FZD6

Frizzled class receptor 6 O60353 FZD6_HUMAN
Protein Coding Chr 8 8q22.3 Swiss-Prot reviewed Entrez 8323
Mutations
878
CL 120 · Tissue 739
Samples
302
CL 52 · Tissue 242
Peptides
231
unique mutant peptides
Transcripts
3
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
Mutations878120739
Samples30252242
Peptides23136192

Function

FZD6 · Frizzled class receptor 6

This gene represents a member of the 'frizzled' gene family, which encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The protein encoded by this family member contains a signal peptide, a cysteine-rich domain in the N-terminal extracellular region, and seven transmembrane domains, but unlike other family members, this protein does not contain a C-terminal PDZ domain-binding motif. This protein functions as a negative regulator of the canonical Wnt/beta-catenin signaling cascade, thereby inhibiting the processes that trigger oncogenic transformation, cell proliferation, and inhibition of apoptosis. Alternative splicing results in multiple transcript variants, some of which do not encode a protein with a predicted signal peptide.[provided by RefSeq, Aug 2011].

Isoforms & Proteins

3 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
ENST00000358755 O60353 320 230
ENST00000522566 O60353 291 215
ENST00000523739 O60353-2 267 204

Gene Properties

Type
Protein Coding
Chromosome
8
Cytoband
8q22.3
Entrez ID
Aliases
FZ-6FZ6HFZ6NDNC1NDNC10

Recurrent Mutations

All 230 amino-acid changes on canonical ENST00000358755 · 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 FZD6 · 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 FZD6 – 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
Endometrial Carcinoma
3/42 7%
27/612 4%
Glioblastoma
4/98 4%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Cervical Carcinoma
5/35 14%
3/422 1%
Bladder Carcinoma
0/58 0%
17/956 2%
Colorectal Carcinoma
6/143 4%
48/3239 1%
Gastric Carcinoma
1/74 1%
25/1809 1%
Non-Small Cell Lung Carcinoma
13/304 4%
8/1390 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Melanoma
0/210 0%
21/1899 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Other Solid Cancers
3/94 3%
9/1515 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Other Sarcomas
1/69 1%
4/699 1%
Head and Neck Carcinoma
1/85 1%
8/1574 1%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Breast Carcinoma
5/144 3%
12/3264 0%
Osteosarcoma
1/45 2%
0/166 0%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
11/2550 0%
Glioma
0/52 0%
9/2127 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Neuroblastoma
2/87 2%
2/1331 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
5/2534 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Kidney Carcinoma
0/85 0%
5/1862 0%
Prostate Carcinoma
1/13 8%
4/2105 0%
Non-Cancerous
0/104 0%
2/830 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%

Mutation Distribution

Where FZD6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in FZD6 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 878 mutations in FZD6

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