EDARADD

EDAR associated via death domain Q8WWZ3 EDAD_HUMAN
Protein Coding Chr 1 1q42.3-q43 Swiss-Prot reviewed Entrez 128178
Mutations
469
CL 28 · Tissue 438
Samples
182
CL 20 · Tissue 161
Peptides
127
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
Mutations46928438
Samples18220161
Peptides12712114

Function

EDARADD · EDAR associated via death domain

This gene was identified by its association with ectodermal dysplasia, a genetic disorder characterized by defective development of hair, teeth, and eccrine sweat glands. The protein encoded by this gene is a death domain-containing protein, and is found to interact with EDAR, a death domain receptor known to be required for the development of hair, teeth and other ectodermal derivatives. This protein and EDAR are coexpressed in epithelial cells during the formation of hair follicles and teeth. Through its interaction with EDAR, this protein acts as an adaptor, and links the receptor to downstream signaling pathways. Two alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008].

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
ENST00000334232 Q8WWZ3 179 114
ENST00000359362 Q8WWZ3-2 148 103
ENST00000637660 A0A1B0GV26* 142 98

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q42.3-q43
Entrez ID
Aliases
CRECTD11AECTD11BED3EDA3

Recurrent Mutations

All 114 amino-acid changes on canonical ENST00000334232 · 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 EDARADD · 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 EDARADD – 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%
Melanoma
4/210 2%
22/1899 1%
Chondrosarcoma
0/14 0%
1/75 1%
Endometrial Carcinoma
0/42 0%
7/612 1%
Non-Small Cell Lung Carcinoma
3/304 1%
13/1390 1%
Non-Cancerous
0/104 0%
8/830 1%
Neuroendocrine Tumour
3/154 2%
3/577 1%
Squamous Cell Lung Carcinoma
3/57 5%
3/810 0%
Colorectal Carcinoma
2/143 1%
19/3239 1%
Ewings Sarcoma
0/63 0%
2/262 1%
Other Sarcomas
0/69 0%
4/699 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Cervical Carcinoma
0/35 0%
2/422 0%
Hepatocellular Carcinoma
1/46 2%
8/2210 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Glioma
0/52 0%
8/2127 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
7/2550 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Other Solid Cancers
1/94 1%
4/1515 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Ovarian Carcinoma
0/109 0%
3/998 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Medulloblastoma
0/0 0%
1/450 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
4/2534 0%
Prostate Carcinoma
1/13 8%
2/2105 0%
Breast Carcinoma
0/144 0%
4/3264 0%
B-Lymphoblastic Leukemia
0/55 0%
3/2640 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in EDARADD 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 469 mutations in EDARADD

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