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: RGD1563590 ENSRNOG00000071183

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Description

similar to melanoma antigen 2 [Source:RGD Symbol;Acc:1563590]

Gene Synonyms

LOC302435

Location

Primary_assembly X: 56,619,985-56,621,013 reverse strand.

mRatBN7.2:CM026994.1

About this gene

This gene has 1 transcript (splice variant), 131 orthologues and 38 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000045816.5	RGD1563590-201	1029	342aa	ENSRNOP00000097626.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GM54	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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