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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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
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Molecular interactions
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ID History
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Gene: LOC134486296 ENSRNOG00000032177

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Description

uncharacterized LOC134486296 [Source:RGD Symbol;Acc:402423633]

Location

Primary_assembly 3: 107,917,471-107,947,240 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 1 transcript (splice variant) and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000040741.3	LOC134486296-201	831	276aa	ENSRNOP00000048432.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HNL8 F7ERC1	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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