PDCD5

Programmed cell death 5 O14737 PDCD5_HUMAN
Protein Coding Chr 19 19q13.11 Swiss-Prot reviewed Entrez 9141
Mutations
116
CL 15 · Tissue 101
Samples
49
CL 10 · Tissue 39
Peptides
56
unique mutant peptides
Transcripts
5
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
Mutations11615101
Samples491039
Peptides56848

Function

PDCD5 · Programmed cell death 5

This gene encodes a protein that is upregulated during apoptosis where it translocates rapidly from the cytoplasm to the nucleus. The encoded protein may be an important regulator of K(lysine) acetyltransferase 5 (a protein involved in transcription, DNA damage response and cell cycle control) by inhibiting its proteasome-dependent degradation. Pseudogenes have been identified on chromosomes 5 and 12 [provided by RefSeq, Dec 2010].

Isoforms & Proteins

5 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
ENST00000590247 O14737 36 31
ENST00000419343 O14737-2 33 25
ENST00000586035 K7EQA1* 27 26
ENST00000592786 K7ESJ4* 14 13
ENST00000379316 F6W1R2* 6 5

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.11
Entrez ID
Aliases
TFAR19

Recurrent Mutations

All 31 amino-acid changes on canonical ENST00000590247 · 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 PDCD5 · 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 PDCD5 – 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
Bladder Carcinoma
0/58 0%
4/956 0%
Non-Small Cell Lung Carcinoma
3/304 1%
3/1390 0%
Endometrial Carcinoma
1/42 2%
1/612 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
7/2550 0%
Neuroendocrine Tumour
1/154 1%
1/577 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Non-Cancerous
2/104 2%
0/830 0%
Melanoma
1/210 0%
3/1899 0%
Other Solid Cancers
2/94 2%
1/1515 0%
Colorectal Carcinoma
0/143 0%
5/3239 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
Gastric Carcinoma
0/74 0%
1/1809 0%
B-Lymphoblastic Leukemia
0/55 0%
1/2640 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where PDCD5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PDCD5 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 116 mutations in PDCD5

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