MGA

MAX dimerization protein MGA Q8IWI9 MGAP_HUMAN
Protein Coding Chr 15 15q15.1 Swiss-Prot reviewed Entrez 23269
Mutations
3,177
CL 495 · Tissue 2,604
Samples
1,186
CL 223 · Tissue 930
Peptides
1,087
unique mutant peptides
Transcripts
5
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
Mutations3,1774952,604
Samples1,186223930
Peptides1,087187895

Function

MGA · MAX dimerization protein MGA

Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in cell fate specification and positive regulation of transcription by RNA polymerase II. Predicted to act upstream of or within cellular response to leukemia inhibitory factor. Part of MLL1 complex. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

5 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
ENST00000219905 Q8IWI9 1,288 992
ENST00000566586 Q8IWI9-3 1,164 894
ENST00000570161 A0A8C8P5L8* 579 465
ENST00000703841 A0A994J6L2* 144 133
ENST00000566718 H3BP52* 2 2

Gene Properties

Type
Protein Coding
Chromosome
15
Cytoband
15q15.1
Entrez ID
Aliases
MAD5MXD5POF26

Recurrent Mutations

All 992 amino-acid changes on canonical ENST00000219905 · 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 MGA · 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 MGA – 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
10/40 25%
0/0 0%
Endometrial Carcinoma
8/42 19%
57/612 9%
Glioblastoma
9/98 9%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
2/26 8%
0/0 0%
Melanoma
16/210 8%
114/1899 6%
Unknown
1/10 10%
1/29 3%
Other Solid Cancers
4/94 4%
72/1515 5%
Colorectal Carcinoma
30/143 21%
123/3239 4%
Acute Myeloid Leukemia
4/90 4%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Gastric Carcinoma
9/74 12%
65/1809 4%
Cervical Carcinoma
0/35 0%
17/422 4%
Bladder Carcinoma
5/58 9%
32/956 3%
Non-Small Cell Lung Carcinoma
14/304 5%
43/1390 3%
Squamous Cell Lung Carcinoma
8/57 14%
20/810 2%
Biliary Tract Carcinoma
0/54 0%
32/950 3%
Burkitts Lymphoma
5/32 16%
2/196 1%
Small Cell Lung Carcinoma
0/9 0%
22/752 3%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Neuroendocrine Tumour
9/154 6%
8/577 1%
Plasma Cell Myeloma
5/44 11%
3/305 1%
Esophageal Carcinoma
2/23 9%
16/769 2%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Ovarian Carcinoma
4/109 4%
21/998 2%
Hodgkins Lymphoma
0/16 0%
3/122 2%
Germ Cell Tumour
0/25 0%
4/169 2%
Non-Cancerous
3/104 3%
16/830 2%
Other Sarcomas
4/69 6%
11/699 2%
Head and Neck Carcinoma
12/85 14%
20/1574 1%
Hepatocellular Carcinoma
3/46 7%
39/2210 2%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in MGA 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 3,177 mutations in MGA

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