MGLL

Monoglyceride lipase Q99685 MGLL_HUMAN
Protein Coding Chr 3 3q21.3 Swiss-Prot reviewed Entrez 11343
Mutations
477
CL 50 · Tissue 412
Samples
161
CL 25 · Tissue 131
Peptides
144
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
Mutations47750412
Samples16125131
Peptides14419128

Function

MGLL · Monoglyceride lipase

This gene encodes a serine hydrolase of the AB hydrolase superfamily that catalyzes the conversion of monoacylglycerides to free fatty acids and glycerol. The encoded protein plays a critical role in several physiological processes including pain and nociperception through hydrolysis of the endocannabinoid 2-arachidonoylglycerol. Expression of this gene may play a role in cancer tumorigenesis and metastasis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012].

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
ENST00000265052 A0A0C4DFN3* 163 115
ENST00000398104 Q99685 157 116
ENST00000453507 Q99685-2 157 113

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3q21.3
Entrez ID
Aliases
HU-K5HUK5MAGLMGL

Recurrent Mutations

All 113 amino-acid changes on canonical ENST00000453507 · 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 MGLL · 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 MGLL – 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
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Endometrial Carcinoma
3/42 7%
10/612 2%
Melanoma
1/210 0%
27/1899 1%
Colorectal Carcinoma
8/143 6%
23/3239 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Other Solid Cancers
0/94 0%
9/1515 1%
Ovarian Carcinoma
3/109 3%
3/998 0%
Bladder Carcinoma
0/58 0%
5/956 1%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Burkitts Lymphoma
1/32 3%
0/196 0%
Hepatocellular Carcinoma
0/46 0%
9/2210 0%
Meningioma
0/3 0%
1/252 0%
Glioma
0/52 0%
7/2127 0%
Non-Cancerous
0/104 0%
3/830 0%
Gastric Carcinoma
1/74 1%
5/1809 0%
Thyroid Gland Carcinoma
0/45 0%
5/1592 0%
Non-Small Cell Lung Carcinoma
2/304 1%
2/1390 0%
Medulloblastoma
0/0 0%
1/450 0%
Wilms Tumour
0/5 0%
1/474 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
4/2550 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Neuroblastoma
2/87 2%
0/1331 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
3/2534 0%
Kidney Carcinoma
2/85 2%
0/1862 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
B-Lymphoblastic Leukemia
0/55 0%
2/2640 0%
Other Blood Cancers
0/61 0%
2/2725 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in MGLL 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 477 mutations in MGLL

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