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Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

Authors: Eudy, JD  Weston, MD  Yao, S  Hoover, DM  Rehm, HL  Ma-Edmonds, M  Yan, D  Ahmad, I  Cheng, JJ  Ayuso, C  Cremers, C  Davenport, S  Moller, C  Talmadge, CB  Beisel, KW  Tamayo, M  Morton, CC  Swaroop, A  Kimberling, WJ  Sumegi, J 
Citation: Eudy JD, etal., Science. 1998 Jun 12;280(5370):1753-7.
Pubmed: (View Article at PubMed) PMID:9624053

Usher syndrome type IIa (OMIM 276901), an autosomal recessive disorder characterized by moderate to severe sensorineural hearing loss and progressive retinitis pigmentosa, maps to the long arm of human chromosome 1q41 between markers AFM268ZD1 and AFM144XF2. Three biologically important mutations in Usher syndrome type IIa patients were identified in a gene (USH2A) isolated from this critical region. The USH2A gene encodes a protein with a predicted size of 171.5 kilodaltons that has laminin epidermal growth factor and fibronectin type III motifs; these motifs are most commonly observed in proteins comprising components of the basal lamina and extracellular matrixes and in cell adhesion molecules.


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CRRD Object Information
CRRD ID: 8547987
Created: 2014-03-04
Species: All species
Last Modified: 2014-03-04
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.