Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Lrrc38 ENSRNOG00000015264

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Description

leucine rich repeat containing 38 [Source:RGD Symbol;Acc:1311416]

Gene Synonyms

LOC313681, RGD1311416

Location

Primary_assembly 5: 160,968,790-160,990,871 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 1 transcript (splice variant), 154 orthologues and 24 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000020483.9	Lrrc38-201	2350	298aa	ENSRNOP00000020483.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6ITZ6 D3ZYA6	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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