ADGRL3 Adhesion G protein-coupled receptor L3 Q9HAR2-4 AGRL3_HUMAN
Protein Coding Chr 4 4q13.1 Swiss-Prot reviewed Entrez 23284
Mutations
18,373
CL 1,979 · Tissue 15,422
Samples
1,419
CL 270 · Tissue 1,088
Peptides
1,171
unique mutant peptides
Transcripts
15
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
Mutations18,3731,97915,422
Samples1,4192701,088
Peptides1,171211988

Function

ADGRL3 · Adhesion G protein-coupled receptor L3

This gene encodes a member of the latrophilin subfamily of G-protein coupled receptors (GPCR). Latrophilins may function in both cell adhesion and signal transduction. In experiments with non-human species, endogenous proteolytic cleavage within a cysteine-rich GPS (G-protein-coupled-receptor proteolysis site) domain resulted in two subunits (a large extracellular N-terminal cell adhesion subunit and a subunit with substantial similarity to the secretin/calcitonin family of GPCRs) being non-covalently bound at the cell membrane. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

15 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
ENST00000506720 E7EUW2* 1,424 1,035
ENST00000506746 E7ETE3* 1,418 1,029
ENST00000507625 E7EVD6* 1,407 1,021
ENST00000508946 E7EW95* 1,391 1,013
ENST00000514996 E9PBG4* 1,385 1,007
ENST00000514591 Q9HAR2-4 1,381 1,005
ENST00000508693 E7EN28* 1,247 897
ENST00000507164 E7EX52* 1,241 891
ENST00000509896 E7EUP0* 1,236 889
ENST00000511324 E7ESV6* 1,230 883
ENST00000504896 E7ENK1* 1,214 875
ENST00000514157 E7ES20* 1,208 869
ENST00000512091 Q9HAR2-2 1,203 867
ENST00000506700 E7EMR3* 1,197 861
ENST00000683033 A0A804HKL8* 191 170

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4q13.1
Entrez ID
Aliases
CIRL3CL3LEC3LPHN3

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 ADGRL3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ADGRL3 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 18,373 mutations in ADGRL3

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