FGR

FGR proto-oncogene, Src family tyrosine kinase P09769 FGR_HUMAN
Protein Coding Chr 1 1p35.3 Swiss-Prot reviewed Entrez 2268
Mutations
816
CL 127 · Tissue 681
Samples
283
CL 65 · Tissue 213
Peptides
220
unique mutant peptides
Transcripts
3
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
Mutations816127681
Samples28365213
Peptides22043178

Function

FGR · FGR proto-oncogene, Src family tyrosine kinase

This gene is a member of the Src family of protein tyrosine kinases (PTKs). The encoded protein contains N-terminal sites for myristylation and palmitylation, a PTK domain, and SH2 and SH3 domains which are involved in mediating protein-protein interactions with phosphotyrosine-containing and proline-rich motifs, respectively. The protein localizes to plasma membrane ruffles, and functions as a negative regulator of cell migration and adhesion triggered by the beta-2 integrin signal transduction pathway. Infection with Epstein-Barr virus results in the overexpression of this gene. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

3 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
ENST00000374005 P09769 302 220
ENST00000374004 P09769 257 200
ENST00000399173 P09769 257 200

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p35.3
Entrez ID
Aliases
SRC2c-fgrc-src2p55-Fgrp55c-fgrp58-Fgr

Recurrent Mutations

All 220 amino-acid changes on canonical ENST00000374005 · 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 FGR · 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 FGR – 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%
T-Cell Non-Hodgkins Lymphoma
3/26 12%
0/0 0%
Melanoma
2/210 1%
53/1899 3%
Endometrial Carcinoma
4/42 10%
13/612 2%
Unknown
1/10 10%
0/29 0%
Glioblastoma
2/98 2%
0/0 0%
Bladder Carcinoma
4/58 7%
9/956 1%
Colorectal Carcinoma
6/143 4%
28/3239 1%
Non-Small Cell Lung Carcinoma
12/304 4%
5/1390 0%
Cervical Carcinoma
0/35 0%
4/422 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Other Solid Cancers
2/94 2%
11/1515 1%
Gastric Carcinoma
0/74 0%
13/1809 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Ovarian Carcinoma
1/109 1%
5/998 0%
Germ Cell Tumour
1/25 4%
0/169 0%
Other Sarcomas
4/69 6%
0/699 0%
Prostate Carcinoma
0/13 0%
10/2105 0%
Thyroid Gland Carcinoma
0/45 0%
7/1592 0%
Neuroendocrine Tumour
2/154 1%
1/577 0%
Kidney Carcinoma
2/85 2%
6/1862 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
B-Cell Non-Hodgkins Lymphoma
4/88 5%
5/2534 0%
Glioma
0/52 0%
5/2127 0%
Breast Carcinoma
0/144 0%
7/3264 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
5/2550 0%
Other Blood Cancers
0/61 0%
5/2725 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in FGR 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 816 mutations in FGR

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