ADGRL2 Adhesion G protein-coupled receptor L2 O95490 AGRL2_HUMAN
Protein Coding Chr 1 1p31.1 Swiss-Prot reviewed Entrez 23266
Mutations
13,221
CL 1,196 · Tissue 11,712
Samples
1,095
CL 190 · Tissue 880
Peptides
1,002
unique mutant peptides
Transcripts
13
isoforms mutated

Stats by Source

Global, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Global = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Global can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

GlobalCell lineTissue
Mutations13,2211,19611,712
Samples1,095190880
Peptides1,002147868

Function

ADGRL2 · Adhesion G protein-coupled receptor L2

This gene encodes a member of the latrophilin subfamily of G-protein coupled receptors. The encoded protein participates in the regulation of exocytosis. The proprotein is thought to be further cleaved within a cysteine-rich G-protein-coupled receptor proteolysis site into two chains that are non-covalently bound at the cell membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014].

Isoforms & Proteins

13 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
ENST00000370725 O95490-6 1,145 863
ENST00000370717 O95490 1,137 858
ENST00000370728 O95490 1,137 858
ENST00000370723 O95490-7 1,136 857
ENST00000370727 B1ALU3* 1,127 846
ENST00000627151 B1ALU3* 1,127 846
ENST00000370730 O95490-5 1,119 841
ENST00000319517 O95490-2 1,110 835
ENST00000359929 O95490-2 1,110 835
ENST00000370721 B1ALU1* 1,092 820
ENST00000370715 O95490-4 948 704
ENST00000370713 O95490-3 916 681
ENST00000686636 A0A8I5KUX3* 117 112

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p31.1
Entrez ID
Aliases
CIRL2CL2LEC1LPHH1LPHN2

Recurrent Mutations

Top recurrent amino-acid changes along the protein · needle height = number of mutations

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 Distribution

Where ADGRL2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ADGRL2 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 13,221 mutations in ADGRL2

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 CDSTypeSourcePeptide