GLOD5

Glyoxalase domain containing 5 A6NK44 GLOD5_HUMAN
Protein Coding Chr X Xp11.23 Swiss-Prot reviewed Entrez 392465
Mutations
88
CL 26 · Tissue 61
Samples
87
CL 25 · Tissue 61
Peptides
66
unique mutant peptides
Transcripts
1
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
Mutations882661
Samples872561
Peptides661853

Function

GLOD5 · Glyoxalase domain containing 5

This gene encodes a protein with a glyoxalase domain. [provided by RefSeq, Sep 2011].

Isoforms & Proteins

1 transcript · 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
ENST00000303227 A6NK44 88 66

Gene Properties

Type
Protein Coding
Chromosome
X
Cytoband
Xp11.23
Entrez ID

Recurrent Mutations

All 66 amino-acid changes on canonical ENST00000303227 · 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 GLOD5 · 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 GLOD5 – 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
3/40 8%
0/0 0%
Endometrial Carcinoma
2/42 5%
6/612 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Melanoma
1/210 0%
12/1899 1%
Other Solid Cancers
1/94 1%
6/1515 0%
Bladder Carcinoma
0/58 0%
4/956 0%
Colorectal Carcinoma
8/143 6%
5/3239 0%
Non-Small Cell Lung Carcinoma
1/304 0%
4/1390 0%
Biliary Tract Carcinoma
1/54 2%
2/950 0%
Other Sarcomas
0/69 0%
2/699 0%
Cervical Carcinoma
0/35 0%
1/422 0%
B-Cell Non-Hodgkins Lymphoma
4/88 5%
1/2534 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
Glioma
0/52 0%
3/2127 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Non-Cancerous
0/104 0%
1/830 0%
Gastric Carcinoma
0/74 0%
2/1809 0%
Breast Carcinoma
2/144 1%
1/3264 0%
B-Lymphoblastic Leukemia
0/55 0%
2/2640 0%
Thyroid Gland Carcinoma
1/45 2%
0/1592 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%

Mutation Distribution

Where GLOD5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in GLOD5 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 24 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 88 mutations in GLOD5

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