DPY30

Dpy-30 histone methyltransferase complex regulatory subunit Q9C005 DPY30_HUMAN
Protein Coding Chr 2 2p22.3 Swiss-Prot reviewed Entrez 84661
Mutations
72
CL 12 · Tissue 60
Samples
38
CL 9 · Tissue 29
Peptides
32
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
Mutations721260
Samples38929
Peptides32626

Function

DPY30 · Dpy-30 histone methyltransferase complex regulatory subunit

This gene encodes an integral core subunit of the SET1/MLL family of H3K4 methyltransferases. The encoded protein directly controls cell cycle regulators and plays an important role in the proliferation and differentiation of human hematopoietic progenitor cells. [provided by RefSeq, Mar 2016].

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
ENST00000342166 Q9C005 39 32
ENST00000295066 Q9C005 33 29

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2p22.3
Entrez ID
Aliases
Cps25HDPY-30Saf19

Recurrent Mutations

All 32 amino-acid changes on canonical ENST00000342166 · 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 DPY30 · 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 DPY30 – 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
Endometrial Carcinoma
4/42 10%
2/612 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Other Sarcomas
0/69 0%
2/699 0%
Colorectal Carcinoma
2/143 1%
6/3239 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Melanoma
0/210 0%
3/1899 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
3/2550 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Bladder Carcinoma
0/58 0%
1/956 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
B-Lymphoblastic Leukemia
2/55 4%
0/2640 0%
Non-Small Cell Lung Carcinoma
0/304 0%
1/1390 0%
Head and Neck Carcinoma
1/85 1%
0/1574 0%
Other Solid Cancers
0/94 0%
1/1515 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Gastric Carcinoma
0/74 0%
1/1809 0%

Mutation Distribution

Where DPY30 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DPY30 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 72 mutations in DPY30

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