FTL
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn FTL yw FTL a elwir hefyd yn Ferritin light chain (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn blaen o gromosom dynol 19, band 19q13.33.[2]
FTL | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | FTL, LFTD, NBIA3, ferritin, light polypeptide, ferritin light chain | ||||||||||||||||
Dynodwyr allanol | OMIM: 134790 HomoloGene: 79330 GeneCards: FTL | ||||||||||||||||
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Species | Bod dynol | Llygoden | |||||||||||||||
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RefSeq (mRNA) |
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RefSeq (protein) |
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Lleoliad (UCSC) | n/a | n/a | |||||||||||||||
PubMed search | [1] | n/a | |||||||||||||||
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Cyfystyron
golyguYn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn FTL.
- LFTD
- NBIA3
Llyfryddiaeth
golygu- "Impact of non-transferrin-bound iron (NTBI) in comparison to serum ferritin on outcome after allogeneic stem cell transplantation (ASCT). ". Ann Hematol. 2017. PMID 28585071.
- "Hepatitis E virus ORF1 encoded macro domain protein interacts with light chain subunit of human ferritin and inhibits its secretion. ". Mol Cell Biochem. 2016. PMID 27170377.
- "Ferritin light chain gene mutation in a large Australian family with hereditary hyperferritinemia-cataract syndrome. ". Ophthalmic Genet. 2017. PMID 27096259.
- "Relationships between typical histopathological hallmarks and the ferritin in the hippocampus from patients with Alzheimer's disease. ". Acta Neurobiol Exp (Wars). 2015. PMID 26994418.
- "Expression of Ferritin Light Chain (FTL) Is Elevated in Glioblastoma, and FTL Silencing Inhibits Glioblastoma Cell Proliferation via the GADD45/JNK Pathway.". PLoS One. 2016. PMID 26871431.