GRIA3

Glutamate ionotropic receptor AMPA type subunit 3 P42263 GRIA3_HUMAN
Protein Coding Chr X Xq25 Swiss-Prot reviewed Entrez 2892
Mutations
1,902
CL 219 · Tissue 1,668
Samples
616
CL 106 · Tissue 504
Peptides
498
unique mutant peptides
Transcripts
5
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
Mutations1,9022191,668
Samples616106504
Peptides49868441

Function

GRIA3 · Glutamate ionotropic receptor AMPA type subunit 3

Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. These receptors are heteromeric protein complexes composed of multiple subunits, arranged to form ligand-gated ion channels. The classification of glutamate receptors is based on their activation by different pharmacologic agonists. The subunit encoded by this gene belongs to a family of AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate)-sensitive glutamate receptors, and is subject to RNA editing (AGA->GGA; R->G). Alternative splicing at this locus results in different isoforms, which may vary in their signal transduction properties. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

5 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
ENST00000620443 P42263-2 646 439
ENST00000622768 P42263 585 422
ENST00000620581 A0A087WYJ6* 537 382
ENST00000611689 A0A087WUM1* 67 55
ENST00000616590 A0A087WUM1* 67 55

Gene Properties

Type
Protein Coding
Chromosome
X
Cytoband
Xq25
Entrez ID
Aliases
GLUR-CGLUR-K3GLUR3GLURCGluA3MRX94

Recurrent Mutations

All 439 amino-acid changes on canonical ENST00000620443 · 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 GRIA3 · 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 GRIA3 – 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
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Acute Monocytic Leukemia
0/1 0%
2/25 8%
Endometrial Carcinoma
6/42 14%
35/612 6%
Melanoma
8/210 4%
89/1899 5%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Squamous Cell Lung Carcinoma
2/57 4%
23/810 3%
Non-Small Cell Lung Carcinoma
13/304 4%
34/1390 2%
Small Cell Lung Carcinoma
0/9 0%
19/752 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Colorectal Carcinoma
16/143 11%
67/3239 2%
Cervical Carcinoma
2/35 6%
8/422 2%
Glioblastoma
2/98 2%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Ewings Sarcoma
6/63 10%
0/262 0%
Gastric Carcinoma
3/74 4%
31/1809 2%
Other Solid Cancers
3/94 3%
22/1515 1%
Thyroid Gland Carcinoma
0/45 0%
21/1592 1%
Neuroendocrine Tumour
7/154 5%
2/577 0%
Other Sarcomas
2/69 3%
7/699 1%
Ovarian Carcinoma
4/109 4%
9/998 1%
Glioma
0/52 0%
24/2127 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
24/2550 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Pancreatic Carcinoma
4/89 4%
9/1611 1%
Hepatocellular Carcinoma
2/46 4%
14/2210 1%
Biliary Tract Carcinoma
0/54 0%
7/950 1%
Head and Neck Carcinoma
1/85 1%
10/1574 1%
Esophageal Carcinoma
1/23 4%
4/769 1%
Breast Carcinoma
3/144 2%
18/3264 1%

Mutation Distribution

Where GRIA3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in GRIA3 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 1,902 mutations in GRIA3

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