KCNK4

Potassium two pore domain channel subfamily K member 4 Q9NYG8 KCNK4_HUMAN
Protein Coding Chr 11 11q13.1 Swiss-Prot reviewed Entrez 50801
Mutations
731
CL 148 · Tissue 569
Samples
271
CL 64 · Tissue 203
Peptides
253
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
Mutations731148569
Samples27164203
Peptides25365192

Function

KCNK4 · Potassium two pore domain channel subfamily K member 4

This gene encodes a member of the TWIK-related arachidonic acid-stimulated two pore potassium channel subfamily. The encoded protein homodimerizes and functions as an outwardly rectifying channel. This channel is regulated by polyunsaturated fatty acids, temperature and mechanical deformation of the lipid membrane. This protein is expressed primarily in neural tissues and may be involved in regulating the noxious input threshold in dorsal root ganglia neurons. Alternate splicing results in multiple transcript variants. Naturally occurring read-through transcripts also exist between this gene and the downstream testis expressed 40 (TEX40) gene, as represented in GeneID: 106780802. [provided by RefSeq, Nov 2015].

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
ENST00000422670 Q9NYG8 224 148
ENST00000394525 Q9NYG8 184 126
ENST00000539216 Q9NYG8 184 126
ENST00000538767 F5GYE0* 139 105

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q13.1
Entrez ID
Aliases
FHEIGK2p4.1TRAAKTRAAK1

Recurrent Mutations

All 148 amino-acid changes on canonical ENST00000422670 · 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 KCNK4 · 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 KCNK4 – 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
10/40 25%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Burkitts Lymphoma
4/32 12%
0/196 0%
Endometrial Carcinoma
3/42 7%
8/612 1%
Other Solid Cancers
2/94 2%
18/1515 1%
Gastric Carcinoma
4/74 5%
18/1809 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Cervical Carcinoma
2/35 6%
3/422 1%
Bladder Carcinoma
0/58 0%
11/956 1%
Glioblastoma
1/98 1%
0/0 0%
Melanoma
0/210 0%
20/1899 1%
Squamous Cell Lung Carcinoma
3/57 5%
5/810 1%
Colorectal Carcinoma
4/143 3%
26/3239 1%
Thyroid Gland Carcinoma
0/45 0%
14/1592 1%
Small Cell Lung Carcinoma
0/9 0%
6/752 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Glioma
1/52 2%
12/2127 1%
Hepatocellular Carcinoma
6/46 13%
6/2210 0%
Other Sarcomas
2/69 3%
2/699 0%
Esophageal Carcinoma
0/23 0%
4/769 1%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
12/2550 0%
Mesothelioma
0/62 0%
1/165 1%
Non-Cancerous
0/104 0%
4/830 0%
Head and Neck Carcinoma
0/85 0%
7/1574 0%
Neuroendocrine Tumour
2/154 1%
1/577 0%
Non-Small Cell Lung Carcinoma
3/304 1%
4/1390 0%
Ovarian Carcinoma
3/109 3%
0/998 0%

Mutation Distribution

Where KCNK4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KCNK4 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 53 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 731 mutations in KCNK4

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