Gene: Pias2 ENSMUSG00000025423

Description

protein inhibitor of activated STAT 2 [Source:MGI Symbol;Acc:MGI:1096566]

Gene Synonyms

6330408K17Rik, ARIP3, Dib, Miz1, PIASxalpha, PIASxb, PIASxbeta

Location

Chromosome 18: 77,152,904-77,241,496 forward strand.

GRCm39:CM001011.3

About this gene

This gene has 4 transcripts (splice variants), 221 orthologues, 5 paralogues and is associated with 26 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000114777.10	Pias2-202	3060	621aa	ENSMUSP00000110425.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS37866	Q8C5D8-1	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,
ENSMUST00000168882.9	Pias2-203	2254	614aa	ENSMUSP00000131485.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS50324	G3UWE3	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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,
ENSMUST00000114776.4	Pias2-201	2077	565aa	ENSMUSP00000110424.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS50323	F8WHS8	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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,
ENSMUST00000235135.2	Pias2-204	2633	252aa	ENSMUSP00000157458.2	Nonsense mediated decay		A0A494B929	-

Gene: Pias2 ENSMUSG00000025423

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Gene: Pias2 ENSMUSG00000025423

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