
FTL Gene - GeneCards | FRIL Protein | FRIL Antibody
2024年12月25日 · FTL (Ferritin Light Chain) is a Protein Coding gene. Diseases associated with FTL include Hyperferritinemia With Or Without Cataract and Neurodegeneration With Brain …
Ferritin light chain - Wikipedia
Ferritin light chain is a protein that in humans is encoded by the FTL gene. [4] [5] [6] Ferritin is the major protein responsible for storing intracellular iron in prokaryotes and eukaryotes. It is a …
L-Ferritin: One Gene, Five Diseases; from Hereditary …
A variety of mutations have been reported in the L-ferritin subunit gene (FTL gene) that cause the following five diseases: (1) hereditary hyperferritinemia with cataract syndrome (HHCS), (2) …
FTL ferritin light chain [Homo sapiens (human)] - Gene - NCBI
2025年2月9日 · This gene encodes the light subunit of the ferritin protein. Ferritin is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits …
FTL gene: MedlinePlus Genetics
2012年8月1日 · The FTL gene provides instructions for making the ferritin light chain, which is one part (subunit) of a protein called ferritin. Learn about this gene and related health conditions.
FTL - ferritin light chain Gene - MCE-生物活性分子大师
This gene encodes the light subunit of the ferritin protein. Ferritin is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and …
FTL ferritin light chain - NIH Genetic Testing Registry (GTR) - NCBI
2013年8月22日 · Clinical resource with information about FTL, Hereditary hyperferritinemia with congenital cataracts, L-ferritin deficiency, Neuroferritinopathy, and available tests. There are …
2512 - Gene ResultFTL ferritin light chain [ (human)]
FTL is a marker gene useful for stratifying osteosarcoma patients into low- and high-risk groups and predicting therapy outcome. We have detected a significant inverse correlation of -0.565 …
Hyperferritinemia-cataract syndrome - MedlinePlus
2012年8月1日 · Hyperferritinemia-cataract syndrome is caused by mutations in the FTL gene. This gene provides instructions for making the ferritin light chain, which is one part (subunit) of …
FTL人源基因|FTL基因突变_致病性_靶点-RDDC官网
铁蛋白是原核生物和真核生物中主要的细胞内铁储存蛋白。 它由24个重链和轻链铁蛋白亚基组成。 铁蛋白亚基组成的变化可能会影响不同组织中铁的摄取和释放速度。 铁蛋白的主要功能是将 …