Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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- GO: Anatomical entity
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Genetic Variation
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Gene: RGD1562699 ENSRNOG00000042716

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Description

RGD1562699 [Source:RGD Symbol;Acc:1562699]

Gene Synonyms

LOC291558

Location

Primary_assembly 18: 60,097,332-60,098,204 reverse strand.

GRCr8:CM070408.1

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000065939.3	RGD1562699-201	389	116aa	ENSRNOP00000059990.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IXN6 D3ZWR7	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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