Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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- GO: Anatomical entity
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Genetic Variation
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Molecular interactions
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ID History
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Gene: RGD1560775 ENSRNOG00000042726

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Description

similar to RIKEN cDNA 4930579C12 gene [Source:RGD Symbol;Acc:1560775]

Gene Synonyms

LOC501031

Location

Primary_assembly 8: 98,483,284-98,562,296 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 1 transcript (splice variant) and 3 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000067996.3	RGD1560775-201	1731	516aa	ENSRNOP00000061288.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1A5Q3	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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