Gene: Tcf20 ENSMUSG00000041852

Description

transcription factor 20 [Source:MGI Symbol;Acc:MGI:108399]

Gene Synonyms

2810438H08Rik, SPBP, stromelysin 1 PDGF responsive element binding protein

Location

Chromosome 15: 82,692,637-82,872,073 reverse strand.

GRCm39:CM001008.3

About this gene

This gene has 5 transcripts (splice variants), 206 orthologues, 2 paralogues and is associated with 29 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000109510.10	Tcf20-202	7323	1987aa	ENSMUSP00000105136.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS49681	Q9EPQ8-1	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2, 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,
ENSMUST00000048966.7	Tcf20-201	7417	1965aa	ENSMUSP00000048486.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS27693	Q9EPQ8-2	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2, 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,
ENSMUST00000230403.2	Tcf20-205	687	113aa	ENSMUSP00000155055.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A2R8W6K2	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSMUST00000229547.2	Tcf20-204	630	152aa	ENSMUSP00000154966.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A2R8VHC6	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSMUST00000229439.2	Tcf20-203	412	39aa	ENSMUSP00000155508.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A2R8VKG9	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

Gene: Tcf20 ENSMUSG00000041852

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Gene: Tcf20 ENSMUSG00000041852

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