Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
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Supporting evidence
ID History
- Gene history

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Gene: Rpl39-ps12 ENSRNOG00000029267

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Description

ribosomal protein L39, pseudogene 12 [Source:RGD Symbol;Acc:9201561]

Gene Synonyms

LOC100361880, LOC100363391, LOC103692785, LOC103692831, LOC103693375, LOC103694169

Location

Primary_assembly 15: 20,118,923-20,119,078 reverse strand.

mRatBN7.2:CM026988.1

About this gene

This gene has 1 transcript (splice variant), 27 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000050345.2	Rpl39-ps12-201	156	51aa	ENSRNOP00000044553.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P62893	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