Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Lrrc66 ENSRNOG00000026585

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Description

leucine rich repeat containing 66 [Source:RGD Symbol;Acc:1306094]

Gene Synonyms

LOC103693755, LOC289587, RGD1306094

Location

Primary_assembly 14: 34,933,161-34,959,044 forward strand.

GRCr8:CM070404.1

About this gene

This gene has 1 transcript (splice variant), 134 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000031756.5	Lrrc66-201	3304	866aa	ENSRNOP00000030477.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2UKS8	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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