ZNF185

Zinc finger protein 185 with LIM domain O15231 ZN185_HUMAN
Protein Coding Chr X Xq28 Swiss-Prot reviewed Entrez 7739
Mutations
1,679
CL 259 · Tissue 1,406
Samples
313
CL 80 · Tissue 228
Peptides
347
unique mutant peptides
Transcripts
9
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
Mutations1,6792591,406
Samples31380228
Peptides34773285

Function

ZNF185 · Zinc finger protein 185 with LIM domain

Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a LIM-domain zinc finger protein. The LIM domain is composed of two contiguous zinc finger domains, separated by a two-amino acid residue hydrophobic linker. The LIM domain mediates protein:protein interactions. Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, May 2010].

Isoforms & Proteins

9 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
ENST00000535861 O15231-6 281 224
ENST00000449285 O15231-3 264 211
ENST00000370268 O15231 257 205
ENST00000539731 O15231-8 255 202
ENST00000318504 O15231-4 238 191
ENST00000318529 O15231-5 201 160
ENST00000454925 O15231-9 141 118
ENST00000695776 A0A8Q3WKR1* 39 35
ENST00000710013 O15231 3 3

Gene Properties

Type
Protein Coding
Chromosome
X
Cytoband
Xq28
Entrez ID
Aliases
SCELL

Recurrent Mutations

All 224 amino-acid changes on canonical ENST00000535861 · 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 ZNF185 · 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 ZNF185 – 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
Oral Cavity Carcinoma
6/54 11%
0/0 0%
T-Lymphoblastic Leukemia
4/40 10%
0/0 0%
Acute Myeloid Leukemia
4/90 4%
0/0 0%
Endometrial Carcinoma
3/42 7%
19/612 3%
Unknown
0/10 0%
1/29 3%
Glioblastoma
2/98 2%
0/0 0%
Melanoma
9/210 4%
27/1899 1%
Germ Cell Tumour
2/25 8%
1/169 1%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Other Sarcomas
2/69 3%
8/699 1%
Colorectal Carcinoma
13/143 9%
28/3239 1%
Cervical Carcinoma
0/35 0%
5/422 1%
Non-Small Cell Lung Carcinoma
7/304 2%
11/1390 1%
Squamous Cell Lung Carcinoma
2/57 4%
6/810 1%
Adrenocortical Carcinoma
1/3 33%
0/112 0%
Plasma Cell Myeloma
1/44 2%
2/305 1%
Other Solid Cancers
2/94 2%
11/1515 1%
Gastric Carcinoma
3/74 4%
12/1809 1%
Thyroid Gland Carcinoma
1/45 2%
12/1592 1%
Ovarian Carcinoma
4/109 4%
4/998 0%
Biliary Tract Carcinoma
0/54 0%
7/950 1%
Medulloblastoma
0/0 0%
3/450 1%
Esophageal Carcinoma
0/23 0%
5/769 1%
Hepatocellular Carcinoma
0/46 0%
13/2210 1%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Bladder Carcinoma
0/58 0%
5/956 1%
Head and Neck Carcinoma
1/85 1%
7/1574 0%
Osteosarcoma
1/45 2%
0/166 0%
Breast Carcinoma
3/144 2%
12/3264 0%
Non-Cancerous
0/104 0%
3/830 0%

Mutation Distribution

Where ZNF185 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZNF185 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 1,679 mutations in ZNF185

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