Skip Navigation
Genetics Home Reference: your guide to understanding genetic conditions About   Site Map   Contact Us
 
Home A service of the U.S. National Library of Medicine®

Cell part

Cell part

  • Apical part of cell
    • CFTR: cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
    • PKHD1: polycystic kidney and hepatic disease 1 (autosomal recessive)
    • SLC26A4: solute carrier family 26, member 4
    • SLC46A1: solute carrier family 46 (folate transporter), member 1
    • USH1C: Usher syndrome 1C (autosomal recessive, severe)
  • Basal part of cell
    • LDLRAP1: low density lipoprotein receptor adaptor protein 1
  • Cell division site
    • MEN1: multiple endocrine neoplasia I
  • Cell division site part
    • MEN1: multiple endocrine neoplasia I
  • Cell fraction
  • Cell leading edge
    • ALS2: amyotrophic lateral sclerosis 2 (juvenile)
    • FGD1: FYVE, RhoGEF and PH domain containing 1
    • TSC1: tuberous sclerosis 1
  • Cell projection
  • Cell projection part
    • GNAT2: guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
    • PKD2: polycystic kidney disease 2 (autosomal dominant)
    • PKHD1: polycystic kidney and hepatic disease 1 (autosomal recessive)
    • SOD1: superoxide dismutase 1, soluble
  • Cell soma
  • Cell surface
  • Endomembrane system
  • Intracellular
  • Intracellular part
  • Membrane
  • Membrane part
  • Perikaryon
    • TH: tyrosine hydroxylase
  • Photoreceptor inner segment
    • GNAT2: guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
    • MYO7A: myosin VIIA
  • Site of polarized growth
    • ANG: angiogenin, ribonuclease, RNase A family, 5
    • SNCA: synuclein, alpha (non A4 component of amyloid precursor)

Source: Gene Ontology ConsortiumThis link leads to a site outside Genetics Home Reference. (June 2009).

 
Published: November 20, 2009