Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Gene tree
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Pathway
Molecular interactions
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ID History
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Gene: 9030612E09Rikl ENSRNOG00000026080

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Description

RIKEN cDNA 9030612E09 gene like [Source:RGD Symbol;Acc:1589988]

Gene Synonyms

LOC688390

Location

Primary_assembly 20: 48,243,688-48,245,638 forward strand.

GRCr8:CM070410.1

About this gene

This gene has 1 transcript (splice variant) and 5 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000038842.5	9030612E09Rikl-201	1951	147aa	ENSRNOP00000034919.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6K6X4 D3Z996	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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