FYVE, RhoGEF And PH Domain Containing protein 1 (FGD1)
[Edit]FGDY; ZFYVE3; Faciogenital Dysplasia; Rho/Rac guanine nucleotide exchange factor FGD1; Zinc finger FYVE domain-containing protein 3
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 |
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- "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]
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- "A quantitative atlas of mitotic phosphorylation."Proc. Natl. Acad. Sci. U.S.A. 105:10762-10767(2008) [PubMed] [Europe PMC] [Abstract]
- "Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis."Sci. Signal. 3:RA3-RA3(2010) [PubMed] [Europe PMC] [Abstract]
- "Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome."Eur. J. Hum. Genet. 8:869-874(2000) [PubMed] [Europe PMC] [Abstract]
- "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]
- "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]
- "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]