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: Rps13l1 ENSRNOG00000048698

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Description

ribosomal protein S13 like 1 [Source:RGD Symbol;Acc:1596535]

Gene Synonyms

AABR07048031.1, LOC683961

Location

Primary_assembly 5: 61,247,396-61,256,975 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 3 transcripts (splice variants), 26 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000153679.1	Rps13l1-202	728	180aa	ENSRNOP00000112806.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000162788.1	Rps13l1-203	1149	163aa	ENSRNOP00000106623.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000073017.3	Rps13l1-201	581	155aa	ENSRNOP00000067470.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RCY2	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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