DNM2

Dynamin 2 P50570 DYN2_HUMAN
Protein Coding Chr 19 19p13.2 Swiss-Prot reviewed Entrez 1785
Mutations
2,748
CL 278 · Tissue 2,420
Samples
592
CL 106 · Tissue 472
Peptides
445
unique mutant peptides
Transcripts
6
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
Mutations2,7482782,420
Samples592106472
Peptides44570377

Function

DNM2 · Dynamin 2

Dynamins represent one of the subfamilies of GTP-binding proteins. These proteins share considerable sequence similarity over the N-terminal portion of the molecule, which contains the GTPase domain. Dynamins are associated with microtubules. They have been implicated in cell processes such as endocytosis and cell motility, and in alterations of the membrane that accompany certain activities such as bone resorption by osteoclasts. Dynamins bind many proteins that bind actin and other cytoskeletal proteins. Dynamins can also self-assemble, a process that stimulates GTPase activity. Five alternatively spliced transcripts encoding different proteins have been described. Additional alternatively spliced transcripts may exist, but their full-length nature has not been determined. [provided by RefSeq, Jun 2010].

Isoforms & Proteins

6 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
ENST00000389253 P50570-4 612 407
ENST00000408974 P50570-3 542 386
ENST00000585892 P50570-5 532 373
ENST00000355667 P50570 531 371
ENST00000359692 P50570-2 530 371
ENST00000591818 K7EMR9* 1 1

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19p13.2
Entrez ID
Aliases
CMT2MCMTDI1CMTDIBDI-CMTBDYN2DYNII

Recurrent Mutations

All 407 amino-acid changes on canonical ENST00000389253 · 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 DNM2 · 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 DNM2 – 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
Chronic Myelogenous Leukemia
6/25 24%
0/0 0%
T-Lymphoblastic Leukemia
5/40 12%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
2/26 8%
0/0 0%
Glioblastoma
4/98 4%
0/0 0%
Endometrial Carcinoma
6/42 14%
19/612 3%
Melanoma
10/210 5%
49/1899 3%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Esophageal Squamous Cell Carcinoma
0/51 0%
66/2550 3%
Colorectal Carcinoma
17/143 12%
65/3239 2%
Bladder Carcinoma
2/58 3%
21/956 2%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Plasma Cell Myeloma
2/44 5%
4/305 1%
Other Solid Cancers
1/94 1%
25/1515 2%
Germ Cell Tumour
3/25 12%
0/169 0%
Gastric Carcinoma
0/74 0%
28/1809 2%
Thyroid Gland Carcinoma
0/45 0%
24/1592 2%
Squamous Cell Lung Carcinoma
2/57 4%
10/810 1%
Ovarian Carcinoma
3/109 3%
11/998 1%
Neuroendocrine Tumour
7/154 5%
2/577 0%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
B-Lymphoblastic Leukemia
4/55 7%
26/2640 1%
Small Cell Lung Carcinoma
0/9 0%
8/752 1%
Head and Neck Carcinoma
2/85 2%
14/1574 1%
Cervical Carcinoma
0/35 0%
4/422 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Kidney Carcinoma
4/85 5%
11/1862 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Other Sarcomas
0/69 0%
5/699 1%
Non-Small Cell Lung Carcinoma
6/304 2%
5/1390 0%
Glioma
2/52 4%
12/2127 1%

Mutation Distribution

Where DNM2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DNM2 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 2,748 mutations in DNM2

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