Sequence Detail

ID/Version

Q9JII1 Q3TCC9 (UniProt | EBI)

Last sequence update: 2000-10-01
Last annotation update: 2025-02-05

Sequence description from provider

RecName: Full=Phosphatidylinositol polyphosphate 5-phosphatase type IV;AltName: Full=72 kDa inositol polyphosphate 5-phosphatase {ECO:0000303|PubMed:10806194};AltName: Full=Inositol polyphosphate-5-phosphatase E;AltName: Full=Phosphatidylinositol 4,5-bisp

Provider

SWISS-PROT

Sequence

Polypeptide 647 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Inpp5e	inositol polyphosphate-5-phosphatase E	54	107	3	8

Sequence references in MGI

J:63827 Kong AM, et al., Cloning and characterization of a 72-kDa inositol-polyphosphate 5-phosphatase localized to the Golgi network. J Biol Chem. 2000 Aug 4;275(31):24052-64
J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:152712 Jacoby M, et al., INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse. Nat Genet. 2009 Sep;41(9):1027-31
J:249381 Yang AW, et al., Deletion of Inpp5a causes ataxia and cerebellar degeneration in mice. Neurogenetics. 2015 Oct;16(4):277-85
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89