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Index > Protein center > Ush1g(Gene name) > Mouse
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  • Ush1g (Gene name),
  • Usher syndrome type-1G protein homolog (Protein name ),  USH1G_MOUSE from NCBI database.
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  • General Annotation
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  • Antigen Annotation
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  • Vaild Sequence
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  • Gene name:
    Ush1g(Sans);
    Protein name:
    Usher syndrome type-1G protein homolog;
    Alternative:
    Scaffold protein containing ankyrin repeats and SAM domain;Jackson shaker protein;
    Organism:
    Mouse (Mus musculus). 
    General Annotation
    Sub Unit:
    Associates with USH1C by binding to its first PDZ domain. Interacts with PDZD7.
    Function:
    Unknown. Required for normal hearing. May have a role in the development and maintenance of the stereocilia bundles. Might function as an anchoring/scaffolding protein in hair cells. Could be involved in the functional network formed by USH1C, CDH23 and MYO7A that is required for cohesion of the growing hair bundle.
    Subcellular Location:
    N/A
    Protein Attributes:
    Sequence length:
    461
    Sequence:
    50:
    MNDQYHRAAR | DGYLELLKEA | TRKELNAPDE | DGMTPTLWAA | YHGNLESLRL | 
    100:
    IVSRGGDPDK | CDIWGNTPLH | LAASNGHLHC | LSFLVSFGAN | IWCLDNDYHT | 
    150:
    PLDMAAMKGH | MECVRYLDSI | AAKQSSLNPK | LVGKLKDKAF | REAERRIREC | 
    200:
    AKMQRKHHER | MERRYRRELA | ERSDTLSFSS | LTSSTLSRRL | QHMTLGSQLP | 
    250:
    YSQATLHGTA | KGKAKIQKKL | ERRKQGGEGT | FKVSEDGRKS | VRSLSGLQLG | 
    300:
    SDVMFVRQGT | YANPKEWGRA | PLRDMFLSDE | DSVSRATLAA | EPAHSEVSTD | 
    350:
    SGHDSLFTRP | GLGTMVFRRN | YVSSGLHGLG | REDGGLDGAG | TPRGRLHSSP | 
    400:
    SLDDDSLGSA | NSLQDRSCGE | ELPWDELDLG | LDEDLEPETS | PLETFLASLH | 
    450:
    MEDFASLLRH | EKIDLEALML | CSDLDLRSIS | VPLGPRKKIL | GAVRRRRQAL | 
    461:
    ERPLALEDTE | L
    3D Structure:
    N/A
    Predicted Eptitope:
    Please Sign in.
    EIAab Sequence  Vaild Sequence:
    Please Sign in.
    Related Databases
    KEGG:
    SMR:
    Pfam:
    UniGene:
    String:
    Uniprot:
     
    FOR
    ELISA Kit for Mouse Usher syndrome type-1G protein homolog
    ELISA Kit for Mouse Usher syndrome type-1G protein homolog
    CLIA Kit for Mouse Usher syndrome type-1G protein homolog
    CLIA Kit for Mouse Usher syndrome type-1G protein homolog
    Polyclonal Antibody for Mouse Usher syndrome type-1G protein homolog
    Polyclonal Antibody for Mouse Usher syndrome type-1G protein homolog
    Monoclonal Antibody for Mouse Usher syndrome type-1G protein homolog
    Monoclonal Antibody for Mouse Usher syndrome type-1G protein homolog
    Protein for Mouse Usher syndrome type-1G protein homolog
    Protein for Mouse Usher syndrome type-1G protein homolog

    R&D Technical Data
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    Precision
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    Recovery
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    Linearity
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    For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.
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    References
    1. 1.
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA];TISSUE SPECIFICITY;POSSIBLE FUNCTION
    2. 2.
      "Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin."
      Weil D. , El-Amraoui A. , Masmoudi S. , Mustapha M. , Kikkawa Y. , Laine S. , Delmaghani S. , Adato A. , Nadifi S. , Zina Z.B. , Hamel C. , Gal A. , Ayadi H. , Yonekawa H. , Petit C.
      Hum. Mol. Genet.12:463-471(2003) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: INTERACTION WITH USH1C;POSSIBLE FUNCTION
    3. 3.
      "Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia."
      Caberlotto E. , Michel V. , Foucher I. , Bahloul A. , Goodyear R.J. , Pepermans E. , Michalski N. , Perfettini I. , Alegria-Prevot O. , Chardenoux S. , Do Cruzeiro M. , Hardelin J.P. , Richardson G.P. , Avan P. , Weil D. , Petit C.
      Proc. Natl. Acad. Sci. U.S.A.108:5825-5830(2011) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: FUNCTION;DISRUPTION PHENOTYPE;TISSUE SPECIFICITY;SUBCELLULAR LOCATION;INTERACTION WITH CDH23 AND PCDH15
    4. 4.
      "Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction."
      Grati M. , Kachar B.
      Proc. Natl. Acad. Sci. U.S.A.108:11476-11481(2011) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: FUNCTION;TISSUE SPECIFICITY;SUBCELLULAR LOCATION
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