We use cookies to enhance the usability of our website. If you continue, we'll assume that you are happy to receive all cookies. More information. Don't show this again.
USP13
HPA
RESOURCES
  • TISSUE
  • BRAIN
  • SINGLE CELL
  • SUBCELLULAR
  • CANCER
  • BLOOD
  • CELL LINE
  • STRUCTURE
  • INTERACTION
ABOUT
  • INTRODUCTION
  • HISTORY
  • ORGANIZATION
  • PUBLICATIONS
  • ACKNOWLEDGMENTS
  • CONTACT
NEWS
  • NEWS ARTICLES
  • PRESS ROOM
LEARN
  • DICTIONARY
  • PROTEIN CLASSES
  • PROTEIN EVIDENCE
  • METHODS
  • EDUCATIONAL VIDEOS
DATA
  • DOWNLOADABLE DATA
  • PUBLICATION DATA
  • RELEASE HISTORY
HELP
  • HELP & FAQ
  • ANTIBODY AVAILABILITY
  • DISCLAIMER
  • PRIVACY STATEMENT
  • LICENCE & CITATION
Fields »
Search result

Field
Term
Gene name
Class
Subclass
Category
Keyword
Chromosome
External id
Tissue
Cell type
Expression
Antibody panel
Tissue
Main location
Patient ID
Annotation
Tissue
Category
Tau score
Cluster
Reliability
Brain region
Category
Tau score
Brain region
Category
Tau score
Brain region
Category
Tau score
Cluster
Reliability
Tissue
Cell type
Enrichment
Cell type
Category
Tau score
Cell type group
Category
Tau score
Cell type
Category
Tau score
Cell type
Category
Tau score
Cell lineage
Category
Tau score
Cluster
Cluster
Location
Searches
Location
Cell line
Class
Type
Phase
Reliability
Cancer
Prognosis
Cancer
Category
Cancer
Category
Tau score
Cluster
Variants
Interacting gene (ensg_id)
Type
Number of interactions
Pathway
ipTM
Category
Category
Category
Category
Validation
Validation
Validation
Validation
Antibodies
Data type
Column


  • SUMMARY

  • TISSUE

  • BRAIN

  • SINGLE CELL

  • SUBCELL

  • CANCER

  • BLOOD

  • CELL LINE

  • STRUCTURE

  • INTERACTION

  • USP13
STRUCTURE STRUCTURE
Protein structures
Structure methods
GENERAL INFORMATIONi

General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.

Gene namei

Official gene symbol, which is typically a short form of the gene name, according to HGNC.

USP13
Synonyms IsoT-3
Gene descriptioni

Full gene name according to HGNC.

Ubiquitin specific peptidase 13
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Read more
Enzymes
Metabolic proteins
Plasma proteins
Predicted locationi

All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.

  • Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.
  • Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).

The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.

Intracellular
Protein evidence Evidence at protein level (all genes)

HUMAN PROTEIN ATLAS INFORMATIONi

Summary of RNA expression analysis and annotation data generated within the Human Protein Atlas project.

Single cell type
expression clusteri

The RNA data was used to cluster genes according to their expression across single cell types. Clusters contain genes that have similar expression patterns, and each cluster has been manually annotated to describe common features in terms of function and specificity.

Skeletal myocytes - Muscle structure & formation (mainly)
Single cell type specificityi

The RNA specificity category is based on mRNA expression levels in the analyzed cell types based on scRNA-seq data from normal tissues. The categories include: cell type enriched, group enriched, cell type enhanced, low cell type specificity and not detected.

Cell type enhanced (Alveolar cells type 2, Cardiomyocytes, Myonuclei, Oligodendrocyte progenitor cells, Oligodendrocytes, Thymic myoid cells)
Tissue expression
cluster (RNA)i

The RNA data was used to cluster genes according to their expression across tissues. Clusters contain genes that have similar expression patterns, and each cluster has been manually annotated to describe common features in terms of function and specificity.

Skeletal muscle - Striated muscle contraction (mainly)
Tissue specificity (RNA)i

The RNA specificity category is based on mRNA expression levels in the consensus dataset which is calculated from the RNA expression levels in samples from HPA and GTEX. The categories include: tissue enriched, group enriched, tissue enhanced, low tissue specificity and not detected.

Group enriched (Heart muscle, Skeletal muscle, Tongue)
Subcellular locationi

Main subcellular location based on data generated in the subcellular section of the Human Protein Atlas.

Localized to the Nucleoplasm, Cytosol
Secretome annotationi

All genes with at least one predicted secreted isoform have been annotated and classified with the aim to determine if the corresponding protein(s) are:

  • secreted into blood
  • locally secreted
  • or actually being attached to membrane or retained in intracellular locations like mitochondria, endoplasmatic reticulum (ER), Golgi apparatus or lysosomes.
Not available
GENE INFORMATIONi

Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.

Chromosome 3
Cytoband q26.33
Chromosome location (bp) 179653032 - 179804366
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

23
Ensembl ENSG00000058056 (version 109)
Entrez gene 8975
HGNC HGNC:12611
UniProt Q92995
GeneCards USP13
PROTEIN BROWSERi

The Structure section provides in-house generated structures, predicted using the Alphafold source code, for the majority of the proteins and their related isoforms.

Displaying protein features on the AlphaFold structures

Individual splice variants can be selected in the top part of the Protein Browser (see below) and different transcript-related features such as transmembrane regions, InterPro domains and antigen sequences for antibodies can be displayed in the structure by clicking on the respective features in the Protein Browser.

Clinical and population-based amino acid variants based on data from the Ensembl variation database and AlphaMissense (AM) predictions can be highlighted using the sliders to the right of the structure. These can also be used to colour the entire structure by residue index or make the structure autorotate.The structures are displayed using the NGL Viewer and can also be zoomed-in and rotated manually.

The Protein Browser

The ProteinBrowser displays the antigen location on the target protein(s) and the features of the target protein. Transcript names and schematic transcript structures including exons, introns and UTRs for the different isoforms are shown on top, and can be used to switch between the structures for the different splice variants.

At the top of the view, the position of the antigen (identified by the corresponding HPA identifier) is shown as a green bar. A yellow triangle on the bar indicates a <100% sequence identity to the protein target.

Below the antigens, the maximum percent sequence identity of the protein to all other proteins from other human genes is displayed, using a sliding window of 10 aa residues (HsID 10) or 50 aa residues (HsID 50). The region with the lowest possible identity is always selected for antigen design, with a maximum identity of 60% allowed for designing a single-target antigen (read more).

The curve in blue displays the predicted antigenicity i.e. the tendency for different regions of the protein to generate an immune response, with peak regions being predicted to be more antigenic.The curve shows average values based on a sliding window approach using an in-house propensity scale. (read more).

Signal peptides (turquoise) and membrane regions (orange) based on predictions using the majority decision methods MDM and MDSEC are also displayed.

Low complexity regions are shown in yellow and InterPro regions in green. Common (purple) and unique (grey) regions between different splice variants of the gene are also displayed (read more), and at the bottom of the protein view is the protein scale.

«
USP13-201
USP13-203
USP13-204
USP13-206
USP13-209
USP13-212
USP13-214
USP13-215
USP13-216
USP13-222
USP13-226
USP13-230
USP13-236
USP13-237
USP13-238
USP13-240
USP13-244
USP13-249
USP13-251
USP13-256
USP13-259
USP13-265
USP13-271
»

Description:

Color scheme:
Confidence
Residue index
Your selection
Variants:
Off
Population
Clinical
Alphamissense variants:
Off
Benign
Pathogenic
Autorotate:
Off
On
PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.

The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.

The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.

Splice variant SwissProt TrEMBL Protein class Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
USP13-201 Q92995
A0A0A6YZ17
Enzymes
Metabolic proteins
Predicted intracellular proteins
Plasma proteins
Mapped to neXtProt
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
863 aa
97.3 kDa
No 0
USP13-203 Q92995
Enzymes
Metabolic proteins
Predicted intracellular proteins
Plasma proteins
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
Show all
798 aa
90.4 kDa
No 0
USP13-204 H7C5J3
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
299 aa
34.2 kDa
No 0
USP13-206 A0A7P0Z4M1
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
15 aa
1.7 kDa
No 0
USP13-209 A0A7P0TBG5
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
145 aa
16.5 kDa
No 0
USP13-212 A0A7P0TB18
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
64 aa
7.2 kDa
No 0
USP13-214 A0A7P0T8B2
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
40 aa
4.5 kDa
No 0
USP13-215 A0A7P0TB48
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
71 aa
8.1 kDa
No 0
USP13-216 A0A7P0TAJ9
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
226 aa
24.9 kDa
No 0
USP13-222 A0A7P0T8S4
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
53 aa
5.9 kDa
No 0
USP13-226 A0A7P0TB69
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
819 aa
92.1 kDa
No 0
USP13-230 A0A7P0T9S5
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
83 aa
9.5 kDa
No 0
USP13-236 A0A7P0T9N7
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
65 aa
6.7 kDa
No 0
USP13-237 A0A7P0TB82
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
131 aa
14.1 kDa
No 0
USP13-238 A0A7P0TAJ4
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
80 aa
8.8 kDa
No 0
USP13-240 A0A7P0TAP9
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
862 aa
97.2 kDa
No 0
USP13-244 A0A7P0T8Y7
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
71 aa
7.4 kDa
No 0
USP13-249 A0A7P0T873
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
92 aa
10.6 kDa
No 0
USP13-251 A0A7P0TB92
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
103 aa
11.3 kDa
No 0
USP13-256 A0A7P0T9V0
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
52 aa
5.8 kDa
No 0
USP13-259 A0A7P0Z4C0
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
75 aa
8 kDa
No 0
USP13-265 A0A7P0T9H6
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
89 aa
10.2 kDa
No 0
USP13-271 A0A7P0T863
Metabolic proteins
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
76 aa
8.4 kDa
No 0
Show allShow less

Contact

  • NEWS ARTICLES
  • PRESS ROOM

The Project

  • INTRODUCTION
  • ORGANIZATION
  • PUBLICATIONS

The Human Protein Atlas

  • DOWNLOADABLE DATA
  • LICENCE & CITATION
  • HELP & FAQ
KAW logo The Human Protein Atlas project is funded
by the Knut & Alice Wallenberg Foundation.

Facebook logo X logo Bluesky logo Linkedin logo RSS feed logo contact@proteinatlas.org
GCBR logo Elixir core logo SciLifeLab logo Uppsala university logo KI logo KTH logo