UNIPROT:P02794 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P02794 (ferritin)
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Human Gene/Protein
CAG-isl 7	10.8
Ferritin light polypeptide	10.8
tryptase-I	10.8
keratinocyte associated protein 2	10.8
ferritin	10.8
Glyceronephosphate O-acyltransferase	10.8
ubiquitin-conjugating enzyme E2D 3	10.8
collagen alpha 1(I) chain precursor	10.8
NADH-ubiquinone oxidoreductase B22 subunit	10.8
ferritin L-chain	10.5
Ferritin	10.5
ferritin light polypeptide	10.1
nuclear receptor coactivator 4	10.1
ferritin repressor protein	10.0
mitochondrial ferritin	9.9
NCOA4 protein	9.8
DCYTB	9.8
truncated coagulation factor VIII	9.8
GLYCOLATE OXIDASE 1	9.8
HUMPPA	9.8
NAALAD2	9.8
ferritin light chain	9.6
ferritin heavy chain	9.6
FTH	9.5
ferroxidase	9.5
IRP protein	9.5
IRP1	9.4
IRP2	9.3
transmembrane protease, serine 6	9.2
dihydrodiol dehydrogenase 3	9.2
Apo M	9.2
ferroportin 1	9.2
iron regulatory protein 1	9.2
ferritin-like protein	9.1
TfR	9.0
ferroportin1	9.0
FTH1	9.0
SLC40A1	8.9
human ribosomal protein L38	8.8
heterogeneous nuclear ribonucleoprotein H2	8.8

Disease
Autoimmune leukopenia	10.8
Anemias due to chronic disorders	10.8
Secondary hemosiderosis	10.8
HFE4	10.4
Cardiac siderosis	10.2
Hepatic hemosiderosis	10.1
Hepatic siderosis	10.0
Other nutritional deficiencies	9.8
Bantu siderosis	9.8
Iron deficiency without anemia	9.5
Congenital atransferrinemia	9.2
Hypoproliferative anemia	9.2
Klauder	9.2
iron overload	9.0
iron deficiency	8.9
Anemia of chronic renal failure	8.8
Acquired sideroblastic anemia	8.8
Renal hemosiderosis	8.8
Trichophagia	8.8
acquired hemochromatosis	8.8
anemia of chronic disease	8.8
disorders of iron metabolism	8.6
hereditary hemochromatosis	8.5
sideroblastosis	8.5
Epstein-Barr viremia	8.5
hemochromatosis	8.5
iron deficiency anemia	8.5
Sports anemia	8.4
Adult-onset Still's disease	8.3
HFE2	8.3
siderosis	8.3
Macrophage activation syndrome	8.3
anaemia in pregnancy	8.2
Anemia during pregnancy	8.1
Still's disease	8.1
POF3	8.0
Gastrointestinal amyloidosis	8.0
Familial porphyria cutanea tarda	8.0
Uroporphyria	8.0
thalassemia major	8.0

Symptom
Gastrointestinal distress	7.2
Paroxysmal hypertension	7.1
toe pain	6.4
unable to sleep	6.3
Poor weight gain	6.2
Bitot's spots	5.8
hepatosplenomegaly	5.7
Postural tremor	5.7
male puberty	5.4
Reticulocytosis	5.2
cardiovascular impairment	5.1
Flu-like symptoms	5.0
Gasping	4.9
brittle nails	4.8
fever of unknown origin	4.8
Grimace	4.8
pedal edema	4.7
generalized rash	4.7
menometrorrhagia	4.5
sore throat	4.5
lumbar back pain	4.4
splenomegaly	4.3
impaired motor coordination	4.2
arthralgia	4.2
phosphatemia	4.1
generalized erythema	3.9
hepatomegaly	3.9
hypoproteinemia	3.7
chromosome marker	3.7
leg cramps	3.6
pallor	3.6
No adverse effect	3.5
meningism	3.4
night sweats	3.4
rales	3.1
Spots	3.0
disturbed balance	3.0
aphonia	2.9
myalgia	2.8
periorbital edema	2.8

Enzyme
IDS3	8.8
proprotein convertase 7	8.5
ceruloplasmin	7.6
trimetaphosphatase	7.4
nicotianamine synthase	7.3
CEAS	6.7
aconitase	6.7
ALA synthase	6.0
heme oxygenase	5.9
methylmalonate-semialdehyde dehydrogenase	5.9
biliverdin reductase	5.9
ferric chelate reductase	5.7
destabilase	5.5
caffeoyl-CoA O-methyltransferase	5.4
uroporphyrinogen decarboxylase	5.4
arginine kinase	5.4
NAAT	5.4
nicotinamide N-methyltransferase	5.3
6-pyruvoyltetrahydropterin synthase	5.3
aureolysin	5.2
DMT	5.2
dihydroneopterin aldolase	5.2
pantothenate kinase	5.2
lactic acid dehydrogenase	5.2
ferrochelatase	5.2
lactic acid dehydrogenase	5.1
serum carnosinase	5.0
porphobilinogenase	5.0
cathepsin F	4.8
deoxyhypusine hydroxylase	4.8
10-formyltetrahydrofolate dehydrogenase	4.7
glutathione-insulin transhydrogenase	4.7
carboxyl proteinase	4.6
threonine synthase	4.6
lactic acid dehydrogenase	4.6
isoflavone reductase	4.5
ribonucleotide reductase	4.5
ribonucleotide reductase	4.4
6-phosphogluconolactonase	4.4
chondroitin ABC lyase	4.3