KCNK3

Potassium two pore domain channel subfamily K member 3 O14649 KCNK3_HUMAN
Protein Coding Chr 2 2p23.3 Swiss-Prot reviewed Entrez 3777
Mutations
303
CL 79 · Tissue 207
Samples
271
CL 73 · Tissue 193
Peptides
206
unique mutant peptides
Transcripts
1
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
Mutations30379207
Samples27173193
Peptides20653150

Function

KCNK3 · Potassium two pore domain channel subfamily K member 3

This gene encodes a member of the superfamily of potassium channel proteins that contain two pore-forming P domains. The encoded protein is an outwardly rectifying channel that is sensitive to changes in extracellular pH and is inhibited by extracellular acidification. Also referred to as an acid-sensitive potassium channel, it is activated by the anesthetics halothane and isoflurane. Although three transcripts are detected in northern blots, there is currently no sequence available to confirm transcript variants for this gene. [provided by RefSeq, Aug 2008].

Isoforms & Proteins

1 transcript · 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
ENST00000302909 O14649 303 206

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2p23.3
Entrez ID
Aliases
DDSAK2p3.1OAT1PPH4TASKTASK-1

Recurrent Mutations

All 206 amino-acid changes on canonical ENST00000302909 · 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 KCNK3 · 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 KCNK3 – 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
9/40 22%
0/0 0%
Endometrial Carcinoma
9/42 21%
11/612 2%
Colorectal Carcinoma
15/143 10%
36/3239 1%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Osteosarcoma
2/45 4%
1/166 1%
Gastric Carcinoma
0/74 0%
23/1809 1%
Glioblastoma
1/98 1%
0/0 0%
Neuroendocrine Tumour
3/154 2%
4/577 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
24/2550 1%
Melanoma
3/210 1%
16/1899 1%
Non-Small Cell Lung Carcinoma
6/304 2%
9/1390 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Squamous Cell Lung Carcinoma
0/57 0%
6/810 1%
Non-Cancerous
1/104 1%
5/830 1%
Thyroid Gland Carcinoma
2/45 4%
8/1592 0%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Ovarian Carcinoma
2/109 2%
3/998 0%
Burkitts Lymphoma
1/32 3%
0/196 0%
Mesothelioma
0/62 0%
1/165 1%
Hepatocellular Carcinoma
0/46 0%
9/2210 0%
Meningioma
1/3 33%
0/252 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Ewings Sarcoma
1/63 2%
0/262 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
7/2534 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Breast Carcinoma
4/144 3%
5/3264 0%
Other Solid Cancers
0/94 0%
4/1515 0%
Head and Neck Carcinoma
1/85 1%
3/1574 0%
Pancreatic Carcinoma
0/89 0%
4/1611 0%

Mutation Distribution

Where KCNK3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KCNK3 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 303 mutations in KCNK3

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