ZFY

Zinc finger protein Y-linked P08048 ZFY_HUMAN
Protein Coding Chr Y Yp11.2 Swiss-Prot reviewed Entrez 7544
Mutations
350
CL 36 · Tissue 311
Samples
100
CL 16 · Tissue 81
Peptides
91
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
Mutations35036311
Samples1001681
Peptides911080

Function

ZFY · Zinc finger protein Y-linked

This gene encodes a zinc finger-containing protein that may function as a transcription factor. This gene was once a candidate gene for the testis-determining factor (TDF) and was erroneously referred to as TDF. [provided by RefSeq, Jul 2008].

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
ENST00000155093 P08048 100 81
ENST00000383052 P08048 94 79
ENST00000449237 P08048-3 84 70
ENST00000625061 P08048-2 72 59

Gene Properties

Type
Protein Coding
Chromosome
Y
Cytoband
Yp11.2
Entrez ID
Aliases
ZNF911

Recurrent Mutations

All 81 amino-acid changes on canonical ENST00000155093 · 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 ZFY · 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 ZFY – 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
2/40 5%
0/0 0%
Burkitts Lymphoma
2/32 6%
0/196 0%
Bladder Carcinoma
0/58 0%
7/956 1%
Melanoma
2/210 1%
12/1899 1%
Non-Small Cell Lung Carcinoma
4/304 1%
7/1390 0%
Other Solid Cancers
0/94 0%
9/1515 1%
Head and Neck Carcinoma
3/85 4%
3/1574 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Colorectal Carcinoma
0/143 0%
10/3239 0%
Kidney Carcinoma
1/85 1%
4/1862 0%
Prostate Carcinoma
0/13 0%
5/2105 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Non-Cancerous
0/104 0%
2/830 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%
Gastric Carcinoma
0/74 0%
3/1809 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Pancreatic Carcinoma
0/89 0%
2/1611 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
1/2550 0%
Glioma
0/52 0%
1/2127 0%
Other Blood Cancers
0/61 0%
1/2725 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in ZFY 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 350 mutations in ZFY

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