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

Configure this page

Share this page

Bookmark this page

.

Gene: RGD1559622 ENSRNOG00000025219

.

Description

similar to hypothetical protein C130079G13 [Source:RGD Symbol;Acc:1559622]

Gene Synonyms

LOC295071

Location

Primary_assembly 2: 143,761,608-143,800,682 reverse strand.

mRatBN7.2:CM026975.1

About this gene

This gene has 1 transcript (splice variant), 160 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000035057.7	RGD1559622-201	1710	346aa	ENSRNOP00000032213.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZXW5	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,

.

Summary

.

.