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OCRL

From Wikipedia, the free encyclopedia
OCRL
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesOCRL, LOCR, NPHL2, OCRL-1, OCRL1, oculocerebrorenal syndrome of Lowe, inositol polyphosphate-5-phosphatase, OCRL inositol polyphosphate-5-phosphatase, INPP5F, Dent-2, DENT2
External IDsOMIM: 300535; MGI: 109589; HomoloGene: 233; GeneCards: OCRL; OMA:OCRL - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000276
NM_001587
NM_001318784

NM_177215

RefSeq (protein)

NP_000267
NP_001305713
NP_001578

NP_796189

Location (UCSC)Chr X: 129.54 – 129.59 MbChr X: 47.91 – 47.97 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Inositol 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 in humans.[5]

This gene encodes an inositol polyphosphate 5-phosphatase. The responsible gene locus is at Xq26.1. This phosphatase enzyme is in part responsible for regulating membrane trafficking actin polymerization, and is located in several subcellular parts of the trans-Golgi network.

Deficiencies in OCRL-1 may cause with oculocerebrorenal syndrome[6] and also have been linked to Dent's disease.[7][8]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000122126Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000001173Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: oculocerebrorenal syndrome of Lowe".
  6. ^ Kawano T, Indo Y, Nakazato H, Shimadzu M, Matsuda I (June 1998). "Oculocerebrorenal syndrome of Lowe: three mutations in the OCRL1 gene derived from three patients with different phenotypes". Am. J. Med. Genet. 77 (5): 348–55. doi:10.1002/(SICI)1096-8628(19980605)77:5<348::AID-AJMG2>3.0.CO;2-J. PMID 9632163.
  7. ^ Online Mendelian Inheritance in Man (OMIM): 300555
  8. ^ Hoopes RR, Shrimpton AE, Knohl SJ, et al. (February 2005). "Dent Disease with mutations in OCRL1". Am. J. Hum. Genet. 76 (2): 260–7. doi:10.1086/427887. PMC 1196371. PMID 15627218.

Further reading

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