Organelle: Difference between revisions
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| Rough endoplasmic reticulum || || || || || || || || || | | Rough endoplasmic reticulum || || || || || || || || || | ||
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| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome || | | Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome<ref>{{cite journal|last1=Bexiga|first1=Mariana G.|last2=Simpson|first2=Jeremy C.|title=Human Diseases Associated with Form and Function of the Golgi Complex|doi=10.3390/ijms140918670|url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/|accessdate=25 November 2017|pmc=3794802}}</ref> || | ||
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| Smooth endoplasmic reticulum || || || || || || || || || | | Smooth endoplasmic reticulum || || || || || || || || || | ||
Revision as of 20:10, 25 November 2017
| Organelle | Plant/Animal or both | Location in the cell | Units per cell | Size | Membrane | Components | Function | Associated illness | Year of discovery |
|---|---|---|---|---|---|---|---|---|---|
| Nucleus | |||||||||
| Ribosomes | |||||||||
| Rough endoplasmic reticulum | |||||||||
| Golgi aparatus | Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[1] | ||||||||
| Smooth endoplasmic reticulum | |||||||||
| Lysosomes | |||||||||
| Peroxisomes | |||||||||
| Vacuoles | |||||||||
| Mitochondria | |||||||||
| Chloroplasts | |||||||||
| Cytoskeleton | |||||||||
| Plasma membrane | |||||||||
| Cell wall |
Source pages
For organelle associated diseases [1]
- ↑ <templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>Bexiga, Mariana G.; Simpson, Jeremy C. "Human Diseases Associated with Form and Function of the Golgi Complex". doi:10.3390/ijms140918670. PMC 3794802. Retrieved 25 November 2017.
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