Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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ID History
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Gene: LOC100912266 ENSRNOG00000059441

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Description

uncharacterized LOC100912266 [Source:RGD Symbol;Acc:6488109]

Gene Synonyms

LRRG00123, LRRGT00103

Location

Primary_assembly 2: 28,288,798-28,297,873 forward strand.

GRCr8:CM070392.1

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
ENSRNOT00000078413.3	LOC100912266-201	279	92aa	ENSRNOP00000070141.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JX55 Q6QI85	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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