Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Gene tree
  - Orthologues
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Ontologies
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ID History
- Gene history

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Gene: Lrrc73 ENSMUSG00000071073

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Description

leucine rich repeat containing 73 [Source:MGI Symbol;Acc:MGI:2684934]

Gene Synonyms

Gm88, LOC224813

Location

Chromosome 17: 46,564,457-46,568,241 forward strand.

GRCm39:CM001010.3

About this gene

This gene has 4 transcripts (splice variants) and 195 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000233692.2	Lrrc73-204	2010	316aa	ENSMUSP00000156533.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS50123	B2RWC4	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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,
ENSMUST00000095262.6	Lrrc73-201	1317	289aa	ENSMUSP00000092896.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding		F6U1P7	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000233543.2	Lrrc73-203	1116	188aa	ENSMUSP00000156631.2	Nonsense mediated decay		A0A3B2W7N5	-
ENSMUST00000233341.2	Lrrc73-202	2445	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-

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Summary

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