MARCH7

E3 ubiquitin-protein ligase MARCHF7 Q9H992 MARH7_HUMAN
Swiss-Prot reviewed
Mutations
1,078
CL 152 · Tissue 913
Samples
278
CL 39 · Tissue 235
Peptides
245
unique mutant peptides
Transcripts
4
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
Mutations1,078152913
Samples27839235
Peptides24534214

Function

MARCH7 · E3 ubiquitin-protein ligase MARCHF7

E3 ubiquitin-protein ligase which may specifically enhance the E2 activity of HIP2. E3 ubiquitin ligases accept ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfer the ubiquitin to targeted substrates (PubMed:16868077). May be involved in T-cell proliferation by regulating LIF secretion (By similarity). May play a role in lysosome homeostasis (PubMed:31270356). Promotes 'Lys-6', 'Lys-11' and 'Lys-63'-linked mixed polyubiquitination on ATG14 leading to the inhibition of autophagy by impairing the interaction between ATG14 and STX7 (PubMed:37632749). Participates in the dopamine-mediated negative regulation of the NLRP3 inflammasome by promoting its ubiquitination and subsequent degradation (PubMed:25594175)

Isoforms & Proteins

4 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
ENST00000259050 Q9H992 278 220
ENST00000409175 Q9H992 278 220
ENST00000409591 Q9H992-2 264 207
ENST00000539065 F5H6W4* 258 203

Gene Properties

Recurrent Mutations

All 220 amino-acid changes on canonical ENST00000259050 · 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 MARCH7 · 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 MARCH7 – 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
Endometrial Carcinoma
0/42 0%
17/612 3%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Non-Small Cell Lung Carcinoma
13/304 4%
14/1390 1%
Melanoma
4/210 2%
28/1899 1%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Bladder Carcinoma
0/58 0%
13/956 1%
Chondrosarcoma
1/14 7%
0/75 0%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Gastric Carcinoma
0/74 0%
20/1809 1%
Colorectal Carcinoma
2/143 1%
32/3239 1%
Osteosarcoma
1/45 2%
1/166 1%
Other Solid Cancers
1/94 1%
14/1515 1%
Biliary Tract Carcinoma
1/54 2%
8/950 1%
Non-Cancerous
0/104 0%
8/830 1%
Head and Neck Carcinoma
1/85 1%
11/1574 1%
Squamous Cell Lung Carcinoma
2/57 4%
3/810 0%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Esophageal Carcinoma
0/23 0%
4/769 1%
Hepatocellular Carcinoma
0/46 0%
11/2210 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Kidney Carcinoma
1/85 1%
7/1862 0%
Meningioma
0/3 0%
1/252 0%
Other Sarcomas
0/69 0%
3/699 0%
Breast Carcinoma
2/144 1%
11/3264 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
9/2550 0%
Glioma
0/52 0%
7/2127 0%
Thyroid Gland Carcinoma
1/45 2%
4/1592 0%

Mutation Distribution

Where MARCH7 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MARCH7 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 1,078 mutations in MARCH7

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