ART4

ADP-ribosyltransferase 4 (inactive) (Dombrock blood group) Q93070 NAR4_HUMAN
Protein Coding Chr 12 12p12.3 Swiss-Prot reviewed Entrez 420
Mutations
168
CL 34 · Tissue 133
Samples
165
CL 34 · Tissue 130
Peptides
121
unique mutant peptides
Transcripts
1
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
Mutations16834133
Samples16534130
Peptides12119104

Function

ART4 · ADP-ribosyltransferase 4 (inactive) (Dombrock blood group)

This gene encodes a protein that contains a mono-ADP-ribosylation (ART) motif. It is a member of the ADP-ribosyltransferase gene family but enzymatic activity has not been demonstrated experimentally. Antigens of the Dombrock blood group system are located on the gene product, which is glycosylphosphatidylinosotol-anchored to the erythrocyte membrane. Allelic variants, some of which lead to adverse transfusion reactions, are known. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

1 transcript · 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
ENST00000228936 Q93070 168 121

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12p12.3
Entrez ID
Aliases
ARTC4CD297DODO/ART4DOK1

Recurrent Mutations

All 121 amino-acid changes on canonical ENST00000228936 · 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 ART4 · 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 ART4 – 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%
4/133 3%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Rhabdomyosarcoma
0/33 0%
4/171 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Melanoma
5/210 2%
24/1899 1%
Squamous Cell Lung Carcinoma
1/57 2%
7/810 1%
Endometrial Carcinoma
0/42 0%
6/612 1%
Colorectal Carcinoma
7/143 5%
17/3239 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Other Solid Cancers
0/94 0%
9/1515 1%
Gastric Carcinoma
0/74 0%
9/1809 0%
Head and Neck Carcinoma
0/85 0%
7/1574 0%
Neuroendocrine Tumour
3/154 2%
0/577 0%
Non-Small Cell Lung Carcinoma
0/304 0%
7/1390 0%
Bladder Carcinoma
2/58 3%
2/956 0%
Kidney Carcinoma
5/85 6%
2/1862 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Other Sarcomas
2/69 3%
0/699 0%
Breast Carcinoma
3/144 2%
4/3264 0%
Prostate Carcinoma
0/13 0%
4/2105 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
Other Blood Cancers
0/61 0%
4/2725 0%
Glioma
0/52 0%
3/2127 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Non-Cancerous
0/104 0%
1/830 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Thyroid Gland Carcinoma
1/45 2%
0/1592 0%

Mutation Distribution

Where ART4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ART4 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 168 mutations in ART4

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