NABP1

Nucleic acid binding protein 1 Q96AH0 SOSB2_HUMAN
Protein Coding Chr 2 2q32.3 Swiss-Prot reviewed Entrez 64859
Mutations
182
CL 41 · Tissue 140
Samples
88
CL 22 · Tissue 65
Peptides
69
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
Mutations18241140
Samples882265
Peptides691257

Function

NABP1 · Nucleic acid binding protein 1

Single-stranded DNA (ssDNA)-binding proteins, such as OBFC2A, are ubiquitous and essential for a variety of DNA metabolic processes, including replication, recombination, and detection and repair of damage (Richard et al., 2008 [PubMed 18449195]).[supplied by OMIM, Jun 2008].

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
ENST00000425611 Q96AH0 89 67
ENST00000409510 Q96AH0-2 46 38
ENST00000410026 Q96AH0-2 46 38
ENST00000674172 Q96AH0 1 1

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q32.3
Entrez ID
Aliases
NABP1-OT1OBFC2ASOSS-B2SSB2

Recurrent Mutations

All 67 amino-acid changes on canonical ENST00000425611 · 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 NABP1 · 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 NABP1 – 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
Glioblastoma
2/98 2%
0/0 0%
Endometrial Carcinoma
0/42 0%
6/612 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Melanoma
1/210 0%
13/1899 1%
Plasma Cell Myeloma
0/44 0%
2/305 1%
Neuroendocrine Tumour
4/154 3%
0/577 0%
Non-Small Cell Lung Carcinoma
4/304 1%
4/1390 0%
Osteosarcoma
1/45 2%
0/166 0%
Gastric Carcinoma
0/74 0%
8/1809 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Colorectal Carcinoma
4/143 3%
4/3239 0%
Breast Carcinoma
3/144 2%
5/3264 0%
Kidney Carcinoma
0/85 0%
4/1862 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Glioma
0/52 0%
4/2127 0%
Other Sarcomas
1/69 1%
0/699 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
0/2534 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%

Mutation Distribution

Where NABP1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in NABP1 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 182 mutations in NABP1

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