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: Lrrc10b ENSRNOG00000030180

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Description

leucine rich repeat containing 10B [Source:RGD Symbol;Acc:1564983]

Gene Synonyms

LOC309208, RGD1564983

Location

Primary_assembly 1: 216,520,677-216,524,310 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 1 transcript (splice variant), 144 orthologues and 31 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000050716.6	Lrrc10b-201	3498	292aa	ENSRNOP00000048468.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6I032 D3ZED9	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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