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KERA

Official Full Name
keratocan
Organism
Homo sapiens
GeneID
11081
Background
The protein encoded by this gene is a keratan sulfate proteoglycan that is involved in corneal transparency. Defects in this gene are a cause of autosomal recessive cornea plana 2 (CNA2).[provided by RefSeq, May 2010]
Synonyms
KTN; CNA2; SLRR2B;

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