ZDHHC5

ZDHHC palmitoyltransferase 5 Q9C0B5 ZDHC5_HUMAN
Protein Coding Chr 11 11q12.1 Swiss-Prot reviewed Entrez 25921
Mutations
581
CL 110 · Tissue 464
Samples
305
CL 68 · Tissue 233
Peptides
241
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
Mutations581110464
Samples30568233
Peptides24147199

Function

ZDHHC5 · ZDHHC palmitoyltransferase 5

Enables palmitoyltransferase activity. Involved in positive regulation of pattern recognition receptor signaling pathway and positive regulation of protein localization to plasma membrane. Acts upstream of or within protein palmitoylation. Located in phagocytic vesicle and plasma membrane. [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
ENST00000287169 Q9C0B5 322 237
ENST00000527985 Q9C0B5-2 259 207

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q12.1
Entrez ID
Aliases
DHHC5ZNF375

Recurrent Mutations

All 237 amino-acid changes on canonical ENST00000287169 · 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 ZDHHC5 · 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 ZDHHC5 – 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
Endometrial Carcinoma
5/42 12%
24/612 4%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Colorectal Carcinoma
10/143 7%
44/3239 1%
Gastric Carcinoma
7/74 9%
20/1809 1%
Melanoma
5/210 2%
25/1899 1%
Burkitts Lymphoma
1/32 3%
2/196 1%
Chondrosarcoma
1/14 7%
0/75 0%
Cervical Carcinoma
1/35 3%
4/422 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Glioblastoma
1/98 1%
0/0 0%
Bladder Carcinoma
1/58 2%
8/956 1%
Other Sarcomas
3/69 4%
3/699 0%
Head and Neck Carcinoma
0/85 0%
12/1574 1%
Non-Small Cell Lung Carcinoma
5/304 2%
7/1390 0%
Glioma
0/52 0%
12/2127 1%
Esophageal Carcinoma
0/23 0%
4/769 1%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Pancreatic Carcinoma
0/89 0%
8/1611 0%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Neuroendocrine Tumour
1/154 1%
2/577 0%
Kidney Carcinoma
1/85 1%
6/1862 0%
Breast Carcinoma
5/144 3%
7/3264 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
7/2534 0%
Other Solid Cancers
1/94 1%
4/1515 0%
Ewings Sarcoma
0/63 0%
1/262 0%

Mutation Distribution

Where ZDHHC5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZDHHC5 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 581 mutations in ZDHHC5

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