FTO Recombinant Rabbit Monoclonal Antibody [JM98-30] (ET1705-89)

UNIPROT #

Q9C0B1

PROTEIN NAME

FTO

SYNONYMS

AlkB homolog 9 antibody;ALKBH9 antibody;Alpha-ketoglutarate-dependent dioxygenase FTO antibody;AW743446 antibody;Fat mass and obesity-associated protein antibody;FATSO, MOUSE, HOMOLOG OF antibody;Fto antibody;FTO_HUMAN antibody;GDFD antibody;KIAA1752 antibody;mKIAA1752 antibody;Protein fatso antibody

SEQUENCE SIMILARITIES

Belongs to the fto family.

TISSUE SPECIFICITY

Ubiquitously expressed, with relatively high expression in adrenal glands and brain; especially in hypothalamus and pituitary. Highly expressed in highly expressed in acute myeloid leukemias (AML) with t(11;11)(q23;23) with KMT2A/MLL1 rearrangements, t(15;17)(q21;q21)/PML-RARA, FLT3-ITD, and/or NPM1 mutations.

SUBCELLULAR LOCATION

Cytoplasm, Nucleus.

FUNCTION

FTO, also known as Fatso or KIAA1752, is a 505 amino acid protein that has an N-terminal nuclear localization signal. Expressed in a variety of tissues, with highest levels present in brain and pancreatic tissue, Fatso exists as four alternatively spliced isoforms, one of which is associated with a predisposition to childhood and adult obesity. Due to its involvement in the development of obesity, Fatso is associated with an increased BMI and may be involved in the pathogenesis of type 2 diabetes. The gene encoding Fatso maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.