HDAC3

Histone deacetylase 3 O15379 HDAC3_HUMAN
Protein Coding Chr 5 5q31.3 Swiss-Prot reviewed Entrez 8841
Mutations
188
CL 39 · Tissue 145
Samples
180
CL 39 · Tissue 137
Peptides
144
unique mutant peptides
Transcripts
1
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
Mutations18839145
Samples18039137
Peptides14422123

Function

HDAC3 · Histone deacetylase 3

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 the histone deacetylase/acuc/apha family. It has histone deacetylase activity and represses transcription when tethered to a promoter. It may participate in the regulation of transcription through its binding with the zinc-finger transcription factor YY1. This protein can also down-regulate p53 function and thus modulate cell growth and apoptosis. This gene is regarded as a potential tumor suppressor gene. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

1 transcript · 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
ENST00000305264 O15379 188 144

Gene Properties

Type
Protein Coding
Chromosome
5
Cytoband
5q31.3
Entrez ID
Aliases
HD3KDAC3RPD3RPD3-2

Recurrent Mutations

All 144 amino-acid changes on canonical ENST00000305264 · 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 HDAC3 · 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 HDAC3 – 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%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Endometrial Carcinoma
1/42 2%
19/612 3%
Hodgkins Lymphoma
2/16 12%
2/122 2%
Glioblastoma
1/98 1%
0/0 0%
Melanoma
1/210 0%
20/1899 1%
Non-Small Cell Lung Carcinoma
11/304 4%
4/1390 0%
Cervical Carcinoma
0/35 0%
4/422 1%
Neuroendocrine Tumour
4/154 3%
2/577 0%
Colorectal Carcinoma
4/143 3%
23/3239 1%
Gastric Carcinoma
0/74 0%
14/1809 1%
Other Sarcomas
4/69 6%
1/699 0%
Germ Cell Tumour
1/25 4%
0/169 0%
Other Solid Cancers
1/94 1%
6/1515 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Ovarian Carcinoma
1/109 1%
3/998 0%
Thyroid Gland Carcinoma
0/45 0%
5/1592 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%
Squamous Cell Lung Carcinoma
1/57 2%
1/810 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
4/2550 0%
Medulloblastoma
0/0 0%
1/450 0%
Non-Cancerous
0/104 0%
2/830 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Prostate Carcinoma
0/13 0%
4/2105 0%
Glioma
0/52 0%
3/2127 0%
Other Blood Cancers
1/61 2%
3/2725 0%
Kidney Carcinoma
1/85 1%
1/1862 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Breast Carcinoma
0/144 0%
3/3264 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%

Mutation Distribution

Where HDAC3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in HDAC3 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 188 mutations in HDAC3

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