Summary
- Splice variants
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- Gene alleles
Sequence
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Phenotypes
Genetic Variation
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Gene: Rpl38-ps8 ENSRNOG00000049047

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Description

ribosomal protein L38, pseudogene 8 [Source:RGD Symbol;Acc:1596041]

Gene Synonyms

LOC366919, LOC685963, LOC690468, MGC125176, Rpl38_predicted

Location

Primary_assembly 16: 10,188,932-10,189,144 reverse strand.

GRCr8:CM070406.1

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
ENSRNOT00000023369.6	Rpl38-ps8-202	213	70aa	ENSRNOP00000023368.3	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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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data