Transcript: ENST00000585937.1

Description

novel transcript, readthrough between UQCR11 and MBD3

Location

About this transcript

This transcript has 7 exons, is annotated with 1 domain and feature, is associated with 16549 variant alleles and maps to 350 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	RefSeq Match	Flags
ENST00000585937.1	-	1002	56aa	ENSP00000468614.1	Nonsense mediated decay	CCDS12073	-	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, 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 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,

Summary

Statistics

Exons: 7, Coding exons: 2, Transcript length: 1,002 bps, Translation length: 56 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS12073

Transcript Support Level (TSL)

TSL:3

Version

ENST00000585937.1

Type

Nonsense mediated decay

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Annotation Attributes

dotter confirmed [Definitions]

GENCODE basic gene

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