FTO - FTO alpha-ketoglutarate dependent dioxygenase Gene

Also Known as GDFD; ALKBH9; BMIQ14

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79068

About FTO

Cytogenetic location: 16q12.2 Genomic coordinates (GRCh38): 16:53,703,963-54,121,941 (from NCBI)

This gene has 23 transcripts (splice variants), 202 orthologues and is associated with 4 phenotypes. Ubiquitous expression in brain (RPKM 7.3), adrenal (RPKM 4.2) and 25 other tissues.

Summary

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]

FTO Products (25)

mRNA Protein Name
XM_011523316.4 XP_011521618.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform X6
NM_001363896.1 NP_001350825.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 4
NM_001363905.1 NP_001350834.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 11
XR_007064911.1
NR_156761.1
NM_001363894.1 NP_001350823.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 1
XM_017023654.3 XP_016879143.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform X1
XM_047434607.1 XP_047290563.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform X3
NM_001363898.1 NP_001350827.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 6
NM_001080432.3 NP_001073901.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 3
NM_001363900.1 NP_001350829.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 8
XM_011523315.4 XP_011521617.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform X5
XM_017023656.3 XP_016879145.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform X7
NM_001363901.1 NP_001350830.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 9
XM_047434606.1 XP_047290562.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform X2
XM_047434609.1 XP_047290565.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform X8
NM_001363891.1 NP_001350820.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 2
XM_011523314.4 XP_011521616.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform X4
XM_024450437.2 XP_024306205.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform X9
NM_001363903.1 NP_001350832.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 10
NM_001363988.1 NP_001350917.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 12
NM_001363897.1 NP_001350826.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 5
NM_001363899.1 NP_001350828.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform 7
XM_017023657.3 XP_016879146.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform X8
XM_047434608.1 XP_047290564.1 alpha-ketoglutarate-dependent dioxygenase FTO isoform X5
Molecular Function GO Annotation Evidence References Source
enables broad specificity oxidative DNA demethylase activity IDA
IDA: Inferred from direct assay
18775698 GOA
enables ferrous iron binding IDA
IDA: Inferred from direct assay
20376003 GOA
enables mRNA N6-methyladenosine dioxygenase activity IDA
IDA: Inferred from direct assay
25452335 GOA
enables mRNA N6-methyladenosine dioxygenase activity IMP
IMP: Inferred from mutant phenotype
26458103 GOA
enables oxidative RNA demethylase activity IDA
IDA: Inferred from direct assay
18775698 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables tRNA demethylase activity IDA
IDA: Inferred from direct assay
30197295 GOA
Biological Process GO Annotation Evidence References Source
involved in DNA alkylation repair IDA
IDA: Inferred from direct assay
18775698 GOA
involved in RNA repair IDA
IDA: Inferred from direct assay
18775698 GOA
involved in mRNA destabilization IDA
IDA: Inferred from direct assay
28002401 GOA
involved in regulation of brown fat cell differentiation IMP
IMP: Inferred from mutant phenotype
26287746 GOA
involved in regulation of lipid storage IMP
IMP: Inferred from mutant phenotype
26287746 GOA
involved in snRNA processing IDA
IDA: Inferred from direct assay
30197295 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
28002401 GOA
located in nuclear speck IDA
IDA: Inferred from direct assay
22002720 GOA
located in nucleus IDA
IDA: Inferred from direct assay
26458103 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

FTO Protein Structure

FTO_NTD

FTO_NTD: FTO catalytic domain (35 - 326)

FTO_CTD

FTO_CTD: FTO C-terminal domain (329 - 499)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 505 a.a.
Protein Preferred Names Protein Names

alpha-ketoglutarate-dependent dioxygenase FTO

  • AlkB homolog 9

  • U6 small nuclear RNA (2'-O-methyladenosine-N(6)-)-demethylase FTO

  • U6 small nuclear RNA N(6)-methyladenosine-demethylase FTO

  • fat mass and obesity associated

  • fat mass and obesity-associated protein

  • m6A(m)-demethylase FTO

  • mRNA (2'-O-methyladenosine-N(6)-)-demethylase FTO

  • mRNA N(6)-methyladenosine demethylase FTO

  • tRNA N1-methyl adenine demethylase FTO

FTO Antibodies

Cat. No. Product Name Application Reactivity
HY-P80680 FTO Antibody (YA424) WB, IHC-P Human
HY-P80680A FTO Antibody (YA424)(PBS only) WB, IHC-P Human
HY-P86495 FTO Antibody (YA6187) WB, IHC-P, ICC/IF, IP, ELISA Human, Mouse, Rat

Related Diseases

Diseases Alias
Type 2 Diabetes Mellitus
  • Insulin Resistance

  • NIDDM

  • Diabetes Mellitus, Non-Insulin-Dependent

  • Type 2 Diabetes

  • T2D

  • Noninsulin-Dependent Diabetes Mellitus

  • Diabetes Mellitus, Type Ii

  • Maturity-Onset Diabetes

  • Insulin Resistance, Severe, Digenic

  • Diabetes Mellitus, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent

  • Diabetes Mellitus, Noninsulin-Dependent, Association With

  • Diabetes Mellitus, Noninsulin-Dependent, Late Onset

  • Hypertension, Insulin Resistance-Related, Susceptibility To

  • Insulin Resistance, Susceptibility To

  • Non-Insulin-Dependent Diabetes Mellitus

  • Type Ii Diabetes Mellitus

  • Adult-Onset Diabetes Mellitus

  • Maturity-Onset Diabetes Mellitus

  • Diabetes Mellitus Type 2

  • Type Ii Diabetes

  • Type 2 Diabetes Mellitus, Susceptibility To

  • Diabetes, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Type 2, Susceptibility To

  • Diabetes Mellitus, Noninsulin-Dependent, 2

  • Diabetes Mellitus, Type Ii, Susceptibility To

  • Hypertension, Insulin Resistance-Related

  • Adult-Onset Diabetes

  • Aodm

  • Diabetes Mellitus, Adult-Onset

  • Diabetes Mellitus Type Ii

  • Diabetes Mellitus Type 2, Susceptibility To

  • Diabetes, Type Ii, Susceptibility To

  • Diabetes Type 2

  • Diabetes Mellitus

  • Adult Onset Diabetes

  • Maturity Onset Diabetes

  • Nonketotic Diabetes

  • Non-Insulin Dependent Diabetes Mellitus

  • T2dm - [Type 2 Diabetes Mellitus]

  • Niddm - [Non Insulin Dependent Diabetes Mellitus]

  • Dm2

  • Dm Type Ii

  • Diabetic Type 2

  • Insulin Requiring Type 2 Diabetes

  • Noninsulin Dependent Diabetes

  • Non-Insulin-Dependent Diabetes Mellitus Without Complications

  • Diabetes Due To Insulin Secretory Defect

  • Diabetes Mellitus Due To Insulin Secretory Defect

  • Non-Insulin-Dependent Diabetes Of The Young

  • Senile Diabetes

  • Nonketotic Hyperglycaemia

  • Stable Diabetes

Growth Retardation, Developmental Delay, And Facial Dysmorphism
  • Lethal Polymalformative Syndrome, Boissel Type

  • Growth Retardation, Developmental Delay, Coarse Facies, And Early Death

  • GDFD

  • Growth Retardation, Developmental Delay, Facial Dysmorphism

  • Growth Retardation Developmental Delay Coarse Facies Early Death

  • Lethal Polymalformative Syndrome Boissel Type

Acquired Metabolic Disease
Body Mass Index Quantitative Trait Locus 11
  • OBESITY

  • Obesity, Susceptibility To

  • Leanness, Inherited

  • Obesity, Susceptibility To, Bmiq11

  • Obesity, Mild, Early-Onset

  • Obesity, Association With

  • Obesity, Early-Onset, Susceptibility To

  • Obesity, Severe

  • Obesity, Severe, And Type Ii Diabetes

  • Obesity, Late-Onset

  • BMIQ11

  • Obesity Bmiq11

  • Obesity, Early-Onset

  • Obesity , Susceptibility To

  • Simple Obesity Nos

  • Excess Fat

  • Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified

  • Adiposis

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Body Mass Index Quantitative Trait Locus 14
  • Obesity

  • BMIQ14

  • Obesity, Susceptibility To

  • Obesity, Susceptibility To, Bmiq14

  • Obesity Bmiq14

  • {Obesity, Susceptibility To, Bmiq14}

Eating Disorder
  • Eating Disorders

  • Feeding And Eating Disorders

Osteoporosis
  • Postmenopausal Osteoporosis

  • Osteoporosis, Postmenopausal

  • Bone Mineral Density Quantitative Trait Locus

  • Bmnd

  • Osteoporosis, Involutional

  • Osteoporosis, Susceptibility To

  • Osteoporosis, Postmenopausal, Susceptibility

  • Bone Mineral Density Variation Qtl, Osteoporosis

  • OSTEOP

  • Involutional Osteoporosis

  • Senile Osteoporosis

  • Osteoporosis Postmenopausal

  • Bone Mineral Density, Quantitative Trait Locus

  • Osteoporosis, Senile

  • Idiopathic Osteoporosis

  • Bone Rarefaction Nos

  • Type 1 Osteoporosis

Overnutrition
Wilms Tumor 1
  • Nephroblastoma

  • Wilms Tumor

  • WT1

  • Wilms' Tumor

  • Bilateral Wilms Tumor

  • Wilms Tumor, Type 1

  • Wilms Tumor, Somatic

  • Adult Nephroblastoma

  • Wt1 Disorder

  • Renal Embryonic Tumor

  • Adult Kidney Wilms Tumor

  • Childhood Kidney Wilms Tumor

  • Nonanaplastic Kidney Wilms Tumor

Bardet-Biedl Syndrome
  • Bbs

  • Biedl-Bardet Syndrome

Diabetes Mellitus
  • Diabetes

Glucose Intolerance
  • Glucose: Intolerance

  • Glucose: Malabsorption

  • Malabsorption Of Glucose

  • Impaired Glucose Tolerance

Microcephaly
  • Microencephaly

  • Microcephalus

  • Microcephalic

  • Nanocephaly

  • Congenital Microcephaly

  • Brain Hypoplasia

  • Brain Nondevelopment

  • Cephalic Hypoplasia

  • Undeveloped Cerebrum

  • Undeveloped Brain

  • Micrencephalon

  • Micrencephaly

Maturity-Onset Diabetes Of The Young
  • MODY

  • Maturity Onset Diabetes Mellitus In Young

  • Mason-Type Diabetes

  • Mason Type Diabetes

  • Maturity Onset Diabetes Of The Young

  • Mody Syndrome

  • Diabetes Of The Young, Maturity-Onset

Cervix Carcinoma
  • Cancer Of Cervix

  • Carcinoma Of Cervix

  • Carcinoma Cervix Uteri

  • Carcinoma Of The Cervix Uteri

Leukemia, Acute Myeloid
  • Acute Myeloid Leukemia

  • Leukemia, Acute Myelogenous

  • Acute Myelogenous Leukemia

  • AML

  • Leukemia, Acute Myeloid, Susceptibility To

  • Acute Myeloblastic Leukemia

  • Leukemia, Acute Myeloid, Reduced Survival In, Somatic

  • Acute Myeloid Leukaemia

  • Leukemia, Myelocytic, Acute

  • Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

  • Secondary Aml

  • Acute Myelocytic Leukemia

  • Leukemia, Myeloid, Acute

  • Acute Myeloid Leukemia, Somatic

  • Leukemia, Acute Myeloid, Somatic

  • Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

  • Acute Myeloblastic Leukaemia

  • Acute Myelogenous Leukaemia

  • Aml - Acute Myeloid Leukemia

  • Acute Myeloid Leukemia With Cebpa Somatic Mutations

  • Aml With Cebpa Somatic Mutations

  • Inherited Acute Myeloid Leukemia

  • Familial Aml

  • Inherited Aml

  • Pure Familial Aml

  • Pure Familial Acute Myeloid Leukemia

  • Secondary Acute Myeloid Leukemia

  • Therapy-Related Aml And Myelodysplastic Syndrome

  • Acute Myeloid Leukemia, Secondary

  • Acute Non-Lymphoblastic Leukemia

  • Acute Non-Lymphocytic Leukemia

  • Acute Biphenotypic Leukemia

  • Acute Undifferentiated Leukemia

  • Acute Myeloblastic Leukaemia With Multilineage Dysplasia

  • Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

  • Acute Myeloid Leukaemia With Myelodysplasia-Related Features

Leptin Deficiency Or Dysfunction
  • Morbid Obesity

  • Obesity Due To Congenital Leptin Deficiency

  • LEPD

  • Congenital Leptin Deficiency

  • Obesity, Morbid

  • Obesity, Morbid, Due To Leptin Deficiency

  • Severe Obesity

  • Obesity, Morbid, Nonsyndromic 1

  • Leptin Deficiency

  • Obesity, Severe, Due To Leptin Deficiency

  • Morbid Obesity Due To Leptin Deficiency

  • Obesity Morbid

  • Leptin Dysfunction

  • Leptin

Adult Spinal Cord Glioblastoma Multiforme
  • Glioblastoma Multiforme Of Spinal Cord

  • Adult Spinal Cord Glioblastoma

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus FTO VGNC VGNC:29138
Canis familiaris FTO VGNC VGNC:41003
Rattus norvegicus FTO RGD RGD:1305121
Felis catus FTO VGNC VGNC:62384
Macaca mulatta FTO VGNC VGNC:72772
Mus musculus FTO MGD MGI:1347093
Others FTO NCBI