BASP1

Brain abundant membrane attached signal protein 1 P80723 BASP1_HUMAN
Protein Coding Chr 5 5p15.1 Swiss-Prot reviewed Entrez 10409
Mutations
400
CL 56 · Tissue 342
Samples
209
CL 39 · Tissue 169
Peptides
133
unique mutant peptides
Transcripts
2
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
Mutations40056342
Samples20939169
Peptides13325112

Function

BASP1 · Brain abundant membrane attached signal protein 1

This gene encodes a membrane bound protein with several transient phosphorylation sites and PEST motifs. Conservation of proteins with PEST sequences among different species supports their functional significance. PEST sequences typically occur in proteins with high turnover rates. Immunological characteristics of this protein are species specific. This protein also undergoes N-terminal myristoylation. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Oct 2012].

Isoforms & Proteins

2 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
ENST00000322611 P80723 212 133
ENST00000616743 P80723 188 119

Gene Properties

Type
Protein Coding
Chromosome
5
Cytoband
5p15.1
Entrez ID
Aliases
CAP-23CAP23NAP-22NAP22

Recurrent Mutations

All 133 amino-acid changes on canonical ENST00000322611 · 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 BASP1 · 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 BASP1 – 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
2/40 5%
0/0 0%
Melanoma
3/210 1%
27/1899 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
28/2550 1%
Glioblastoma
1/98 1%
0/0 0%
Colorectal Carcinoma
9/143 6%
25/3239 1%
Endometrial Carcinoma
0/42 0%
6/612 1%
Non-Small Cell Lung Carcinoma
4/304 1%
10/1390 1%
Gastric Carcinoma
2/74 3%
13/1809 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Hepatocellular Carcinoma
0/46 0%
13/2210 1%
Squamous Cell Lung Carcinoma
3/57 5%
2/810 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Ovarian Carcinoma
3/109 3%
2/998 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Mesothelioma
1/62 2%
0/165 0%
Neuroendocrine Tumour
2/154 1%
1/577 0%
Other Solid Cancers
1/94 1%
5/1515 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Non-Cancerous
0/104 0%
3/830 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Cervical Carcinoma
0/35 0%
1/422 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
5/2534 0%
Breast Carcinoma
3/144 2%
2/3264 0%
Glioma
0/52 0%
3/2127 0%
Other Sarcomas
0/69 0%
1/699 0%
Pancreatic Carcinoma
0/89 0%
2/1611 0%
B-Lymphoblastic Leukemia
3/55 5%
0/2640 0%

Mutation Distribution

Where BASP1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in BASP1 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 400 mutations in BASP1

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