PIK3IP1

PIK3IP1
Identifiers
Aliases	PIK3IP1 , HGFL, hHGFL(S), phosphoinositide-3-kinase interacting protein 1, TrIP
External IDs	MGI: 1917016; HomoloGene: 14166; GeneCards: PIK3IP1; OMA:PIK3IP1 - orthologs
Gene location (Human) Chr. Chromosome 22 (human) [1] Band 22q12.2 Start 31,281,594 bp [1] End 31,292,534 bp [1]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in lymph node olfactory zone of nasal mucosa right lung granulocyte blood gastric mucosa spleen tibial nerve skin of leg skin of abdomen n/a More reference expression data BioGPS More reference expression data
Gene ontology Molecular function phosphatidylinositol 3-kinase catalytic subunit binding protein binding Cellular component integral component of membrane plasma membrane membrane Biological process negative regulation of phosphatidylinositol 3-kinase signaling negative regulation of phosphatidylinositol 3-kinase activity Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 113791 216505 Ensembl ENSG00000100100 n/a UniProt Q96FE7 Q7TMJ8 RefSeq (mRNA) NM_052880 NM_001135911 NM_178149 RefSeq (protein) NP_001129383 NP_443112 NP_835362 Location (UCSC) Chr 22: 31.28 – 31.29 Mb n/a PubMed search [2] [3]
Wikidata
View/Edit Human View/Edit Mouse

Phosphoinositide-3-kinase-interacting protein 1 (PIK3IP1) is an enzyme that in humans is encoded by the PIK3IP1 gene. ^{[4] [5]}

PIK3IP1 is a transmembrane protein that binds to PI3K, reducing signal to the PI3K/AKT/mTOR pathway. ^[6] Through this mechanism, PIK3IP1 inhibits cell proliferation in tumor cells and is associated with cancer. PIK3IP1 is also associated with the inflammatory response and autoimmune diseases. ^[6]

References

1. GRCh38: Ensembl release 89: ENSG00000100100 – Ensembl, May 2017
2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
3. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, Wagner L, Shenmen CM, Schuler GD, Altschul SF, Zeeberg B, Buetow KH, Schaefer CF, Bhat NK, Hopkins RF, Jordan H, Moore T, Max SI, Wang J, Hsieh F, Diatchenko L, Marusina K, Farmer AA, Rubin GM, Hong L, Stapleton M, Soares MB, Bonaldo MF, Casavant TL, Scheetz TE, Brownstein MJ, Usdin TB, Toshiyuki S, Carninci P, Prange C, Raha SS, Loquellano NA, Peters GJ, Abramson RD, Mullahy SJ, Bosak SA, McEwan PJ, McKernan KJ, Malek JA, Gunaratne PH, Richards S, Worley KC, Hale S, Garcia AM, Gay LJ, Hulyk SW, Villalon DK, Muzny DM, Sodergren EJ, Lu X, Gibbs RA, Fahey J, Helton E, Ketteman M, Madan A, Rodrigues S, Sanchez A, Whiting M, Madan A, Young AC, Shevchenko Y, Bouffard GG, Blakesley RW, Touchman JW, Green ED, Dickson MC, Rodriguez AC, Grimwood J, Schmutz J, Myers RM, Butterfield YS, Krzywinski MI, Skalska U, Smailus DE, Schnerch A, Schein JE, Jones SJ, Marra MA (Dec 2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc Natl Acad Sci U S A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi: 10.1073/pnas.242603899 . PMC   139241 . PMID   12477932.
5. "Entrez Gene: MGC17330 HGFL gene".
6. Jia, Yingjie; He, Pengxing; Ma, Xubin; Lv, Kaili; Liu, Ying; Xu, Yichao (2024-08-15). "PIK3IP1: structure, aberration, function, and regulation in diseases". European Journal of Pharmacology. 977 176753. doi:10.1016/j.ejphar.2024.176753. ISSN   1879-0712. PMID   38897445.

Further reading

• Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi: 10.1101/gr.6.9.791 . PMID   8889548.
• Dunham I, Shimizu N, Roe BA, et al. (1999). "The DNA sequence of human chromosome 22". Nature. 402 (6761): 489–95. Bibcode:1999Natur.402..489D. doi: 10.1038/990031 . PMID   10591208.
• Collins JE, Goward ME, Cole CG, et al. (2003). "Reevaluating human gene annotation: a second-generation analysis of chromosome 22". Genome Res. 13 (1): 27–36. doi:10.1101/gr.695703. PMC   430954 . PMID   12529303.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi: 10.1038/ng1285 . PMID   14702039.
• Zhang Z, Henzel WJ (2005). "Signal peptide prediction based on analysis of experimentally verified cleavage sites". Protein Sci. 13 (10): 2819–24. doi:10.1110/ps.04682504. PMC   2286551 . PMID   15340161.
• Collins JE, Wright CL, Edwards CA, et al. (2005). "A genome annotation-driven approach to cloning the human ORFeome". Genome Biol. 5 (10) R84. doi: 10.1186/gb-2004-5-10-r84 . PMC   545604 . PMID   15461802.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC   528928 . PMID   15489334.
• Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries". DNA Res. 12 (2): 117–26. doi: 10.1093/dnares/12.2.117 . PMID   16303743.
• Zhu Z, He X, Johnson C, et al. (2007). "PI3K is negatively regulated by PIK3IP1, a novel p110 interacting protein". Biochem. Biophys. Res. Commun. 358 (1): 66–72. doi:10.1016/j.bbrc.2007.04.096. PMC   1978172 . PMID   17475214.