DNAJC5

DnaJ heat shock protein family (Hsp40) member C5 Q9H3Z4 DNJC5_HUMAN
Protein Coding Chr 20 20q13.33 Swiss-Prot reviewed Entrez 80331
Mutations
96
CL 13 · Tissue 82
Samples
94
CL 13 · Tissue 80
Peptides
68
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
Mutations961382
Samples941380
Peptides681061

Function

DNAJC5 · DnaJ heat shock protein family (Hsp40) member C5

This gene is a member of the J protein family. J proteins function in many cellular processes by regulating the ATPase activity of 70 kDa heat shock proteins. The encoded protein plays a role in membrane trafficking and protein folding, and has been shown to have anti-neurodegenerative properties. The encoded protein is known to play a role in cystic fibrosis and Huntington's disease. A pseudogene of this gene is located on the short arm of chromosome 8. [provided by RefSeq, Nov 2010].

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
ENST00000360864 Q9H3Z4 96 68

Gene Properties

Type
Protein Coding
Chromosome
20
Cytoband
20q13.33
Entrez ID
Aliases
CLN4CLN4BCSPDNAJC5Amir-941-2mir-941-3

Recurrent Mutations

All 68 amino-acid changes on canonical ENST00000360864 · 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 DNAJC5 · 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 DNAJC5 – 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%
Gastric Carcinoma
1/74 1%
12/1809 1%
Colorectal Carcinoma
4/143 3%
19/3239 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Melanoma
1/210 0%
9/1899 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Other Solid Cancers
0/94 0%
5/1515 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Hepatocellular Carcinoma
1/46 2%
4/2210 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Pancreatic Carcinoma
2/89 2%
1/1611 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
4/2534 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Neuroblastoma
1/87 1%
0/1331 0%
Breast Carcinoma
0/144 0%
2/3264 0%
Non-Small Cell Lung Carcinoma
0/304 0%
1/1390 0%
Glioma
0/52 0%
1/2127 0%

Mutation Distribution

Where DNAJC5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DNAJC5 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 96 mutations in DNAJC5

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