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:
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 |
Vaild Sequence:
Related Databases
Uniprot:
ELISA Kit
CLIA Kit
Polyclonal Antibody
Monoclonal Antibody
Protein
FOR
Mouse
Human
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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References
1.
"Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice."
Kikkawa Y.
,
Shitara H.
,
Wakana S.
,
Kohara Y.
,
Takada T.
,
Okamoto M.
,
Taya C.
,
Kamiya K.
,
Yoshikawa Y.
,
Tokano H.
,
Kitamura K.
,
Shimizu K.
,
Wakabayashi Y.
,
Shiroishi T.
,
Kominami R.
,
Yonekawa H.
Hum. Mol. Genet.12:453-461(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 : NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA];TISSUE SPECIFICITY;POSSIBLE FUNCTION
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.
"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.
[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