Cell part

Cell part

• Apical part of cell
  • CLCN5: chloride channel, voltage-sensitive 5
  • HFE: hemochromatosis
  • USH1C: Usher syndrome 1C (autosomal recessive, severe)
  • Apical plasma membrane
• Basal part of cell
  • HFE: hemochromatosis
  • Basal cortex
    • PKD2: polycystic kidney disease 2 (autosomal dominant)
  • Basal plasma membrane
    • LDLRAP1: low density lipoprotein receptor adaptor protein 1
    • PKD2: polycystic kidney disease 2 (autosomal dominant)
    • TEK: TEK tyrosine kinase, endothelial
• Cell body
  • Neuronal cell body
• Cell division site
• Cell division site part
  • Actomyosin contractile ring
    • MYH9: myosin, heavy chain 9, non-muscle
  • Cleavage furrow
    • MEN1: multiple endocrine neoplasia I
    • MYH9: myosin, heavy chain 9, non-muscle
• Cell leading edge
  • ITGB4: integrin, beta 4
  • MYH9: myosin, heavy chain 9, non-muscle
  • PAFAH1B1: platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
  • Lamellipodium
  • Leading edge membrane
    • APC: adenomatous polyposis coli
    • CDKL5: cyclin-dependent kinase-like 5
    • TRPV4: transient receptor potential cation channel, subfamily V, member 4
  • Ruffle
• Cell periphery
  • CTNNB1: catenin (cadherin-associated protein), beta 1, 88kDa
  • Cell cortex
  • Plasma membrane
• Cell projection
• Cell projection part
• Cell surface
• Coated pit
  • LDLR: low density lipoprotein receptor
  • Clathrin coat of coated pit
    • LDLRAP1: low density lipoprotein receptor adaptor protein 1
• Compact myelin
  • Schmidt-Lanterman incisure
    • PTEN: phosphatase and tensin homolog
• Contractile ring
  • Actomyosin contractile ring
    • MYH9: myosin, heavy chain 9, non-muscle
• Endomembrane system
  • Coated pit
    • LDLR: low density lipoprotein receptor
    • LDLRAP1: low density lipoprotein receptor adaptor protein 1
  • Golgi membrane
  • Nuclear envelope
  • Vesicle membrane
• Envelope
  • Organelle envelope
• Intracellular
• Intracellular part
• Midbody
• Myelin sheath
• Myelin sheath adaxonal region
  • PTEN: phosphatase and tensin homolog
• Neuron part
  • NBAF complex
    • ARID1A: AT rich interactive domain 1A (SWI-like)
    • SMARCA4: SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
    • SMARCB1: SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
    • SMARCE1: SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1
  • Neurofilament cytoskeleton
    • GAN: gigaxonin
    • LDLRAP1: low density lipoprotein receptor adaptor protein 1
    • NEFH: neurofilament, heavy polypeptide
    • NEFL: neurofilament, light polypeptide
  • Neuronal cell body
  • Neuron projection
  • Presynaptic membrane
    • SNCAIP: synuclein, alpha interacting protein
• Nuclear outer membrane-endoplasmic reticulum membrane network
  • Endoplasmic reticulum membrane
  • Nuclear outer membrane
    • DHCR7: 7-dehydrocholesterol reductase
    • EMD: emerin
    • GHRHR: growth hormone releasing hormone receptor
    • GUCY2D: guanylate cyclase 2D, membrane (retina-specific)
    • PSEN1: presenilin 1
• Perikaryon
  • TH: tyrosine hydroxylase
• Photoreceptor inner segment
  • ARMS2: age-related maculopathy susceptibility 2
  • GNAT2: guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
  • MYO7A: myosin VIIA
  • RHO: rhodopsin
  • Photoreceptor inner segment membrane
    • RHO: rhodopsin
• Photoreceptor inner segment membrane
  • RHO: rhodopsin
• Plasma membrane
• Plasma membrane part
• Protein serine/threonine phosphatase complex
  • PTW/PP1 phosphatase complex
    • PPP1R12A: protein phosphatase 1, regulatory subunit 12A
• Schmidt-Lanterman incisure
  • PTEN: phosphatase and tensin homolog
• Site of polarized growth
  • Growth cone
• Sperm part
  • Sperm flagellum
    • RPGR: retinitis pigmentosa GTPase regulator
• Stereocilia ankle link complex
  • USH2A: Usher syndrome 2A (autosomal recessive, mild)
• Stereocilia coupling link
  • Stereocilia ankle link
    • USH2A: Usher syndrome 2A (autosomal recessive, mild)
• Trailing edge
  • Uropod
    • MYH9: myosin, heavy chain 9, non-muscle
• Vesicle membrane
  • Cytoplasmic vesicle membrane

Source: Gene Ontology Consortium.