ush2a
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  • Official Full Name
  • Usher syndrome 2A (autosomal recessive, mild)
  • Background
  • This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs. The protein is found in the basement membrane, and may be important in development and homeostasis of the inner ear and retina. Mutations within this gene have been associated with Usher syndrome type IIa and retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene.
  • Synonyms
  • USH2A; Usher syndrome 2A (autosomal recessive, mild); USH2; usherin; RP39; dJ1111A8.1; US2; Usher syndrome type IIa protein; Usher syndrome type-2A protein; OTTHUMP00000035145; OTTHUMP00000063383
Cat.#:USH2A-17894MTag:His
Source (Host):Mammalian CellsSpecies:Mouse
Product nameRecombinant Mouse USH2A Protein
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Cat.#:USH2A-6464RTag:His
Source (Host):Mammalian CellsSpecies:Rat
Product nameRecombinant Rat USH2A Protein
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Protein Function

USH2A has several biochemical functions, for example, collagen binding, myosin binding, protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by USH2A itself. We selected most functions USH2A had, and list some proteins which have the same functions with USH2A. You can find most of the proteins on our site.
Function
Related Protein
Function collagen binding
Related Protein ITGA3; SRGN; SMAD3; USH2A; GP6; CTSS; DDR1; HSD17B12; CCBE1; C1QTNF1
Function myosin binding
Related Protein CALD1; TRIM32; ACTA1; MYBPC3; SLC6A4; STX4A; VETZ; USH2A; NPHS1; CALD1B
Function protein binding
Related Protein CD200R4; SPINLW1; TACSTD2; COMMD10; COP1; OTX1; TMEM8A; FDX1L; RAB6B; PHAX
Function protein homodimerization activity
Related Protein EXT1; PVRL3; PLD6; IKBKG; STOM; Trl; TREX2; SNX2; ACOT7; TWIST1