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 | 1,699 | 152 | 1,512 |
| Samples | 461 | 59 | 391 |
| Peptides | 399 | 46 | 350 |
Function
PHF8 · PHD finger protein 8
The protein encoded by this gene is a histone lysine demethylase that preferentially acts on histones in the monomethyl or dimethyl states. The encoded protein requires Fe(2+) ion, 2-oxoglutarate, and oxygen for its catalytic activity. The protein has an N-terminal PHD finger and a central Jumonji C domain. This gene is thought to function as a transcription activator. Defects in this gene are a cause of syndromic X-linked Siderius type intellectual disability (MRXSSD) and over-expression of this gene is associated with several forms of cancer. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017].
Isoforms & Proteins
4 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.
| Transcript | UniProt | Mutations | Peptides |
|---|---|---|---|
| ENST00000338154 | Q9UPP1-2 | 487 | 356 |
| ENST00000357988 | Q9UPP1 | 462 | 354 |
| ENST00000338946 | A0A8J8YW94* | 382 | 298 |
| ENST00000322659 | Q9UPP1-5 | 368 | 277 |
Gene Properties
Recurrent Mutations
All 356 amino-acid changes on canonical ENST00000338154 · 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 PHF8 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in PHF8 – 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 |
|---|---|---|
| Endometrial Carcinoma | 6/42 14% | 36/612 6% |
| Chronic Myelogenous Leukemia | 1/25 4% | 0/0 0% |
| Acute Myeloid Leukemia | 3/90 3% | 0/0 0% |
| T-Lymphoblastic Leukemia | 1/40 2% | 0/0 0% |
| Other Solid Cancers | 3/94 3% | 34/1515 2% |
| Cervical Carcinoma | 0/35 0% | 10/422 2% |
| Glioblastoma | 2/98 2% | 0/0 0% |
| Melanoma | 5/210 2% | 37/1899 2% |
| Non-Small Cell Lung Carcinoma | 4/304 1% | 24/1390 2% |
| Colorectal Carcinoma | 15/143 10% | 39/3239 1% |
| Gastric Carcinoma | 1/74 1% | 29/1809 2% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 2/133 2% |
| Thyroid Gland Carcinoma | 0/45 0% | 22/1592 1% |
| Small Cell Lung Carcinoma | 1/9 11% | 9/752 1% |
| Squamous Cell Lung Carcinoma | 0/57 0% | 9/810 1% |
| Germ Cell Tumour | 1/25 4% | 1/169 1% |
| Hepatocellular Carcinoma | 0/46 0% | 21/2210 1% |
| Biliary Tract Carcinoma | 0/54 0% | 9/950 1% |
| Bladder Carcinoma | 0/58 0% | 9/956 1% |
| Burkitts Lymphoma | 2/32 6% | 0/196 0% |
| Pancreatic Carcinoma | 0/89 0% | 14/1611 1% |
| Neuroendocrine Tumour | 2/154 1% | 4/577 1% |
| Ovarian Carcinoma | 0/109 0% | 9/998 1% |
| Hodgkins Lymphoma | 1/16 6% | 0/122 0% |
| Breast Carcinoma | 3/144 2% | 19/3264 1% |
| Ewings Sarcoma | 2/63 3% | 0/262 0% |
| Plasma Cell Myeloma | 0/44 0% | 2/305 1% |
| Head and Neck Carcinoma | 2/85 2% | 7/1574 0% |
| B-Lymphoblastic Leukemia | 4/55 7% | 7/2640 0% |
| Glioma | 0/52 0% | 9/2127 0% |
Mutation Distribution
Where PHF8 is mutated · all tissues, split by cell line vs tissue
How many mutations in PHF8 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 1,699 mutations in PHF8
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 |
|---|