ANO7

Anoctamin 7 Q6IWH7 ANO7_HUMAN
Protein Coding Chr 2 2q37.3 Swiss-Prot reviewed Entrez 50636
Mutations
656
CL 121 · Tissue 520
Samples
540
CL 103 · Tissue 428
Peptides
447
unique mutant peptides
Transcripts
4
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
Mutations656121520
Samples540103428
Peptides44789371

Function

ANO7 · Anoctamin 7

This prostate-specific gene encodes a cytoplasmic protein, as well as a polytopic membrane protein which may serve as a target in prostate cancer diagnosis and immunotherapy. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2011].

Isoforms & Proteins

4 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
ENST00000274979 Q6IWH7 552 385
ENST00000674324 A0A6I8PRE6* 61 55
ENST00000402430 A0A6Q8JTU6* 35 27
ENST00000402530 A0A6Q8JT31* 8 7

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q37.3
Entrez ID
Aliases
D-TMPPDTMPPIPCA-5IPCA5NGEPPCANAP5

Recurrent Mutations

All 385 amino-acid changes on canonical ENST00000274979 · 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 ANO7 · 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 ANO7 – 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
4/40 10%
0/0 0%
Endometrial Carcinoma
14/42 33%
25/612 4%
Acute Myeloid Leukemia
4/90 4%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Acute Monocytic Leukemia
0/1 0%
1/25 4%
Gastrointestinal Stromal Tumour
0/0 0%
4/133 3%
Non-Small Cell Lung Carcinoma
14/304 5%
34/1390 2%
Colorectal Carcinoma
15/143 10%
77/3239 2%
Cervical Carcinoma
0/35 0%
10/422 2%
Melanoma
4/210 2%
42/1899 2%
Gastric Carcinoma
2/74 3%
35/1809 2%
Non-Cancerous
2/104 2%
16/830 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Other Solid Cancers
1/94 1%
25/1515 2%
Squamous Cell Lung Carcinoma
2/57 4%
9/810 1%
Ovarian Carcinoma
5/109 5%
9/998 1%
Bladder Carcinoma
3/58 5%
9/956 1%
Hepatocellular Carcinoma
2/46 4%
23/2210 1%
Small Cell Lung Carcinoma
1/9 11%
7/752 1%
Germ Cell Tumour
2/25 8%
0/169 0%
Glioma
3/52 6%
19/2127 1%
Thyroid Gland Carcinoma
0/45 0%
16/1592 1%
Neuroendocrine Tumour
5/154 3%
2/577 0%
Other Sarcomas
0/69 0%
7/699 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
16/2550 1%
Ewings Sarcoma
1/63 2%
1/262 0%
Head and Neck Carcinoma
0/85 0%
9/1574 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Pancreatic Carcinoma
3/89 3%
5/1611 0%
Burkitts Lymphoma
1/32 3%
0/196 0%

Mutation Distribution

Where ANO7 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ANO7 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 656 mutations in ANO7

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