AP1S2

Adaptor related protein complex 1 subunit sigma 2 P56377 AP1S2_HUMAN
Protein Coding Chr X Xp22.2 Swiss-Prot reviewed Entrez 8905
Mutations
82
CL 5 · Tissue 76
Samples
48
CL 5 · Tissue 42
Peptides
46
unique mutant peptides
Transcripts
3
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
Mutations82576
Samples48542
Peptides46540

Function

AP1S2 · Adaptor related protein complex 1 subunit sigma 2

Adaptor protein complex 1 is found at the cytoplasmic face of coated vesicles located at the Golgi complex, where it mediates both the recruitment of clathrin to the membrane and the recognition of sorting signals within the cytosolic tails of transmembrane receptors. This complex is a heterotetramer composed of two large, one medium, and one small adaptin subunit. The protein encoded by this gene serves as the small subunit of this complex and is a member of the adaptin protein family. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2013].

Isoforms & Proteins

3 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
ENST00000329235 P56377 42 37
ENST00000380291 A6NH01* 36 34
ENST00000672987 A0A5F9ZHW1* 4 4

Gene Properties

Type
Protein Coding
Chromosome
X
Cytoband
Xp22.2
Entrez ID
Aliases
DC22MRX59MRXS21MRXS5MRXSFPGS

Recurrent Mutations

All 37 amino-acid changes on canonical ENST00000329235 · 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 AP1S2 · 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 AP1S2 – 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
1/42 2%
7/612 1%
Burkitts Lymphoma
1/32 3%
0/196 0%
Bladder Carcinoma
0/58 0%
4/956 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Melanoma
1/210 0%
3/1899 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Other Sarcomas
0/69 0%
1/699 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Colorectal Carcinoma
0/143 0%
4/3239 0%
Non-Small Cell Lung Carcinoma
1/304 0%
1/1390 0%
Prostate Carcinoma
0/13 0%
2/2105 0%
Neuroblastoma
0/87 0%
1/1331 0%
Breast Carcinoma
0/144 0%
2/3264 0%
Other Blood Cancers
1/61 2%
0/2725 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%

Mutation Distribution

Where AP1S2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in AP1S2 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 82 mutations in AP1S2

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