MUC19

Mucin 19, oligomeric (gene/pseudogene)
Protein Coding Chr 12 12q12 Entrez 283463
Mutations
695
CL 695 · Tissue 0
Samples
517
CL 517 · Tissue 0
Peptides
421
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
Mutations6956950
Samples5175170
Peptides4214210

Function

MUC19 · Mucin 19, oligomeric (gene/pseudogene)

This gene encodes a member of the gel-forming mucin protein family. Mucin family members are glycoproteins that have tandem repeats which are extensively O-glycosylated. The structural features of mucin proteins are responsible for the gel-like properties of mucus. The encoded protein may be involved in disruption of the ocular surface in Sjogren syndrome. [provided by RefSeq, Apr 2014].

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
ENST00000454784 - 695 421

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12q12
Entrez ID
Aliases
MUC-19

Recurrent Mutations

All 422 amino-acid changes on canonical ENST00000454784 · 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 MUC19 · 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 MUC19 – 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
9/40 22%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
5/26 19%
0/0 0%
Glioblastoma
18/98 18%
0/0 0%
Oral Cavity Carcinoma
9/54 17%
0/0 0%
Acute Myeloid Leukemia
12/90 13%
0/0 0%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Neuroendocrine Tumour
38/154 25%
0/577 0%
Rhabdomyosarcoma
10/33 30%
0/171 0%
Hodgkins Lymphoma
4/16 25%
0/122 0%
Non-Small Cell Lung Carcinoma
46/304 15%
0/1390 0%
Unknown
1/10 10%
0/29 0%
Melanoma
53/210 25%
0/1899 0%
Osteosarcoma
5/45 11%
0/166 0%
Burkitts Lymphoma
5/32 16%
0/196 0%
Ewings Sarcoma
7/63 11%
0/262 0%
Endometrial Carcinoma
14/42 33%
0/612 0%
Plasma Cell Myeloma
7/44 16%
0/305 0%
Mesothelioma
4/62 6%
0/165 0%
Germ Cell Tumour
3/25 12%
0/169 0%
Ovarian Carcinoma
17/109 16%
0/998 0%
Cervical Carcinoma
6/35 17%
0/422 0%
Non-Cancerous
11/104 11%
0/830 0%
Pancreatic Carcinoma
20/89 22%
0/1611 0%
Chondrosarcoma
1/14 7%
0/75 0%
Colorectal Carcinoma
36/143 25%
0/3239 0%
Squamous Cell Lung Carcinoma
9/57 16%
0/810 0%
Other Sarcomas
8/69 12%
0/699 0%
Other Solid Cancers
16/94 17%
0/1515 0%
Adrenocortical Carcinoma
1/3 33%
0/112 0%
Head and Neck Carcinoma
14/85 16%
0/1574 0%

Mutation Distribution

Where MUC19 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MUC19 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 695 mutations in MUC19

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