FYVE, RhoGEF and PH domain-containing protein 2 (FGD2), also known as zinc finger FYVE domain-containing protein 4 (ZFYVE4), is a protein that in humans is encoded by the FGD2 gene.[5]
It is a member of the FYVE, RhoGEF and PH domain containing family.
See also
edit- FYVE domain (zinc finger domain)
- RhoGEF domain (with guanine nucleotide exchange factor activity)
- PH domain (pleckstrin homology domain)
References
edit- ^ a b c GRCh38: Ensembl release 89: ENSG00000146192 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024013 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: FYVE".
Further reading
edit- Salehi AH, Xanthoudakis S, Barker PA (2002). "NRAGE, a p75 neurotrophin receptor-interacting protein, induces caspase activation and cell death through a JNK-dependent mitochondrial pathway". J. Biol. Chem. 277 (50): 48043–50. doi:10.1074/jbc.M205324200. PMID 12376548.48043-50&rft.date=2002&rft_id=info:doi/10.1074/jbc.M205324200&rft_id=info:pmid/12376548&rft.aulast=Salehi&rft.aufirst=AH&rft.au=Xanthoudakis, S&rft.au=Barker, PA&rft_id=https://doi.org/10.1074%2Fjbc.M205324200&rfr_id=info:sid/en.wikipedia.org:FGD2" class="Z3988">
- Mungall AJ, Palmer SA, Sims SK, et al. (2003). "The DNA sequence and analysis of human chromosome 6". Nature. 425 (6960): 805–11. Bibcode:2003Natur.425..805M. doi:10.1038/nature02055. PMID 14574404.805-11&rft.date=2003&rft_id=info:pmid/14574404&rft_id=info:doi/10.1038/nature02055&rft_id=info:bibcode/2003Natur.425..805M&rft.aulast=Mungall&rft.aufirst=AJ&rft.au=Palmer, SA&rft.au=Sims, SK&rft_id=https://doi.org/10.1038%2Fnature02055&rfr_id=info:sid/en.wikipedia.org:FGD2" class="Z3988">
- Hattori A, Okumura K, Nagase T, et al. (2000). "Characterization of long cDNA clones from human adult spleen". DNA Res. 7 (6): 357–66. doi:10.1093/dnares/7.6.357. PMID 11214971.357-66&rft.date=2000&rft_id=info:doi/10.1093/dnares/7.6.357&rft_id=info:pmid/11214971&rft.aulast=Hattori&rft.aufirst=A&rft.au=Okumura, K&rft.au=Nagase, T&rft_id=https://doi.org/10.1093%2Fdnares%2F7.6.357&rfr_id=info:sid/en.wikipedia.org:FGD2" class="Z3988">
- Pasteris NG, Gorski JL (1999). "Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues". Genomics. 60 (1): 57–66. doi:10.1006/geno.1999.5903. PMID 10458911.57-66&rft.date=1999&rft_id=info:doi/10.1006/geno.1999.5903&rft_id=info:pmid/10458911&rft.aulast=Pasteris&rft.aufirst=NG&rft.au=Gorski, JL&rfr_id=info:sid/en.wikipedia.org:FGD2" class="Z3988">
- 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 15489334.2121-7&rft.date=2004&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC528928#id-name=PMC&rft_id=info:pmid/15489334&rft_id=info:doi/10.1101/gr.2596504&rft.aulast=Gerhard&rft.aufirst=DS&rft.au=Wagner, L&rft.au=Feingold, EA&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC528928&rfr_id=info:sid/en.wikipedia.org:FGD2" class="Z3988">
- 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 14702039.40-5&rft.date=2004&rft_id=info:doi/10.1038/ng1285&rft_id=info:pmid/14702039&rft.aulast=Ota&rft.aufirst=T&rft.au=Suzuki, Y&rft.au=Nishikawa, T&rft_id=https://doi.org/10.1038%2Fng1285&rfr_id=info:sid/en.wikipedia.org:FGD2" class="Z3988">
- Harrington AW, Kim JY, Yoon SO (2002). "Activation of Rac GTPase by p75 is necessary for c-jun N-terminal kinase-mediated apoptosis". J. Neurosci. 22 (1): 156–66. doi:10.1523/JNEUROSCI.22-01-00156.2002. PMC 6757583. PMID 11756498.156-66&rft.date=2002&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757583#id-name=PMC&rft_id=info:pmid/11756498&rft_id=info:doi/10.1523/JNEUROSCI.22-01-00156.2002&rft.aulast=Harrington&rft.aufirst=AW&rft.au=Kim, JY&rft.au=Yoon, SO&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757583&rfr_id=info:sid/en.wikipedia.org:FGD2" class="Z3988">
- Strausberg RL, Feingold EA, Grouse LH, et al. (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 12477932.16899-903&rft.date=2002&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139241#id-name=PMC&rft_id=info:pmid/12477932&rft_id=info:doi/10.1073/pnas.242603899&rft_id=info:bibcode/2002PNAS...9916899M&rft.aulast=Strausberg&rft.aufirst=RL&rft.au=Feingold, EA&rft.au=Grouse, LH&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139241&rfr_id=info:sid/en.wikipedia.org:FGD2" class="Z3988">
- Rabizadeh S, Bredesen DE (2003). "Ten years on: mediation of cell death by the common neurotrophin receptor p75(NTR)". Cytokine Growth Factor Rev. 14 (3–4): 225–39. doi:10.1016/S1359-6101(03)00018-2. PMID 12787561.3–4&rft.pages=225-39&rft.date=2003&rft_id=info:doi/10.1016/S1359-6101(03)50018-2&rft_id=info:pmid/12787561&rft.aulast=Rabizadeh&rft.aufirst=S&rft.au=Bredesen, DE&rfr_id=info:sid/en.wikipedia.org:FGD2" class="Z3988">
- Huber C, Mårtensson A, Bokoch GM, et al. (2008). "FGD2, a CDC42-specific exchange factor expressed by antigen-presenting cells, localizes to early endosomes and active membrane ruffles". J. Biol. Chem. 283 (49): 34002–12. doi:10.1074/jbc.M803957200. PMC 2590680. PMID 18838382.34002-12&rft.date=2008&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2590680#id-name=PMC&rft_id=info:pmid/18838382&rft_id=info:doi/10.1074/jbc.M803957200&rft.aulast=Huber&rft.aufirst=C&rft.au=Mårtensson, A&rft.au=Bokoch, GM&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2590680&rfr_id=info:sid/en.wikipedia.org:FGD2" class="Z3988">
- Delague V, Jacquier A, Hamadouche T, et al. (2007). "Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H". Am. J. Hum. Genet. 81 (1): 1–16. doi:10.1086/518428. PMC 1950914. PMID 17564959.1-16&rft.date=2007&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950914#id-name=PMC&rft_id=info:pmid/17564959&rft_id=info:doi/10.1086/518428&rft.aulast=Delague&rft.aufirst=V&rft.au=Jacquier, A&rft.au=Hamadouche, T&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950914&rfr_id=info:sid/en.wikipedia.org:FGD2" class="Z3988">