Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: RGD1565459 ENSRNOG00000033613

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Description

similar to ribosomal protein L10a [Source:RGD Symbol;Acc:1565459]

Gene Synonyms

AABR07030647.1, LOC287782

Location

Primary_assembly 10: 94,192,152-94,192,520 reverse strand.

mRatBN7.2:CM026983.1

About this gene

This gene has 1 transcript (splice variant), 210 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000042056.2	RGD1565459-201	369	122aa	ENSRNOP00000049509.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZXK6	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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