SOLH2 Rabbit Polyclonal Antibody, 20ul Culture Plate Inserts Mutations in a related gene

Mutations in a related gene on chromosome X cause X-linked amelogenesis imperfecta

Members of this family contain a C-terminal DNA-binding domain with three Kruppel-like zinc fingers

protein tyrosine kinase 2 beta undergoes rapid tyrosine phosphorylation and activation in response to increases in the intracellular calcium concentration

Alternate transcription initiation sites result in two transcript variants of this gene

|Contains 1 PID domain

SOLH2 Rabbit Polyclonal Antibody, 20ul Culture Plate Inserts Mutations in a related geneThis gene encodes one of testis specific transcription factors which are essential for spermatogenesis oogenesis and folliculogenesis. This gene is located on chromosome 13. The proteins encoded by this gene and another testis specific transcription factor SOHLH1 can form heterodimers in addition to homodimers. There is a read through locus (GeneID: 100526761) that shares sequence identity with this gene and the upstream CCDC169 (GeneID: 728591).