ocrl Gene Set

Dataset	GeneRIF Biological Term Annotations
Category	structural or functional annotations
Type	biological term
Description	oculocerebrorenal syndrome of Lowe\|This gene encodes a phosphatase enzyme that is involved in actin polymerization and is found in the trans-Golgi network. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. [provided by RefSeq, Jul 2008] (NCBI Entrez Gene Database, 4952)
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Genes

11 genes co-occuring with the biological term ocrl in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol	Name
APPL1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1
FAM109A	family with sequence similarity 109, member A
FAM109B	family with sequence similarity 109, member B
GRB2	growth factor receptor-bound protein 2
IGF2R	insulin-like growth factor 2 receptor
INPP5B	inositol polyphosphate-5-phosphatase, 75kDa
OCRL	oculocerebrorenal syndrome of Lowe
RAB35	RAB35, member RAS oncogene family
RAB5A	RAB5A, member RAS oncogene family
TRPV4	transient receptor potential cation channel, subfamily V, member 4
TRPV6	transient receptor potential cation channel, subfamily V, member 6