Stats by Source
Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)
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.
| Total | Cell line | Tissue | |
|---|---|---|---|
| Mutations | 2,626 | 405 | 2,181 |
| Samples | 1,277 | 238 | 1,017 |
| Peptides | 1,075 | 191 | 897 |
Function
AKAP6 · A-kinase anchoring protein 6
The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. The encoded protein is highly expressed in various brain regions and cardiac and skeletal muscle. It is specifically localized to the sarcoplasmic reticulum and nuclear membrane, and is involved in anchoring PKA to the nuclear membrane or sarcoplasmic reticulum. [provided by RefSeq, Jul 2008].
Isoforms & Proteins
3 transcripts · UniProt mapping is sequence-verified (AA-safe)
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.
Gene Properties
Recurrent Mutations
All 1040 amino-acid changes on canonical ENST00000280979 · needle height = samples · drag the mini-map to zoom
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 AKAP6 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in AKAP6 – 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 type | Cell lines | Tissue samples |
|---|---|---|
| T-Lymphoblastic Leukemia | 13/40 32% | 0/0 0% |
| T-Cell Non-Hodgkins Lymphoma | 4/26 15% | 0/0 0% |
| Endometrial Carcinoma | 10/42 24% | 49/612 8% |
| Melanoma | 13/210 6% | 163/1899 9% |
| Chronic Myelogenous Leukemia | 2/25 8% | 0/0 0% |
| Non-Small Cell Lung Carcinoma | 24/304 8% | 74/1390 5% |
| Unknown | 0/10 0% | 2/29 7% |
| Glioblastoma | 5/98 5% | 0/0 0% |
| Squamous Cell Lung Carcinoma | 7/57 12% | 36/810 4% |
| Other Solid Cancers | 9/94 10% | 69/1515 5% |
| Colorectal Carcinoma | 30/143 21% | 130/3239 4% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 6/133 5% |
| Acute Myeloid Leukemia | 4/90 4% | 0/0 0% |
| Neuroendocrine Tumour | 17/154 11% | 15/577 3% |
| Bladder Carcinoma | 3/58 5% | 40/956 4% |
| Gastric Carcinoma | 6/74 8% | 69/1809 4% |
| Oral Cavity Carcinoma | 2/54 4% | 0/0 0% |
| Hodgkins Lymphoma | 0/16 0% | 5/122 4% |
| Germ Cell Tumour | 2/25 8% | 5/169 3% |
| Esophageal Carcinoma | 0/23 0% | 25/769 3% |
| Small Cell Lung Carcinoma | 2/9 22% | 21/752 3% |
| Ovarian Carcinoma | 8/109 7% | 22/998 2% |
| Cervical Carcinoma | 2/35 6% | 10/422 2% |
| Head and Neck Carcinoma | 7/85 8% | 31/1574 2% |
| Other Sarcomas | 3/69 4% | 13/699 2% |
| Adrenocortical Carcinoma | 1/3 33% | 1/112 1% |
| Plasma Cell Myeloma | 1/44 2% | 5/305 2% |
| Esophageal Squamous Cell Carcinoma | 7/51 14% | 35/2550 1% |
| Rhabdomyosarcoma | 1/33 3% | 2/171 1% |
| Breast Carcinoma | 15/144 10% | 34/3264 1% |
Mutation Distribution
Where AKAP6 is mutated · all tissues, split by cell line vs tissue
How many mutations in AKAP6 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
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 2,626 mutations in AKAP6
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.
| ID | Sample | Transcript | AA Change | CDS | Type | Source | Mutant Peptide | Wild-type Peptide |
|---|