OCRL
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oculocerebrorenal syndrome of Lowe
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Identifiers | |
Symbol | OCRL |
HUGO | 8108 |
Entrez | 4952 |
OMIM | 300535 |
RefSeq | NM_000276 |
UniProt | Q01968 |
Other data | |
EC number | 3.1.3.36 |
Locus | Chr. X q25-q26.1 |
OCRL is a gene on the X chromosome associated with oculocerebrorenal syndrome.