gene

USH1G

Entity Detail — Knowledge Graph Node

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This page aggregates everything SciDEX knows about USH1G: its mechanistic relationships (Knowledge Graph edges), hypotheses targeting it, analyses mentioning it, and supporting scientific papers. The interactive graph below shows its immediate neighbors. All content is AI-synthesized from peer-reviewed literature.

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🧬 Gene Info
Gene SymbolUSH1G
Full NameUSHER Syndrome 1G Protein (SANS)
Chromosome17q25.1
Protein TypeGene
Functionis a critical gene involved in the development and maintenance of the auditory and visual systems.
Primary Expressionboth inner and outer hair cells of the cochlea - Stereocilia: Localizes to the stereociliary tips and shafts - Vestibular system: Present in h
Molecular Weight51 kDa
Amino Acids460 aa
GeneCardsUSH1G
Human Protein AtlasUSH1G
Ankyrin (ANK) repeat domainThree ankyrin repeats (residues 50-180) that mediate protein-protein interactions
SAM (Sterile Alpha Motif) domainLocated in the central region (residues 200-260)
PDZ-binding motifThe extreme C-terminus contains a canonical PDZ-binding sequence (S/T-X-L/V)
Hair cellsExpressed in both inner and outer hair cells of the cochlea
StereociliaLocalizes to the stereociliary tips and shafts
Associated Diseasesneurodegeneration
DatabasesGeneCardsUniProtNCBI GeneHPASTRING

Wiki Pages (2)

Knowledge base pages for this entity

Canonical Page

USH1G — USHER Syndrome 1G Protein (SANS)

gene · 3073 words

USH1G Protein

protein · 748 words

Pathway Diagram

graph TD
    USH1G["USH1G"]
    neurodegeneration["neurodegeneration"]
    USH1G -->|"implicated_in"| neurodegeneration
    style USH1G fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0

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Targeting Hypotheses (0)

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Mentioning Analyses (0)

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Experiments (0)

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