ATPSCKMT

ATP synthase c subunit lysine N-methyltransferase Q6P4H8 ACKMT_HUMAN
Protein Coding Chr 5 5p15.2 Swiss-Prot reviewed Entrez 134145
Mutations
34
CL 20 · Tissue 0
Samples
29
CL 20 · Tissue 0
Peptides
33
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
Mutations34200
Samples29200
Peptides33190

Function

ATPSCKMT · ATP synthase c subunit lysine N-methyltransferase

Enables protein-lysine N-methyltransferase activity. Involved in peptidyl-lysine trimethylation; positive regulation of sensory perception of pain; and regulation of proton transport. Located in mitochondrial crista. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000511437 Q6P4H8 34 33

Gene Properties

Type
Protein Coding
Chromosome
5
Cytoband
5p15.2
Entrez ID
Aliases
FAM173BJS-2hFAM173B

Recurrent Mutations

All 33 amino-acid changes on canonical ENST00000511437 · 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 ATPSCKMT · 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 ATPSCKMT – 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
2/42 5%
1/612 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Non-Small Cell Lung Carcinoma
3/304 1%
2/1390 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Ovarian Carcinoma
2/109 2%
0/998 0%
Colorectal Carcinoma
3/143 2%
1/3239 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Biliary Tract Carcinoma
1/54 2%
0/950 0%
Melanoma
1/210 0%
1/1899 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Gastric Carcinoma
1/74 1%
0/1809 0%
Prostate Carcinoma
1/13 8%
0/2105 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
0/2534 0%
Hepatocellular Carcinoma
1/46 2%
0/2210 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in ATPSCKMT 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.

Mutations

All 34 mutations in ATPSCKMT

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