ACP4

Acid phosphatase 4 Q9BZG2 PPAT_HUMAN
Protein Coding Chr 19 19q13.33 Swiss-Prot reviewed Entrez 93650
Mutations
308
CL 66 · Tissue 240
Samples
284
CL 59 · Tissue 223
Peptides
187
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
Mutations30866240
Samples28459223
Peptides18744153

Function

ACP4 · Acid phosphatase 4

Acid phosphatases are enzymes capable of hydrolyzing orthophosphoric acid esters in an acid medium. This gene is up-regulated by androgens and is down-regulated by estrogens in the prostate cancer cell line. This gene exhibits a lower level of expression in testicular cancer tissues than in normal tissues. The protein encoded by this gene has structural similarity to prostatic and lysosomal acid phosphatases. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008].

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
ENST00000270593 Q9BZG2 308 187

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.33
Entrez ID
Aliases
ACPTAI1J

Recurrent Mutations

All 187 amino-acid changes on canonical ENST00000270593 · 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 ACP4 · 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 ACP4 – 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
3/40 8%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
Adrenocortical Carcinoma
2/3 67%
1/112 1%
Endometrial Carcinoma
4/42 10%
10/612 2%
Cervical Carcinoma
1/35 3%
8/422 2%
Melanoma
7/210 3%
31/1899 2%
Bladder Carcinoma
0/58 0%
13/956 1%
Non-Small Cell Lung Carcinoma
8/304 3%
12/1390 1%
Germ Cell Tumour
2/25 8%
0/169 0%
Rhabdomyosarcoma
0/33 0%
2/171 1%
Colorectal Carcinoma
4/143 3%
24/3239 1%
Esophageal Carcinoma
0/23 0%
6/769 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Hepatocellular Carcinoma
0/46 0%
15/2210 1%
Other Sarcomas
3/69 4%
2/699 0%
Gastric Carcinoma
1/74 1%
11/1809 1%
Squamous Cell Lung Carcinoma
0/57 0%
5/810 1%
Thyroid Gland Carcinoma
0/45 0%
9/1592 1%
Glioma
0/52 0%
11/2127 1%
Ovarian Carcinoma
4/109 4%
1/998 0%
Medulloblastoma
0/0 0%
2/450 0%
Neuroendocrine Tumour
1/154 1%
2/577 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
9/2550 0%
Prostate Carcinoma
4/13 31%
4/2105 0%
Other Solid Cancers
0/94 0%
6/1515 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
7/2534 0%
Non-Cancerous
0/104 0%
3/830 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%

Mutation Distribution

Where ACP4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ACP4 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 308 mutations in ACP4

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