KLRC3

Killer cell lectin like receptor C3 Q07444 NKG2E_HUMAN
Protein Coding Chr 12 12p13.2 Swiss-Prot reviewed Entrez 3823
Mutations
323
CL 38 · Tissue 285
Samples
148
CL 21 · Tissue 127
Peptides
96
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
Mutations32338285
Samples14821127
Peptides961584

Function

KLRC3 · Killer cell lectin like receptor C3

Natural killer (NK) cells are lymphocytes that can mediate lysis of certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. NK cells preferentially express several calcium-dependent (C-type) lectins, which have been implicated in the regulation of NK cell function. KLRC3 is a member of the NKG2 group which are expressed primarily in natural killer (NK) cells and encodes a family of transmembrane proteins characterized by a type II membrane orientation (extracellular C terminus) and the presence of a C-type lectin domain. The NKG2 gene family is located within the NK complex, a region that contains several C-type lectin genes preferentially expressed on NK cells. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008].

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
ENST00000381903 Q07444-2 164 88
ENST00000396439 Q07444 159 86

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12p13.2
Entrez ID
Aliases
NKG2-ENKG2E

Recurrent Mutations

All 88 amino-acid changes on canonical ENST00000381903 · 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 KLRC3 · 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 KLRC3 – 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
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Endometrial Carcinoma
1/42 2%
8/612 1%
Esophageal Carcinoma
0/23 0%
10/769 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Bladder Carcinoma
2/58 3%
8/956 1%
Non-Small Cell Lung Carcinoma
5/304 2%
8/1390 1%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Ewings Sarcoma
2/63 3%
0/262 0%
Melanoma
0/210 0%
13/1899 1%
Other Solid Cancers
1/94 1%
8/1515 1%
Osteosarcoma
0/45 0%
1/166 1%
Colorectal Carcinoma
1/143 1%
15/3239 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Thyroid Gland Carcinoma
1/45 2%
4/1592 0%
Glioma
0/52 0%
6/2127 0%
Gastric Carcinoma
1/74 1%
4/1809 0%
Neuroendocrine Tumour
1/154 1%
1/577 0%
Pancreatic Carcinoma
0/89 0%
4/1611 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Prostate Carcinoma
1/13 8%
3/2105 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
4/2550 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
4/2534 0%
Other Sarcomas
0/69 0%
1/699 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Non-Cancerous
0/104 0%
1/830 0%

Mutation Distribution

Where KLRC3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KLRC3 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 52 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 323 mutations in KLRC3

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