ZNF180

Zinc finger protein 180 Q9UJW8 ZN180_HUMAN
Protein Coding Chr 19 19q13.31 Swiss-Prot reviewed Entrez 7733
Mutations
1,168
CL 128 · Tissue 1,035
Samples
362
CL 58 · Tissue 301
Peptides
305
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
Mutations1,1681281,035
Samples36258301
Peptides30542274

Function

ZNF180 · Zinc finger protein 180

Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See MIM 604749 for additional information on zinc finger proteins.[supplied by OMIM, Jul 2002].

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
ENST00000592529 Q9UJW8-2 399 261
ENST00000221327 Q9UJW8 381 265
ENST00000391956 Q9UJW8-3 362 248
ENST00000587047 K7ES30* 26 22

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.31
Entrez ID
Aliases
HHZ168

Recurrent Mutations

All 261 amino-acid changes on canonical ENST00000592529 · 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 ZNF180 · 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 ZNF180 – 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
4/40 10%
0/0 0%
Endometrial Carcinoma
3/42 7%
30/612 5%
Unknown
1/10 10%
0/29 0%
Colorectal Carcinoma
14/143 10%
47/3239 1%
Bladder Carcinoma
0/58 0%
18/956 2%
Melanoma
2/210 1%
31/1899 2%
Squamous Cell Lung Carcinoma
2/57 4%
9/810 1%
Non-Small Cell Lung Carcinoma
5/304 2%
14/1390 1%
Chondrosarcoma
1/14 7%
0/75 0%
Cervical Carcinoma
0/35 0%
5/422 1%
Glioblastoma
1/98 1%
0/0 0%
Head and Neck Carcinoma
1/85 1%
14/1574 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Other Solid Cancers
0/94 0%
14/1515 1%
Gastric Carcinoma
0/74 0%
15/1809 1%
Other Sarcomas
2/69 3%
4/699 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
20/2550 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Biliary Tract Carcinoma
0/54 0%
7/950 1%
Breast Carcinoma
7/144 5%
17/3264 1%
Ewings Sarcoma
0/63 0%
2/262 1%
Neuroendocrine Tumour
4/154 3%
0/577 0%
Ovarian Carcinoma
2/109 2%
4/998 0%
Hepatocellular Carcinoma
1/46 2%
11/2210 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Medulloblastoma
0/0 0%
2/450 0%
Thyroid Gland Carcinoma
0/45 0%
7/1592 0%
Kidney Carcinoma
1/85 1%
7/1862 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%

Mutation Distribution

Where ZNF180 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZNF180 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 1,168 mutations in ZNF180

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