HDAC11

Histone deacetylase 11 Q96DB2 HDA11_HUMAN
Protein Coding Chr 3 3p25.1 Swiss-Prot reviewed Entrez 79885
Mutations
1,198
CL 87 · Tissue 1,092
Samples
203
CL 27 · Tissue 173
Peptides
221
unique mutant peptides
Transcripts
10
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
Mutations1,198871,092
Samples20327173
Peptides22123205

Function

HDAC11 · Histone deacetylase 11

This gene encodes a class IV histone deacetylase. The encoded protein is localized to the nucleus and may be involved in regulating the expression of interleukin 10. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Apr 2009].

Isoforms & Proteins

10 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
ENST00000295757 Q96DB2 186 125
ENST00000437379 E7ETT9* 154 109
ENST00000402271 B5MCQ6* 146 101
ENST00000522202 Q96DB2-2 146 103
ENST00000404040 B5MCU6* 135 92
ENST00000433119 A0ACM8Q5M3* 104 70
ENST00000446613 A0ACM8Q5M3* 104 70
ENST00000402259 B5MCS3* 95 68
ENST00000404548 B5MC52* 72 46
ENST00000405025 B5MD06* 56 36

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3p25.1
Entrez ID
Aliases
HD11

Recurrent Mutations

All 125 amino-acid changes on canonical ENST00000295757 · 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 HDAC11 · 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 HDAC11 – 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
4/42 10%
11/612 2%
Melanoma
2/210 1%
25/1899 1%
Gastric Carcinoma
4/74 5%
19/1809 1%
Bladder Carcinoma
0/58 0%
9/956 1%
Mesothelioma
0/62 0%
2/165 1%
Colorectal Carcinoma
3/143 2%
26/3239 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Glioma
0/52 0%
12/2127 1%
Non-Small Cell Lung Carcinoma
0/304 0%
9/1390 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
13/2550 1%
Ovarian Carcinoma
2/109 2%
3/998 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Prostate Carcinoma
2/13 15%
5/2105 0%
Non-Cancerous
0/104 0%
3/830 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Other Sarcomas
0/69 0%
2/699 0%
Head and Neck Carcinoma
1/85 1%
3/1574 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Medulloblastoma
0/0 0%
1/450 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Neuroblastoma
2/87 2%
0/1331 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
B-Lymphoblastic Leukemia
2/55 4%
1/2640 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Breast Carcinoma
0/144 0%
3/3264 0%

Mutation Distribution

Where HDAC11 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in HDAC11 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 1,198 mutations in HDAC11

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