HDAC4

Histone deacetylase 4 P56524 HDAC4_HUMAN
Protein Coding Chr 2 2q37.3 Swiss-Prot reviewed Entrez 9759
Mutations
742
CL 143 · Tissue 580
Samples
618
CL 124 · Tissue 480
Peptides
531
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
Mutations742143580
Samples618124480
Peptides531102433

Function

HDAC4 · Histone deacetylase 4

Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to class II of the histone deacetylase/acuc/apha family. It possesses histone deacetylase activity and represses transcription when tethered to a promoter. This protein does not bind DNA directly, but through transcription factors MEF2C and MEF2D. It seems to interact in a multiprotein complex with RbAp48 and HDAC3. [provided by RefSeq, Jul 2008].

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
ENST00000345617 P56524 623 468
ENST00000543185 A0A7I2SVS4* 119 101

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q37.3
Entrez ID
Aliases
AHO3BDMRHA6116HD4HDAC-4HDAC-A

Recurrent Mutations

All 468 amino-acid changes on canonical ENST00000345617 · 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 HDAC4 · 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 HDAC4 – 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
3/26 12%
0/0 0%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
8/42 19%
36/612 6%
Melanoma
13/210 6%
56/1899 3%
Gastric Carcinoma
7/74 9%
49/1809 3%
Colorectal Carcinoma
22/143 15%
68/3239 2%
Non-Small Cell Lung Carcinoma
12/304 4%
30/1390 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Neuroendocrine Tumour
9/154 6%
7/577 1%
Other Solid Cancers
3/94 3%
32/1515 2%
Squamous Cell Lung Carcinoma
1/57 2%
16/810 2%
Cervical Carcinoma
2/35 6%
6/422 1%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Thyroid Gland Carcinoma
0/45 0%
22/1592 1%
Bladder Carcinoma
1/58 2%
11/956 1%
Other Sarcomas
1/69 1%
8/699 1%
Glioblastoma
1/98 1%
0/0 0%
Biliary Tract Carcinoma
0/54 0%
10/950 1%
Ovarian Carcinoma
4/109 4%
7/998 1%
Hepatocellular Carcinoma
1/46 2%
21/2210 1%
Osteosarcoma
2/45 4%
0/166 0%
Head and Neck Carcinoma
2/85 2%
13/1574 1%
Esophageal Carcinoma
1/23 4%
6/769 1%
Small Cell Lung Carcinoma
0/9 0%
6/752 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
16/2550 1%
Glioma
1/52 2%
13/2127 1%
Ewings Sarcoma
1/63 2%
1/262 0%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Breast Carcinoma
4/144 3%
15/3264 0%

Mutation Distribution

Where HDAC4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in HDAC4 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 742 mutations in HDAC4

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