VPS45

Vacuolar protein sorting 45 homolog Q9NRW7 VPS45_HUMAN
Protein Coding Chr 1 1q21.2 Swiss-Prot reviewed Entrez 11311
Mutations
949
CL 125 · Tissue 801
Samples
261
CL 49 · Tissue 204
Peptides
253
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
Mutations949125801
Samples26149204
Peptides25337214

Function

VPS45 · Vacuolar protein sorting 45 homolog

Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene is a member of the Sec1 domain family, and shows a high degree of sequence similarity to mouse, rat and yeast Vps45. The exact function of this gene is not known, but its high expression in peripheral blood mononuclear cells suggests a role in trafficking proteins, including inflammatory mediators. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2013].

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
ENST00000644510 Q9NRW7 275 208
ENST00000644526 A0A2R8YD95* 241 195
ENST00000643970 A0A2R8YE10* 206 167
ENST00000369128 Q9NRW7-2 196 161
ENST00000643611 A0A2R8Y7W9* 31 25

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q21.2
Entrez ID
Aliases
H1H1VPS45SCN5VPS45AVPS45BVPS54A

Recurrent Mutations

All 208 amino-acid changes on canonical ENST00000644510 · 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 VPS45 · 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 VPS45 – 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
T-Lymphoblastic Leukemia
3/40 8%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Endometrial Carcinoma
1/42 2%
16/612 3%
Glioblastoma
2/98 2%
0/0 0%
Melanoma
9/210 4%
26/1899 1%
Colorectal Carcinoma
11/143 8%
34/3239 1%
Bladder Carcinoma
2/58 3%
9/956 1%
Gastric Carcinoma
0/74 0%
20/1809 1%
Non-Small Cell Lung Carcinoma
2/304 1%
14/1390 1%
Mesothelioma
2/62 3%
0/165 0%
Other Solid Cancers
0/94 0%
14/1515 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Squamous Cell Lung Carcinoma
0/57 0%
6/810 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Ovarian Carcinoma
2/109 2%
5/998 0%
Hepatocellular Carcinoma
3/46 7%
11/2210 0%
Plasma Cell Myeloma
0/44 0%
2/305 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Osteosarcoma
0/45 0%
1/166 1%
Head and Neck Carcinoma
1/85 1%
6/1574 0%
Glioma
0/52 0%
8/2127 0%
Breast Carcinoma
3/144 2%
7/3264 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
7/2550 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Medulloblastoma
0/0 0%
1/450 0%
Prostate Carcinoma
2/13 15%
2/2105 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Neuroblastoma
1/87 1%
1/1331 0%

Mutation Distribution

Where VPS45 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in VPS45 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 949 mutations in VPS45

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