ZFAND6

Zinc finger AN1-type containing 6 Q6FIF0 ZFAN6_HUMAN
Protein Coding Chr 15 15q25.1 Swiss-Prot reviewed Entrez 54469
Mutations
820
CL 43 · Tissue 766
Samples
85
CL 13 · Tissue 71
Peptides
80
unique mutant peptides
Transcripts
11
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
Mutations82043766
Samples851371
Peptides801171

Function

ZFAND6 · Zinc finger AN1-type containing 6

Predicted to enable polyubiquitin modification-dependent protein binding activity. Involved in cellular response to tumor necrosis factor; negative regulation of apoptotic process; and regulation of I-kappaB kinase/NF-kappaB signaling. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

11 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
ENST00000261749 Q6FIF0 84 64
ENST00000561060 Q6FIF0 76 61
ENST00000558087 Q6FIF0 75 60
ENST00000558494 Q6FIF0 75 60
ENST00000559775 Q6FIF0 75 60
ENST00000559835 Q6FIF0 75 60
ENST00000613266 Q6FIF0 75 60
ENST00000616533 Q6FIF0 75 60
ENST00000618205 Q6FIF0 75 60
ENST00000559157 Q6FIF0-2 72 58
ENST00000558688 H0YK54* 63 49

Gene Properties

Type
Protein Coding
Chromosome
15
Cytoband
15q25.1
Entrez ID
Aliases
AWP1ZA20D3ZFAND5B

Recurrent Mutations

All 64 amino-acid changes on canonical ENST00000261749 · 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 ZFAND6 · 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 ZFAND6 – 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
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Melanoma
2/210 1%
11/1899 1%
Endometrial Carcinoma
0/42 0%
4/612 1%
Squamous Cell Lung Carcinoma
0/57 0%
5/810 1%
Other Solid Cancers
3/94 3%
6/1515 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Bladder Carcinoma
0/58 0%
4/956 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Non-Small Cell Lung Carcinoma
0/304 0%
6/1390 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Glioma
2/52 4%
2/2127 0%
Breast Carcinoma
2/144 1%
4/3264 0%
Colorectal Carcinoma
0/143 0%
5/3239 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Non-Cancerous
0/104 0%
1/830 0%
Gastric Carcinoma
0/74 0%
2/1809 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Kidney Carcinoma
0/85 0%
1/1862 0%

Mutation Distribution

Where ZFAND6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZFAND6 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 820 mutations in ZFAND6

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