GALR3

Galanin receptor 3 O60755 GALR3_HUMAN
Protein Coding Chr 22 22q13.1 Swiss-Prot reviewed Entrez 8484
Mutations
127
CL 48 · Tissue 78
Samples
121
CL 42 · Tissue 78
Peptides
92
unique mutant peptides
Transcripts
1
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
Mutations1274878
Samples1214278
Peptides923066

Function

GALR3 · Galanin receptor 3

The neuropeptide galanin modulates a variety of physiologic processes including cognition/memory, sensory/pain processing, hormone secretion, and feeding behavior. The human galanin receptors are G protein-coupled receptors that functionally couple to their intracellular effector through distinct signaling pathways. GALR3 is found in many tissues and may be expressed as 1.4-, 2.4-, and 5-kb transcripts [provided by RefSeq, Jul 2008].

Isoforms & Proteins

1 transcript · 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
ENST00000249041 O60755 127 92

Gene Properties

Type
Protein Coding
Chromosome
22
Cytoband
22q13.1
Entrez ID

Recurrent Mutations

All 92 amino-acid changes on canonical ENST00000249041 · 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 GALR3 · 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 GALR3 – 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
7/40 18%
0/0 0%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Endometrial Carcinoma
1/42 2%
4/612 1%
Gastric Carcinoma
1/74 1%
13/1809 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Colorectal Carcinoma
8/143 6%
14/3239 0%
Thyroid Gland Carcinoma
0/45 0%
10/1592 1%
Other Solid Cancers
3/94 3%
6/1515 0%
Germ Cell Tumour
1/25 4%
0/169 0%
Melanoma
2/210 1%
7/1899 0%
Non-Small Cell Lung Carcinoma
5/304 2%
2/1390 0%
Bladder Carcinoma
2/58 3%
2/956 0%
Other Sarcomas
2/69 3%
1/699 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
3/2534 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Glioma
0/52 0%
2/2127 0%
B-Lymphoblastic Leukemia
1/55 2%
1/2640 0%
Neuroblastoma
1/87 1%
0/1331 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
Other Blood Cancers
1/61 2%
0/2725 0%

Mutation Distribution

Where GALR3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in GALR3 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 47 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 127 mutations in GALR3

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