TEKT1 Rabbit Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification Defects in MEF2A could be

Defects in MEF2A could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

is related to mutations in the ALMS1 gene

A pseudogene of this gene is located on the short arm of chromosome 2

the protein encoded by DYSF binds caveolin-3

SEMA3C (Semaphorin 3C) is a Protein Coding gene

TEKT1 Rabbit Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification Defects in MEF2A could beThis gene product belongs to the tektin family of proteins. Tektins comprise a family of filament forming proteins that are coassembled with tubulins to form ciliary and flagellar microtubules. This gene is predominantly expressed in the testis and in mouse tektin 1 mRNA was localized to the spermatocytes and round spermatids in the seminiferous tubules indicating that it may play a role in spermatogenesis.