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Myosin Id Polyclonal Antibody, 50ul Pathway and Network Analysis Prader-Willi syndrome

SKU: 1021894567

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Myosin Id Polyclonal Antibody, 50ul Pathway and Network Analysis Prader-Willi syndromeMYO1D (Myosin ID) is a Protein Coding gene. Diseases associated with MYO1D include visceral heterotaxy. Among its related pathways are Actin Nucleation by ARP WASP Complex and PAK Pathway. GO annotations related to this gene include actin binding and calmodulin binding. An important paralog of this gene is MYO3B.

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Description

Prader-Willi syndrome

Interacts with the phosphorylated carboxyterminal domain of POLR2A

X-linked distal spinal muscular atrophy

as well as with proliferating cell nuclear antigen

PTM:Binds keratan sulfate chains

Myosin Id Polyclonal Antibody, 50ul Pathway and Network Analysis Prader-Willi syndromeMYO1D (Myosin ID) is a Protein Coding gene. Diseases associated with MYO1D include visceral heterotaxy. Among its related pathways are Actin Nucleation by ARP WASP Complex and PAK Pathway. GO annotations related to this gene include actin binding and calmodulin binding. An important paralog of this gene is MYO3B.

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