GPR149

G protein-coupled receptor 149 Q86SP6 GP149_HUMAN
Protein Coding Chr 3 3q25.2 Swiss-Prot reviewed Entrez 344758
Mutations
659
CL 140 · Tissue 504
Samples
614
CL 131 · Tissue 473
Peptides
454
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
Mutations659140504
Samples614131473
Peptides45478384

Function

GPR149 · G protein-coupled receptor 149

This gene encodes a seven-transmembrane G protein coupled receptor (GPCR) class A family member. Although categorized as a class A GPCR, the encoded protein lacks the first two charged amino acids of the highly conserved Asp-Arg-Tyr (DRY) motif found in the third transmembrane helix of class A receptors which is important for efficient G protein-coupled signal transduction. Mice with a knockout of the orthologous gene are viable and have normal maturation of the ovarian follicle, but show enhanced fertility and ovulation. All GPCRs have a common structural architecture consisting of seven transmembrane alpha-helices interconnected by three extracellular and three intracellular loops. A general feature of GPCR signaling is agonist-induced conformational changes in the receptor, leading to activation of the heterotrimeric G proteins, which consist of the guanine nucleotide-binding G-alpha subunit and the dimeric G-beta-gamma subunits. The activated G proteins then bind to and activate numerous downstream effector proteins, which generate second messengers that mediate a broad range of cellular and physiological processes. [provided by RefSeq, Jul 2017].

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
ENST00000389740 Q86SP6 659 454

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3q25.2
Entrez ID
Aliases
IEDAPGR10R35

Recurrent Mutations

All 454 amino-acid changes on canonical ENST00000389740 · 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 GPR149 · 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 GPR149 – 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
11/40 28%
0/0 0%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
6/42 14%
25/612 4%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Colorectal Carcinoma
23/143 16%
90/3239 3%
Glioblastoma
3/98 3%
0/0 0%
Melanoma
7/210 3%
57/1899 3%
Non-Small Cell Lung Carcinoma
13/304 4%
32/1390 2%
Squamous Cell Lung Carcinoma
1/57 2%
22/810 3%
Neuroendocrine Tumour
14/154 9%
4/577 1%
Gastric Carcinoma
2/74 3%
38/1809 2%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Plasma Cell Myeloma
2/44 5%
3/305 1%
Cervical Carcinoma
0/35 0%
6/422 1%
Other Sarcomas
3/69 4%
7/699 1%
Ovarian Carcinoma
3/109 3%
11/998 1%
Biliary Tract Carcinoma
3/54 6%
9/950 1%
Other Solid Cancers
0/94 0%
19/1515 1%
Small Cell Lung Carcinoma
0/9 0%
9/752 1%
Bladder Carcinoma
3/58 5%
9/956 1%
Non-Cancerous
3/104 3%
6/830 1%
Ewings Sarcoma
2/63 3%
1/262 0%
Mesothelioma
0/62 0%
2/165 1%
Head and Neck Carcinoma
3/85 4%
11/1574 1%
Hepatocellular Carcinoma
1/46 2%
18/2210 1%
Esophageal Squamous Cell Carcinoma
3/51 6%
16/2550 1%
Glioma
2/52 4%
12/2127 1%
Esophageal Carcinoma
1/23 4%
4/769 1%

Mutation Distribution

Where GPR149 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in GPR149 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 18 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 659 mutations in GPR149

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