ANKK1

Ankyrin repeat and kinase domain containing 1 Q8NFD2 ANKK1_HUMAN
Protein Coding Chr 11 11q23.2 Swiss-Prot reviewed Entrez 255239
Mutations
437
CL 79 · Tissue 346
Samples
393
CL 74 · Tissue 307
Peptides
304
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
Mutations43779346
Samples39374307
Peptides30448259

Function

ANKK1 · Ankyrin repeat and kinase domain containing 1

The protein encoded by this gene belongs to the Ser/Thr protein kinase family, and protein kinase superfamily involved in signal transduction pathways. This gene is closely linked to DRD2 gene (GeneID:1813) on chr 11, and a well studied restriction fragment length polymorphism (RFLP) designated TaqIA, was originally associated with the DRD2 gene, however, later was determined to be located in exon 8 of ANKK1 gene (PMIDs: 18621654, 15146457), where it causes a nonconservative amino acid substitution. It is not clear if this gene plays any role in neuropsychiatric disorders previously associated with Taq1A RFLP. [provided by RefSeq, Sep 2009].

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
ENST00000303941 Q8NFD2 437 304

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q23.2
Entrez ID
Aliases
PKK2sgK288

Recurrent Mutations

All 304 amino-acid changes on canonical ENST00000303941 · 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 ANKK1 · 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 ANKK1 – 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-Cell Non-Hodgkins Lymphoma
2/26 8%
0/0 0%
T-Lymphoblastic Leukemia
3/40 8%
0/0 0%
Endometrial Carcinoma
2/42 5%
18/612 3%
Melanoma
5/210 2%
50/1899 3%
Non-Small Cell Lung Carcinoma
17/304 6%
27/1390 2%
Unknown
0/10 0%
1/29 3%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Colorectal Carcinoma
12/143 8%
44/3239 1%
Ewings Sarcoma
4/63 6%
0/262 0%
Gastric Carcinoma
3/74 4%
20/1809 1%
Squamous Cell Lung Carcinoma
3/57 5%
7/810 1%
Esophageal Carcinoma
0/23 0%
9/769 1%
Glioblastoma
1/98 1%
0/0 0%
Hepatocellular Carcinoma
2/46 4%
20/2210 1%
Neuroendocrine Tumour
4/154 3%
3/577 1%
Osteosarcoma
2/45 4%
0/166 0%
Thyroid Gland Carcinoma
1/45 2%
14/1592 1%
Plasma Cell Myeloma
1/44 2%
2/305 1%
Other Solid Cancers
0/94 0%
12/1515 1%
Other Sarcomas
0/69 0%
5/699 1%
Ovarian Carcinoma
3/109 3%
4/998 0%
Biliary Tract Carcinoma
0/54 0%
6/950 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Bladder Carcinoma
1/58 2%
4/956 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Non-Cancerous
0/104 0%
4/830 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
11/2534 0%
Head and Neck Carcinoma
1/85 1%
6/1574 0%
Kidney Carcinoma
1/85 1%
7/1862 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%

Mutation Distribution

Where ANKK1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ANKK1 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 437 mutations in ANKK1

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