Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Orphanet Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol HYLS1 contributors: mct/npt - updated : 06-01-2010
HGNC name hydrolethalus syndrome 1
HGNC id 26558
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
HOMOLOGY
Homologene
FAMILY
  • HYLS1 family
  • CATEGORY motor/contractile
    SUBCELLULAR LOCALIZATION     intracellular
    intracellular,cytoplasm
    intracellular,nucleus
    text localization to centrioles (Dammermann 2009)
    basic FUNCTION
  • plays an essential role in cilia formation (Dammermann 2009)
  • required for the apical targeting/anchoring of centrioles at the plasma membrane but not for the intraflagellar transport-dependent extension of the ciliary axoneme (Dammermann 2009)
  • dispensable for centriole duplication, centrosome function in cell division, and embryonic viability (Dammermann 2009)
  • contributes to basal body organization at the cell surface and helps initiate cilia formation (Dammermann 2009)
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
    protein
    cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) HYLS1
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS