OARD1

O-acyl-ADP-ribose deacylase 1 Q9Y530 OARD1_HUMAN
Protein Coding Chr 6 6p21.1 Swiss-Prot reviewed Entrez 221443
Mutations
439
CL 66 · Tissue 372
Samples
68
CL 18 · Tissue 49
Peptides
68
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
Mutations43966372
Samples681849
Peptides681454

Function

OARD1 · O-acyl-ADP-ribose deacylase 1

The protein encoded by this gene is a deacylase that can convert O-acetyl-ADP-ribose to ADP-ribose and acetate, O-propionyl-ADP-ribose to ADP-ribose and propionate, and O-butyryl-ADP-ribose to ADP-ribose and butyrate. The ADP-ribose product is able to inhibit these reactions through a competitive feedback loop. [provided by RefSeq, Jul 2016].

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
ENST00000424266 Q9Y530 63 49
ENST00000463088 Q9Y530 52 43
ENST00000468811 Q9Y530 52 43
ENST00000479950 Q9Y530 52 43
ENST00000486443 C9JXC3* 38 32
ENST00000373154 C9J5P1* 28 23
ENST00000480585 C9J5P1* 28 23
ENST00000628419 C9J5P1* 28 23
ENST00000469104 C9IZY1* 25 20
ENST00000471367 C9IZY1* 25 20
ENST00000464633 C9JA90* 24 19
ENST00000482515 C9JA90* 24 19

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6p21.1
Entrez ID
Aliases
C6orf130TARG1dJ34B21.3

Recurrent Mutations

All 49 amino-acid changes on canonical ENST00000424266 · 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 OARD1 · 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 OARD1 – 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
2/26 8%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Endometrial Carcinoma
4/42 10%
3/612 0%
Glioblastoma
1/98 1%
0/0 0%
Bladder Carcinoma
1/58 2%
9/956 1%
Mesothelioma
2/62 3%
0/165 0%
Other Sarcomas
2/69 3%
2/699 0%
Gastric Carcinoma
0/74 0%
5/1809 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Pancreatic Carcinoma
0/89 0%
3/1611 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
4/2550 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Colorectal Carcinoma
0/143 0%
4/3239 0%
Other Solid Cancers
1/94 1%
1/1515 0%
Non-Small Cell Lung Carcinoma
0/304 0%
2/1390 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
2/2534 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Melanoma
0/210 0%
2/1899 0%
Glioma
0/52 0%
2/2127 0%
Breast Carcinoma
2/144 1%
1/3264 0%
Kidney Carcinoma
1/85 1%
0/1862 0%

Mutation Distribution

Where OARD1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in OARD1 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 439 mutations in OARD1

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