Stats by Source
Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)
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.
| Total | Cell line | Tissue | |
|---|---|---|---|
| Mutations | 331 | 41 | 288 |
| Samples | 128 | 20 | 107 |
| Peptides | 122 | 15 | 106 |
Function
NFKBIA · NFKB inhibitor alpha
This gene encodes a member of the NF-kappa-B inhibitor family, which contain multiple ankrin repeat domains. The encoded protein interacts with REL dimers to inhibit NF-kappa-B/REL complexes which are involved in inflammatory responses. The encoded protein moves between the cytoplasm and the nucleus via a nuclear localization signal and CRM1-mediated nuclear export. Mutations in this gene have been found in ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant disease. [provided by RefSeq, Aug 2011].
Isoforms & Proteins
3 transcripts · UniProt mapping is sequence-verified (AA-safe)
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.
Gene Properties
Recurrent Mutations
All 110 amino-acid changes on canonical ENST00000216797 · needle height = samples · drag the mini-map to zoom
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 NFKBIA · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in NFKBIA – 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 type | Cell lines | Tissue samples |
|---|---|---|
| T-Lymphoblastic Leukemia | 3/40 8% | 0/0 0% |
| Burkitts Lymphoma | 2/32 6% | 0/196 0% |
| Bladder Carcinoma | 0/58 0% | 8/956 1% |
| Endometrial Carcinoma | 0/42 0% | 5/612 1% |
| Non-Cancerous | 0/104 0% | 5/830 1% |
| Germ Cell Tumour | 0/25 0% | 1/169 1% |
| Colorectal Carcinoma | 6/143 4% | 11/3239 0% |
| Non-Small Cell Lung Carcinoma | 2/304 1% | 6/1390 0% |
| Cervical Carcinoma | 0/35 0% | 2/422 0% |
| Melanoma | 1/210 0% | 8/1899 0% |
| B-Cell Non-Hodgkins Lymphoma | 3/88 3% | 8/2534 0% |
| Meningioma | 1/3 33% | 0/252 0% |
| Thyroid Gland Carcinoma | 0/45 0% | 6/1592 0% |
| Hepatocellular Carcinoma | 0/46 0% | 7/2210 0% |
| Other Solid Cancers | 0/94 0% | 5/1515 0% |
| Head and Neck Carcinoma | 0/85 0% | 5/1574 0% |
| Glioma | 0/52 0% | 6/2127 0% |
| Gastric Carcinoma | 0/74 0% | 5/1809 0% |
| Breast Carcinoma | 0/144 0% | 8/3264 0% |
| Neuroendocrine Tumour | 1/154 1% | 0/577 0% |
| Small Cell Lung Carcinoma | 0/9 0% | 1/752 0% |
| Pancreatic Carcinoma | 0/89 0% | 2/1611 0% |
| Esophageal Squamous Cell Carcinoma | 0/51 0% | 3/2550 0% |
| Squamous Cell Lung Carcinoma | 1/57 2% | 0/810 0% |
| Kidney Carcinoma | 0/85 0% | 2/1862 0% |
| Ovarian Carcinoma | 0/109 0% | 1/998 0% |
| Neuroblastoma | 0/87 0% | 1/1331 0% |
| Other Blood Cancers | 0/61 0% | 2/2725 0% |
Mutation Distribution
Where NFKBIA is mutated · all tissues, split by cell line vs tissue
How many mutations in NFKBIA 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
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 331 mutations in NFKBIA
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.
| ID | Sample | Transcript | AA Change | CDS | Type | Source | Mutant Peptide | Wild-type Peptide |
|---|