ADH4

Alcohol dehydrogenase 4 (class II), pi polypeptide P08319 ADH4_HUMAN
Protein Coding Chr 4 4q23 Swiss-Prot reviewed Entrez 127
Mutations
590
CL 65 · Tissue 522
Samples
198
CL 36 · Tissue 161
Peptides
148
unique mutant peptides
Transcripts
3
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
Mutations59065522
Samples19836161
Peptides14825127

Function

ADH4 · Alcohol dehydrogenase 4 (class II), pi polypeptide

This gene encodes class II alcohol dehydrogenase 4 pi subunit, which is a member of the alcohol dehydrogenase family. Members of this enzyme family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. Class II alcohol dehydrogenase is a homodimer composed of 2 pi subunits. It exhibits a high activity for oxidation of long-chain aliphatic alcohols and aromatic alcohols and is less sensitive to pyrazole. This gene is localized to chromosome 4 in the cluster of alcohol dehydrogenase genes. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

3 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
ENST00000265512 P08319 212 141
ENST00000505590 P08319-2 189 133
ENST00000508393 P08319-2 189 133

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4q23
Entrez ID
Aliases
ADH-2HEL-S-4

Recurrent Mutations

All 141 amino-acid changes on canonical ENST00000265512 · 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 ADH4 · 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 ADH4 – 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
Gastrointestinal Stromal Tumour
0/0 0%
7/133 5%
Glioblastoma
2/98 2%
0/0 0%
Melanoma
6/210 3%
33/1899 2%
Germ Cell Tumour
2/25 8%
1/169 1%
Endometrial Carcinoma
2/42 5%
7/612 1%
Plasma Cell Myeloma
2/44 5%
2/305 1%
Cervical Carcinoma
2/35 6%
3/422 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Squamous Cell Lung Carcinoma
1/57 2%
6/810 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
18/2550 1%
Hepatocellular Carcinoma
0/46 0%
14/2210 1%
Non-Small Cell Lung Carcinoma
3/304 1%
5/1390 0%
Other Solid Cancers
2/94 2%
5/1515 0%
Thyroid Gland Carcinoma
0/45 0%
7/1592 0%
Colorectal Carcinoma
2/143 1%
12/3239 0%
Other Sarcomas
0/69 0%
3/699 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Bladder Carcinoma
0/58 0%
4/956 0%
Gastric Carcinoma
0/74 0%
7/1809 0%
Non-Cancerous
0/104 0%
3/830 0%
Head and Neck Carcinoma
2/85 2%
2/1574 0%
Medulloblastoma
0/0 0%
1/450 0%
Breast Carcinoma
2/144 1%
5/3264 0%
Biliary Tract Carcinoma
2/54 4%
0/950 0%
Prostate Carcinoma
0/13 0%
4/2105 0%
Neuroblastoma
0/87 0%
2/1331 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Pancreatic Carcinoma
1/89 1%
1/1611 0%

Mutation Distribution

Where ADH4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ADH4 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 51 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 590 mutations in ADH4

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