PLOD2

Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 O00469 PLOD2_HUMAN
Protein Coding Chr 3 3q24 Swiss-Prot reviewed Entrez 5352
Mutations
1,315
CL 178 · Tissue 1,104
Samples
409
CL 81 · Tissue 317
Peptides
339
unique mutant peptides
Transcripts
6
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
Mutations1,3151781,104
Samples40981317
Peptides33957290

Function

PLOD2 · Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2

The protein encoded by this gene is a membrane-bound homodimeric enzyme that is localized to the cisternae of the rough endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VIB have deficiencies in lysyl hydroxylase activity. Mutations in the coding region of this gene are associated with Bruck syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

6 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
ENST00000282903 O00469-2 415 304
ENST00000360060 O00469 362 282
ENST00000494950 E7ETU9* 346 269
ENST00000461497 O00469-3 190 148
ENST00000469350 C9JXZ0* 1 1
ENST00000703523 O00469 1 1

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3q24
Entrez ID
Aliases
BRKS2LH2TLH

Recurrent Mutations

All 304 amino-acid changes on canonical ENST00000282903 · 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 PLOD2 · 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 PLOD2 – 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
9/42 21%
18/612 3%
Non-Small Cell Lung Carcinoma
16/304 5%
29/1390 2%
Melanoma
3/210 1%
36/1899 2%
Squamous Cell Lung Carcinoma
3/57 5%
12/810 1%
Colorectal Carcinoma
13/143 9%
43/3239 1%
Gastric Carcinoma
2/74 3%
28/1809 2%
Small Cell Lung Carcinoma
0/9 0%
10/752 1%
Neuroendocrine Tumour
8/154 5%
1/577 0%
Chondrosarcoma
0/14 0%
1/75 1%
Other Solid Cancers
2/94 2%
15/1515 1%
Head and Neck Carcinoma
3/85 4%
13/1574 1%
Esophageal Carcinoma
0/23 0%
7/769 1%
Bladder Carcinoma
2/58 3%
6/956 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Hepatocellular Carcinoma
1/46 2%
15/2210 1%
Cervical Carcinoma
1/35 3%
2/422 0%
Non-Cancerous
2/104 2%
4/830 0%
Kidney Carcinoma
0/85 0%
12/1862 1%
Esophageal Squamous Cell Carcinoma
1/51 2%
14/2550 1%
Plasma Cell Myeloma
0/44 0%
2/305 1%
Ovarian Carcinoma
4/109 4%
2/998 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Other Sarcomas
1/69 1%
3/699 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Glioma
0/52 0%
10/2127 0%
Meningioma
0/3 0%
1/252 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
9/2534 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Pancreatic Carcinoma
0/89 0%
6/1611 0%

Mutation Distribution

Where PLOD2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PLOD2 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 1,315 mutations in PLOD2

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