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: Rpl4 ENSRNOG00000009378

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Description

ribosomal protein L4 [Source:RGD Symbol;Acc:619824]

Gene Synonyms

L1

Location

Primary_assembly 8: 73,566,466-73,571,788 forward strand.

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants), 166 orthologues, 1 paralogue and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000106792.2	Rpl4-202	1441	421aa	ENSRNOP00000083420.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GAR6 Q6P3V9	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,
ENSRNOT00000013461.9	Rpl4-201	1547	408aa	ENSRNOP00000013462.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6P3V9	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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