Transcript: ENST00000527954.1 EXOSC4-203

Description

exosome component 4 [Source:HGNC Symbol;Acc:HGNC:18189]

Gene Synonyms

FLJ20591, HRRP41P, P12A, RRP41, RRP41A, RRP41P, SKI6, SKI6P

Location

Chromosome 8: 144,079,423-144,080,579 forward strand.

About this transcript

This transcript has 2 exons, is annotated with 10 domains and features, is associated with 684 variant alleles and maps to 299 oligo probes.

Gene

This transcript is a product of gene ENSG00000178896.9 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000316052.6	EXOSC4-201	842	245aa	ENSP00000315476.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS6414	Q9NPD3	NM_019037.3	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, 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 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,
ENST00000527954.1	EXOSC4-203	1065	261aa	ENSP00000436539.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9PI41	-	TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs 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:2, 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000525936.1	EXOSC4-202	606	156aa	ENSP00000432661.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9PPI9	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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: 2, Coding exons: 2, Transcript length: 1,065 bps, Translation length: 261 residues

Transcript Support Level (TSL)

TSL:2

Incomplete CDS

3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete

Version

ENST00000527954.1

Type

Protein coding

Annotation Method

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

Transcript: ENST00000527954.1 EXOSC4-203

Summary

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Transcript: ENST00000527954.1 EXOSC4-203

Summary

About Us

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