Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Rps8l1 ENSRNOG00000005017

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Description

ribosomal protein S8 like 1 [Source:RGD Symbol;Acc:1566369]

Gene Synonyms

LOC291353, RGD1566369

Location

Primary_assembly 17: 88,667,623-88,668,273 reverse strand.

GRCr8:CM070407.1

About this gene

This gene has 1 transcript (splice variant), 145 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000006662.8	Rps8l1-201	651	208aa	ENSRNOP00000006662.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZIE1	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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