IKBKG

Inhibitor of nuclear factor kappa B kinase regulatory subunit gamma Q9Y6K9 NEMO_HUMAN
Protein Coding Chr X Xq28 Swiss-Prot reviewed Entrez 8517
Mutations
204
CL 28 · Tissue 167
Samples
43
CL 9 · Tissue 32
Peptides
36
unique mutant peptides
Transcripts
9
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
Mutations20428167
Samples43932
Peptides36926

Function

IKBKG · Inhibitor of nuclear factor kappa B kinase regulatory subunit gamma

This gene encodes the regulatory subunit of the inhibitor of kappaB kinase (IKK) complex, which activates NF-kappaB resulting in activation of genes involved in inflammation, immunity, cell survival, and other pathways. Mutations in this gene result in incontinentia pigmenti, hypohidrotic ectodermal dysplasia, and several other types of immunodeficiencies. A pseudogene highly similar to this locus is located in an adjacent region of the X chromosome. [provided by RefSeq, Mar 2016].

Isoforms & Proteins

9 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
ENST00000618670 Q9Y6K9-2 38 29
ENST00000594239 Q9Y6K9 32 22
ENST00000611071 Q9Y6K9 27 18
ENST00000611176 Q9Y6K9-3 27 18
ENST00000617207 A0A087X1B1* 27 18
ENST00000615874 A0A087X0G7* 25 17
ENST00000619941 A0A087WUW6* 25 17
ENST00000440286 Q9Y6K9 2 2
ENST00000422680 Q9Y6K9 1 1

Gene Properties

Type
Protein Coding
Chromosome
X
Cytoband
Xq28
Entrez ID
Aliases
AMCBX1EDAID1FIP-3FIP3Fip3pIKK-gamma

Recurrent Mutations

All 29 amino-acid changes on canonical ENST00000618670 · 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 IKBKG · 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 IKBKG – 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
Unknown
0/10 0%
1/29 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Endometrial Carcinoma
2/42 5%
9/612 1%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Gastric Carcinoma
2/74 3%
1/1809 0%
Colorectal Carcinoma
0/143 0%
5/3239 0%
Melanoma
0/210 0%
3/1899 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Other Solid Cancers
0/94 0%
2/1515 0%
Non-Cancerous
0/104 0%
1/830 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
0/2534 0%
Non-Small Cell Lung Carcinoma
0/304 0%
1/1390 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Glioma
0/52 0%
1/2127 0%
Breast Carcinoma
1/144 1%
0/3264 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in IKBKG 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 204 mutations in IKBKG

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