WAC

WW domain containing adaptor with coiled-coil Q9BTA9 WAC_HUMAN
Protein Coding Chr 10 10p12.1|10p12.1-p11.2 Swiss-Prot reviewed Entrez 51322
Mutations
1,009
CL 122 · Tissue 853
Samples
276
CL 47 · Tissue 217
Peptides
255
unique mutant peptides
Transcripts
6
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
Mutations1,009122853
Samples27647217
Peptides25540218

Function

WAC · WW domain containing adaptor with coiled-coil

The protein encoded by this gene contains a WW domain, which is a protein module found in a wide range of signaling proteins. This domain mediates protein-protein interactions and binds proteins containing short linear peptide motifs that are proline-rich or contain at least one proline. This gene product shares 94% sequence identity with the WAC protein in mouse, however, its exact function is not known. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008].

Isoforms & Proteins

6 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
ENST00000354911 Q9BTA9 307 234
ENST00000375664 Q9BTA9-2 258 204
ENST00000347934 Q9BTA9-5 228 186
ENST00000375646 A0A0A0MRT2* 212 171
ENST00000628285 A0A0D9SFY7* 3 2
ENST00000428935 A0A0A0MSR1* 1 1

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10p12.1|10p12.1-p11.2
Entrez ID
Aliases
BM-016DESSHPRO1741Wwp4

Recurrent Mutations

All 234 amino-acid changes on canonical ENST00000354911 · 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 WAC · 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 WAC – 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%
Endometrial Carcinoma
5/42 12%
16/612 3%
Unknown
0/10 0%
1/29 3%
Bladder Carcinoma
2/58 3%
13/956 1%
Squamous Cell Lung Carcinoma
3/57 5%
9/810 1%
Burkitts Lymphoma
3/32 9%
0/196 0%
Non-Small Cell Lung Carcinoma
2/304 1%
19/1390 1%
Melanoma
2/210 1%
22/1899 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Cervical Carcinoma
0/35 0%
5/422 1%
Colorectal Carcinoma
6/143 4%
31/3239 1%
Rhabdomyosarcoma
0/33 0%
2/171 1%
Osteosarcoma
1/45 2%
1/166 1%
Head and Neck Carcinoma
2/85 2%
12/1574 1%
Gastric Carcinoma
0/74 0%
13/1809 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Other Sarcomas
2/69 3%
3/699 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Non-Cancerous
0/104 0%
4/830 0%
Glioma
0/52 0%
9/2127 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Meningioma
1/3 33%
0/252 0%
Breast Carcinoma
2/144 1%
11/3264 0%
Other Solid Cancers
0/94 0%
6/1515 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
6/2534 0%
Hepatocellular Carcinoma
0/46 0%
7/2210 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Kidney Carcinoma
0/85 0%
6/1862 0%
Neuroendocrine Tumour
1/154 1%
1/577 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in WAC 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 1,009 mutations in WAC

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