ANKS6

Ankyrin repeat and sterile alpha motif domain containing 6 Q68DC2 ANKS6_HUMAN
Protein Coding Chr 9 9q22.33 Swiss-Prot reviewed Entrez 203286
Mutations
755
CL 128 · Tissue 612
Samples
419
CL 84 · Tissue 324
Peptides
310
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
Mutations755128612
Samples41984324
Peptides31069248

Function

ANKS6 · Ankyrin repeat and sterile alpha motif domain containing 6

This gene encodes a protein containing multiple ankyrin repeats and a SAM domain. It is thought that this protein may localize to the proximal region of the primary cilium, and may play a role in renal and cardiovascular development. Mutations in this gene have been shown to cause a form of nephronophthisis (NPHP16), a chronic tubulo-interstitial nephritis. [provided by RefSeq, Jul 2015].

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
ENST00000353234 Q68DC2 445 300
ENST00000375019 A0A0A0MRS7* 309 212
ENST00000444472 H7C163* 1 1

Gene Properties

Type
Protein Coding
Chromosome
9
Cytoband
9q22.33
Entrez ID
Aliases
ANKRD14NPHP16PKDR1SAMD6

Recurrent Mutations

All 300 amino-acid changes on canonical ENST00000353234 · 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 ANKS6 · 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 ANKS6 – 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
3/40 8%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Endometrial Carcinoma
6/42 14%
18/612 3%
Colorectal Carcinoma
13/143 9%
52/3239 2%
Melanoma
2/210 1%
34/1899 2%
Gastric Carcinoma
1/74 1%
31/1809 2%
Hodgkins Lymphoma
1/16 6%
1/122 1%
Pheochromocytoma and Paraganglioma
0/0 0%
1/71 1%
Other Solid Cancers
1/94 1%
21/1515 1%
Bladder Carcinoma
2/58 3%
11/956 1%
Esophageal Squamous Cell Carcinoma
3/51 6%
25/2550 1%
Other Sarcomas
2/69 3%
6/699 1%
Glioblastoma
1/98 1%
0/0 0%
Non-Small Cell Lung Carcinoma
6/304 2%
11/1390 1%
Neuroendocrine Tumour
6/154 4%
1/577 0%
Squamous Cell Lung Carcinoma
2/57 4%
5/810 1%
Ovarian Carcinoma
5/109 5%
4/998 0%
Meningioma
0/3 0%
2/252 1%
Non-Cancerous
2/104 2%
5/830 1%
Biliary Tract Carcinoma
4/54 7%
3/950 0%
Thyroid Gland Carcinoma
0/45 0%
11/1592 1%
Kidney Carcinoma
2/85 2%
10/1862 1%
Head and Neck Carcinoma
1/85 1%
9/1574 1%
Plasma Cell Myeloma
0/44 0%
2/305 1%
Hepatocellular Carcinoma
1/46 2%
11/2210 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Breast Carcinoma
5/144 3%
11/3264 0%
B-Cell Non-Hodgkins Lymphoma
4/88 5%
8/2534 0%
Mesothelioma
1/62 2%
0/165 0%

Mutation Distribution

Where ANKS6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ANKS6 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 755 mutations in ANKS6

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