KCNN3

Potassium calcium-activated channel subfamily N member 3 Q9UGI6 KCNN3_HUMAN
Protein Coding Chr 1 1q21.3 Swiss-Prot reviewed Entrez 3782
Mutations
1,770
CL 278 · Tissue 1,415
Samples
580
CL 160 · Tissue 409
Peptides
354
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
Mutations1,7702781,415
Samples580160409
Peptides35458288

Function

KCNN3 · Potassium calcium-activated channel subfamily N member 3

Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. This gene belongs to the KCNN family of potassium channels. It encodes an integral membrane protein that forms a voltage-independent calcium-activated channel, which is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. This gene contains two CAG repeat regions in the coding sequence. It was thought that expansion of one or both of these repeats could lead to an increased susceptibility to schizophrenia or bipolar disorder, but studies indicate that this is probably not the case. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011].

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
ENST00000271915 Q9UGI6 676 331
ENST00000618040 A0A087WYJ0* 519 312
ENST00000361147 Q9UGI6-2 290 203
ENST00000358505 Q9UGI6-3 285 199

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q21.3
Entrez ID
Aliases
KCa2.3SK3SKCA3ZLS3hSK3

Recurrent Mutations

All 331 amino-acid changes on canonical ENST00000271915 · 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 KCNN3 · 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 KCNN3 – 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
Oral Cavity Carcinoma
6/54 11%
0/0 0%
Chordoma
2/7 29%
0/13 0%
Acute Myeloid Leukemia
7/90 8%
0/0 0%
Glioblastoma
7/98 7%
0/0 0%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Rhabdomyosarcoma
0/33 0%
9/171 5%
Melanoma
13/210 6%
60/1899 3%
Endometrial Carcinoma
4/42 10%
17/612 3%
Colorectal Carcinoma
14/143 10%
80/3239 2%
Germ Cell Tumour
0/25 0%
5/169 3%
Hodgkins Lymphoma
3/16 19%
0/122 0%
Gastric Carcinoma
9/74 12%
28/1809 2%
Non-Small Cell Lung Carcinoma
15/304 5%
16/1390 1%
Squamous Cell Lung Carcinoma
8/57 14%
7/810 1%
Non-Cancerous
2/104 2%
13/830 2%
Neuroendocrine Tumour
10/154 6%
1/577 0%
Thyroid Gland Carcinoma
1/45 2%
22/1592 1%
Mesothelioma
3/62 5%
0/165 0%
Other Solid Cancers
1/94 1%
17/1515 1%
Chondrosarcoma
0/14 0%
1/75 1%
Hepatocellular Carcinoma
3/46 7%
22/2210 1%
B-Cell Non-Hodgkins Lymphoma
8/88 9%
20/2534 1%
Osteosarcoma
1/45 2%
1/166 1%
Ewings Sarcoma
3/63 5%
0/262 0%
Burkitts Lymphoma
2/32 6%
0/196 0%
Cervical Carcinoma
1/35 3%
3/422 1%
Plasma Cell Myeloma
2/44 5%
1/305 0%
Bladder Carcinoma
1/58 2%
7/956 1%
Other Sarcomas
5/69 7%
1/699 0%
Glioma
3/52 6%
13/2127 1%

Mutation Distribution

Where KCNN3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KCNN3 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 1,770 mutations in KCNN3

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