ADGRG5

Adhesion G protein-coupled receptor G5 Q8IZF4 AGRG5_HUMAN
Protein Coding Chr 16 16q21 Swiss-Prot reviewed Entrez 221188
Mutations
566
CL 76 · Tissue 484
Samples
244
CL 39 · Tissue 202
Peptides
192
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
Mutations56676484
Samples24439202
Peptides19228168

Function

ADGRG5 · Adhesion G protein-coupled receptor G5

This gene encodes a member of the adhesion family of G-protein coupled receptors. Members of this family are characterized by long N-termini and multiple functional domains. They may play a role in the immune system as well as in the central nervous system. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016].

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
ENST00000349457 Q8IZF4 257 190
ENST00000340339 Q8IZF4 239 184
ENST00000615867 A0A087WZA0* 70 59

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16q21
Entrez ID
Aliases
GPR114PGR27

Recurrent Mutations

All 190 amino-acid changes on canonical ENST00000349457 · 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 ADGRG5 · 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 ADGRG5 – 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%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Glioblastoma
2/98 2%
0/0 0%
Melanoma
4/210 2%
33/1899 2%
Endometrial Carcinoma
1/42 2%
9/612 1%
Gastric Carcinoma
1/74 1%
20/1809 1%
Colorectal Carcinoma
8/143 6%
28/3239 1%
Non-Small Cell Lung Carcinoma
7/304 2%
8/1390 1%
Cervical Carcinoma
2/35 6%
2/422 0%
Small Cell Lung Carcinoma
0/9 0%
6/752 1%
Glioma
3/52 6%
13/2127 1%
Squamous Cell Lung Carcinoma
1/57 2%
5/810 1%
Bladder Carcinoma
1/58 2%
6/956 1%
Other Solid Cancers
0/94 0%
10/1515 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Esophageal Carcinoma
0/23 0%
4/769 1%
Osteosarcoma
1/45 2%
0/166 0%
Mesothelioma
1/62 2%
0/165 0%
Non-Cancerous
0/104 0%
4/830 0%
Neuroendocrine Tumour
1/154 1%
2/577 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
6/2550 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Other Sarcomas
1/69 1%
1/699 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
6/2534 0%
Medulloblastoma
0/0 0%
1/450 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%
Ovarian Carcinoma
0/109 0%
2/998 0%

Mutation Distribution

Where ADGRG5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ADGRG5 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 566 mutations in ADGRG5

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