ICAM2

Intercellular adhesion molecule 2 P13598 ICAM2_HUMAN
Protein Coding Chr 17 17q23.3 Swiss-Prot reviewed Entrez 3384
Mutations
921
CL 170 · Tissue 743
Samples
155
CL 43 · Tissue 110
Peptides
111
unique mutant peptides
Transcripts
7
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
Mutations921170743
Samples15543110
Peptides1112987

Function

ICAM2 · Intercellular adhesion molecule 2

The protein encoded by this gene is a member of the intercellular adhesion molecule (ICAM) family. All ICAM proteins are type I transmembrane glycoproteins, contain 2-9 immunoglobulin-like C2-type domains, and bind to the leukocyte adhesion LFA-1 protein. This protein may play a role in lymphocyte recirculation by blocking LFA-1-dependent cell adhesion. It mediates adhesive interactions important for antigen-specific immune response, NK-cell mediated clearance, lymphocyte recirculation, and other cellular interactions important for immune response and surveillance. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

7 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
ENST00000579788 P13598 155 99
ENST00000412356 P13598 136 94
ENST00000418105 P13598 135 94
ENST00000449662 P13598 135 94
ENST00000579687 P13598 135 94
ENST00000578892 J3QRT5* 127 86
ENST00000578379 J3QKR4* 98 66

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q23.3
Entrez ID
Aliases
CD102

Recurrent Mutations

All 99 amino-acid changes on canonical ENST00000579788 · 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 ICAM2 · 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 ICAM2 – 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
4/40 10%
0/0 0%
Cervical Carcinoma
4/35 11%
3/422 1%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Endometrial Carcinoma
1/42 2%
7/612 1%
Melanoma
2/210 1%
22/1899 1%
Mesothelioma
2/62 3%
0/165 0%
Squamous Cell Lung Carcinoma
4/57 7%
3/810 0%
Other Solid Cancers
0/94 0%
11/1515 1%
Colorectal Carcinoma
6/143 4%
14/3239 0%
Ovarian Carcinoma
3/109 3%
2/998 0%
Gastric Carcinoma
1/74 1%
7/1809 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
9/2550 0%
Non-Small Cell Lung Carcinoma
4/304 1%
2/1390 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Prostate Carcinoma
0/13 0%
6/2105 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Breast Carcinoma
3/144 2%
5/3264 0%
Non-Cancerous
0/104 0%
2/830 0%
B-Lymphoblastic Leukemia
4/55 7%
0/2640 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Glioma
0/52 0%
3/2127 0%
Other Sarcomas
1/69 1%
0/699 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Neuroblastoma
0/87 0%
1/1331 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Kidney Carcinoma
0/85 0%
1/1862 0%

Mutation Distribution

Where ICAM2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ICAM2 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 921 mutations in ICAM2

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