KLF4

KLF transcription factor 4 O43474-1 KLF4_HUMAN
Protein Coding Chr 9 9q31.2 Swiss-Prot reviewed Entrez 9314
Mutations
482
CL 97 · Tissue 377
Samples
316
CL 80 · Tissue 232
Peptides
207
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
Mutations48297377
Samples31680232
Peptides20754157

Function

KLF4 · KLF transcription factor 4

This gene encodes a protein that belongs to the Kruppel family of transcription factors. The encoded zinc finger protein is required for normal development of the barrier function of skin. The encoded protein is thought to control the G1-to-S transition of the cell cycle following DNA damage by mediating the tumor suppressor gene p53. Mice lacking this gene have a normal appearance but lose weight rapidly, and die shortly after birth due to fluid evaporation resulting from compromised epidermal barrier function. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015].

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
ENST00000374672 O43474-1 326 196
ENST00000610832 A0A087X0S4* 156 76

Gene Properties

Type
Protein Coding
Chromosome
9
Cytoband
9q31.2
Entrez ID
Aliases
EZFGKLF

Recurrent Mutations

All 196 amino-acid changes on canonical ENST00000374672 · 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 KLF4 · 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 KLF4 – 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
6/40 15%
0/0 0%
Chordoma
2/7 29%
0/13 0%
Meningioma
0/3 0%
21/252 8%
Endometrial Carcinoma
7/42 17%
11/612 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Pancreatic Carcinoma
1/89 1%
36/1611 2%
Neuroendocrine Tumour
7/154 5%
3/577 1%
Gastric Carcinoma
3/74 4%
17/1809 1%
Glioblastoma
1/98 1%
0/0 0%
Melanoma
3/210 1%
18/1899 1%
Colorectal Carcinoma
10/143 7%
21/3239 1%
Non-Small Cell Lung Carcinoma
4/304 1%
11/1390 1%
Esophageal Carcinoma
0/23 0%
7/769 1%
Bladder Carcinoma
1/58 2%
7/956 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Prostate Carcinoma
4/13 31%
8/2105 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
13/2550 1%
Ovarian Carcinoma
5/109 5%
1/998 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Other Sarcomas
2/69 3%
2/699 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Neuroblastoma
1/87 1%
6/1331 0%
Osteosarcoma
1/45 2%
0/166 0%
Mesothelioma
1/62 2%
0/165 0%
Non-Cancerous
0/104 0%
4/830 0%
Squamous Cell Lung Carcinoma
2/57 4%
1/810 0%
Breast Carcinoma
0/144 0%
11/3264 0%
B-Cell Non-Hodgkins Lymphoma
4/88 5%
4/2534 0%
B-Lymphoblastic Leukemia
3/55 5%
5/2640 0%

Mutation Distribution

Where KLF4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KLF4 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 482 mutations in KLF4

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