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Multicellular organismal process

Multicellular organismal process

  • Coagulation
  • Cytokine production
  • Digestion
    • LDLR: low density lipoprotein receptor (familial hypercholesterolemia)
  • Molting cycle
    • ATP7A: ATPase, Cu++ transporting, alpha polypeptide (Menkes syndrome)
  • Multicellular organismal development
  • Multicellular organismal homeostasis
    • BARD1: BRCA1 associated RING domain 1
    • DFNB31: deafness, autosomal recessive 31
    • NF1: neurofibromin 1 (neurofibromatosis, von Recklinghausen disease, Watson disease)
    • SOD1: superoxide dismutase 1, soluble (amyotrophic lateral sclerosis 1 (adult))
  • Multicellular organismal response to stress
    • GCH1: GTP cyclohydrolase 1 (dopa-responsive dystonia)
  • Multicellular organism growth
    • PTCH1: patched homolog 1 (Drosophila)
    • SOD1: superoxide dismutase 1, soluble (amyotrophic lateral sclerosis 1 (adult))
  • Multicellular organism reproduction
    • ANG: angiogenin, ribonuclease, RNase A family, 5
    • EIF2B2: eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
    • EIF2B4: eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
    • EIF2B5: eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
    • FOXL2: forkhead box L2
    • SOD1: superoxide dismutase 1, soluble (amyotrophic lateral sclerosis 1 (adult))
  • Negative regulation of multicellular organismal process
    • APOE: apolipoprotein E
    • BMPR2: bone morphogenetic protein receptor, type II (serine/threonine kinase)
    • F2: coagulation factor II (thrombin)
    • FOXP3: forkhead box P3
    • PTCH1: patched homolog 1 (Drosophila)
    • SOD1: superoxide dismutase 1, soluble (amyotrophic lateral sclerosis 1 (adult))
  • Positive regulation of multicellular organismal process
  • Regulation of body fluid levels
  • Regulation of multicellular organismal process
  • Reproductive process in a multicellular organism
    • ANG: angiogenin, ribonuclease, RNase A family, 5
    • EIF2B2: eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
    • EIF2B4: eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
    • EIF2B5: eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
    • FOXL2: forkhead box L2
    • SOD1: superoxide dismutase 1, soluble (amyotrophic lateral sclerosis 1 (adult))
  • Respiratory gaseous exchange
    • CFTR: cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
    • ELN: elastin (supravalvular aortic stenosis, Williams-Beuren syndrome)
  • System process
  • Tissue remodeling
    • ACVR1: activin A receptor, type I
    • ATP7A: ATPase, Cu++ transporting, alpha polypeptide (Menkes syndrome)
    • BMPR2: bone morphogenetic protein receptor, type II (serine/threonine kinase)
    • NF1: neurofibromin 1 (neurofibromatosis, von Recklinghausen disease, Watson disease)
    • TGFB1: transforming growth factor, beta 1
  • Visual behavior
    • NF1: neurofibromin 1 (neurofibromatosis, von Recklinghausen disease, Watson disease)

Source: Gene Ontology ConsortiumThis link leads to a site outside Genetics Home Reference. (September 2008).

 
Published: January 30, 2009