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Human(GRCh38.p14)

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Transcript: ENST00000392894.8RNF13-203

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Description

ring finger protein 13 [Source:HGNC Symbol;Acc:HGNC:10057]

Gene Synonyms

RZF

About this transcript

This transcript has10 exons, is annotated with23 domains and features, is associated with58921 variant alleles and maps to561 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000392894.8RNF13-2032336381aaENSP00000376628.3
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
CCDS3146O43567-1NM_183381.3The 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 SelectA 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 CanonicalGENCODE 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 PrimaryA 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
ENST00000344229.7RNF13-2012866381aaENSP00000341361.3
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
CCDS3146O43567-1-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
ENST00000361785.10RNF13-2021939262aaENSP00000355268.6
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
CCDS87154O43567-2-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 PrimaryA subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic

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
ENST00000491086.5RNF13-2151104233aaENSP00000420667.1
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
C9JCY0-

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
ENST00000459632.5RNF13-2041008165aaENSP00000419069.1
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
C9JYN7-

TSL 4: A transcript where the best supporting EST is flagged as suspect

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:4
3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete
ENST00000468289.1RNF13-209820183aaENSP00000420510.1
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
H7C5Q6-

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
5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete
ENST00000482083.7RNF13-213777232aaENSP00000418863.3
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
C9IY58-

TSL 5: A transcript where no single transcript supports the model structure.

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:5
3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete
ENST00000467977.5RNF13-207761150aaENSP00000418308.1
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
C9J7B4-

TSL 5: A transcript where no single transcript supports the model structure.

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:5
3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete
ENST00000470151.5RNF13-21170180aaENSP00000419836.1
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
C9JYY4-

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
3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete
ENST00000466478.5RNF13-20559372aaENSP00000419508.1
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
C9JU37-

TSL 5: A transcript where no single transcript supports the model structure.

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:5
3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete
ENST00000466795.5RNF13-206586163aaENSP00000417655.1
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
C9J8T4-

TSL 4: A transcript where the best supporting EST is flagged as suspect

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:4
3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete
ENST00000490631.5RNF13-214583192aaENSP00000417294.1
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
C9J383-

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
3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete
ENST00000468648.5RNF13-210570115aaENSP00000420067.1
 
Gene/transcipt that contains an open reading frame (ORF).Protein coding
C9JRV0-

TSL 5: A transcript where no single transcript supports the model structure.

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:5
3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete
ENST00000474348.5RNF13-2121027140aaENSP00000420124.1
 
Nonsense mediated decay
F8WDJ5-

TSL 5: A transcript where no single transcript supports the model structure.

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:5
ENST00000467996.1RNF13-20876717aaENSP00000419809.1
 
Nonsense mediated decay
F8WEX6-

TSL 5: A transcript where no single transcript supports the model structure.

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:5
ENST00000493238.1RNF13-216815No protein-
 
An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron
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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

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Statistics

Exons: 10,Coding exons: 9,Transcript length: 2,336 bps,Translation length: 381 residues

MANE

This MANE Select transcript containsENSP00000376628 and matches toNM_183381.3 andNP_899237.1

Uniprot

This transcript corresponds to the following Uniprot identifiers:O43567

CCDS

This transcript is a member of the Human CCDS set:CCDS3146

Transcript Support Level (TSL)

TSL:1

Version

ENST00000392894.8

Type

Protein coding

Annotation Method

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

GENCODE basic gene

This transcript is a member of theGencode basic gene set.

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Ensembl release 113 - October 2024 ©EMBL-EBIEMBL-EBI
http://asia.ensembl.org

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