Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
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External references
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ID History
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Gene: RGD1561151 ENSRNOG00000034183

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Description

similar to hypothetical protein 4932411N23 [Source:RGD Symbol;Acc:1561151]

Gene Synonyms

AABR07040266.1, LOC302774

Location

Primary_assembly X: 89,737,134-89,781,886 forward strand.

mRatBN7.2:CM026994.1

About this gene

This gene has 2 transcripts (splice variants), 204 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000110924.1	RGD1561151-202	2694	485aa	ENSRNOP00000081716.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RCD4	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,
ENSRNOT00000042552.5	RGD1561151-201	2690	485aa	ENSRNOP00000067248.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RCD4	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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