FTO

FTO alpha-ketoglutarate dependent dioxygenase Q9C0B1 FTO_HUMAN
Protein Coding Chr 16 16q12.2 Swiss-Prot reviewed Entrez 79068
Mutations
1,089
CL 177 · Tissue 909
Samples
230
CL 58 · Tissue 169
Peptides
196
unique mutant peptides
Transcripts
8
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
Mutations1,089177909
Samples23058169
Peptides19638158

Function

FTO · FTO alpha-ketoglutarate dependent dioxygenase

This gene is a nuclear protein of the AlkB related non-haem iron and 2-oxoglutarate-dependent oxygenase superfamily but the exact physiological function of this gene is not known. Other non-heme iron enzymes function to reverse alkylated DNA and RNA damage by oxidative demethylation. Studies in mice and humans indicate a role in nervous and cardiovascular systems and a strong association with body mass index, obesity risk, and type 2 diabetes. [provided by RefSeq, Jul 2011].

Isoforms & Proteins

8 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
ENST00000471389 Q9C0B1 236 170
ENST00000637969 A0A1B0GVH5* 200 156
ENST00000637001 A0A1B0GU26* 179 144
ENST00000636218 A0A1B0GTC5* 178 143
ENST00000636491 A0A1B0GUC3* 177 142
ENST00000431610 Q9C0B1-4 40 28
ENST00000460382 Q9C0B1-4 40 28
ENST00000463855 Q9C0B1-2 39 27

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16q12.2
Entrez ID
Aliases
ALKBH9BMIQ14GDFDIFEX9

Recurrent Mutations

All 170 amino-acid changes on canonical ENST00000471389 · 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 FTO · 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 FTO – 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
1/25 4%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Glioblastoma
3/98 3%
0/0 0%
Endometrial Carcinoma
6/42 14%
11/612 2%
Squamous Cell Lung Carcinoma
3/57 5%
9/810 1%
Burkitts Lymphoma
0/32 0%
3/196 2%
Colorectal Carcinoma
8/143 6%
30/3239 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Melanoma
4/210 2%
18/1899 1%
Non-Small Cell Lung Carcinoma
5/304 2%
10/1390 1%
Bladder Carcinoma
0/58 0%
7/956 1%
Cervical Carcinoma
2/35 6%
1/422 0%
Ovarian Carcinoma
1/109 1%
6/998 1%
Esophageal Carcinoma
0/23 0%
5/769 1%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Neuroendocrine Tumour
3/154 2%
1/577 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Gastric Carcinoma
3/74 4%
6/1809 0%
Glioma
0/52 0%
10/2127 0%
Mesothelioma
1/62 2%
0/165 0%
Medulloblastoma
0/0 0%
2/450 0%
Head and Neck Carcinoma
0/85 0%
7/1574 0%
Other Solid Cancers
0/94 0%
6/1515 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
7/2550 0%
Hepatocellular Carcinoma
0/46 0%
7/2210 0%
Thyroid Gland Carcinoma
0/45 0%
5/1592 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Other Sarcomas
2/69 3%
0/699 0%
B-Lymphoblastic Leukemia
6/55 11%
0/2640 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in FTO 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 1,089 mutations in FTO

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