ZMYM1

Zinc finger MYM-type containing 1 Q5SVZ6 ZMYM1_HUMAN
Protein Coding Chr 1 1p34.3 Swiss-Prot reviewed Entrez 79830
Mutations
1,181
CL 169 · Tissue 1,005
Samples
381
CL 77 · Tissue 301
Peptides
320
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
Mutations1,1811691,005
Samples38177301
Peptides32053272

Function

ZMYM1 · Zinc finger MYM-type containing 1

Predicted to enable protein dimerization activity and zinc ion binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000359858 Q5SVZ6 416 319
ENST00000373330 Q5SVZ6 382 307
ENST00000611874 Q5SVZ6 382 307
ENST00000650449 Q5SVZ6 1 1

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p34.3
Entrez ID
Aliases
MYM

Recurrent Mutations

All 319 amino-acid changes on canonical ENST00000359858 · 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 ZMYM1 · 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 ZMYM1 – 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
10/42 24%
23/612 4%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Unknown
1/10 10%
0/29 0%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Squamous Cell Lung Carcinoma
3/57 5%
15/810 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Cervical Carcinoma
2/35 6%
6/422 1%
Melanoma
2/210 1%
32/1899 2%
Bladder Carcinoma
3/58 5%
13/956 1%
Colorectal Carcinoma
11/143 8%
42/3239 1%
Germ Cell Tumour
1/25 4%
2/169 1%
Non-Small Cell Lung Carcinoma
9/304 3%
17/1390 1%
Plasma Cell Myeloma
4/44 9%
0/305 0%
Other Solid Cancers
0/94 0%
17/1515 1%
Gastric Carcinoma
2/74 3%
16/1809 1%
Osteosarcoma
2/45 4%
0/166 0%
Burkitts Lymphoma
2/32 6%
0/196 0%
Other Sarcomas
2/69 3%
4/699 1%
Hepatocellular Carcinoma
0/46 0%
17/2210 1%
Head and Neck Carcinoma
2/85 2%
9/1574 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
15/2550 1%
Neuroendocrine Tumour
3/154 2%
1/577 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Kidney Carcinoma
1/85 1%
9/1862 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Mesothelioma
1/62 2%
0/165 0%
Medulloblastoma
0/0 0%
2/450 0%

Mutation Distribution

Where ZMYM1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZMYM1 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 1,181 mutations in ZMYM1

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