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OCRL

OCRL

Protein-coding gene in the species Homo sapiens

polyphosphate 5-phosphatase OCRL-1, also known as Lowe oculocerebrorenal syndrome protein, is an enzyme encoded by the OCRL gene located on the X chromosome

OCRL

Oculocerebrorenal syndrome

Medical condition

dysfunction.[medical citation needed] This syndrome is caused by mutations in the OCRL gene which encodes an inositol polyphosphate-5-phosphatase. At least one

Oculocerebrorenal syndrome

Oculocerebrorenal_syndrome

Dent's disease

Medical condition

with the OCRL gene. Both Lowe syndrome (oculocerebrorenal syndrome) and Dent disease can be caused by truncating or missense mutations in OCRL. Diagnosis

Dent's disease

Dent's_disease

List of genetic disorders

1:30,000-100,000 Dent's disease (Genetic hypercalciuria) Xp11.22 CLCN5, OCRL Denys–Drash syndrome WT1 De Grouchy syndrome 18q D Dolichonychia Down syndrome

List of genetic disorders

List_of_genetic_disorders

List of public library systems in Georgia

Ocmulgee Regional Library System orls.org PINES Oconee Regional Library System ocrl.org PINES Ohoopee Regional Library System ohoopeelibrary.org PINES Okefenokee

List of public library systems in Georgia

List_of_public_library_systems_in_Georgia

Cytokinesis

Final stage of cell division

and its effector, the phosphatidylinositol-4,5-bisphosphate 5-phosphatase OCRL. The final step of abscission is controlled by the recruitment and polymerization

Cytokinesis

Oconee Regional Library System

The Oconee Regional Library System (OCRL) is a public library system that serves the counties of Glascock, Laurens, Johnson, Treutlen, and Washington Georgia

Oconee Regional Library System

Oconee_Regional_Library_System

Synaptojanin

Protein involved in vesicle uncoating in neurons

Other members of the family of 5'phosphoinositide phosphatases include OCRL, SHIP1, SHIP2, INPP5J, INPP5E, INPP5B, INPP5A and SKIP.[citation needed]

Synaptojanin

RhoGAP domain

Evolutionary conserved protein domain

FAM13A1; FKSG42; GMIP; GRLF1; HMHA1; INPP5B; KIAA1688; LOC553158; MYO9A; MYO9B; OCRL; OPHN1; PIK3R1; PIK3R2; PRR5; RACGAP1; RACGAP1P; RALBP1; RICH2; RICS; SH3BP1;

RhoGAP domain

RhoGAP_domain

Endonuclease/Exonuclease/phosphatase family

Protein family

DNASE1L1; DNASE1L2; DNASE1L3; INPP5A; INPP5B; INPP5D; INPP5E; INPPL1; KIAA1706; OCRL; PIB5PA; SKIP; SMPD2; SMPD3; SYNJ1; SYNJ2; TTRAP; Nocturnin; Mol CD, Kuo

Endonuclease/Exonuclease/phosphatase family

Endonuclease/Exonuclease/phosphatase_family

APPL1

Protein-coding gene in the species Homo sapiens

interact with Deleted in Colorectal Cancer, AKT2, but also Rab5, Rab21, OCRL and almost 30 other proteins. GRCh38: Ensembl release 89: ENSG00000157500

APPL1

List of human protein-coding genes 5

HGNC:8104; Q16625 11007 OCM HGNC:8105; P0CE72 11008 OCM2 HGNC:34396; P0CE71 11009 OCRL HGNC:8108; Q01968 11010 OCSTAMP HGNC:16116; Q9BR26 11011 ODAD1 HGNC:26560;

List of human protein-coding genes 5

List_of_human_protein-coding_genes_5

List of OMIM disorder codes

127750; SNCA Dementia, Lewy body; 127750; SNCB Dent's disease 2; 300555; OCRL Dent's disease; 300009; CLCN5 Dentatorubr–pallidoluysian atrophy; 125370;

List of OMIM disorder codes

List_of_OMIM_disorder_codes