atransferrinemia Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050649)
Similar Terms
Downloads & Tools

Genes

18 genes co-occuring with the disease atransferrinemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TF transferrin 1.39389
HEPH hephaestin 1.36161
TFR2 transferrin receptor 2 1.30226
HFE2 hemochromatosis type 2 (juvenile) 1.09251
HAMP hepcidin antimicrobial peptide 0.9238
PANK2 pantothenate kinase 2 0.825768
HFE hemochromatosis 0.820847
ALAS2 5'-aminolevulinate synthase 2 0.811411
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1 0.781888
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like 0.772479
SLC11A2 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2 0.728547
FTL ferritin, light polypeptide 0.582773
FTH1 ferritin, heavy polypeptide 1 0.582384
TFRC transferrin receptor 0.575383
FXN frataxin 0.471468
CP ceruloplasmin (ferroxidase) 0.223853
HP haptoglobin 0.214297
HPR haptoglobin-related protein 0.208914