CLDN19

Claudin 19 Q8N6F1 CLD19_HUMAN
Protein Coding Chr 1 1p34.2 Swiss-Prot reviewed Entrez 149461
Mutations
302
CL 22 · Tissue 280
Samples
138
CL 17 · Tissue 121
Peptides
120
unique mutant peptides
Transcripts
3
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
Mutations30222280
Samples13817121
Peptides12014106

Function

CLDN19 · Claudin 19

The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010].

Isoforms & Proteins

3 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
ENST00000296387 Q8N6F1 111 87
ENST00000539749 Q8N6F1-3 102 71
ENST00000372539 Q8N6F1-2 89 69

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p34.2
Entrez ID
Aliases
HOMG5

Recurrent Mutations

All 87 amino-acid changes on canonical ENST00000296387 · 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 CLDN19 · 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 CLDN19 – 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
2/40 5%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Germ Cell Tumour
0/25 0%
2/169 1%
Osteosarcoma
1/45 2%
1/166 1%
Melanoma
1/210 0%
18/1899 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Squamous Cell Lung Carcinoma
0/57 0%
7/810 1%
Endometrial Carcinoma
0/42 0%
5/612 1%
Colorectal Carcinoma
3/143 2%
16/3239 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Gastric Carcinoma
1/74 1%
8/1809 0%
Glioma
0/52 0%
10/2127 0%
Ovarian Carcinoma
0/109 0%
5/998 0%
Non-Small Cell Lung Carcinoma
2/304 1%
5/1390 0%
Bladder Carcinoma
0/58 0%
4/956 0%
Hepatocellular Carcinoma
1/46 2%
6/2210 0%
Thyroid Gland Carcinoma
1/45 2%
4/1592 0%
Biliary Tract Carcinoma
1/54 2%
2/950 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
7/2550 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Head and Neck Carcinoma
1/85 1%
3/1574 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Medulloblastoma
0/0 0%
1/450 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Pancreatic Carcinoma
0/89 0%
2/1611 0%
Other Solid Cancers
0/94 0%
2/1515 0%
Non-Cancerous
0/104 0%
1/830 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
0/2534 0%

Mutation Distribution

Where CLDN19 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CLDN19 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 53 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 302 mutations in CLDN19

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