ALPG

Alkaline phosphatase, germ cell P10696 PPBN_HUMAN
Protein Coding Chr 2 2q37.1 Swiss-Prot reviewed Entrez 251
Mutations
423
CL 70 · Tissue 339
Samples
387
CL 69 · Tissue 307
Peptides
219
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
Mutations42370339
Samples38769307
Peptides21942186

Function

ALPG · Alkaline phosphatase, germ cell

There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The product of this gene is a membrane bound glycosylated enzyme, localized to testis, thymus and certain germ cell tumors, that is closely related to both the placental and intestinal forms of alkaline phosphatase. [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
ENST00000295453 P10696 423 219

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q37.1
Entrez ID
Aliases
ALPPLALPPL2GCAP

Recurrent Mutations

All 219 amino-acid changes on canonical ENST00000295453 · 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 ALPG · 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 ALPG – 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
6/40 15%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
4/133 3%
Melanoma
6/210 3%
45/1899 2%
Thyroid Gland Carcinoma
1/45 2%
35/1592 2%
Endometrial Carcinoma
2/42 5%
10/612 2%
Colorectal Carcinoma
10/143 7%
48/3239 1%
Non-Small Cell Lung Carcinoma
11/304 4%
12/1390 1%
Gastric Carcinoma
1/74 1%
19/1809 1%
Glioblastoma
1/98 1%
0/0 0%
Neuroendocrine Tumour
4/154 3%
3/577 1%
Ovarian Carcinoma
8/109 7%
2/998 0%
Burkitts Lymphoma
2/32 6%
0/196 0%
Cervical Carcinoma
0/35 0%
4/422 1%
Small Cell Lung Carcinoma
0/9 0%
6/752 1%
Esophageal Carcinoma
0/23 0%
6/769 1%
Hepatocellular Carcinoma
0/46 0%
17/2210 1%
Biliary Tract Carcinoma
0/54 0%
7/950 1%
Other Solid Cancers
0/94 0%
11/1515 1%
Head and Neck Carcinoma
0/85 0%
11/1574 1%
Glioma
0/52 0%
13/2127 1%
Squamous Cell Lung Carcinoma
0/57 0%
5/810 1%
Non-Cancerous
0/104 0%
5/830 1%
Other Sarcomas
1/69 1%
3/699 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
11/2534 0%
Osteosarcoma
1/45 2%
0/166 0%
Pancreatic Carcinoma
3/89 3%
4/1611 0%
Kidney Carcinoma
2/85 2%
5/1862 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
9/2550 0%
Other Blood Cancers
3/61 5%
6/2725 0%
Breast Carcinoma
2/144 1%
9/3264 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in ALPG 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 423 mutations in ALPG

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