Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: 1700006A11Rikl ENSRNOG00000024928

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Description

RIKEN cDNA 1700006A11 gene like [Source:RGD Symbol;Acc:1306519]

Gene Synonyms

LOC295437, RGD1306519

Location

Primary_assembly 2: 215,293,391-215,318,229 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 1 transcript (splice variant), 40 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000106313.2	1700006A11Rikl-201	1635	545aa	ENSRNOP00000095579.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6B305	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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