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: Rpl38-ps9 ENSRNOG00000048701

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Description

ribosomal protein L38, pseudogene 9 [Source:RGD Symbol;Acc:1587812]

Gene Synonyms

LOC366919, LOC685963, LOC690468, MGC125176, Rpl38_predicted

Location

Primary_assembly 3: 176,399,692-176,400,005 forward strand.

GRCr8:CM070393.1

About this gene

This gene has 1 transcript (splice variant), 335 orthologues and 10 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000044141.6	Rpl38-ps9-201	314	70aa	ENSRNOP00000042288.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HKI5 P63174	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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