DLGAP3

DLG associated protein 3 O95886 DLGP3_HUMAN
Protein Coding Chr 1 1p34.3 Swiss-Prot reviewed Entrez 58512
Mutations
1,233
CL 180 · Tissue 1,042
Samples
617
CL 130 · Tissue 481
Peptides
471
unique mutant peptides
Transcripts
2
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations1,2331801,042
Samples617130481
Peptides471102381

Function

DLGAP3 · DLG associated protein 3

Predicted to enable PDZ domain binding activity; molecular adaptor activity; and scaffold protein binding activity. Predicted to be involved in protein-containing complex assembly and regulation of postsynaptic neurotransmitter receptor activity. Predicted to be located in synapse. Predicted to be part of postsynaptic density. Predicted to be active in several cellular components, including cholinergic synapse; glutamatergic synapse; and neuromuscular junction. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

2 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000373347 O95886 665 471
ENST00000235180 O95886 568 414

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p34.3
Entrez ID
Aliases
DAP3SAPAP3SPAPA3

Recurrent Mutations

All 471 amino-acid changes on canonical ENST00000373347 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in DLGAP3 · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in DLGAP3 – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
T-Cell Non-Hodgkins Lymphoma
2/26 8%
0/0 0%
T-Lymphoblastic Leukemia
3/40 8%
0/0 0%
Acute Myeloid Leukemia
4/90 4%
0/0 0%
Melanoma
15/210 7%
78/1899 4%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Acute Monocytic Leukemia
0/1 0%
1/25 4%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Endometrial Carcinoma
4/42 10%
18/612 3%
Non-Small Cell Lung Carcinoma
17/304 6%
35/1390 3%
Colorectal Carcinoma
14/143 10%
70/3239 2%
Gastric Carcinoma
5/74 7%
37/1809 2%
Other Solid Cancers
1/94 1%
32/1515 2%
Cervical Carcinoma
0/35 0%
8/422 2%
Squamous Cell Lung Carcinoma
3/57 5%
12/810 1%
Ovarian Carcinoma
7/109 6%
9/998 1%
Neuroendocrine Tumour
8/154 5%
2/577 0%
Mesothelioma
1/62 2%
2/165 1%
Bladder Carcinoma
0/58 0%
11/956 1%
Small Cell Lung Carcinoma
0/9 0%
8/752 1%
Thyroid Gland Carcinoma
1/45 2%
16/1592 1%
Other Sarcomas
5/69 7%
3/699 0%
Glioblastoma
1/98 1%
0/0 0%
Non-Cancerous
1/104 1%
8/830 1%
Breast Carcinoma
9/144 6%
23/3264 1%
Prostate Carcinoma
0/13 0%
19/2105 1%
Head and Neck Carcinoma
2/85 2%
13/1574 1%
Hepatocellular Carcinoma
0/46 0%
20/2210 1%
Medulloblastoma
0/0 0%
4/450 1%
Esophageal Carcinoma
1/23 4%
5/769 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%

Mutation Distribution

Where DLGAP3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DLGAP3 were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 1,233 mutations in DLGAP3

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide