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DLG2
HPA
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  • SUMMARY

  • TISSUE

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  • DLG2
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.

DLG2
Synonyms chapsyn-110, PPP1R58, PSD-93, PSD93
Gene descriptioni

Full gene name according to HGNC.

Discs large MAGUK scaffold protein 2
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.

Retinal bipolar cells - Synaptic signal transduction (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 (Brain excitatory neurons, Brain inhibitory neurons, Cone photoreceptor cells, Oligodendrocyte progenitor cells, Oligodendrocytes, Other brain neurons, Pituicytes/FSCs, Podocytes, Retinal bipolar 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.

Brain - Neuronal signaling (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 enhanced (Brain)
Subcellular locationi

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

Localized to the Plasma membrane In addition localized to the Vesicles
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 11
Cytoband q14.1
Chromosome location (bp) 83455012 - 85628335
Number of transcriptsi

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

32
Ensembl ENSG00000150672 (version 109)
Entrez gene 1740
HGNC HGNC:2901
UniProt Q15700
GeneCards DLG2
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.

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DLG2-201
DLG2-202
DLG2-203
DLG2-204
DLG2-206
DLG2-207
DLG2-208
DLG2-209
DLG2-210
DLG2-211
DLG2-212
DLG2-214
DLG2-215
DLG2-216
DLG2-218
DLG2-220
DLG2-221
DLG2-224
DLG2-228
DLG2-229
DLG2-230
DLG2-231
DLG2-232
DLG2-234
DLG2-237
DLG2-239
DLG2-244
DLG2-245
DLG2-246
DLG2-247
DLG2-249
DLG2-250
»

Description:

Color scheme:
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Alphamissense variants:
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Autorotate:
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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)
DLG2-201 Q15700
Predicted intracellular proteins
Mapped to neXtProt
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
909 aa
101 kDa
No 0
DLG2-202 F8VYC1
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
797 aa
88.5 kDa
No 0
DLG2-203 Q15700
Predicted intracellular proteins
Mapped to neXtProt
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
975 aa
109.4 kDa
No 0
DLG2-204 A8MUT9
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
232 aa
25.1 kDa
No 0
DLG2-206 A8MVA8
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
129 aa
14.5 kDa
No 0
DLG2-207 Q15700
Predicted intracellular proteins
Mapped to neXtProt
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
870 aa
97.6 kDa
No 0
DLG2-208 B5MCC5
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
348 aa
39.9 kDa
No 0
DLG2-209 Q15700
Predicted intracellular proteins
Mapped to neXtProt
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
749 aa
83.4 kDa
No 0
DLG2-210 F8W750
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
221 aa
25.8 kDa
No 0
DLG2-211 Q15700
Predicted intracellular proteins
Mapped to neXtProt
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
334 aa
38.4 kDa
No 0
DLG2-212 C9JFF9
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
108 aa
12.4 kDa
No 0
DLG2-214 H7C325
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
165 aa
19.4 kDa
No 0
DLG2-215 A0A3B3ITF4
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
52 aa
5.9 kDa
No 0
DLG2-216 E9PRL2
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
109 aa
12.4 kDa
No 0
DLG2-218 E9PN83
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
866 aa
96.5 kDa
No 0
DLG2-220 E9PIJ9
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
821 aa
91.3 kDa
No 0
DLG2-221 A0A5F9ZH92
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
810 aa
90.2 kDa
No 0
DLG2-224 E9PQT9
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
93 aa
10.7 kDa
No 0
DLG2-228 E9PPV7
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
142 aa
16.3 kDa
No 0
DLG2-229 E9PIW2
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
811 aa
90.7 kDa
No 0
DLG2-230 B7Z2T4
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
852 aa
95 kDa
No 0
DLG2-231 A0A3B3ISW2
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
890 aa
99.6 kDa
No 0
DLG2-232 A0A3B3ITF1
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
1012 aa
113.7 kDa
No 0
DLG2-234 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
645 aa
70.9 kDa
No 0
DLG2-237 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
857 aa
95.1 kDa
No 0
DLG2-239 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
68 aa
7.7 kDa
No 0
DLG2-244 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
969 aa
108.4 kDa
No 0
DLG2-245 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
512 aa
55.8 kDa
No 0
DLG2-246 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
968 aa
108.3 kDa
No 0
DLG2-247 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
891 aa
98.4 kDa
No 0
DLG2-249 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
820 aa
91.2 kDa
No 0
DLG2-250 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
872 aa
97.1 kDa
No 0
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