Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
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- Strains
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  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: 1700067P10Rikl ENSRNOG00000040095

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Description

RIKEN cDNA 1700067P10 gene like [Source:RGD Symbol;Acc:1585834]

Gene Synonyms

LOC680955

Location

Primary_assembly 9: 20,392,050-20,394,414 reverse strand.

GRCr8:CM070399.1

About this gene

This gene has 1 transcript (splice variant) and 37 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000061674.4	1700067P10Rikl-201	1932	195aa	ENSRNOP00000058386.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZHC6	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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Gene tree

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