Gene: Hmga2 ENSMUSG00000056758

Description

high mobility group AT-hook 2 [Source:MGI Symbol;Acc:MGI:101761]

Gene Synonyms

9430083A20Rik, HMGI-C, Hmgic

Location

Chromosome 10: 120,197,180-120,312,374 reverse strand.

GRCm39:CM001003.3

About this gene

This gene has 3 transcripts (splice variants), 137 orthologues and is associated with 52 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000159699.2	Hmga2-203	3810	129aa	ENSMUSP00000123998.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS83758	Q6NSP9	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, 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,
ENSMUST00000072777.14	Hmga2-201	3710	108aa	ENSMUSP00000072556.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS36073	P52927	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,
ENSMUST00000159310.2	Hmga2-202	3389	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	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: Hmga2 ENSMUSG00000056758

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Gene: Hmga2 ENSMUSG00000056758

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