Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Lrit2 ENSRNOG00000022726

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Description

leucine-rich repeat, Ig-like and transmembrane domains 2 [Source:RGD Symbol;Acc:1564668]

Gene Synonyms

LOC498594, RGD1564668

Location

Primary_assembly 16: 12,855,257-12,860,289 forward strand.

GRCr8:CM070406.1

About this gene

This gene has 1 transcript (splice variant), 232 orthologues and 26 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000038771.3	Lrit2-201	2251	549aa	ENSRNOP00000035539.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A7B9	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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