SOX5 Rabbit Polyclonal Antibody, 100ul Antibodies Mutations in this gene cause

Mutations in this gene cause early infantile epileptic encephalopathy 25

and IL1RL1 (T1/ST2)

and seems to be involved in angiogenesis and vascular patterning

neuromedin N and neurotensin

Additional isoforms resulting from the use of alternate in-frame translation initiation sites have also been described

SOX5 Rabbit Polyclonal Antibody, 100ul Antibodies Mutations in this gene causeThis gene encodes a member of the SOX (SRY related HMG box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. The encoded protein may play a role in chondrogenesis. A pseudogene of this gene is located on chromosome 8. Multiple transcript variants encoding distinct