• Official Full Name
  • Usher syndrome 1G (autosomal recessive)
  • Background
  • This gene encodes a protein that contains three ankyrin domains, a class I PDZ-binding motif and a sterile alpha motif. The encoded protein interacts with harmonin, which is associated with Usher syndrome type 1C. This protein plays a role in the development and maintenance of the auditory and visual systems and functions in the cohesion of hair bundles formed by inner ear sensory cells. Mutations in this gene are associated with Usher syndrome type 1G (USH1G).
  • Synonyms
  • USH1G; Usher syndrome 1G (autosomal recessive); Usher syndrome type-1G protein; ANKS4A; FLJ33924; Sans; scaffold protein containing ankyrin repeats and SAM domain
Source (Host):E. coliSpecies:Human
Product nameRecombinant Human USH1G, His-tagged
Source (Host):Species:Human
Product nameRecombinant Human USH1G 293 Cell Lysate

Protein Function

USH1G has several biochemical functions, for example, protein binding, protein homodimerization activity, spectrin binding. Some of the functions are cooperated with other proteins, some of the functions could acted by USH1G itself. We selected most functions USH1G had, and list some proteins which have the same functions with USH1G. You can find most of the proteins on our site.
Related Protein
Function protein binding
Related Protein CCL20; FANCC; THBS2; CRMP1; ZNF394; NUP98; ZKSCAN5; SLC25A6; ZNF10; FEM1C
Function protein homodimerization activity
Related Protein ATPIF1B; HPRT1; MAP3K13; CRYAB; CRTAM; NKX2-5; CBX5; NTSR1; AP1S2; SEPT12
Function spectrin binding
Related Protein STX4A; DCTN2; CAMSAP1; SPTAN1; DYNC1I1; SLC26A5; ADD1; EPB49; GNB1; ADD2

Interacting Protein

USH1G has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with USH1G here. Most of them are supplied by our site. Hope this information will be useful for your research of USH1G.