Transcript: ENSMUST00000061639.11 Spty2d1-201

Description

SPT2 chromatin protein domain containing 1 [Source:MGI Symbol;Acc:MGI:2142062]

Gene Synonyms

5830435K17Rik

Location

Chromosome 7: 46,640,144-46,658,169 reverse strand.

About this transcript

This transcript has 6 exons, is annotated with 37 domains and features, is associated with 1519 variant alleles and maps to 298 oligo probes.

Gene

This transcript is a product of gene ENSMUSG00000049516.11 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000061639.11	Spty2d1-201	5233	682aa	ENSMUSP00000059457.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS21293	Q68FG3	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,
ENSMUST00000510577.1	Spty2d1-203	5066	46aa	ENSMUSP00000288940.1	Nonsense mediated decay		-	-
ENSMUST00000208588.2	Spty2d1-202	1726	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	TSL NA: A transcript that was not analysed for TSL. 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:NA,

Summary

Statistics

Exons: 6, Coding exons: 6, Transcript length: 5,233 bps, Translation length: 682 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q68FG3

CCDS

This transcript is a member of the Mouse CCDS set: CCDS21293

Transcript Support Level (TSL)

TSL:1

Version

ENSMUST00000061639.11

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

GENCODE primary gene

This transcript is a member of the Gencode Primary gene set.

Upcoming Ensembl Platform Transition

Transcript: ENSMUST00000061639.11 Spty2d1-201

Summary

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Transcript: ENSMUST00000061639.11 Spty2d1-201

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