HDAC10

Histone deacetylase 10 Q969S8 HDA10_HUMAN
Protein Coding Chr 22 22q13.33 Swiss-Prot reviewed Entrez 83933
Mutations
773
CL 102 · Tissue 666
Samples
260
CL 58 · Tissue 199
Peptides
232
unique mutant peptides
Transcripts
4
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
Mutations773102666
Samples26058199
Peptides23249188

Function

HDAC10 · Histone deacetylase 10

The protein encoded by this gene belongs to the histone deacetylase family, members of which deacetylate lysine residues on the N-terminal part of the core histones. Histone deacetylation modulates chromatin structure, and plays an important role in transcriptional regulation, cell cycle progression, and developmental events. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011].

Isoforms & Proteins

4 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
ENST00000216271 Q969S8 285 211
ENST00000349505 Q969S8-2 239 179
ENST00000448072 C9J8B8* 227 172
ENST00000626012 A0A0D9SFS6* 22 20

Gene Properties

Type
Protein Coding
Chromosome
22
Cytoband
22q13.33
Entrez ID
Aliases
HD10

Recurrent Mutations

All 211 amino-acid changes on canonical ENST00000216271 · 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 HDAC10 · 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 HDAC10 – 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
3/40 8%
0/0 0%
Endometrial Carcinoma
5/42 12%
14/612 2%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Ewings Sarcoma
4/63 6%
2/262 1%
Pheochromocytoma and Paraganglioma
0/0 0%
1/71 1%
Melanoma
7/210 3%
20/1899 1%
Non-Small Cell Lung Carcinoma
8/304 3%
12/1390 1%
Colorectal Carcinoma
7/143 5%
26/3239 1%
Neuroendocrine Tumour
4/154 3%
2/577 0%
Small Cell Lung Carcinoma
1/9 11%
5/752 1%
Non-Cancerous
1/104 1%
6/830 1%
Other Solid Cancers
2/94 2%
10/1515 1%
Squamous Cell Lung Carcinoma
0/57 0%
6/810 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Head and Neck Carcinoma
2/85 2%
8/1574 1%
Bladder Carcinoma
1/58 2%
5/956 1%
Ovarian Carcinoma
3/109 3%
3/998 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
14/2550 1%
Gastric Carcinoma
2/74 3%
8/1809 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
8/2534 0%
Breast Carcinoma
3/144 2%
7/3264 0%
Other Sarcomas
0/69 0%
2/699 0%
Glioma
0/52 0%
5/2127 0%
Medulloblastoma
0/0 0%
1/450 0%
Wilms Tumour
0/5 0%
1/474 0%
Kidney Carcinoma
0/85 0%
4/1862 0%

Mutation Distribution

Where HDAC10 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in HDAC10 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 773 mutations in HDAC10

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