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Intracellular part

Intracellular part

  • AMP-activated protein kinase complex
    • PRKAG2: protein kinase, AMP-activated, gamma 2 non-catalytic subunit
  • BRCA2-MAGE-D1 complex
    • BRCA2: breast cancer 2, early onset
  • Cytoplasm
  • Cytoplasmic part
  • Inclusion body
  • Intracellular ferritin complex
    • FTL: ferritin, light polypeptide
  • Intracellular organelle
  • Intracellular organelle part
  • Methyltransferase complex
    • MEN1: multiple endocrine neoplasia I
  • Mismatch repair complex
    • MSH2: mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)
    • MSH6: mutS homolog 6 (E. coli)
    • WRN: Werner syndrome, RecQ helicase-like
  • NADH dehydrogenase complex
    • MT-ND1: mitochondrially encoded NADH dehydrogenase 1
    • MT-ND4: mitochondrially encoded NADH dehydrogenase 4
    • MT-ND4L: mitochondrially encoded NADH dehydrogenase 4L
    • MT-ND5: mitochondrially encoded NADH dehydrogenase 5
    • MT-ND6: mitochondrially encoded NADH dehydrogenase 6
  • Nucleoid
    • ACADVL: acyl-coenzyme A dehydrogenase, very long chain
    • CPS1: carbamoyl-phosphate synthetase 1, mitochondrial
    • DBT: dihydrolipoamide branched chain transacylase E2
    • HADHA: hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A thiolase/enoyl-Coenzyme A hydratase (trifunctional protein), alpha subunit
    • HADHB: hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A thiolase/enoyl-Coenzyme A hydratase (trifunctional protein), beta subunit
  • Organelle inner membrane
  • Organelle outer membrane
    • DHCR7: 7-dehydrocholesterol reductase
    • MFN2: mitofusin 2
    • OPA1: optic atrophy 1 (autosomal dominant)
    • PSEN1: presenilin 1
    • RAF1: v-raf-1 murine leukemia viral oncogene homolog 1
  • Proton-transporting ATP synthase complex
    • MT-ATP6: mitochondrially encoded ATP synthase 6
  • Proton-transporting ATP synthase complex, coupling factor F(o)
    • MT-ATP6: mitochondrially encoded ATP synthase 6
  • Ribonucleoprotein complex
  • Stereocilium
    • CDH23: cadherin-like 23
    • DFNB31: deafness, autosomal recessive 31
    • PCDH15: protocadherin 15
    • USH1C: Usher syndrome 1C (autosomal recessive, severe)
  • Ubiquitin ligase complex
    • BARD1: BRCA1 associated RING domain 1
    • BRCA1: breast cancer 1, early onset
    • CUL7: cullin 7

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

 
Published: November 20, 2009