PDZK1

PDZ domain containing 1 Q5T2W1 NHRF3_HUMAN
Protein Coding Chr 1 1q21.1 Swiss-Prot reviewed Entrez 5174
Mutations
271
CL 54 · Tissue 216
Samples
94
CL 21 · Tissue 72
Peptides
85
unique mutant peptides
Transcripts
3
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
Mutations27154216
Samples942172
Peptides851871

Function

PDZK1 · PDZ domain containing 1

This gene encodes a PDZ domain-containing scaffolding protein. PDZ domain-containing molecules bind to and mediate the subcellular localization of target proteins. The encoded protein mediates the localization of cell surface proteins and plays a critical role in cholesterol metabolism by regulating the HDL receptor, scavenger receptor class B type 1. Single nucleotide polymorphisms in this gene may be associated with metabolic syndrome, and overexpression of this gene may play a role in drug resistance of multiple myeloma. Pseudogenes of this gene are located on the long arm of chromosome 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011].

Isoforms & Proteins

3 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
ENST00000417171 Q5T2W1 100 81
ENST00000344770 Q5T2W1 94 78
ENST00000451928 Q5T2W1-2 77 67

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q21.1
Entrez ID
Aliases
CAP70CLAMPNHERF-3NHERF3PDZD1

Recurrent Mutations

All 81 amino-acid changes on canonical ENST00000417171 · 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 PDZK1 · 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 PDZK1 – 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-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Unknown
0/10 0%
1/29 3%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Endometrial Carcinoma
1/42 2%
13/612 2%
Glioblastoma
2/98 2%
0/0 0%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Bladder Carcinoma
1/58 2%
4/956 0%
Melanoma
2/210 1%
8/1899 0%
Non-Small Cell Lung Carcinoma
4/304 1%
3/1390 0%
Colorectal Carcinoma
3/143 2%
9/3239 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Prostate Carcinoma
0/13 0%
4/2105 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
Pancreatic Carcinoma
0/89 0%
3/1611 0%
Esophageal Carcinoma
1/23 4%
0/769 0%
Other Sarcomas
0/69 0%
1/699 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Squamous Cell Lung Carcinoma
1/57 2%
0/810 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Ovarian Carcinoma
1/109 1%
0/998 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Other Blood Cancers
0/61 0%
2/2725 0%
Breast Carcinoma
0/144 0%
2/3264 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Glioma
0/52 0%
1/2127 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%

Mutation Distribution

Where PDZK1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PDZK1 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 271 mutations in PDZK1

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