CELSR2

Cadherin EGF LAG seven-pass G-type receptor 2 Q9HCU4 CELR2_HUMAN
Protein Coding Chr 1 1p13.3 Swiss-Prot reviewed Entrez 1952
Mutations
1,552
CL 401 · Tissue 1,087
Samples
1,255
CL 324 · Tissue 915
Peptides
1,086
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
Mutations1,5524011,087
Samples1,255324915
Peptides1,086209865

Function

CELSR2 · Cadherin EGF LAG seven-pass G-type receptor 2

The protein encoded by this gene is a member of the flamingo subfamily, part of the cadherin superfamily. The flamingo subfamily consists of nonclassic-type cadherins; a subpopulation that does not interact with catenins. The flamingo cadherins are located at the plasma membrane and have nine cadherin domains, seven epidermal growth factor-like repeats and two laminin A G-type repeats in their ectodomain. They also have seven transmembrane domains, a characteristic unique to this subfamily. It is postulated that these proteins are receptors involved in contact-mediated communication, with cadherin domains acting as homophilic binding regions and the EGF-like domains involved in cell adhesion and receptor-ligand interactions. The specific function of this particular member has not been determined. [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
ENST00000271332 Q9HCU4 1,552 1,086

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p13.3
Entrez ID
Aliases
ADGRC2CDHF10EGFL2Flamingo1MEGF3

Recurrent Mutations

All 1086 amino-acid changes on canonical ENST00000271332 · 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 CELSR2 · 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 CELSR2 – 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
12/40 30%
0/0 0%
Chronic Myelogenous Leukemia
6/25 24%
0/0 0%
Endometrial Carcinoma
19/42 45%
55/612 9%
Glioblastoma
11/98 11%
0/0 0%
Acute Myeloid Leukemia
8/90 9%
0/0 0%
Oral Cavity Carcinoma
4/54 7%
0/0 0%
Non-Small Cell Lung Carcinoma
42/304 14%
48/1390 3%
Colorectal Carcinoma
33/143 23%
146/3239 5%
Gastric Carcinoma
10/74 14%
82/1809 5%
Melanoma
20/210 10%
82/1899 4%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Other Solid Cancers
4/94 4%
52/1515 3%
Squamous Cell Lung Carcinoma
4/57 7%
25/810 3%
Cervical Carcinoma
2/35 6%
13/422 3%
Bladder Carcinoma
9/58 16%
24/956 3%
Germ Cell Tumour
2/25 8%
4/169 2%
Hodgkins Lymphoma
2/16 12%
2/122 2%
Plasma Cell Myeloma
6/44 14%
4/305 1%
Neuroendocrine Tumour
13/154 8%
8/577 1%
Pheochromocytoma and Paraganglioma
0/0 0%
2/71 3%
Head and Neck Carcinoma
10/85 12%
31/1574 2%
Ovarian Carcinoma
13/109 12%
14/998 1%
Biliary Tract Carcinoma
3/54 6%
20/950 2%
Esophageal Carcinoma
0/23 0%
18/769 2%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Other Sarcomas
6/69 9%
11/699 2%
Mesothelioma
4/62 6%
1/165 1%
Non-Cancerous
6/104 6%
13/830 2%
Prostate Carcinoma
2/13 15%
31/2105 1%
Ewings Sarcoma
3/63 5%
2/262 1%

Mutation Distribution

Where CELSR2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CELSR2 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 1,552 mutations in CELSR2

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