RAP2A

RAP2A, member of RAS oncogene family P10114 RAP2A_HUMAN
Protein Coding Chr 13 13q32.1 Swiss-Prot reviewed Entrez 5911
Mutations
62
CL 19 · Tissue 38
Samples
60
CL 19 · Tissue 37
Peptides
47
unique mutant peptides
Transcripts
1
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
Mutations621938
Samples601937
Peptides471132

Function

RAP2A · RAP2A, member of RAS oncogene family

Enables GTPase activity; guanyl ribonucleotide binding activity; and magnesium ion binding activity. Involved in several processes, including actin cytoskeleton reorganization; microvillus assembly; and positive regulation of protein autophosphorylation. Acts upstream of or within establishment of protein localization. Located in plasma membrane and recycling endosome membrane. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

1 transcript · 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
ENST00000245304 P10114 62 47

Gene Properties

Type
Protein Coding
Chromosome
13
Cytoband
13q32.1
Entrez ID
Aliases
K-REVKREVRAP2RbBP-30

Recurrent Mutations

All 47 amino-acid changes on canonical ENST00000245304 · 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 RAP2A · 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 RAP2A – 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
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Non-Small Cell Lung Carcinoma
6/304 2%
5/1390 0%
Gastric Carcinoma
2/74 3%
10/1809 1%
Endometrial Carcinoma
2/42 5%
2/612 0%
Burkitts Lymphoma
1/32 3%
0/196 0%
Colorectal Carcinoma
4/143 3%
7/3239 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Glioma
0/52 0%
3/2127 0%
Melanoma
1/210 0%
2/1899 0%
Other Sarcomas
0/69 0%
1/699 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Hepatocellular Carcinoma
2/46 4%
0/2210 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Other Solid Cancers
0/94 0%
1/1515 0%
Kidney Carcinoma
0/85 0%
1/1862 0%

Mutation Distribution

Where RAP2A is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RAP2A 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 62 mutations in RAP2A

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