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.
CLN5
SECTIONS
  • TISSUE
  • BRAIN
  • SINGLE CELL TYPE
  • TISSUE CELL TYPE
  • PATHOLOGY
  • DISEASE
  • IMMUNE CELL
  • BLOOD PROTEIN
  • SUBCELLULAR
  • CELL LINE
  • STRUCTURE
  • METABOLIC
ABOUT
  • INTRODUCTION
  • HISTORY
  • ORGANIZATION
  • PUBLICATIONS
  • ANTIBODY SUBMISSION
  • ANTIBODY AVAILABILITY
  • ACKNOWLEDGMENTS
  • CONTACT
NEWS
  • NEWS ARTICLES
  • PRESS ROOM
LEARN
  • DICTIONARY
  • PROTEIN CLASSES
  • PROTEIN EVIDENCE
  • METHODS
  • EDUCATIONAL VIDEOS
DATA
  • DOWNLOADABLE DATA
  • PUBLICATION DATA
  • RELEASE HISTORY
  • SARS-COV-2
HELP
  • ANTIBODY VALIDATION
  • ASSAYS & ANNOTATION
  • DISCLAIMER
  • HELP & FAQ
  • PRIVACY STATEMENT
  • LICENCE & CITATION
Fields »
Search result

Field
Term
Gene name
Class
Subclass
Class
Keyword
Chromosome
External id
Tissue
Cell type
Expression
Patient ID
Tissue
Category
Cluster
Reliability
Brain region
Category
Brain region
Category
Brain region
Category
Reliability
Cell type
Category
Cluster
Tissue
Cell type
Enrichment
Cancer
Prognosis
Cancer
Category
Cell type
Category
Cell lineage
Category
Cluster
Annotation
Disease
Location
Searches
Location
Cell line
Type
Phase
Reliability
Cancer type
Category
Cluster
Pathway
Category
Score
Score
Score
Validation
Validation
Validation
Validation
Antibodies
Protein structure
In atlas
Column


  • SUMMARY

  • TISSUE

  • BRAIN

  • SINGLE CELL

  • TISSUE CELL

  • PATHOLOGY

  • DISEASE

  • IMMUNE

  • BLOOD

  • SUBCELL

  • CELL LINE

  • STRUCTURE

  • METABOLIC

  • CLN5
PROTEIN STRUCTURE
ANTIBODIES
AND
VALIDATION
Protein structures
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.

CLN5
Synonyms
Gene descriptioni

Full gene name according to HGNC.

CLN5 intracellular trafficking protein
Protein classi

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

Read more
Disease related genes
Human disease related genes
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.

Read more
Intracellular
Protein evidence Evidence at protein level (all genes)
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 13
Cytoband q22.3
Chromosome location (bp) 76990660 - 77019143
Number of transcriptsi

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

10
Ensembl ENSG00000102805 (version 103.38)
Entrez gene 1203
HGNC HGNC:2076
UniProt O75503 (UniProt - Evidence at protein level)
neXtProt NX_O75503
Antibodypedia CLN5 antibodies


PROTEIN STRUCTUREi

The Structure section provides predicted structures from the Alphafold protein structure database and available experimental structures from Protein Data Bank (PDB).

In the Structure drop-down menu all experimental structures from PDB are available for selection and display. The structures are displayed using the NGL Viewer and can be zoomed-in and rotated either manually or by checking the Autorotate box. The Color scheme can be selected to show the residue index, chain name or confidence score (as B-factors and pLDDT score for experimental and predicted structures, respectively). The positions for available antigen sequences in the structure are shown if Antigens is turned to ON, and the Variants slider can be used to show the positions of clinical and population variants.https://github.com/nglviewer/ngl

Read more

Predicted


Description: Structure prediction from Alphafold project. Structure version 2

# Chains: 1      # Clinical variants: 7      # Population variants: 226

Antigens:

Off
On

Variants:

Off
Clinical
Population

Color scheme:

Confidence
Residue index
Chain name

Autorotate:

Off
On



PROTEIN BROWSERi

The protein browser displays the antigen location on the target protein(s) and the features of the target protein. The tabs at the top of the protein view section can be used to switch between the different splice variants to which an antigen has been mapped.

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).

If a signal peptide is predicted by a majority of the signal peptide predictors SPOCTOPUS, SignalP 4.0, and Phobius (turquoise) and/or transmembrane regions (orange) are predicted by MDM, these are 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.
CLN5-201
CLN5-202
CLN5-203
CLN5-208
CLN5-211
CLN5-214
CLN5-215
CLN5-216
CLN5-218
CLN5-219


PROTEIN INFORMATIONi

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

The ENSP identifier links to the Ensembl website protein summary, while the ENST identifier links to the Ensembl website transcript summary for the selected splice variant. The data in the UniProt column can be expanded to show links to all matching UniProt identifiers for this protein.

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 Gene Ontology terms assigned to this protein are listed if expanding the Gene ontology column. The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide (according to a majority of the signal peptide predictors SPOCTOPUS, SignalP 4.0, and Phobius) and the number of predicted transmembrane region(s) (according to MDM) are also reported.
Splice variant UniProt Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
CLN5-201
ENSP00000366673
ENST00000377453
O75503 [Direct mapping]
Ceroid-lipofuscinosis neuronal protein 5 Ceroid-lipofuscinosis neuronal protein 5, secreted form
Show all
   MEMSAT3 predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Disease related genes
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of lipid/glycolipid metabolism
   Lysosomal storage diseases
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005515 [protein binding]
GO:0005537 [mannose binding]
GO:0005764 [lysosome]
GO:0005765 [lysosomal membrane]
GO:0005783 [endoplasmic reticulum]
GO:0005794 [Golgi apparatus]
GO:0005829 [cytosol]
GO:0006465 [signal peptide processing]
GO:0007040 [lysosome organization]
GO:0007042 [lysosomal lumen acidification]
GO:0007420 [brain development]
GO:0016020 [membrane]
GO:0016021 [integral component of membrane]
GO:0016798 [hydrolase activity, acting on glycosyl bonds]
GO:0022008 [neurogenesis]
GO:0030163 [protein catabolic process]
GO:0042147 [retrograde transport, endosome to Golgi]
GO:0042551 [neuron maturation]
GO:0048471 [perinuclear region of cytoplasm]
GO:0070062 [extracellular exosome]
GO:0070085 [glycosylation]
GO:1904426 [positive regulation of GTP binding]
Show all
358 aa
41.5 kDa
Yes 0
CLN5-202
ENSP00000482959
ENST00000485938
A0A087WZY0 [Direct mapping]
Ceroid-lipofuscinosis neuronal protein 5
Show all
   MEMSAT3 predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of lipid/glycolipid metabolism
   Lysosomal storage diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005764 [lysosome]
GO:0016020 [membrane]
GO:0016021 [integral component of membrane]
Show all
191 aa
21.7 kDa
Yes 0
CLN5-203
ENSP00000479547
ENST00000616833
A0A1C7CYZ2 [Direct mapping]
Ceroid-lipofuscinosis neuronal protein 5
Show all
   MEMSAT3 predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of lipid/glycolipid metabolism
   Lysosomal storage diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005764 [lysosome]
GO:0016020 [membrane]
GO:0016021 [integral component of membrane]
Show all
207 aa
23.4 kDa
Yes 0
CLN5-208
ENSP00000490181
ENST00000636183
O75503 [Direct mapping]
Ceroid-lipofuscinosis neuronal protein 5 Ceroid-lipofuscinosis neuronal protein 5, secreted form
Show all
   MEMSAT3 predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Disease related genes
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of lipid/glycolipid metabolism
   Lysosomal storage diseases
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005515 [protein binding]
GO:0005537 [mannose binding]
GO:0005764 [lysosome]
GO:0005765 [lysosomal membrane]
GO:0005783 [endoplasmic reticulum]
GO:0005794 [Golgi apparatus]
GO:0005829 [cytosol]
GO:0006465 [signal peptide processing]
GO:0007040 [lysosome organization]
GO:0007042 [lysosomal lumen acidification]
GO:0007420 [brain development]
GO:0016020 [membrane]
GO:0016021 [integral component of membrane]
GO:0016798 [hydrolase activity, acting on glycosyl bonds]
GO:0022008 [neurogenesis]
GO:0030163 [protein catabolic process]
GO:0042147 [retrograde transport, endosome to Golgi]
GO:0042551 [neuron maturation]
GO:0048471 [perinuclear region of cytoplasm]
GO:0070062 [extracellular exosome]
GO:0070085 [glycosylation]
GO:1904426 [positive regulation of GTP binding]
Show all
358 aa
41.5 kDa
Yes 0
CLN5-211
ENSP00000490078
ENST00000636525
A0A1B0GUE8 [Direct mapping]
Ceroid-lipofuscinosis neuronal protein 5
Show all
   MEMSAT3 predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of lipid/glycolipid metabolism
   Lysosomal storage diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005764 [lysosome]
GO:0016020 [membrane]
GO:0016021 [integral component of membrane]
Show all
270 aa
30.7 kDa
Yes 0
CLN5-214
ENSP00000490937
ENST00000636705
A0A1B0GWI2 [Direct mapping]
Ceroid-lipofuscinosis neuronal protein 5
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of lipid/glycolipid metabolism
   Lysosomal storage diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005764 [lysosome]
Show all
304 aa
35.4 kDa
No 0
CLN5-215
ENSP00000489855
ENST00000636767
A0A1B0GTV7 [Direct mapping]
Ceroid-lipofuscinosis neuronal protein 5
Show all
   MEMSAT3 predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of lipid/glycolipid metabolism
   Lysosomal storage diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005764 [lysosome]
GO:0016020 [membrane]
GO:0016021 [integral component of membrane]
Show all
248 aa
28 kDa
Yes 0
CLN5-216
ENSP00000489809
ENST00000636780
A0A1B0GTR6 [Direct mapping]
Ceroid-lipofuscinosis neuronal protein 5
Show all
   MEMSAT3 predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of lipid/glycolipid metabolism
   Lysosomal storage diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005764 [lysosome]
GO:0016020 [membrane]
GO:0016021 [integral component of membrane]
Show all
197 aa
22.4 kDa
Yes 0
CLN5-218
ENSP00000490422
ENST00000637397
A0A1B0GV94 [Direct mapping]
Ceroid-lipofuscinosis neuronal protein 5
Show all
   MEMSAT3 predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of lipid/glycolipid metabolism
   Lysosomal storage diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005764 [lysosome]
GO:0016020 [membrane]
GO:0016021 [integral component of membrane]
Show all
273 aa
30.7 kDa
Yes 0
CLN5-219
ENSP00000489711
ENST00000637537
A0A1B0GTR6 [Direct mapping]
Ceroid-lipofuscinosis neuronal protein 5
Show all
   MEMSAT3 predicted membrane proteins
   Phobius predicted membrane proteins
   SCAMPI predicted membrane proteins
   THUMBUP predicted membrane proteins
   TMHMM predicted membrane proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
Predicted intracellular proteins
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of lipid/glycolipid metabolism
   Lysosomal storage diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005764 [lysosome]
GO:0016020 [membrane]
GO:0016021 [integral component of membrane]
Show all
197 aa
22.4 kDa
Yes 0

Contact

  • NEWS ARTICLES
  • PRESS ROOM
  • contact@proteinatlas.org

The Project

  • INTRODUCTION
  • ORGANIZATION
  • PUBLICATIONS

The Human Protein Atlas

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