DHRS4

Dehydrogenase/reductase 4 Q9BTZ2 DHRS4_HUMAN
Protein Coding Chr 14 14q11.2 Swiss-Prot reviewed Entrez 10901
Mutations
785
CL 101 · Tissue 682
Samples
171
CL 34 · Tissue 136
Peptides
157
unique mutant peptides
Transcripts
9
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
Mutations785101682
Samples17134136
Peptides15732126

Function

DHRS4 · Dehydrogenase/reductase 4

Enables identical protein binding activity; oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor; and oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor. Involved in several processes, including cellular ketone metabolic process; positive regulation of reactive oxygen species metabolic process; and steroid metabolic process. Located in nucleus and peroxisomal membrane. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

9 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
ENST00000313250 Q9BTZ2 163 98
ENST00000558581 Q9BTZ2-4 117 73
ENST00000558263 Q9BTZ2-7 115 67
ENST00000397075 Q9BTZ2-2 112 69
ENST00000543741 F5GWZ1* 98 59
ENST00000559632 Q9BTZ2-5 94 55
ENST00000397074 Q9BTZ2-3 84 49
ENST00000645602 Q9BTZ2-2 1 1
ENST00000710584 Q9BTZ2 1 1

Gene Properties

Type
Protein Coding
Chromosome
14
Cytoband
14q11.2
Entrez ID
Aliases
CRNRDRPHCRPSCDSCAD-SRLSDR-SRL

Recurrent Mutations

All 98 amino-acid changes on canonical ENST00000313250 · 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 DHRS4 · 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 DHRS4 – 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%
Rhabdomyosarcoma
1/33 3%
3/171 2%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Pheochromocytoma and Paraganglioma
0/0 0%
1/71 1%
Endometrial Carcinoma
4/42 10%
5/612 1%
Cervical Carcinoma
0/35 0%
5/422 1%
Glioblastoma
1/98 1%
0/0 0%
Neuroendocrine Tumour
3/154 2%
2/577 0%
Other Solid Cancers
0/94 0%
10/1515 1%
Squamous Cell Lung Carcinoma
0/57 0%
5/810 1%
Melanoma
1/210 0%
11/1899 1%
Colorectal Carcinoma
5/143 4%
13/3239 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Bladder Carcinoma
0/58 0%
5/956 1%
Gastric Carcinoma
2/74 3%
7/1809 0%
Osteosarcoma
1/45 2%
0/166 0%
Mesothelioma
0/62 0%
1/165 1%
Medulloblastoma
0/0 0%
2/450 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
10/2550 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Kidney Carcinoma
0/85 0%
7/1862 0%
Ovarian Carcinoma
3/109 3%
1/998 0%
Non-Small Cell Lung Carcinoma
1/304 0%
4/1390 0%
Pancreatic Carcinoma
2/89 2%
3/1611 0%
Glioma
0/52 0%
5/2127 0%
Breast Carcinoma
1/144 1%
7/3264 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Other Blood Cancers
1/61 2%
4/2725 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%

Mutation Distribution

Where DHRS4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DHRS4 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 785 mutations in DHRS4

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