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FTL (ferritin light chain)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2512
Gene nameGene Name - the full gene name approved by the HGNC.
Ferritin light chain
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
FTL
SynonymsGene synonyms aliases
FTL1, LFTD, NBIA3
ChromosomeChromosome number
19
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.33
SummarySummary of gene provided in NCBI Entrez Gene.
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 light ferritin chains. Variation in ferritin subunit compos
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs2230267 T>C Benign, likely-pathogenic Synonymous variant, coding sequence variant
rs104894685 G>A Pathogenic Coding sequence variant, missense variant
rs139732572 A>G Pathogenic Initiator codon variant, missense variant, coding sequence variant
rs199869995 G>C,T Pathogenic Missense variant, coding sequence variant, stop gained
rs201241191 G>A Likely-benign, likely-pathogenic, uncertain-significance Missense variant, coding sequence variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT021706 hsa-miR-133a-3p Microarray 21396852
MIRT031525 hsa-miR-16-5p Proteomics 18668040
MIRT021706 hsa-miR-133a-3p Immunocytochemistry, Western blot 23969999
MIRT021706 hsa-miR-133a-3p Immunocytochemistry, Western blot 23969999
MIRT1005659 hsa-miR-1258 CLIP-seq
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005506 Function Iron ion binding IDA 19923220, 20159981
GO:0005515 Function Protein binding IPI 16169070, 16189514, 17143515, 18486613, 21516116, 23275563, 23685131, 25416956, 25910212, 28514442, 31515488, 32296183, 32814053
GO:0005576 Component Extracellular region TAS
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005829 Component Cytosol TAS
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P02792
Protein name Ferritin light chain (Ferritin L subunit)
Protein function Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation. Also plays a role in delivery of iron to cells. Mediates iron u
PDB 2FFX , 2FG4 , 2FG8 , 3KXU , 4V6B , 5LG8 , 6TR9 , 6TS0 , 6TS1 , 6TSA , 6TSF , 6TSJ , 6WX6
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00210 Ferritin
14 155
Ferritin-like domain
Domain
Sequence
Sequence length 175
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Porphyrin metabolism
Ferroptosis
Necroptosis
Mineral absorption
  Golgi Associated Vesicle Biogenesis
Neutrophil degranulation
Iron uptake and transport
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Arthritis Degenerative polyarthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 18784066
Cataract Cataract, Embryonal nuclear cataract (disorder), Nuclear cataract, Nuclear non-senile cataract rs118203965, rs118203966, rs104893685, rs121908938, rs104894175, rs121909048, rs28937573, rs121909049, rs121909050, rs74315488, rs80358200, rs80358203, rs121434643, rs56141211, rs132630322, rs121917775, rs121917735, rs121917736, rs137853199, rs137853200, rs121917867, rs121917869, rs121913555, rs104893736, rs121909595, rs121909596, rs121909597, rs28931605, rs121909598, rs104893618, rs1695062782, rs74315486, rs74315487, rs74315490, rs74315489, rs745938679, rs1566402656, rs74315439, rs74315441, rs121912973, rs121917823, rs1593332981, rs121917825, rs121917827, rs113994108, rs387906963, rs387906964, rs1240503246, rs387906965, rs387906966, rs750207077, rs387907336, rs387907337, rs387907342, rs140332366, rs397514703, rs398122937, rs398122378, rs398122392, rs398122944, rs137853924, rs398122947, rs397515623, rs397515624, rs397515625, rs397515626, rs398122948, rs587778872, rs398123066, rs587777601, rs370424081, rs786205221, rs786205222, rs864309684, rs864309688, rs864309701, rs864309689, rs864309690, rs864309681, rs864309686, rs864309696, rs864309693, rs864309687, rs864309691, rs864309692, rs864309695, rs864309678, rs864309685, rs864309700, rs864309698, rs864309683, rs864309682, rs864309679, rs111534978, rs864309680, rs864309702, rs864622780, rs756898971, rs869312732, rs775038545, rs878852983, rs1114167312, rs1114167313, rs1114167314, rs1114167315, rs1114167307, rs886041410, rs886041412, rs1057518738, rs1057517926, rs1057518878, rs1057519616, rs12799308, rs1064793935, rs1064797219, rs1085307126, rs1085307127, rs765628635, rs1114167427, rs1114167433, rs1554744860, rs1554743428, rs747093432, rs1411557416, rs1555179713, rs1481963503, rs1555549755, rs1456161420, rs1555547008, rs1555889308, rs1555888762, rs766522434, rs1264025914, rs1553585262, rs1567671947, rs1337897299, rs764945940, rs1307969607, rs949335475, rs1184095219, rs776129797, rs1569203234, rs1567668570, rs749141857, rs764098604, rs1184398243, rs1578956689, rs1568480054, rs1564745688, rs1564722302, rs1564723150, rs1571175950, rs1569602837, rs1576552712, rs1575369255, rs981126461, rs1570403798, rs200557771, rs1477743112, rs1651879427, rs1651881222, rs1651919374, rs2024441691, rs148284531, rs1246080692
Developmental regression Developmental regression rs1224421127
Hereditary hyperferritinemia with congenital cataracts Hereditary hyperferritinemia-cataract syndrome, Hyperferritinemia, hereditary, with congenital cataracts rs398124633, rs398124634, rs398124635, rs1555796939, rs398124636, rs398124637, rs398124638, rs398124639, rs397514540 10759702, 9226182, 10383191, 11849230, 2336358, 19176363, 7493028, 9414313, 22881709, 19800271, 23421845
Unknown
Disease name Disease term dbSNP ID References
Alopecia Alopecia
Anarthria speech disorder Anarthria speech disorder
Blepharospasm Blepharospasm
Cavitation of the basal ganglia Cavitation of the basal ganglia

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