FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1)

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FGDY; ZFYVE3; Faciogenital Dysplasia; Rho/Rac guanine nucleotide exchange factor FGD1; Zinc finger FYVE domain-containing protein 3

FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1)
FGD1 contains Dbl (DH) and pleckstrin (PH) homology domains. It can bind specifically to the Rho family GTPase Cdc42Hs and stimulate the GDP-GTP exchange of the isoprenylated form of Cdc42Hs. It also stimulates the mitogen activated protein kinase cascade leading to c-Jun kinase SAPK/JNK1 activation. FGD1 has an essential role in embryonic development, and FGD1 gene mutations result in the human developmental disorder, Aarskog-Scott syndrome.The mouse cDNA clones contained a 2,880-bp open reading frame predicted to encode a protein of 960 amino acids, 1 amino acid shorter than the human FGD1 open reading frame. Comparison of the mouse and human sequences within the coding region indicated 94.7% identity (96.3% similarity) at the amino acid level.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) CLIA Kit Customized Service Offer
n/a ELISA Kit for FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) CLIA Kit Customized Service Offer
n/a ELISA Kit for FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) CLIA Kit Customized Service Offer
n/a ELISA Kit for FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1) ELISA Kit Customized Service Offer
  1. "Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor."Cell 79:669-678(1994) [PubMed] [Europe PMC] [Abstract]
  2. "The DNA sequence of the human X chromosome." Nature 434:325-337(2005) [PubMed] [Europe PMC] [Abstract]
  3. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  4. "The faciogenital dysplasia gene product FGD1 functions as a Cdc42Hs-specific guanine-nucleotide exchange factor."J. Biol. Chem. 271:33169-33172(1996) [PubMed] [Europe PMC] [Abstract]
  5. "A quantitative atlas of mitotic phosphorylation."Proc. Natl. Acad. Sci. U.S.A. 105:10762-10767(2008) [PubMed] [Europe PMC] [Abstract]
  6. "Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis."Sci. Signal. 3:RA3-RA3(2010) [PubMed] [Europe PMC] [Abstract]
  7. "Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome."Eur. J. Hum. Genet. 8:869-874(2000) [PubMed] [Europe PMC] [Abstract]
  8. "A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome)."FEBS Lett. 478:216-220(2000) [PubMed] [Europe PMC] [Abstract]
  9. "Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene."Clin. Genet. 61:139-145(2002) [PubMed] [Europe PMC] [Abstract]
  10. "Phenotypic and molecular characterisation of the Aarskog-Scott syndrome: a survey of the clinical variability in light of FGD1 mutation analysis in 46 patients."Eur. J. Hum. Genet. 12:16-23(2004) [PubMed] [Europe PMC] [Abstract]