usherin

Summary
Gene Symbol
  • USH2A
Organism
Homo sapiens (human)
NCBI Gene
7399
PubChem
7399
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cell membrane
  • Cell projection
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Hearing
  • Laminin EGF-like domain
  • Reference proteome
  • Repeat
  • Retinitis pigmentosa
  • Secreted
  • Signal
  • Transmembrane helix
  • Usher syndrome
  • Vision
Proteins
Displaying 1 entry
UniProt Protein Name
O75445
  • Usher syndrome type IIa protein
  • Usher syndrome type-2A protein
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
netrin
Functional Category
  • E: Amino acid transport and metabolism
  • G: Carbohydrate transport and metabolism
  • M: Cell wall/membrane/envelope biogenesis
Displaying all 2 entries
Gene Ontology
animal organ morphogenesis
tissue development
Displaying 1 entry
InterPro
Laminin-type EGF domain
Disease
Disease Ontology
Displaying all 6 entries
DO ID Disease Name Source
DOID:0050439 Usher syndrome
DOID:0050563 nonsyndromic deafness
DOID:0110360 retinitis pigmentosa 39
DOID:0110827 Usher syndrome type 2
DOID:0110838 Usher syndrome type 2A
DOID:10584 retinitis pigmentosa

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024