SKIP

INPP5K
Identifiers
Aliases	INPP5K, PPS, SKIP, inositol polyphosphate-5-phosphatase K, MDCCAID
External IDs	MGI: 1194899 HomoloGene: 75059 GeneCards: INPP5K
Gene location (Human)
Chr.	Chromosome 17 (human)[1]
End	1,516,888 bp[1]
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)[2]
End	75,648,871 bp[2]
RNA expression pattern
	; ;
	More reference expression data
Gene ontology
Molecular function	• inositol-1,3,4,5-tetrakisphosphate 5-phosphatase activity; • inositol-1,4,5-trisphosphate 5-phosphatase activity; • inositol bisphosphate phosphatase activity; • inositol-polyphosphate 5-phosphatase activity; • phosphatidylinositol phosphate 5-phosphatase activity; • phosphatidylinositol trisphosphate phosphatase activity; • protein binding; • lipid phosphatase activity; • inositol trisphosphate phosphatase activity; • hydrolase activity; • vasopressin receptor activity; • phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase activity; • phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity;
Cellular component	• cytoplasm; • cytosol; • membrane; • ruffle; • plasma membrane; • ruffle membrane; • trans-Golgi network; • endoplasmic reticulum; • perinuclear region of cytoplasm; • neuron projection; • cell nucleus;
Biological process	• negative regulation of protein phosphorylation; • G-protein coupled receptor signaling pathway; • negative regulation of protein kinase B signaling; • positive regulation of urine volume; • negative regulation of dephosphorylation; • negative regulation of protein kinase activity; • glucose homeostasis; • cellular response to tumor necrosis factor; • negative regulation of peptidyl-threonine phosphorylation; • in utero embryonic development; • negative regulation of glycogen biosynthetic process; • positive regulation of renal water transport; • cellular response to epidermal growth factor stimulus; • positive regulation of transcription, DNA-templated; • response to insulin; • negative regulation of insulin receptor signaling pathway; • negative regulation of protein targeting to membrane; • cellular response to hormone stimulus; • negative regulation of glucose transport; • negative regulation of glycogen (starch) synthase activity; • phosphatidylinositol dephosphorylation; • negative regulation of MAP kinase activity; • negative regulation of calcium ion transport; • negative regulation of peptidyl-serine phosphorylation; • cellular response to insulin stimulus; • phosphatidylinositol biosynthetic process; • regulation of glycogen biosynthetic process; • negative regulation of stress fiber assembly; • negative regulation of transcription, DNA-templated; • ruffle assembly; • inositol phosphate dephosphorylation; • actin cytoskeleton organization; • cellular response to cAMP; • dephosphorylation; • negative regulation of single stranded viral RNA replication via double stranded DNA intermediate; • protein localization to plasma membrane;
	Sources:Amigo / QuickGO
Orthologs
	51763
	19062
	ENSG00000132376
	ENSMUSG00000006127
	Q9BT40
	Q8C5L6
	NM_001135642; NM_016532; NM_130766
	NM_008916
	NP_001129114; NP_057616; NP_570122
	NP_032942
	Wikidata
View/Edit Human	View/Edit Mouse

SKIP is an acronym for Skeletal muscle and kidney enriched inositol phosphatase, which is a human gene.^[5]

Function

This gene encodes a protein with 5-phosphatase activity toward polyphosphate inositol. The protein localizes to the cytosol in regions lacking actin stress fibers. It is thought that this protein may negatively regulate the actin cytoskeleton. Alternative splicing of this gene results in two transcript variants encoding different isoforms.^[5] Overexpression of SKIP in mice affects osmoregulation in kidney collecting ducts.^[6]

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000132376 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000006127 - Ensembl, May 2017
↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
1 2 "Entrez Gene: SKIP skeletal muscle and kidney enriched inositol phosphatase".
↑ Pernot E, Terryn S, Cheong SC, Markadieu N, Janas S, Blockmans M, Jacoby M, Pouillon V, Gayral S, Rossier BC, Beauwens R, Erneux C, Devuyst O, Schurmans S (Dec 2011). "The inositol Inpp5k 5-phosphatase affects osmoregulation through the vasopressin-aquaporin 2 pathway in the collecting system". Pflügers Archiv. 462 (6): 871–83. doi:10.1007/s00424-011-1028-0. PMID 21938401.

Drayer AL, Pesesse X, De Smedt F, Communi D, Moreau C, Erneux C (Nov 1996). "The family of inositol and phosphatidylinositol polyphosphate 5-phosphatases". Biochemical Society Transactions. 24 (4): 1001–5. doi:10.1042/bst0241001. PMID 8968500.
Mitchell CA, Brown S, Campbell JK, Munday AD, Speed CJ (Nov 1996). "Regulation of second messengers by the inositol polyphosphate 5-phosphatases". Biochemical Society Transactions. 24 (4): 994–1000. doi:10.1042/bst0240994. PMID 8968499.
Ewing RM, Chu P, Elisma F, Li H, Taylor P, Climie S, McBroom-Cerajewski L, Robinson MD, O'Connor L, Li M, Taylor R, Dharsee M, Ho Y, Heilbut A, Moore L, Zhang S, Ornatsky O, Bukhman YV, Ethier M, Sheng Y, Vasilescu J, Abu-Farha M, Lambert JP, Duewel HS, Stewart II, Kuehl B, Hogue K, Colwill K, Gladwish K, Muskat B, Kinach R, Adams SL, Moran MF, Morin GB, Topaloglou T, Figeys D (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Molecular Systems Biology. 3 (1): 89. doi:10.1038/msb4100134. PMC 1847948. PMID 17353931.
Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
Chen J, Xu J, Zhao W, Hu G, Cheng H, Kang Y, Xie Y, Lu Y (Nov 2005). "Characterization of human LNX, a novel ligand of Numb protein X that is downregulated in human gliomas". The International Journal of Biochemistry & Cell Biology. 37 (11): 2273–83. doi:10.1016/j.biocel.2005.02.028. PMID 16002321.
Cardoso C, Leventer RJ, Ward HL, Toyo-Oka K, Chung J, Gross A, Martin CL, Allanson J, Pilz DT, Olney AH, Mutchinick OM, Hirotsune S, Wynshaw-Boris A, Dobyns WB, Ledbetter DH (Apr 2003). "Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3". American Journal of Human Genetics. 72 (4): 918–30. doi:10.1086/374320. PMC 1180354. PMID 12621583.
Ijuin T, Takenawa T (Feb 2003). "SKIP negatively regulates insulin-induced GLUT4 translocation and membrane ruffle formation". Molecular and Cellular Biology. 23 (4): 1209–20. doi:10.1128/MCB.23.4.1209-1220.2003. PMC 141139. PMID 12556481.
Gurung R, Tan A, Ooms LM, McGrath MJ, Huysmans RD, Munday AD, Prescott M, Whisstock JC, Mitchell CA (Mar 2003). "Identification of a novel domain in two mammalian inositol-polyphosphate 5-phosphatases that mediates membrane ruffle localization. The inositol 5-phosphatase skip localizes to the endoplasmic reticulum and translocates to membrane ruffles following epidermal growth factor stimulation". The Journal of Biological Chemistry. 278 (13): 11376–85. doi:10.1074/jbc.M209991200. PMID 12536145.
Ijuin T, Mochizuki Y, Fukami K, Funaki M, Asano T, Takenawa T (Apr 2000). "Identification and characterization of a novel inositol polyphosphate 5-phosphatase". The Journal of Biological Chemistry. 275 (15): 10870–5. doi:10.1074/jbc.275.15.10870. PMID 10753883.

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[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000132376 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000006127 - Ensembl, May 2017

[3] "Human PubMed Reference:".

[4] "Mouse PubMed Reference:".

[entrez-5] 1 2 "Entrez Gene: SKIP skeletal muscle and kidney enriched inositol phosphatase".

[Skip-6] Pernot E, Terryn S, Cheong SC, Markadieu N, Janas S, Blockmans M, Jacoby M, Pouillon V, Gayral S, Rossier BC, Beauwens R, Erneux C, Devuyst O, Schurmans S (Dec 2011). "The inositol Inpp5k 5-phosphatase affects osmoregulation through the vasopressin-aquaporin 2 pathway in the collecting system". Pflügers Archiv. 462 (6): 871–83. doi:10.1007/s00424-011-1028-0. PMID 21938401.

SKIP

Function

References

Further reading