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

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Gene: LRRC3B ENSSSCG00000011216

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Description

leucine rich repeat containing 3B [Source:VGNC Symbol;Acc:VGNC:89838]

Location

Primary_assembly 13: 13,327,220-13,420,223 forward strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 1 transcript (splice variant), 195 orthologues and 23 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000012282.2	LRRC3B-201	1843	259aa	ENSSSCP00000011965.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UHX6 F2Z5C4	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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