PTPN22

Protein tyrosine phosphatase non-receptor type 22 Q9Y2R2-5 PTN22_HUMAN
Protein Coding Chr 1 1p13.2 Swiss-Prot reviewed Entrez 26191
Mutations
1,963
CL 235 · Tissue 1,698
Samples
410
CL 73 · Tissue 330
Peptides
357
unique mutant peptides
Transcripts
6
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
Mutations1,9632351,698
Samples41073330
Peptides35758305

Function

PTPN22 · Protein tyrosine phosphatase non-receptor type 22

This gene encodes of member of the non-receptor class 4 subfamily of the protein-tyrosine phosphatase family. The encoded protein is a lymphoid-specific intracellular phosphatase that associates with the molecular adapter protein CBL and may be involved in regulating CBL function in the T-cell receptor signaling pathway. Mutations in this gene may be associated with a range of autoimmune disorders including Type 1 Diabetes, rheumatoid arthritis, systemic lupus erythematosus and Graves' disease. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Mar 2009].

Isoforms & Proteins

6 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
ENST00000359785 A0A0B4J1S7* 439 328
ENST00000420377 E9PMT0* 388 303
ENST00000538253 F5H2S8* 384 302
ENST00000528414 A0A0A0MTE6* 372 296
ENST00000525799 A0A0A0MTD9* 324 249
ENST00000460620 Q9Y2R2-5 56 51

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p13.2
Entrez ID
Aliases
LYPLYP1LYP2PEPPTPN22.5PTPN22.6

Recurrent Mutations

All 51 amino-acid changes on canonical ENST00000460620 · 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 PTPN22 · 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 PTPN22 – 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%
Endometrial Carcinoma
5/42 12%
30/612 5%
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Melanoma
10/210 5%
77/1899 4%
Other Solid Cancers
3/94 3%
39/1515 3%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Bladder Carcinoma
1/58 2%
15/956 2%
Neuroendocrine Tumour
8/154 5%
2/577 0%
Non-Small Cell Lung Carcinoma
8/304 3%
14/1390 1%
Cervical Carcinoma
0/35 0%
5/422 1%
Glioblastoma
1/98 1%
0/0 0%
Gastric Carcinoma
3/74 4%
14/1809 1%
Hepatocellular Carcinoma
0/46 0%
19/2210 1%
Squamous Cell Lung Carcinoma
0/57 0%
7/810 1%
Colorectal Carcinoma
7/143 5%
20/3239 1%
Esophageal Carcinoma
2/23 9%
4/769 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Other Sarcomas
1/69 1%
4/699 1%
Ewings Sarcoma
0/63 0%
2/262 1%
Head and Neck Carcinoma
2/85 2%
8/1574 1%
Non-Cancerous
0/104 0%
5/830 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Osteosarcoma
0/45 0%
1/166 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
10/2550 0%
Medulloblastoma
0/0 0%
2/450 0%
Breast Carcinoma
4/144 3%
11/3264 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Glioma
0/52 0%
9/2127 0%
Kidney Carcinoma
4/85 5%
3/1862 0%

Mutation Distribution

Where PTPN22 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PTPN22 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 1,963 mutations in PTPN22

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