ZNF189

Zinc finger protein 189 O75820 ZN189_HUMAN
Protein Coding Chr 9 9q31.1 Swiss-Prot reviewed Entrez 7743
Mutations
846
CL 150 · Tissue 693
Samples
280
CL 66 · Tissue 211
Peptides
247
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
Mutations846150693
Samples28066211
Peptides24757197

Function

ZNF189 · Zinc finger protein 189

Kruppel-like zinc finger proteins such as ZNF189 contain a conserved stretch of 7 amino acids that connects a variable number of DNA-binding zinc finger repeats of the cys(2)his(2) (C2H2) type (summarized by Odeberg et al., 1998 [PubMed 9653648]). Approximately 30% of human Kruppel-like zinc finger proteins contain an N-terminal Kruppel-associated box (KRAB) domain. The KRAB domain consists of approximately 75 amino acids that may be subdivided into an A box, which is present in every KRAB domain and is essential for transcriptional repression, and a B box, which is not always present.[supplied by OMIM, May 2010].

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
ENST00000339664 O75820 305 217
ENST00000374861 O75820-2 264 203
ENST00000259395 O75820-4 246 190
ENST00000615466 A0A087X0K2* 31 21

Gene Properties

Type
Protein Coding
Chromosome
9
Cytoband
9q31.1
Entrez ID

Recurrent Mutations

All 217 amino-acid changes on canonical ENST00000339664 · 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 ZNF189 · 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 ZNF189 – 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%
Endometrial Carcinoma
4/42 10%
20/612 3%
Glioblastoma
3/98 3%
0/0 0%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Germ Cell Tumour
0/25 0%
3/169 2%
Pheochromocytoma and Paraganglioma
0/0 0%
1/71 1%
Melanoma
9/210 4%
19/1899 1%
Esophageal Squamous Cell Carcinoma
3/51 6%
27/2550 1%
Colorectal Carcinoma
5/143 4%
33/3239 1%
Cervical Carcinoma
0/35 0%
5/422 1%
Neuroendocrine Tumour
4/154 3%
4/577 1%
Squamous Cell Lung Carcinoma
3/57 5%
6/810 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Bladder Carcinoma
1/58 2%
6/956 1%
Other Solid Cancers
4/94 4%
7/1515 0%
Medulloblastoma
0/0 0%
3/450 1%
Head and Neck Carcinoma
1/85 1%
10/1574 1%
Non-Small Cell Lung Carcinoma
2/304 1%
9/1390 1%
Ovarian Carcinoma
3/109 3%
4/998 0%
Gastric Carcinoma
2/74 3%
8/1809 0%
Other Sarcomas
0/69 0%
4/699 1%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Osteosarcoma
1/45 2%
0/166 0%
Mesothelioma
0/62 0%
1/165 1%
Non-Cancerous
1/104 1%
3/830 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
B-Cell Non-Hodgkins Lymphoma
6/88 7%
4/2534 0%
Prostate Carcinoma
0/13 0%
8/2105 0%
Ewings Sarcoma
0/63 0%
1/262 0%

Mutation Distribution

Where ZNF189 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZNF189 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 846 mutations in ZNF189

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