variant), 200 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000047113.5	Rps10-ps22-201	762	165aa	ENSRNOP00000041943.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZJY5	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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