DNM1L

Dynamin 1L O00429 DNM1L_HUMAN
Protein Coding Chr 12 12p11.21 Swiss-Prot reviewed Entrez 10059
Mutations
1,618
CL 171 · Tissue 1,436
Samples
258
CL 52 · Tissue 203
Peptides
258
unique mutant peptides
Transcripts
7
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
Mutations1,6181711,436
Samples25852203
Peptides25838220

Function

DNM1L · Dynamin 1L

This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013].

Isoforms & Proteins

7 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
ENST00000549701 O00429 280 211
ENST00000553257 O00429-6 241 194
ENST00000381000 O00429-8 231 185
ENST00000547312 O00429-2 226 180
ENST00000358214 O00429-9 216 174
ENST00000452533 O00429-3 213 171
ENST00000266481 O00429-4 211 169

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12p11.21
Entrez ID
Aliases
DLP1DRP1DVLPDYMPLEEMPFEMPF1

Recurrent Mutations

All 211 amino-acid changes on canonical ENST00000549701 · 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 DNM1L · 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 DNM1L – 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
9/42 21%
21/612 3%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Cervical Carcinoma
2/35 6%
5/422 1%
Burkitts Lymphoma
1/32 3%
2/196 1%
Colorectal Carcinoma
7/143 5%
35/3239 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Glioblastoma
1/98 1%
0/0 0%
Gastric Carcinoma
1/74 1%
18/1809 1%
Melanoma
4/210 2%
16/1899 1%
Bladder Carcinoma
0/58 0%
9/956 1%
Adrenocortical Carcinoma
1/3 33%
0/112 0%
Ovarian Carcinoma
4/109 4%
5/998 0%
Biliary Tract Carcinoma
1/54 2%
6/950 1%
Non-Cancerous
0/104 0%
5/830 1%
Non-Small Cell Lung Carcinoma
2/304 1%
7/1390 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Prostate Carcinoma
2/13 15%
9/2105 0%
Other Solid Cancers
0/94 0%
8/1515 1%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
11/2550 0%
Other Sarcomas
0/69 0%
3/699 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Thyroid Gland Carcinoma
2/45 4%
4/1592 0%
Head and Neck Carcinoma
2/85 2%
3/1574 0%
Glioma
0/52 0%
6/2127 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
Breast Carcinoma
2/144 1%
7/3264 0%
Hepatocellular Carcinoma
1/46 2%
4/2210 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
3/2534 0%

Mutation Distribution

Where DNM1L is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DNM1L 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 1,618 mutations in DNM1L

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