MYPN

Myopalladin Q86TC9 MYPN_HUMAN
Protein Coding Chr 10 10q21.3 Swiss-Prot reviewed Entrez 84665
Mutations
2,444
CL 252 · Tissue 2,180
Samples
851
CL 143 · Tissue 703
Peptides
748
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
Mutations2,4442522,180
Samples851143703
Peptides748107664

Function

MYPN · Myopalladin

Striated muscle in vertebrates comprises large proteins which must be organized properly to contract efficiently. Z-lines in striated muscle are a sign of this organization, representing the ends of actin thin filaments, titin, nebulin or nebulette and accessory proteins required for structure and function. This gene encodes a protein which interacts with nebulin in skeletal muscle or nebulette in cardiac muscle and alpha-actinin. In addition, this gene product can interact with a protein with the I-band indicating it has a regulatory as well as structural function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011].

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
ENST00000358913 Q86TC9 1,044 644
ENST00000354393 Q86TC9-2 825 505
ENST00000373675 A0A804CFL5* 267 208
ENST00000540630 A0A8J9ASZ5* 233 181
ENST00000613327 Q86TC9 75 35

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10q21.3
Entrez ID
Aliases
CMD1DDCMH22CMYO24CMYP24MYOPNEM11

Recurrent Mutations

All 644 amino-acid changes on canonical ENST00000358913 · 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 MYPN · 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 MYPN – 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
Gastrointestinal Stromal Tumour
0/0 0%
34/133 26%
Oral Cavity Carcinoma
5/54 9%
0/0 0%
Endometrial Carcinoma
6/42 14%
38/612 6%
Melanoma
15/210 7%
98/1899 5%
Non-Small Cell Lung Carcinoma
23/304 8%
63/1390 5%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Squamous Cell Lung Carcinoma
5/57 9%
33/810 4%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Other Solid Cancers
4/94 4%
60/1515 4%
Colorectal Carcinoma
18/143 13%
76/3239 2%
Neuroendocrine Tumour
13/154 8%
7/577 1%
Cervical Carcinoma
4/35 11%
7/422 2%
Bladder Carcinoma
5/58 9%
19/956 2%
Small Cell Lung Carcinoma
2/9 22%
15/752 2%
Gastric Carcinoma
5/74 7%
34/1809 2%
Adrenocortical Carcinoma
2/3 67%
0/112 0%
Head and Neck Carcinoma
2/85 2%
26/1574 2%
Esophageal Squamous Cell Carcinoma
3/51 6%
38/2550 1%
Germ Cell Tumour
1/25 4%
2/169 1%
Plasma Cell Myeloma
0/44 0%
5/305 2%
Non-Cancerous
0/104 0%
12/830 1%
Hepatocellular Carcinoma
2/46 4%
25/2210 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Biliary Tract Carcinoma
1/54 2%
8/950 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
B-Cell Non-Hodgkins Lymphoma
3/88 3%
18/2534 1%
Esophageal Carcinoma
0/23 0%
6/769 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Medulloblastoma
0/0 0%
3/450 1%
Pancreatic Carcinoma
4/89 4%
7/1611 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in MYPN 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 2,444 mutations in MYPN

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