S2542 Rabbit Polyclonal Antibody, 20ul Cell Proliferation Huntingtin is a disease gene

Huntingtin is a disease gene linked to Huntington's disease| a neurodegenerative disorder characterized by loss of striatal neurons

This gene is expressed exclusively in the brain

This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain

non-receptor type 22 is a lymphoid-specific intracellular phosphatase that associates with the molecular adapter protein CBL and may be involved in regulating CBL function in the T-cell receptor signaling pathway

FES encodes the human cellular counterpart of a feline sarcoma retrovirus protein with transforming capabilities

S2542 Rabbit Polyclonal Antibody, 20ul Cell Proliferation Huntingtin is a disease geneThis gene encodes a solute carrier family 25 protein. Solute carrier family 25 proteins are localized to mitochondria and play critical roles in the transport of molecules across the inner mitochondrial membrane. The encoded protein is a mitochondrial transporter for coenzyme A (CoA) and adenosine 3' 5' diphosphate.