THPO

Thrombopoietin P40225 TPO_HUMAN
Protein Coding Chr 3 Swiss-Prot reviewed Entrez 7066
Mutations
498
CL 48 · Tissue 446
Samples
202
CL 29 · Tissue 171
Peptides
210
unique mutant peptides
Transcripts
4
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
Mutations49848446
Samples20229171
Peptides21026191

Function

THPO · Thrombopoietin

Megakaryocytopoiesis is the cellular development process that leads to platelet production. The main functional protein encoded by this gene is a humoral growth factor that is necessary for megakaryocyte proliferation and maturation, as well as for thrombopoiesis. This protein is the ligand for MLP/C_MPL, the product of myeloproliferative leukemia virus oncogene. Mutations in this gene are the cause of thrombocythemia 1. Alternative promoter usage and differential splicing result in multiple transcript variants differing in the 5' UTR and/or coding region. Multiple AUG codons upstream of the main open reading frame (ORF) have been identified, and these upstream AUGs inhibit translation of the main ORF at different extent. [provided by RefSeq, Feb 2014].

Isoforms & Proteins

4 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
ENST00000647395 P40225 190 145
ENST00000445696 P40225-2 172 133
ENST00000421442 F8W6L1* 121 99
ENST00000645603 A0A3B3ITS0* 15 12

Gene Properties

Type
Protein Coding
Chromosome
3
Entrez ID
Aliases
CAMT2MGDFMKCSFMLMPLLGTHC9

Recurrent Mutations

All 145 amino-acid changes on canonical ENST00000647395 · 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 THPO · 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 THPO – 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
1/42 2%
14/612 2%
Melanoma
7/210 3%
38/1899 2%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Cervical Carcinoma
2/35 6%
2/422 0%
Gastric Carcinoma
2/74 3%
14/1809 1%
Bladder Carcinoma
0/58 0%
8/956 1%
Non-Small Cell Lung Carcinoma
3/304 1%
10/1390 1%
Ovarian Carcinoma
2/109 2%
5/998 0%
Ewings Sarcoma
2/63 3%
0/262 0%
Colorectal Carcinoma
0/143 0%
21/3239 1%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Osteosarcoma
1/45 2%
0/166 0%
Mesothelioma
0/62 0%
1/165 1%
Non-Cancerous
0/104 0%
4/830 0%
Other Solid Cancers
0/94 0%
6/1515 0%
Glioma
0/52 0%
7/2127 0%
Head and Neck Carcinoma
1/85 1%
4/1574 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
7/2550 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Thyroid Gland Carcinoma
1/45 2%
2/1592 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
2/2534 0%
Breast Carcinoma
0/144 0%
5/3264 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Other Blood Cancers
1/61 2%
2/2725 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in THPO 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 52 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 498 mutations in THPO

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