ADH6

Alcohol dehydrogenase 6 (class V) P28332 ADH6_HUMAN
Protein Coding Chr 4 4q23 Swiss-Prot reviewed Entrez 130
Mutations
598
CL 110 · Tissue 486
Samples
221
CL 58 · Tissue 161
Peptides
179
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
Mutations598110486
Samples22158161
Peptides17935147

Function

ADH6 · Alcohol dehydrogenase 6 (class V)

This gene encodes class V alcohol dehydrogenase, which is a member of the alcohol dehydrogenase family. Members of this family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. This gene is expressed in the stomach as well as in the liver, and it contains a glucocorticoid response element upstream of its 5' UTR, which is a steroid hormone receptor binding site. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [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
ENST00000394899 P28332-2 233 167
ENST00000237653 P28332 199 158
ENST00000394897 A0ACM8PXG3* 166 132

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4q23
Entrez ID
Aliases
ADH-5

Recurrent Mutations

All 167 amino-acid changes on canonical ENST00000394899 · 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 ADH6 · 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 ADH6 – 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
4/40 10%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Unknown
1/10 10%
0/29 0%
Melanoma
4/210 2%
49/1899 3%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Endometrial Carcinoma
1/42 2%
9/612 1%
Bladder Carcinoma
0/58 0%
11/956 1%
Colorectal Carcinoma
13/143 9%
23/3239 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Non-Small Cell Lung Carcinoma
4/304 1%
8/1390 1%
Gastric Carcinoma
1/74 1%
10/1809 1%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Cervical Carcinoma
2/35 6%
0/422 0%
Other Sarcomas
0/69 0%
3/699 0%
Esophageal Carcinoma
1/23 4%
2/769 0%
Breast Carcinoma
4/144 3%
9/3264 0%
Squamous Cell Lung Carcinoma
1/57 2%
2/810 0%
Other Solid Cancers
0/94 0%
5/1515 0%
Head and Neck Carcinoma
2/85 2%
3/1574 0%
Hepatocellular Carcinoma
2/46 4%
4/2210 0%
Ovarian Carcinoma
2/109 2%
1/998 0%
Kidney Carcinoma
1/85 1%
3/1862 0%
Neuroblastoma
1/87 1%
2/1331 0%
Glioma
1/52 2%
3/2127 0%
Other Blood Cancers
2/61 3%
2/2725 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
3/2550 0%
Non-Cancerous
1/104 1%
0/830 0%

Mutation Distribution

Where ADH6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ADH6 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 598 mutations in ADH6

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