TFII-I(Phospho Tyr248) Polyclonal Antibody, 100ul Plasma and with Stickler syndrome

and with Stickler syndrome

Part of a complex with TIP120A/CAND1 and RBX1

A read-through transcript variant composed of ZFP91 and the downstream CNTF gene sequence has been identified

Seems to have a role in retrograde membrane traffic at the level of the Golgi complex

TFII-I(Phospho Tyr248) Polyclonal Antibody, 100ul Plasma and with Stickler syndromeThis gene encodes a phosphoprotein containing six characteristic repeat motifs. The encoded protein binds to the initiator element (Inr) and E box element in promoters and functions as a regulator of transcription. This locus, along with several other neighboring genes, is deleted in Williams Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21.