Gene: Nptxr ENSMUSG00000022421

Description

neuronal pentraxin receptor [Source:MGI Symbol;Acc:MGI:1920590]

Gene Synonyms

1700036C17Rik, 5730406O18Rik, D15Bwg0580e, NPCD, NPR

Location

Chromosome 15: 79,670,552-79,688,967 reverse strand.

GRCm39:CM001008.3

About this gene

This gene has 2 transcripts (splice variants), 194 orthologues, 8 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000023057.10	Nptxr-201	5006	493aa	ENSMUSP00000023057.10	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS27653	E9PZM8	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, 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,
ENSMUST00000125283.2	Nptxr-202	999	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	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,

Gene: Nptxr ENSMUSG00000022421

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Gene: Nptxr ENSMUSG00000022421

Summary

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