HDAC9

Histone deacetylase 9 Q9UKV0 HDAC9_HUMAN
Protein Coding Chr 7 7p21.1 Swiss-Prot reviewed Entrez 9734
Mutations
7,287
CL 907 · Tissue 6,227
Samples
995
CL 199 · Tissue 768
Peptides
789
unique mutant peptides
Transcripts
12
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
Mutations7,2879076,227
Samples995199768
Peptides789132675

Function

HDAC9 · Histone deacetylase 9

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 has sequence homology to members of the histone deacetylase family. This gene is orthologous to the Xenopus and mouse MITR genes. The MITR protein lacks the histone deacetylase catalytic domain. It represses MEF2 activity through recruitment of multicomponent corepressor complexes that include CtBP and HDACs. This encoded protein may play a role in hematopoiesis. Multiple alternatively spliced transcripts have been described for this gene but the full-length nature of some of them has not been determined. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

12 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
ENST00000441542 Q9UKV0-7 976 652
ENST00000406451 Q9UKV0-5 975 651
ENST00000401921 Q9UKV0-6 939 628
ENST00000432645 Q9UKV0 933 620
ENST00000405010 Q9UKV0-3 509 337
ENST00000406072 B5MCF1* 490 329
ENST00000417496 Q9UKV0-8 489 328
ENST00000456174 Q9UKV0-10 484 317
ENST00000622668 B7Z3P7* 474 315
ENST00000428307 Q9UKV0-9 472 313
ENST00000524023 Q9UKV0-11 444 291
ENST00000686413 Q9UKV0-7 102 99

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7p21.1
Entrez ID
Aliases
HD7HD7bHD9HDACHDAC7BHDAC9B

Recurrent Mutations

All 652 amino-acid changes on canonical ENST00000441542 · 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 HDAC9 · 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 HDAC9 – 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
5/26 19%
0/0 0%
T-Lymphoblastic Leukemia
5/40 12%
0/0 0%
Melanoma
21/210 10%
176/1899 9%
Non-Small Cell Lung Carcinoma
53/304 17%
61/1390 4%
Endometrial Carcinoma
6/42 14%
25/612 4%
Squamous Cell Lung Carcinoma
10/57 18%
30/810 4%
Other Solid Cancers
8/94 9%
58/1515 4%
Colorectal Carcinoma
20/143 14%
97/3239 3%
Neuroendocrine Tumour
15/154 10%
8/577 1%
Gastric Carcinoma
2/74 3%
49/1809 3%
Ovarian Carcinoma
8/109 7%
18/998 2%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Hepatocellular Carcinoma
6/46 13%
40/2210 2%
Glioblastoma
2/98 2%
0/0 0%
Cervical Carcinoma
3/35 9%
6/422 1%
Mesothelioma
3/62 5%
1/165 1%
Small Cell Lung Carcinoma
0/9 0%
12/752 2%
Germ Cell Tumour
1/25 4%
2/169 1%
Biliary Tract Carcinoma
0/54 0%
15/950 2%
Pancreatic Carcinoma
1/89 1%
21/1611 1%
Head and Neck Carcinoma
3/85 4%
18/1574 1%
Esophageal Carcinoma
0/23 0%
10/769 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
28/2550 1%
Bladder Carcinoma
0/58 0%
10/956 1%
Ewings Sarcoma
2/63 3%
1/262 0%
Burkitts Lymphoma
2/32 6%
0/196 0%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Non-Cancerous
1/104 1%
7/830 1%
Glioma
3/52 6%
14/2127 1%
Breast Carcinoma
5/144 3%
21/3264 1%

Mutation Distribution

Where HDAC9 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in HDAC9 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 7,287 mutations in HDAC9

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