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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  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
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Molecular interactions
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Supporting evidence
ID History
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Gene: 1700001K19Rikl ENSRNOG00000007184

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Description

RIKEN cDNA 1700001K19 gene like [Source:RGD Symbol;Acc:1305298]

Gene Synonyms

LOC103690170, LOC299330, RGD1305298, Tsp26

Location

Primary_assembly 6: 135,502,832-135,514,813 reverse strand.

GRCr8:CM070396.1

About this gene

This gene has 1 transcript (splice variant) and 45 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000009444.8	1700001K19Rikl-201	989	224aa	ENSRNOP00000009444.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KBM4 D3ZSX0	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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