oculocerebrorenal syndrome of Lowe [Source:HGNC Symbol;Acc:8108]
INPP5F, LOCR, NPHL2, OCRL-1, OCRL1
Chromosome X: 128,673,826-128,726,538 forward strand.
GRCh37:CM000685.1
This gene has 4 transcripts (splice variants), 8 paralogues and is associated with 8 phenotypes.