SMYD5

SMYD family member 5 Q6GMV2 SMYD5_HUMAN
Protein Coding Chr 2 2p13.2 Swiss-Prot reviewed Entrez 10322
Mutations
210
CL 38 · Tissue 168
Samples
176
CL 35 · Tissue 137
Peptides
144
unique mutant peptides
Transcripts
2
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
Mutations21038168
Samples17635137
Peptides14419123

Function

SMYD5 · SMYD family member 5

Predicted to enable histone methyltransferase activity (H4-K20 specific). Involved in negative regulation of transposition and regulation of stem cell differentiation. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

2 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
ENST00000389501 Q6GMV2 181 139
ENST00000629411 F8WEJ9* 29 23

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2p13.2
Entrez ID
Aliases
NN8-4AGRAI15RRG1ZMYND23

Recurrent Mutations

All 139 amino-acid changes on canonical ENST00000389501 · 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 SMYD5 · 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 SMYD5 – 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
Endometrial Carcinoma
0/42 0%
12/612 2%
Burkitts Lymphoma
3/32 9%
0/196 0%
Colorectal Carcinoma
14/143 10%
27/3239 1%
Non-Small Cell Lung Carcinoma
9/304 3%
9/1390 1%
Head and Neck Carcinoma
2/85 2%
11/1574 1%
Gastric Carcinoma
0/74 0%
11/1809 1%
Melanoma
0/210 0%
12/1899 1%
Osteosarcoma
0/45 0%
1/166 1%
Other Solid Cancers
0/94 0%
7/1515 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Biliary Tract Carcinoma
1/54 2%
3/950 0%
Other Sarcomas
0/69 0%
3/699 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Non-Cancerous
0/104 0%
3/830 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Pancreatic Carcinoma
1/89 1%
4/1611 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
Kidney Carcinoma
0/85 0%
5/1862 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Glioma
0/52 0%
5/2127 0%
Breast Carcinoma
2/144 1%
3/3264 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
B-Cell Non-Hodgkins Lymphoma
3/88 3%
0/2534 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
Other Blood Cancers
0/61 0%
1/2725 0%

Mutation Distribution

Where SMYD5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in SMYD5 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 210 mutations in SMYD5

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