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CLDND1
HPA
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  • SUMMARY

  • TISSUE

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  • SUBCELL

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  • BLOOD

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  • CLDND1
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.

CLDND1
Synonyms C3orf4, Z38
Gene descriptioni

Full gene name according to HGNC.

Claudin domain containing 1
Protein classi

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

Read more
Transporters
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.

Membrane, 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.

NK-cells & T-cells - Adaptive immunity: Cytotoxicity (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 (Esophageal apical cells, Extravillous trophoblasts, Late primary spermatocytes, Oligodendrocytes)
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.

Oligodendrocytes - Myelination (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.

Tissue enriched (Brain)
Subcellular locationi

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

Localized to the Nucleoplasm In addition localized to the Nucleoli, 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 q11.2
Chromosome location (bp) 98497912 - 98523066
Number of transcriptsi

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

25
Ensembl ENSG00000080822 (version 109)
Entrez gene 56650
HGNC HGNC:1322
UniProt Q9NY35
GeneCards CLDND1
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.

«
CLDND1-201
CLDND1-202
CLDND1-203
CLDND1-204
CLDND1-205
CLDND1-206
CLDND1-208
CLDND1-209
CLDND1-211
CLDND1-212
CLDND1-215
CLDND1-216
CLDND1-217
CLDND1-219
CLDND1-220
CLDND1-221
CLDND1-222
CLDND1-223
CLDND1-224
CLDND1-225
CLDND1-226
CLDND1-227
CLDND1-228
CLDND1-230
CLDND1-231
»

Description:

Color scheme:
Confidence
Residue index
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Variants:
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Clinical
Alphamissense variants:
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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)
CLDND1-201 Q9NY35
Transporters
Predicted membrane proteins
Mapped to neXtProt
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
253 aa
28.6 kDa
No 3
CLDND1-202 Q9NY35
Transporters
Predicted membrane proteins
Mapped to neXtProt
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
253 aa
28.6 kDa
No 3
CLDND1-203 A0A0R4J2F2
Predicted membrane proteins
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
276 aa
31.1 kDa
No 3
CLDND1-204 Q9NY35
Transporters
Predicted membrane proteins
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
253 aa
28.6 kDa
No 3
CLDND1-205 D6R9K1
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
87 aa
9.7 kDa
No 1
CLDND1-206 D6RDI6
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
239 aa
26.9 kDa
No 3
CLDND1-208 Q9NY35
Transporters
Predicted membrane proteins
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
253 aa
28.6 kDa
No 3
CLDND1-209 D6RIU2
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
138 aa
16 kDa
No 1
CLDND1-211 D6RD48
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
89 aa
10.3 kDa
No 0
CLDND1-212 H0Y8T9
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
155 aa
18.1 kDa
No 1
CLDND1-215 D6RC11
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
210 aa
23.7 kDa
No 2
CLDND1-216 D6RDY1
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
177 aa
20.3 kDa
No 1
CLDND1-217 D6RDP6
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
145 aa
17 kDa
No 0
CLDND1-219 D6RHU6
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
172 aa
19.8 kDa
No 1
CLDND1-220 D6RFX6
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
236 aa
26.6 kDa
No 3
CLDND1-221 D6RB31
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
100 aa
10.9 kDa
No 1
CLDND1-222 Q9NY35
Transporters
Predicted membrane proteins
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
253 aa
28.6 kDa
No 3
CLDND1-223 Q9NY35
Transporters
Predicted membrane proteins
Mapped to neXtProt
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
158 aa
17.5 kDa
No 3
CLDND1-224 D6RCE6
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
223 aa
25.2 kDa
No 3
CLDND1-225 D6RCP3
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
121 aa
13.2 kDa
No 3
CLDND1-226 Q9NY35
Transporters
Predicted membrane proteins
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
253 aa
28.6 kDa
No 3
CLDND1-227 D6RCR8
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
244 aa
27.6 kDa
No 3
CLDND1-228 H0YA53
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
72 aa
7.5 kDa
No 1
CLDND1-230 D6R9S8
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
213 aa
24 kDa
No 2
CLDND1-231 D6RA76
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
180 aa
20.6 kDa
No 1
Show allShow less

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