FZD7

Frizzled class receptor 7 O75084 FZD7_HUMAN
Protein Coding Chr 2 2q33.1 Swiss-Prot reviewed Entrez 8324
Mutations
365
CL 80 · Tissue 275
Samples
334
CL 78 · Tissue 252
Peptides
255
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
Mutations36580275
Samples33478252
Peptides25552205

Function

FZD7 · Frizzled class receptor 7

Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD7 protein contains an N-terminal signal sequence, 10 cysteine residues typical of the cysteine-rich extracellular domain of Fz family members, 7 putative transmembrane domains, and an intracellular C-terminal tail with a PDZ domain-binding motif. FZD7 gene expression may downregulate APC function and enhance beta-catenin-mediated signals in poorly differentiated human esophageal carcinomas. [provided by RefSeq, Jul 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
ENST00000286201 O75084 365 255

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q33.1
Entrez ID
Aliases
FzE3

Recurrent Mutations

All 254 amino-acid changes on canonical ENST00000286201 · 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 FZD7 · 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 FZD7 – 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
5/40 12%
0/0 0%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
12/42 29%
16/612 3%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Colorectal Carcinoma
12/143 8%
53/3239 2%
Gastric Carcinoma
2/74 3%
26/1809 1%
Non-Small Cell Lung Carcinoma
15/304 5%
10/1390 1%
Melanoma
5/210 2%
25/1899 1%
Bladder Carcinoma
0/58 0%
11/956 1%
Osteosarcoma
2/45 4%
0/166 0%
Esophageal Squamous Cell Carcinoma
4/51 8%
20/2550 1%
Other Sarcomas
2/69 3%
5/699 1%
Non-Cancerous
1/104 1%
7/830 1%
Esophageal Carcinoma
1/23 4%
5/769 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Ovarian Carcinoma
0/109 0%
7/998 1%
Squamous Cell Lung Carcinoma
0/57 0%
5/810 1%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Neuroendocrine Tumour
3/154 2%
1/577 0%
Thyroid Gland Carcinoma
1/45 2%
7/1592 0%
Head and Neck Carcinoma
1/85 1%
7/1574 0%
Other Solid Cancers
1/94 1%
6/1515 0%
Glioma
0/52 0%
8/2127 0%
Hepatocellular Carcinoma
0/46 0%
7/2210 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Kidney Carcinoma
1/85 1%
4/1862 0%
Medulloblastoma
0/0 0%
1/450 0%
Neuroblastoma
0/87 0%
3/1331 0%
Breast Carcinoma
2/144 1%
5/3264 0%

Mutation Distribution

Where FZD7 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in FZD7 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 365 mutations in FZD7

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