Cell part

Cell part

• Apical part of cell
  • USH1C: Usher syndrome 1C (autosomal recessive, severe)
  • Apical plasma membrane
    • CFTR: cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
    • PKHD1: polycystic kidney and hepatic disease 1 (autosomal recessive)
• Basal part of cell
  • Basal plasma membrane
    • LDLRAP1: low density lipoprotein receptor adaptor protein 1
• Cell division site
  • Cell division site part
    • MEN1: multiple endocrine neoplasia I
• Cell division site part
  • Cleavage furrow
    • MEN1: multiple endocrine neoplasia I
• Cell fraction
  • Insoluble fraction
  • Soluble fraction
• Cell projection
• Cell projection part
  • Basal body
    • PKD2: polycystic kidney disease 2 (autosomal dominant)
    • PKHD1: polycystic kidney and hepatic disease 1 (autosomal recessive)
  • Cell projection cytoplasm
    • SOD1: superoxide dismutase 1, soluble (amyotrophic lateral sclerosis 1 (adult))
• Cell soma
  • ANG: angiogenin, ribonuclease, RNase A family, 5
  • APOE: apolipoprotein E
  • ATP7A: ATPase, Cu++ transporting, alpha polypeptide (Menkes syndrome)
  • SNCAIP: synuclein, alpha interacting protein (synphilin)
  • SOD1: superoxide dismutase 1, soluble (amyotrophic lateral sclerosis 1 (adult))
• Cell surface
• Endomembrane system
  • Golgi membrane
    • ARFGEF2: ADP-ribosylation factor guanine nucleotide-exchange factor 2 (brefeldin A-inhibited)
    • GJB2: gap junction protein, beta 2, 26kDa
    • LDLRAP1: low density lipoprotein receptor adaptor protein 1
  • Nuclear envelope
    • DHCR7: 7-dehydrocholesterol reductase
    • MYO6: myosin VI
    • NPC1: Niemann-Pick disease, type C1
    • PSEN1: presenilin 1
    • PSEN2: presenilin 2 (Alzheimer disease 4)
  • Nuclear envelope-endoplasmic reticulum network
  • Vesicle membrane
    • APOB: apolipoprotein B (including Ag(x) antigen)
    • KIF1B: kinesin family member 1B
    • LDLR: low density lipoprotein receptor (familial hypercholesterolemia)
    • LDLRAP1: low density lipoprotein receptor adaptor protein 1
• Intracellular
  • MKKS: McKusick-Kaufman syndrome
  • TNXB: tenascin XB
  • VPS13A: vacuolar protein sorting 13 homolog A (S. cerevisiae)
• Intracellular part
• Leading edge
  • Lamellipodium
    • ALS2: amyotrophic lateral sclerosis 2 (juvenile)
    • FGD1: FYVE, RhoGEF and PH domain containing 1
    • TSC1: tuberous sclerosis 1
  • Ruffle
    • ALS2: amyotrophic lateral sclerosis 2 (juvenile)
    • FGD1: FYVE, RhoGEF and PH domain containing 1
    • MYO6: myosin VI
• Membrane
• Membrane part
• Photoreceptor inner segment
  • MYO7A: myosin VIIA
• Site of polarized growth
  • Growth cone
    • ANG: angiogenin, ribonuclease, RNase A family, 5

Source: Gene Ontology Consortium (September 2008).