ATP5PD

ATP synthase peripheral stalk subunit d O75947 ATP5H_HUMAN
Protein Coding Chr 17 17q25.1 Swiss-Prot reviewed Entrez 10476
Mutations
96
CL 16 · Tissue 79
Samples
51
CL 11 · Tissue 39
Peptides
48
unique mutant peptides
Transcripts
2
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
Mutations961679
Samples511139
Peptides48839

Function

ATP5PD · ATP synthase peripheral stalk subunit d

Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the d subunit of the Fo complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. In addition, three pseudogenes are located on chromosomes 9, 12 and 15. [provided by RefSeq, Jun 2010].

Isoforms & Proteins

2 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
ENST00000301587 O75947 53 43
ENST00000344546 O75947-2 43 36

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q25.1
Entrez ID
Aliases
APT5HATP5HATPQ

Recurrent Mutations

All 43 amino-acid changes on canonical ENST00000301587 · 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 ATP5PD · 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 ATP5PD – 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
1/40 2%
0/0 0%
Endometrial Carcinoma
1/42 2%
4/612 1%
Burkitts Lymphoma
0/32 0%
1/196 1%
Cervical Carcinoma
1/35 3%
1/422 0%
Melanoma
0/210 0%
7/1899 0%
Other Solid Cancers
0/94 0%
5/1515 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Non-Small Cell Lung Carcinoma
2/304 1%
2/1390 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Colorectal Carcinoma
0/143 0%
5/3239 0%
Neuroblastoma
2/87 2%
0/1331 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Gastric Carcinoma
0/74 0%
2/1809 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Breast Carcinoma
2/144 1%
0/3264 0%
Kidney Carcinoma
1/85 1%
0/1862 0%
Glioma
0/52 0%
1/2127 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%
Other Blood Cancers
0/61 0%
1/2725 0%

Mutation Distribution

Where ATP5PD is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ATP5PD 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.

Mutations

All 96 mutations in ATP5PD

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