Gene: Nlrp2 ENSMUSG00000035177

Description

NLR family, pyrin domain containing 2 [Source:MGI Symbol;Acc:MGI:3041206]

Gene Synonyms

E330007A02Rik, Nalp2, Nbs1, PYPAF2, Pan1

Location

Chromosome 7: 5,301,546-5,354,034 reverse strand.

GRCm39:CM001000.3

About this gene

This gene has 3 transcripts (splice variants), 86 orthologues, 22 paralogues and is associated with 18 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000045022.9	Nlrp2-201	3404	1046aa	ENSMUSP00000045077.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS39746	Q4PLS0	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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,
ENSMUST00000207520.2	Nlrp2-202	746	248aa	ENSMUSP00000147102.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A140LJ71	TSL 3: A transcript where the only support is from a single EST 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:3, 5' and 3' truncations in transcript evidence prevent annotation of the start and the end of the CDS.CDS 5' and 3' incomplete,
ENSMUST00000207685.2	Nlrp2-203	581	87aa	ENSMUSP00000146451.2	Nonsense mediated decay		A0A140LHK4	TSL 3: A transcript where the only support is from a single EST 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:3, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

Gene: Nlrp2 ENSMUSG00000035177

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Gene: Nlrp2 ENSMUSG00000035177

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