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: RGD1307595 ENSRNOG00000011239

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Description

similar to RIKEN cDNA 1700018B24 [Source:RGD Symbol;Acc:1307595]

Gene Synonyms

LOC295019

Location

Primary_assembly 2: 132,570,285-132,573,604 reverse strand.

mRatBN7.2:CM026975.1

About this gene

This gene has 1 transcript (splice variant), 40 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000014928.6	RGD1307595-201	603	105aa	ENSRNOP00000014928.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A5C2	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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